A pathology report is a document that contains the diagnosis determined by examining cells and tissues under a microscope. Pathology reports play an important role in cancer diagnosis and staging. A pathologist is a doctor who does this examination and writes the pathology report. Keep reading to understand pathology reports.
Microtome
Image by National Cancer Institute / Leidos Biomedical Research, Inc.
What Is a Pathology Report?
Major topics of pathology informatics
Image by Mikael Häggström, M.D. Author info - Reusing images- Conflicts of interest: NoneMikael Häggström, M.D. et al.1, 2, 31. The work is using source images by Lourenço BC, Guimarães-Teixeira C, Flores BCT, Miranda-Gonçalves V, Guimarães R, Cantante M, Cruz-Roa A, Gilmore H, Basavanhally A, Feldman M, Ganesan S, Shih NNC, Jerome Walker and Public Domain Vectors2. The work is using some AI-generated images3. See Source section for details./Wikimedia
Major topics of pathology informatics
Major topics and processes of pathology informatics: Data management from molecular testing, slide scanning, digital imaging and image analysis, networks, databases and telepathology. See also: Digital pathology.
Image by Mikael Häggström, M.D. Author info - Reusing images- Conflicts of interest: NoneMikael Häggström, M.D. et al.1, 2, 31. The work is using source images by Lourenço BC, Guimarães-Teixeira C, Flores BCT, Miranda-Gonçalves V, Guimarães R, Cantante M, Cruz-Roa A, Gilmore H, Basavanhally A, Feldman M, Ganesan S, Shih NNC, Jerome Walker and Public Domain Vectors2. The work is using some AI-generated images3. See Source section for details./Wikimedia
What Is a Pathology Report?
A pathology report is a document that contains the diagnosis determined by examining cells and tissues under a microscope. The report may also contain information about the size, shape, and appearance of a specimen as it looks to the naked eye. This information is known as the gross description.
A pathologist is a doctor who does this examination and writes the pathology report. Pathology reports play an important role in cancer diagnosis and staging (describing the extent of cancer within the body, especially whether it has spread), which helps determine treatment options.
Source: National Cancer Institute (NCI)
Additional Materials (22)
Histopathology of apocrine metaplasia of breast, annotated
Histopathology of apocrine metaplasia of breast with typical features, H&E stain
Image by Mikael Häggström, M.D. Author info - Reusing images- Conflicts of interest: NoneMikael Häggström, M.D.Consent note: Consent from the patient or patient's relatives is regarded as redundant, because of absence of identifiable features (List of HIPAA identifiers) in the media and case information (See also HIPAA case reports guidance)./Wikimedia
Mammary gland: Carcinoma (anterior view)
Diagnostic original : Épithélioma (avec «peau d'orange»). Diagnostic actualisé : Carcinome canalaire infiltrant. Histoire : Femme de 40 ans avec infiltration néoplasique des deux seins avec extension au thorax. Décédée d'un cancer disséminé avec multiples métastases hépatiques et pulmonaires avec hydrothorax bilatéral et ascite. Description macroscopie : La peau de la région mammaire gauche est infiltrée de multiples nodules néoplasiques ulcérés et suintants. Le sein droit est également envahi, dur. L'envahissement s'étend pratiquement à toute la région thoracique antérieure. Le sein droit présent l'aspect dit en "peau d'orange". Année du prélèvement : 1951.
Image by
Denis Desaulniers et Bernard Têtu/Wikimedia
Optomap-pathology
תמונת רשתית ( Optomap) בה רואים דוגמאות למחלות עיניים הניתנות לגילוי בצילום רשתית אופטוס.
Image by Zg2891/Wikimedia
Atypical ductal hyperplasia
Atypical ductal hyperplasia : Very low magnification micrograph of atypical ductal hyperplasia, abbreviated ADH. Breast core biopsy. H&E stain.The green and blue (seen at low magnification) are marks from a pathologist and a pathology resident.
Image by Nephron
Breast tissue showing fat necrosis 4X
Breast lump showing an area of fat necrosis showing shadowy outlines of necrotic adipocytes surrounded by an inflammatory reaction with cholesterol clefts [H&E stain 4X]
Image by Department of Pathology, Calicut Medical College/Wikimedia
(UNESP-FMB DEO 20180927-05) Breast adenocarcinoma, human
Breast adenocarcinoma, human
Image by Deilson Elgui de Oliveira/Wikimedia
Invasive lobular carcinoma
Invasive lobular carcinoma of the mammary gland with a moderate degree of differentiation. Occurs in the lobules of the mammary gland. The cells are monomorphic and lack cohesion, with round or oval nuclei and a thin rim of cytoplasm. The cytoplasmic lumen may contain central mucin, which is colorless according to this type of staining of histological sections. Tumor cells are often arranged concentrically around normal ducts of the gland. Collagen fibres are colored blue, tumor cells are colored red. Malory coloring. Magnification 400x. Photomicrograph taken at the R.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, National Academy of Sciences of Ukraine (Kyiv, Ukraine); a Carl Zeiss Axio Imager A2 microscope with an Axiocam 712 color camera was used.
Image by Endolysosome/Wikimedia
How Are These Biomarkers Measured?
The role of biomarkers is to increase the certainty of diagnosis at a time when treatments might be most effective. Measures of structural and functional change may be more useful in predicting progression to Alzheimer’s dementia than measures that indicate an Alzheimer’s pathology is present. It should be said that considerable work still needs to be accomplished to decide what will be the most effective ways for biomarkers to be used by your doctor or healthcare professional.
