- Weber–Christian disease
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Weber–Christian disease Classification and external resources ICD-10 M35.6 ICD-9 729.30 DiseasesDB 14055 eMedicine ped/2429 MeSH D010201 Weber–Christian disease (also known as "Relapsing febrile non-suppurative panniculitis") is a cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin.[1]
It is type of panniculitis.[2]
Eponym
It is named for Frederick Parkes Weber and Henry Asbury Christian.[3][4][5]
See also
- Alpha-1 antitrypsin deficiency panniculitis
- List of cutaneous conditions
References
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ "Weber-Christian disease" at Dorland's Medical Dictionary
- ^ synd/1117 at Who Named It?
- ^ F. P. Weber. A case of relapsing non-suppurative nodular panniculitis, showing phagocytosis of subcutaneous fat-cells by macrophages. British Journal of Dermatology and Syphilis, Oxford, 1925, 37: 301-311.
- ^ H. A. Christian. Relapsing febrile nodular nonsuppurative panniculitis. Archives of Internal Medicine, Chicago, 1928, 42: 338-351.
Lipodystrophy Acquiredgeneralized: Acquired generalized lipodystrophy
partial: Acquired partial lipodystrophy · Centrifugal abdominal lipodystrophy · HIV-associated lipodystrophy · Lipoatrophia annularis
localized: Localized lipodystrophyCongenitalCongenital generalized lipodystrophy · Familial partial lipodystrophy
Poland's syndromeCategories:- Cutaneous condition stubs
- Conditions of the subcutaneous fat
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