What Is Nodular Nonsuppurative Panniculitis?
Source: Genetic and Rare Diseases (GARD) Information Center
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Nodular Nonsuppurative Panniculitis
NNP; Idiopathic Nodular Panniculitis; Relapsing Febrile Nodular Nonsuppurative Panniculitis; Pfeiffer-Weber-Christian Syndrome; Weber-Christian Panniculitis
Nodular nonsuppurative panniculitis describes a rare group of skin disorders characterized by tender, painful bumps below the surface of the skin (subcutaneous nodules) that usually lead to inflammation of the subcutaneous layer of fat (panniculitis). Explore symptoms and treatments.
Skin Nodule (medicine)
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Weber christian disease
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Source: Genetic and Rare Diseases (GARD) Information Center
Dermatologist talks with a little girl at a local medical clinic
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Individuals with nodular nonsuppurative panniculitis (NNP) may consult with a pediatric dermatologist and/or a pediatric rheumatologist in order to confirm the diagnosis, determine the cause of the condition and obtain treatment.
Source: Genetic and Rare Diseases (GARD) Information Center
Prednisone: The Double-Edged Sword
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Treatment for nodular nonsuppurative panniculitis (NNP) generally aims at controlling and relieving the symptoms that an individual has. Before treatment is initiated, a work-up should be completed to determine whether the condition is secondary to another underlying disorder. If there is an underlying disorder, treatment of this disorder may relieve the symptoms of NNP. In some cases, skin lesions heal spontaneously (remission) but the lesions often later return. There is no treatment method found to be effective for all individuals with NNP. Medications used to treat the condition may include systemic steroids (such as prednisone) to suppress sudden attacks; nonsteroidal anti-inflammatory drugs (NSAIDs) to reduce fever and other signs of malaise; and/or immunosuppressive drugs. Relief of symptoms in some affected individuals has also been reported with fibrinolytic agents (medications that help prevent blood clots), hydroxychloroquine, azathioprine, thalidomide, cyclophosphamide, tetracycline, cyclosporin, mycophenolate, and clofazimine.
Source: Genetic and Rare Diseases (GARD) Information Center
Treatment and Prognosis varies depending on the type of condition and the age of symptom onset.
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Source: Genetic and Rare Diseases (GARD) Information Center
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