Image by TheVisualMD
How to Read a Pathology Report
Video by RPCICancerTalk/YouTube
How to Understand Your Pathology Report
Video by Dr. Susan Love Foundation/YouTube
Understanding Your Pathology Report: A Patient’s Story
Video by capathologists/YouTube
Pathology Insights: Basics of Thymic Pathology with Sanjay Mukhopadhyay, MD
Oral Pathology | Salivary Gland Benign Diseases | NBDE Part II
Video by Mental Dental/YouTube
Testicular germ cell tumours - Seminoma - Pathology mini tutorial
Video by Pathology mini tutorials/YouTube
Ottitis Media Pathology
Video by Dr. Rishi Mantri/YouTube
Understanding Pathology for Breast Cancer
Video by Swedish/YouTube
Breast Cancer Pathology Reports: What You Need to Know
Video by Breast Cancer School for Patients/YouTube
How to Understand Your Breast Cancer Pathology Report
Video by Yerbba – Breast Cancer/YouTube
What's in your prostate cancer pathology report? - Dr. David Berman
Video by ProstateCancerBC/YouTube
Histopathology of apocrine metaplasia of breast, annotated
Mikael Häggström, M.D. Author info - Reusing images- Conflicts of interest: NoneMikael Häggström, M.D.Consent note: Consent from the patient or patient's relatives is regarded as redundant, because of absence of identifiable features (List of HIPAA identifiers) in the media and case information (See also HIPAA case reports guidance)./Wikimedia
Mammary gland: Carcinoma (anterior view)
Denis Desaulniers et Bernard Têtu/Wikimedia
Optomap-pathology
Zg2891/Wikimedia
Atypical ductal hyperplasia
Nephron
Breast tissue showing fat necrosis 4X
Department of Pathology, Calicut Medical College/Wikimedia
(UNESP-FMB DEO 20180927-05) Breast adenocarcinoma, human
Deilson Elgui de Oliveira/Wikimedia
Invasive lobular carcinoma
Endolysosome/Wikimedia
How Are These Biomarkers Measured?
TheVisualMD
4:57
How to Read a Pathology Report
RPCICancerTalk/YouTube
2:42
How to Understand Your Pathology Report
Dr. Susan Love Foundation/YouTube
3:14
Understanding Your Pathology Report: A Patient’s Story
capathologists/YouTube
5:53
Pathology Insights: Basics of Thymic Pathology with Sanjay Mukhopadhyay, MD
Oral Pathology | Salivary Gland Benign Diseases | NBDE Part II
Mental Dental/YouTube
3:01
Testicular germ cell tumours - Seminoma - Pathology mini tutorial
Pathology mini tutorials/YouTube
3:05
Ottitis Media Pathology
Dr. Rishi Mantri/YouTube
13:21
Understanding Pathology for Breast Cancer
Swedish/YouTube
7:32
Breast Cancer Pathology Reports: What You Need to Know
Breast Cancer School for Patients/YouTube
9:05
How to Understand Your Breast Cancer Pathology Report
Yerbba – Breast Cancer/YouTube
20:43
What's in your prostate cancer pathology report? - Dr. David Berman
ProstateCancerBC/YouTube
FISH Test
FISH Test
Also called: Fluorescence In Situ Hybridization, FISH, FISH Test for Cancer, FISH Study
Fluorescence in situ hybridization (FISH) is a laboratory technique used to detect and locate a specific DNA sequence on a chromosome. It is utilized to diagnose genetic diseases, gene mapping, and identification of chromosomal abnormalities, and may also be used to study comparisons among the chromosomes' arrangements of genes.
FISH Test
Also called: Fluorescence In Situ Hybridization, FISH, FISH Test for Cancer, FISH Study
Fluorescence in situ hybridization (FISH) is a laboratory technique used to detect and locate a specific DNA sequence on a chromosome. It is utilized to diagnose genetic diseases, gene mapping, and identification of chromosomal abnormalities, and may also be used to study comparisons among the chromosomes' arrangements of genes.
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Use the slider below to see how your results affect your
health.
Your result is Normal.
A normal FISH study indicates the amount of cells counted and analyzed and that no gene rearrangements were observed.
Related conditions
Fluorescence in situ hybridization (abbreviated FISH) is a laboratory technique used to detect and locate a specific DNA sequence on a chromosome. In this technique, the full set of chromosomes from an individual is affixed to a glass slide and then exposed to a “probe”—a small piece of purified DNA tagged with a fluorescent dye. The fluorescently labeled probe finds and then binds to its matching sequence within the set of chromosomes. With the use of a special microscope, the chromosome and sub-chromosomal location where the fluorescent probe bound can be seen.
Fluorescence in situ hybridization (FISH) provides researchers with a way to visualize and map the genetic material in an individual's cells, including specific genes or portions of genes. This may be used for understanding a variety of chromosomal abnormalities and other genetic mutations.
FISH is useful, for example, to help a researcher or clinician identify where a particular gene falls within an individual's chromosomes. The first step is to prepare short sequences of single-stranded DNA that match a portion of the gene the researcher is looking for. These are called probes. The next step is to label these probes by attaching one of a number of colors of fluorescent dye.DNA is composed of two strands of complementary molecules that bind to each other like chemical magnets. Since the researchers' probes are single-stranded, they are able to bind to the complementary strand of DNA, wherever it may reside on a person's chromosomes. When a probe binds to a chromosome, its fluorescent tag provides a way for researchers to see its location.
Scientists use three different types of FISH probes, each of which has a different application:
Locus specific probes bind to a particular region of a chromosome. This type of probe is useful when scientists have isolated a small portion of a gene and want to determine on which chromosome the gene is located, or how many copies of a gene exist within a particular genome.
Alphoid or centromeric repeat probes are generated from repetitive sequences found in the middle of each chromosome. Researchers use these probes to determine whether an individual has the correct number of chromosomes. These probes can also be used in combination with "locus specific probes" to determine whether an individual is missing genetic material from a particular chromosome.
Whole chromosome probes are actually collections of smaller probes, each of which binds to a different sequence along the length of a given chromosome. Using multiple probes labeled with a mixture of different fluorescent dyes, scientists are able to label each chromosome in its own unique color. The resulting full-color map of the chromosome is known as a spectral karyotype. Whole chromosome probes are particularly useful for examining chromosomal abnormalities, for example, when a piece of one chromosome is attached to the end of another chromosome.
For many applications, FISH has largely been replaced by the use of microarrays. However, FISH remains useful for some tests. FISH may also be used to study comparisons among the chromosomal arrangements of genes across related species.
