Weber–Christian disease
Weber–Christian Disease
Weber–Christian Disease (pronounced: WEB-er KRIS-chen disease), also known as Relapsing Febrile Nodular Nonsuppurative Panniculitis, is a rare inflammatory disease that affects the body's fat tissues. The exact cause of the disease is unknown, but it is believed to be an autoimmune disorder.
Etymology
The disease is named after the American dermatologists Frederick Parkes Weber and Henry Asbury Christian, who first described the condition in the early 20th century.
Symptoms
The primary symptom of Weber–Christian Disease is the formation of painful, tender nodules under the skin, particularly in the thighs and abdomen. These nodules can lead to skin discoloration and may come and go over time. Other symptoms can include fever, fatigue, weight loss, and malaise.
Diagnosis
Diagnosis of Weber–Christian Disease is typically made through a combination of clinical examination and biopsy of the affected tissue. Other tests, such as blood tests and imaging studies, may also be used to rule out other conditions.
Treatment
Treatment for Weber–Christian Disease primarily involves managing symptoms and may include the use of nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and other immunosuppressive medications.
Related Terms
- Autoimmune disease
- Inflammation
- Nodule
- Biopsy
- Nonsteroidal anti-inflammatory drug
- Corticosteroid
- Immunosuppressive drug
External links
- Medical encyclopedia article on Weber–Christian disease
- Wikipedia's article - Weber–Christian disease
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