Fluorescence In Situ Hybridization Fact Sheet | National Human Genome Research Institute (NHGRI) [accessed on Feb 19, 2022]
Fluorescence In Situ Hybridization (FISH). Genome.gov [accessed on Feb 19, 2022]
PDQ® Adult Treatment Editorial Board. PDQ Chronic Myelogenous Leukemia Treatment. Bethesda, MD: National Cancer Institute. [accessed on Feb 19, 2022]
510669: Fluorescence in situ Hybridization (FISH), Oncology | Labcorp [accessed on Feb 19, 2022]
Blood Work | How This Provides Clues On Your Health | Leukemia & Lymphoma Society® (LLS) [accessed on Feb 18, 2022]
Normal reference ranges can vary depending on the laboratory and the method used for testing. You must use the range supplied by the laboratory that performed your test to evaluate whether your results are "within normal limits."
Additional Materials (41)
FLUORESCENCE IN SITU HYBRIDIZATION (FISH)
Fluorescence in situ hybridization (abbreviated FISH) is a laboratory technique used to detect and locate a specific DNA sequence on a chromosome. In this technique, the full set of chromosomes from an individual is affixed to a glass slide and then exposed to a “probe”—a small piece of purified DNA tagged with a fluorescent dye. The fluorescently labeled probe finds and then binds to its matching sequence within the set of chromosomes. With the use of a special microscope, the chromosome and sub-chromosomal location where the fluorescent probe bound can be seen.
Image by National Human Genome Research Institute
HER2 FISH on Breast Cancer
HER2 FISH on Breast Cancer
Image by Anistalista
Indian Muntjac fibroblast cells
Indian Muntjac cultured cells; DAPI nuclei, Alexa Fluor 488 Phalloidin actin, Mitotracker Red CMXRos; 63x/1.4. Imaged with ZEISS ApoTome.2, Axiocam 702 mono and Axio Imager www.zeiss.com/axiocam Sample courtesy of Michael W. Davidson, Florida State University
Image by ZEISS Microscopy/Flickr
Aspergillosis
Under a magnification of 562X, this photomicrograph, stained using a fluorescent antibody (FA) staining technique, and NOT stained using a Candida conjugate, revealed the presence of Aspergillus sp. organisms, in a case of aspergillosis.
Image by CDC/ Dr. William Kaplan
FISH Confirmation of a Human-Specific Duplication of a Gene Cluster on Chromosome 5q13.3 Detected by Interspecies cDNA aCGH - journal.pbio.0020207.g003
FISH Confirmation of a Human-Specific Duplication of a Gene Cluster on Chromosome 5q13.3 Detected by Interspecies cDNA array CGH
(A) Human duplication of a cluster of genes at Chromosome 5q13.3. is shown by two separate, and sometimes multiple, red BAC probe (CTD-2288G5) signals in interphase cells, with only one green BAC probe signal (RP11-1077O1) for a flanking region. Metaphase FISH shows both probes at band 5q13. The third nucleus in (A) shows four signals of the control probe (green) and eight copies of the BAC probe duplicated in the aCGH assay, consistent with the pattern expected in an S/G2 nucleus.
(B–E) Bonobo (B), chimpanzee (C), gorilla (D), and orangutan (E) interphase FISH studies all show no increased signal for the human duplicated gene cluster, with signals of comparable size for the CTD-2288G5 (red) and the flanking RP11-107701 (green) probes. Metaphase FISH analyses show the gene cluster to be in the p arm of Chromosomes 4 (corresponding to the human Chromosome 5) in both the bonobo and chimpanzee, in the q arm of Chromosome 4 (corresponding to the human Chromosome 5) in the orangutan, and in the p arm of the gorilla Chromosome 19 (syntenic regions to human Chromosomes 5 and 17).
doi:10.1371/journal.pbio.0020207.g003
Image by Fortna, A.; Kim, Y.; MacLaren, E.; Marshall, K.; Hahn, G.; Meltesen, L.; Brenton, M.; Hink, R.; Burgers, S.; Hernandez-Boussard, T.; Karimpour-Fard, A.; Glueck, D.; McGavran, L.; Berry, R.; Pollack, J.; Sikela, J. M./Wikimedia
FISH (Fluorescent In Situ Hybridization)
Scheme of the principle of the FISH (Fluorescent in situ hybridization) Experiment to localize a gene in the nucleus.
Image by MrMatze/Wikimedia
FISH for Bacterial Pathogen Identification
This figure outlines the process of fluorescence in situ hybridization (FISH) used for bacterial pathogen identification. First, a sample of the infected tissue is taken from the patient. Then an oligonucleotide that is complementary to the suspected pathogen’s genetic code is synthesized and chemically tagged with a fluorescent probe. The collected tissue sample must then be chemically treated in order to make the cell membranes permeable to the fluorescently tagged oligonucleotide. After the tissue sample is treated, the tagged complementary oligonucleotide is added. The fluorescently tagged oligonucleotide will only bind to the complementary DNA of the suspected pathogen. If the pathogen is present in the tissue sample, then the pathogen’s cells will glow/fluoresce after treatment with the tagged oligonucleotide. All other cells will not glow after treatment.
Image by Pepetps
Togopic
Ivan Akira
Magnus Manske
Timothy W. Ford/Wikimedia
Results of in situ hybridization of chromosome X and Y BAC probes
Results of in situ hybridization of chromosome X and Y BAC probes. (A) Dual color hybridization showing highly specific signals on the X (red) and Y (green) chromosomes in metaphase cells. The two diploid interphase cell nuclei from a normal male donor show the expected pair of single signals. (B) The approximate locations of the hybridization targets shown along ideograms of the human X and Y chromosomes.
Image by Joanne H. Hsu, Hui Zeng, Kalistyn H. Lemke, Aris A. Polyzos, Jingly F. Weier, Mei Wang, Anna R. Lawin-O’Brien, Heinz-Ulrich G. Weier and Benjamin O’Brien/Wikimedia
Hordeum vulgare stained by fluorescent in situ hybridization
Staining of chromosome Hordeum vulgare by Fluorescent in situ hybridization (FISH)
Image by Karol007 and Marcello002/Wikimedia
FISH versus CISH Detection
Fluorescence in situ hybridization versus chromogenic in situ hybridization
Image by Escott16/Wikimedia
FISH (technique)
Fluorescent in-situ hybridization is a process which vividly paints chromosomes or portions of chromosomes with fluorescent molecules. This technique is useful for identifying chromosomal abnormalities and for gene mapping.
Image by Thomas Ried/Wikimedia
Results of in situ hybridization of a chromosome 16 BAC probe
Results of in situ hybridization of a chromosome 16 BAC probe on metaphase spreads of ‘normal’ cells. (A) The dual color FISH results showing a normal diploid metaphase spread. The DAPI DNA counterstain is shown in gray; (B) Schematic diagram illustrating the relative positions of the chromosome 16 whole chromosome painting probe (Coatasome-16, Oncor) and the biotinylated DNA repeat probe prepared from BAC RP11-486E19 (detected with avidin-FITC, green).
Image by Joanne H. Hsu, Hui Zeng, Kalistyn H. Lemke, Aris A. Polyzos, Jingly F. Weier, Mei Wang, Anna R. Lawin-O’Brien, Heinz-Ulrich G. Weier and Benjamin O’Brien/Wikimedia
FISH human lymphocyte nucleus stained with DAPI with chromosome 13 (green) and 21 (red) centromere probes hybrydized (fluorescent in situ hybridization, FISH)
human lymphocyte nucleus stained with DAPI with chromosome 13 (green) and 21 (red) centromere probes hybrydized (fluorescent in situ hybridization, FISH)
Obraz fluorescencyjny jądra ludzkiego limfocytu barwionego diaminofenyloindolem (DAPI) z sygnałami sond swoistych dla chromosomów 13 (zielony, sonda znakowana fluoresceiną) i 21 (czerwony, sonda znakowana rodaminą), uzyskany w wyniku zastosowania techniki FISH
Image by Gregor1976/Wikimedia
MicroRNA and mRNA visualization in differentiating C1C12 cells
ViewRNA assay for detection of miR-133 microRNA (green) and myogenin mRNA (red) in differentiating C2C12 cells.
Image by Ryan Jeffs/Wikimedia
FISH Her2
Her2 gene amplification by FISH (fluorescent in situ hybridization) in breast cancer cells
Image by IrinaPav/Wikimedia
PLoSBiol3.5.Fig7ChromosomesAluFish
Human metaphase chromosomes were subjected to fluorescence in situ hybridization with a probe to the Alu Sequence (green signals)and counterstained for DNA (red).
Image by Andreas Bolzer, Gregor Kreth, Irina Solovei, Daniela Koehler, Kaan Saracoglu, Christine Fauth, Stefan Müller, Roland Eils, Christoph Cremer, Michael R. Speicher, Thomas Cremer/Wikimedia
Q-FISH workflow
General workflow for Q-FISH with cultured cells.
Image by Jclam at English Wikipedia/Wikimedia
Fluorescence in Situ Hybridization (FISH)
Video by Leukemia & Lymphoma Society/YouTube
Hybridization (microarray) | Biomolecules | MCAT | Khan Academy
Video by khanacademymedicine/YouTube
Fluorescence In Situ Hybridization (FISH)
Video by Abnova/YouTube
FISH Technique Fluorescent In Situ Hybridization HD Animation 1
Video by ПИМУ - Приволжский исследовательский мед.универ./YouTube
Microbiology: Immunofluorescence Detection of Bacteria
Video by biologycourses/YouTube
Fluorescence In Situ Hybridization (FISH)
Fluorescence in situ hybridization (FISH) is a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.
Image by National Human Genome Research Institute (NHGRI)
Hybridization
Hybridization is the process of combining two complementary single-stranded DNA or RNA molecules and allowing them to form a single double-stranded molecule through base pairing.
Image by National Human Genome Research Institute (NHGRI)
FISH Confirmation of a Human-Specific Duplication of a Gene Cluster on Chromosome 5q13.3
FISH Confirmation of a Human-Specific Duplication of a Gene Cluster on Chromosome 5q13.3 Detected by Interspecies cDNA array CGH
(A) Human duplication of a cluster of genes at Chromosome 5q13.3. is shown by two separate, and sometimes multiple, red BAC probe (CTD-2288G5) signals in interphase cells, with only one green BAC probe signal (RP11-1077O1) for a flanking region. Metaphase FISH shows both probes at band 5q13. The third nucleus in (A) shows four signals of the control probe (green) and eight copies of the BAC probe duplicated in the aCGH assay, consistent with the pattern expected in an S/G2 nucleus.
(B–E) Bonobo (B), chimpanzee (C), gorilla (D), and orangutan (E) interphase FISH studies all show no increased signal for the human duplicated gene cluster, with signals of comparable size for the CTD-2288G5 (red) and the flanking RP11-107701 (green) probes. Metaphase FISH analyses show the gene cluster to be in the p arm of Chromosomes 4 (corresponding to the human Chromosome 5) in both the bonobo and chimpanzee, in the q arm of Chromosome 4 (corresponding to the human Chromosome 5) in the orangutan, and in the p arm of the gorilla Chromosome 19 (syntenic regions to human Chromosomes 5 and 17).
Image by Fortna, A.; Kim, Y.; MacLaren, E.; Marshall, K.; Hahn, G.; Meltesen, L.; Brenton, M.; Hink, R.; Burgers, S.; Hernandez-Boussard, T.; Karimpour-Fard, A.; Glueck, D.; McGavran, L.; Berry, R.; Pollack, J.; Sikela, J. M.
FISH18
In situ hybridization. 18p (green) and 18q (red) with subtelomeric probes showing 18p deletion in the patient with De Grouchy syndrome type I (deletion 18p)
Image by /Wikimedia
Kidney section, fluorescence microscopy
Kidney section. IHC stained with Cy3 (red), anti-GFP antibody stained with Alexa 488(green), nuclei stained with DAPI (blue). Fluorescence microscopy with ZEISS Axio Observer, Axiocam, Colibri 7. www.zeiss.com/axioobserver
Image by ZEISS Microscopy
Fish analysis di george syndrome
Figure 2. Result of FISH analysis using LSI probe (TUPLE 1) from DiGeorge/velocardiofacial syndrome critical region. TUPLE 1 (HIRA) probe was labeled in Spectrum Orange and Arylsulfatase A (ARSA) in SpectrumGreen as control. Absence of the orange signal indicates deletion of the TUPLE 1 locus at 22q11.2. Tonelli et al. Journal of Medical Case Reports 2007 1:167 doi:10.1186/1752-1947-1-167
Image by Adriano R Tonelli1 , Kalyan Kosuri1 , Sainan Wei2 and Davoren Chick1/Wikimedia
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Chromosomal Instability in Breast Cancer Cells
Visualization of the enormous degree of chromosomal instability in primary breast cancers using fluorescence in situ hybridization to identify copy number changes of specific chromosomes and oncogenes.
This image was originally submitted as part of the 2015 NCI Cancer Close Up project. This image is part of the NCI Cancer Close Up 2015 collection.
See also https://visualsonline.cancer.gov/closeup.
Image by NCI Center for Cancer Research / Thomas Ried
Mapping a Gene
Mapping the position of genes in the cell nucleus sheds light on basic principles governing the genome. Here, a single gene called Pem (purple) has been localized using fluorescence in situ hybridization. DNA is stained blue; the cell cytoplasm is stained green.
This image was originally submitted as part of the 2015 NCI Cancer Close Up project and selected for exhibit. This image is part of the NCI Cancer Close Up 2015 collection.
See also https://visualsonline.cancer.gov/closeup.
Image by NCI Center for Cancer Research / Tom Misteli
Prokaryotic Diversity
This (a) microbial mat, about one meter in diameter, grows over a hydrothermal vent in the Pacific Ocean in a region known as the “Pacific Ring of Fire.” The mat helps retain microbial nutrients. Chimneys such as the one indicated by the arrow allow gases to escape. (b) In this micrograph, bacteria are visualized using fluorescence microscopy. (credit a: modification of work by Dr. Bob Embley, NOAA PMEL, Chief Scientist; credit b: modification of work by Ricardo Murga, Rodney Donlan, CDC; scale-bar data from Matt Russell)
Image by CNX Openstax
Biofilm formed by a pathogen
A biofilm is a highly organized community of microorganisms that develops naturally on certain surfaces. These communities are common in natural environments and generally do not pose any danger to humans. Many microbes in biofilms have a positive impact on the planet and our societies. Biofilms can be helpful in treatment of wastewater, for example. This dime-sized biofilm, however, was formed by the opportunistic pathogen Pseudomonas aeruginosa. Under some conditions, this bacterium can infect wounds that are caused by severe burns. The bacterial cells release a variety of materials to form an extracellular matrix, which is stained red in this photograph. The matrix holds the biofilm together and protects the bacteria from antibiotics and the immune system. A biofilm is a highly organized community of microorganisms that develops naturally on certain surfaces. These communities are common in natural environments and generally do not pose any danger to humans. Many microbes in biofilms have a positive impact on the planet and our societies. Biofilms can be helpful in treatment of wastewater, for example. This dime-sized biofilm, however, was formed by the opportunistic pathogen Pseudomonas aeruginosa. Under some conditions, this bacterium can infect wounds that are caused by severe burns. The bacterial cells release a variety of materials to form an extracellular matrix, which is stained red in this photograph. The matrix holds the biofilm together and protects the bacteria from antibiotics and the immune system.
Image by Scott Chimileski, Ph.D., and Roberto Kolter, Ph.D., Harvard Medical School.
This browser does not support the video element.
Biofilm blocking fluid flow
This time-lapse movie shows that bacterial communities called biofilms can create blockages that prevent fluid flow in devices such as stents and catheters over a period of about 56 hours. This video was featured in a news release from Princeton University.
Video by NIGMS/Knut Drescher, Princeton University
5 stages of biofilm development
Stage 1, initial attachment; stage 2, irreversible attachment; stage 3, maturation I; stage 4, maturation II; stage 5, dispersion. Each stage of development in the diagram is paired with a photomicrograph of a developing Pseudomonas aeruginosa biofilm. All photomicrographs are shown to same scale
Image by D. Davis
Toxins under microscope
This digitally colorized scanning electron microscopic (SEM) image of an untreated water specimen extracted from a wild stream mainly used to control flooding during inclement weather; revealed the presence of unidentified organisms; which included bacteria; protozoa; and algae. In this particular view; a microorganism is featured; the exterior of which is covered by numerous projections imparting an appearance of a sea urchin. This microscopic pin cushion; was tethered to its surroundings by a biofilm; within which many bacteria; and amoeboid protozoa could be seen enmeshed as well.
Image by CDC/ Janice Haney Carr
Toxins
Under a magnification of 2500X, this digitally colorized scanning electron microscopic (SEM) image of an untreated water specimen extracted from a wild stream mainly used to control flooding during inclement weather, revealed the presence of unidentified organisms, which included bacteria, protozoa, and algae. In this particular view, a microorganism is featured, the exterior of which is covered by numerous projections, imparting an appearance of a sea urchin. This microscopic pincushion was tethered to its surroundings by a biofilm, within which many bacteria and amoeboid protozoa could be seen enmeshed as well. See PHIL 11781 for a greater magnification of this organism’s exterior.
Image by CDC/ Janice Haney Carr
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confocal laser scanning microscope of biofilm of Salmonella enterica (pink) and Erwinia chrysanthemi (green)
Using a confocal laser scanning microscope, microbiologist Maria Brandl examines a mixed biofilm of Salmonella enterica (pink) and Erwinia chrysanthemi (green) in soft rot lesions on cilantro leaves (blue).
Image by USDA Agricultural Research Service/Photo by Peggy Greb.
Flourescence In Situ Hybridization (FISH)
Fluorescence in situ hybridization (FISH) provides researchers with a way to visualize and map the genetic material in an individual's cells, including specifc genes or portions of genes. This is important for understanding a variety of chromosomal abnormalities and other genetic mutations. Unlike most other techniques used to study chromosomes, FISH does not have to be performed on cells that are actively dividing. This makes it a very versatile procedure. Credit: Darryl Leja, NHGRI.
Image by National Human Genome Research Institute (NHGRI) from Bethesda, MD, USA/Wikimedia
Fluorescence in situ hybridization (FISH) image of bcr/abl positive rearranged metaphase
FISH method. The chromosomes are blue in the fluorescence microscope , except for a point on one of the chromosomes, which is green and red. This is where the sequence causing one of the types of leukemia is located
Image by Pmx
In situ hybridization of the Her2 gene (unamplified)
The image shows nuclei of neoplastic cells of a breast cancer with a normal number of copies of the Her2 gene (red signals) (in green, centromere labeling signals). Technique: in situ hybridization of interphase nuclei obtained from paraffin-embedded material from breast cancer.
Image by Manuel Medina Pérez/Wikimedia
Probe
A probe is a single-stranded sequence of DNA or RNA used to search for its complementary sequence in a sample genome.
Image by National Human Genome Research Institute (NHGRI)
FLUORESCENCE IN SITU HYBRIDIZATION (FISH)
National Human Genome Research Institute
HER2 FISH on Breast Cancer
Anistalista
Indian Muntjac fibroblast cells
ZEISS Microscopy/Flickr
Aspergillosis
CDC/ Dr. William Kaplan
FISH Confirmation of a Human-Specific Duplication of a Gene Cluster on Chromosome 5q13.3 Detected by Interspecies cDNA aCGH - journal.pbio.0020207.g003
Pepetps
Togopic
Ivan Akira
Magnus Manske
Timothy W. Ford/Wikimedia
Results of in situ hybridization of chromosome X and Y BAC probes
Joanne H. Hsu, Hui Zeng, Kalistyn H. Lemke, Aris A. Polyzos, Jingly F. Weier, Mei Wang, Anna R. Lawin-O’Brien, Heinz-Ulrich G. Weier and Benjamin O’Brien/Wikimedia
Hordeum vulgare stained by fluorescent in situ hybridization
Karol007 and Marcello002/Wikimedia
FISH versus CISH Detection
Escott16/Wikimedia
FISH (technique)
Thomas Ried/Wikimedia
Results of in situ hybridization of a chromosome 16 BAC probe
Joanne H. Hsu, Hui Zeng, Kalistyn H. Lemke, Aris A. Polyzos, Jingly F. Weier, Mei Wang, Anna R. Lawin-O’Brien, Heinz-Ulrich G. Weier and Benjamin O’Brien/Wikimedia
FISH human lymphocyte nucleus stained with DAPI with chromosome 13 (green) and 21 (red) centromere probes hybrydized (fluorescent in situ hybridization, FISH)
Gregor1976/Wikimedia
MicroRNA and mRNA visualization in differentiating C1C12 cells
Ryan Jeffs/Wikimedia
FISH Her2
IrinaPav/Wikimedia
PLoSBiol3.5.Fig7ChromosomesAluFish
Andreas Bolzer, Gregor Kreth, Irina Solovei, Daniela Koehler, Kaan Saracoglu, Christine Fauth, Stefan Müller, Roland Eils, Christoph Cremer, Michael R. Speicher, Thomas Cremer/Wikimedia
Q-FISH workflow
Jclam at English Wikipedia/Wikimedia
3:22
Fluorescence in Situ Hybridization (FISH)
Leukemia & Lymphoma Society/YouTube
8:57
Hybridization (microarray) | Biomolecules | MCAT | Khan Academy
khanacademymedicine/YouTube
5:01
Fluorescence In Situ Hybridization (FISH)
Abnova/YouTube
1:44
FISH Technique Fluorescent In Situ Hybridization HD Animation 1
Microbiology: Immunofluorescence Detection of Bacteria
biologycourses/YouTube
Fluorescence In Situ Hybridization (FISH)
National Human Genome Research Institute (NHGRI)
Hybridization
National Human Genome Research Institute (NHGRI)
FISH Confirmation of a Human-Specific Duplication of a Gene Cluster on Chromosome 5q13.3
Fortna, A.; Kim, Y.; MacLaren, E.; Marshall, K.; Hahn, G.; Meltesen, L.; Brenton, M.; Hink, R.; Burgers, S.; Hernandez-Boussard, T.; Karimpour-Fard, A.; Glueck, D.; McGavran, L.; Berry, R.; Pollack, J.; Sikela, J. M.
FISH18
/Wikimedia
Kidney section, fluorescence microscopy
ZEISS Microscopy
Fish analysis di george syndrome
Adriano R Tonelli1 , Kalyan Kosuri1 , Sainan Wei2 and Davoren Chick1/Wikimedia
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Chromosomal Instability in Breast Cancer Cells
NCI Center for Cancer Research / Thomas Ried
Mapping a Gene
NCI Center for Cancer Research / Tom Misteli
Prokaryotic Diversity
CNX Openstax
Biofilm formed by a pathogen
Scott Chimileski, Ph.D., and Roberto Kolter, Ph.D., Harvard Medical School.
0:08
Biofilm blocking fluid flow
NIGMS/Knut Drescher, Princeton University
5 stages of biofilm development
D. Davis
Toxins under microscope
CDC/ Janice Haney Carr
Toxins
CDC/ Janice Haney Carr
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confocal laser scanning microscope of biofilm of Salmonella enterica (pink) and Erwinia chrysanthemi (green)
USDA Agricultural Research Service/Photo by Peggy Greb.
Flourescence In Situ Hybridization (FISH)
National Human Genome Research Institute (NHGRI) from Bethesda, MD, USA/Wikimedia
Fluorescence in situ hybridization (FISH) image of bcr/abl positive rearranged metaphase
Pmx
In situ hybridization of the Her2 gene (unamplified)
Manuel Medina Pérez/Wikimedia
Probe
National Human Genome Research Institute (NHGRI)
How Is the Sample Obtained?
Tissue selection from skin excision with lesion less than 4 mm with benign appearance
Tissue selection from skin excision with lesion 4-8 mm with benign appearance
Tissue selection from skin excision with lesion 9-15 mm with benign appearance
1
2
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Skin Excisions - Benign appearance
Interactive by Mikael Häggström
Tissue selection from skin excision with lesion less than 4 mm with benign appearance
Tissue selection from skin excision with lesion 4-8 mm with benign appearance
Tissue selection from skin excision with lesion 9-15 mm with benign appearance
1
2
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Skin Excisions - Benign appearance
Interactive by Mikael Häggström
How Is Tissue Obtained for Examination by the Pathologist?
In most cases, a doctor needs to do a biopsy or surgery to remove cells or tissues for examination under a microscope.
Some common ways a biopsy can be done are as follows:
A needle is used to withdraw tissue or fluid.
An endoscope (a thin, lighted tube) is used to look at areas inside the body and remove cells or tissues.
Surgery is used to remove part of the tumor or the entire tumor. If the entire tumor is removed, typically some normal tissue around the tumor is also removed.
Tissue removed during a biopsy is sent to a pathology laboratory, where it is sliced into thin sections for viewing under a microscope. This is known as histologic (tissue) examination and is usually the best way to tell if cancer is present. The pathologist may also examine cytologic (cell) material. Cytologic material is present in urine, cerebrospinal fluid (the fluid around the brain and spinal cord), sputum (mucus from the lungs), peritoneal (abdominal cavity) fluid, pleural (chest cavity) fluid, cervical/vaginal smears, and in fluid removed during a biopsy.
Source: National Cancer Institute (NCI)
Additional Materials (1)
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Grossing of suspected malignant skin excision
Grossing of a suspected malignant skin excision.
Image by Mikael Häggström, M.D.
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Grossing of suspected malignant skin excision
Mikael Häggström, M.D.
How Is the Sample Processed?
Tissue selection from skin excision with less than 4 mm suspected malignant lesion
Tissue selection from skin excision with 4-8 mm suspected malignant lesion
Tissue selection from skin excision with 9-15 mm suspected malignant lesion
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2
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Skin Excisions - Suspected malignancy
Interactive by Mikael Häggström
Tissue selection from skin excision with less than 4 mm suspected malignant lesion
Tissue selection from skin excision with 4-8 mm suspected malignant lesion
Tissue selection from skin excision with 9-15 mm suspected malignant lesion
1
2
3
Skin Excisions - Suspected malignancy
Interactive by Mikael Häggström
How Is Tissue Processed After a Biopsy or Surgery? What Is a Frozen Section?
The tissue removed during a biopsy or surgery must be cut into thin sections, placed on slides, and stained with dyes before it can be examined under a microscope. Two methods are used to make the tissue firm enough to cut into thin sections: frozen sections and paraffin-embedded (permanent) sections. All tissue samples are prepared as permanent sections, but sometimes frozen sections are also prepared.
Permanent sections are prepared by placing the tissue in fixative (usually formalin) to preserve the tissue, processing it through additional solutions, and then placing it in paraffin wax. After the wax has hardened, the tissue is cut into very thin slices, which are placed on slides and stained. The process normally takes several days. A permanent section provides the best quality for examination by the pathologist and produces more accurate results than a frozen section.
Frozen sections are prepared by freezing and slicing the tissue sample. They can be done in about 15 to 20 minutes while the patient is in the operating room. Frozen sections are done when an immediate answer is needed; for example, to determine whether the tissue is cancerous so as to guide the surgeon during the course of an operation.
Source: National Cancer Institute (NCI)
Additional Materials (1)
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Image of resected colon segment with cancer & 4 nearby polyps plus schematic of field defects with sub-clones
Longitudinally opened freshly resected colon segment showing a cancer and four polyps. Plus a schematic diagram indicating a likely field defect (a region of tissue that precedes and predisposes to the development of cancer) in this colon segment. The diagram indicates sub-clones and sub-sub-clones that were precursors to the tumors.
Image by Bernstein0275/Wikimedia
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Image of resected colon segment with cancer & 4 nearby polyps plus schematic of field defects with sub-clones
Bernstein0275/Wikimedia
How Long Does It Take?
Basal cell carcinoma - intermed mag
Basal cell carcinoma - high mag
1
2
Basal Cell Carcinoma
Interactive by nephron
Basal cell carcinoma - intermed mag
Basal cell carcinoma - high mag
1
2
Basal Cell Carcinoma
Interactive by nephron
How Long After the Tissue Sample Is Taken Will the Pathology Report Be Ready?
The pathologist sends a pathology report to the doctor within 10 days after the biopsy or surgery is performed. Pathology reports are written in technical medical language. Patients may want to ask their doctors to give them a copy of the pathology report and to explain the report to them. Patients also may wish to keep a copy of their pathology report in their own records.
Source: National Cancer Institute (NCI)
Additional Materials (1)
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Polycystic kidneys
Polycystic kidneys
Image by CDC
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Polycystic kidneys
CDC
What Information Does It Give?
Retinoblastoma General Information
Image by The Armed Forces Institute of Pathology (AFIP)
Retinoblastoma General Information
EYE AND OCULAR ADNEXA: RETINOBLASTOMA
Image by The Armed Forces Institute of Pathology (AFIP)
What Information Does a Pathology Report Usually Include?
The pathology report may include the following information:
Patient information: Name, birth date, biopsy date
Gross description: Color, weight, and size of tissue as seen by the naked eye
Microscopic description: How the sample looks under the microscope and how it compares with normal cells
Diagnosis: Type of tumor/cancer and grade (how abnormal the cells look under the microscope and how quickly the tumor is likely to grow and spread)
Tumor size: Measured in centimeters
Tumor margins: There are three possible findings when the biopsy sample is the entire tumor:
Positive margins mean that cancer cells are found at the edge of the material removed
Negative, not involved, clear, or free margins mean that no cancer cells are found at the outer edge
Close margins are neither negative nor positive
Other information: Usually notes about samples that have been sent for other tests or a second opinion
Pathologist’s signature and name and address of the laboratory
Source: National Cancer Institute (NCI)
Additional Materials (1)
Carcinocythemia - malignant tumour cells in peripheral blood
Tumor cells in peripheral blood smear. Noncohesive round tumor cells resembling lymphocytes were identified.
Image by Ogura, Kanako & Amano, Maki & Matsumoto, Toshiharu & Sakaguchi, Asumi & Kosaka, Taijiro & Kitabatake, Toshiaki & Kojima, Kuniaki. (2015). Occult Breast Lobular Carcinoma with Numerous Circulating Tumor Cells in Peripheral Blood. Case reports in pathology. 2015. 135684. 10.1155/2015/135684./Wikimedia
Carcinocythemia - malignant tumour cells in peripheral blood
Ogura, Kanako & Amano, Maki & Matsumoto, Toshiharu & Sakaguchi, Asumi & Kosaka, Taijiro & Kitabatake, Toshiaki & Kojima, Kuniaki. (2015). Occult Breast Lobular Carcinoma with Numerous Circulating Tumor Cells in Peripheral Blood. Case reports in pathology. 2015. 135684. 10.1155/2015/135684./Wikimedia
What Does It Say About the Sample?
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Wilms tumor - NEPHROBLASTOMA
Image by The Armed Forces Institute of Pathology
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Wilms tumor - NEPHROBLASTOMA
KIDNEY-BLADDER-URINARY: NEPHROBLASTOMA Note the prominent septa subdividing the sectioned surface and the protrusion of tumor into the renal pelvis, resembling botryoid rhabdomyosarcoma.
Image by The Armed Forces Institute of Pathology
What Might the Pathology Report Say About the Physical and Chemical Characteristics of the Tissue?
After identifying the tissue as cancerous, the pathologist may perform additional tests to get more information about the tumor that cannot be determined by looking at the tissue with routine stains, such as hematoxylin and eosin (also known as H&E), under a microscope. The pathology report will include the results of these tests. For example, the pathology report may include information obtained from immunochemical stains (IHC). IHC uses antibodies to identify specific antigens on the surface of cancer cells. IHC can often be used to:
Determine where the cancer started
Distinguish among different cancer types, such as carcinoma, melanoma, and lymphoma
Help diagnose and classify leukemias and lymphomas
The pathology report may also include the results of flow cytometry. Flow cytometry is a method of measuring properties of cells in a sample, including the number of cells, percentage of live cells, cell size and shape, and presence of tumor markers on the cell surface. Tumor markers are substances produced by tumor cells or by other cells in the body in response to cancer or certain noncancerous conditions.) Flow cytometry can be used in the diagnosis, classification, and management of cancers such as acute leukemia, chronic lymphoproliferative disorders, and non-Hodgkin lymphoma.
Finally, the pathology report may include the results of molecular diagnostic and cytogenetic studies. Such studies investigate the presence or absence of malignant cells, and genetic or molecular abnormalities in specimens.
Source: National Cancer Institute (NCI)
What Does It Say About Genetics?
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Subependymal giant cell astrocytoma
Image by The Armed Forces Institute of Pathology
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Subependymal giant cell astrocytoma
CNS: SUBEPENDYMAL GIANT CELL ASTROCYTOMA (TUBEROUS SCLEROSIS) This large fleshy mass straddles the midline and produces marked dilatation of the lateral ventricles.
Image by The Armed Forces Institute of Pathology
What Information About the Genetics of the Cells Might Be Included in the Pathology Report?
Cytogenetics uses tissue culture and specialized techniques to provide genetic information about cells, particularly genetic alterations. Some genetic alterations are markers or indicators of a specific cancer. For example, the Philadelphia chromosome is associated with chronic myelogenous leukemia (CML). Some alterations can provide information about prognosis, which helps the doctor make treatment recommendations. Some tests that might be performed on a tissue sample include:
Fluorescence in situ hybridization (FISH): Determines the positions of particular genes. It can be used to identify chromosomal abnormalities and to map genes.
Polymerase chain reaction (PCR): A method of making many copies of particular DNA sequences of relevance to the diagnosis.
Real-time PCR or quantitative PCR: A method of measuring how many copies of a particular DNA sequence are present.
Reverse-transcriptase polymerase chain reaction (RT-PCR): A method of making many copies of a specific RNA sequence.
Southern blot hybridization: Detects specific DNA fragments.
Western blot hybridization: Identifies and analyzes proteins or peptides.
Source: National Cancer Institute (NCI)
Can You Get a Second Opinion?
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Eye and ocular adnexa: malignant melanoma
Image by The Armed Forces Institute of Pathology (AFIP)
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Eye and ocular adnexa: malignant melanoma
Variably pigmented, mushroom-shaped choroidal tumor has ruptured the Bruch membrane and grown into the subretinal space. A form of cancer that begins in melanocytes (cells that make the pigment melanin). It may begin in a mole (skin melanoma), but can also begin in other pigmented tissues, such as in the eye or in the intestines. (National Cancer Institute NCI)
Image by The Armed Forces Institute of Pathology (AFIP)
Can Individuals Get a Second Opinion About Their Pathology Results?
Although most cancers can be easily diagnosed, sometimes patients or their doctors may want to get a second opinion about the pathology results. Patients interested in getting a second opinion should talk with their doctor. They will need to obtain the slides and/or paraffin block from the pathologist who examined the sample or from the hospital where the biopsy or surgery was done.
Many institutions provide second opinions on pathology specimens. NCI-designated cancer centers or academic institutions are reasonable places to consider. Patients should contact the facility in advance to determine if this service is available, the cost, and shipping instructions.
Source: National Cancer Institute (NCI)
What Research Is Being Done?
Optomap-pathology
Image by Zg2891/Wikimedia
Optomap-pathology
תמונת רשתית ( Optomap) בה רואים דוגמאות למחלות עיניים הניתנות לגילוי בצילום רשתית אופטוס.
Image by Zg2891/Wikimedia
What Research Is Being Done to Improve the Diagnosis of Cancer?
NCI, a component of the National Institutes of Health, is sponsoring clinical trials that are designed to improve the accuracy and specificity of cancer diagnoses. Before any new method can be recommended for general use, doctors conduct clinical trials to find out whether it is safe and effective.
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Pathology Reports
A pathology report is a document that contains the diagnosis determined by examining cells and tissues under a microscope. Pathology reports play an important role in cancer diagnosis and staging. A pathologist is a doctor who does this examination and writes the pathology report. Keep reading to understand pathology reports.