Modern approach to diagnosis of idiopathic lobular panniculitis (Weber‑Christian disease)

Author:

Egorova O. N.1,Belov B. S.1,Radenska-Lopovok S. G.2

Affiliation:

1. V. A. Nasonova Research Institute of Rheumatology

2. First Moscow State Medical University n. a. I. M. Sechenov

Abstract

Idiopathic lobular panniculitis (ILP or Weber‑Christian disease) is the least studied disease in the group of systemic connective tissue lesions and is characterized by systemic lesions of subcutaneous fat. The examination of 67 patients (9 men and 58 women aged 20 to 76 years) with a verified diagnosis of ILP allowed to identify the main clinical and laboratory signs of ILP.

Publisher

Alfmed LLC

Subject

Materials Chemistry,Economics and Econometrics,Media Technology,Forestry

Reference12 articles.

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3. Verbenka E. V., Belen'kii G. B. U kliniko-morfologicheskoi kharakteristike bolezni Vebera-Krischena. Vest. dermat. i vener. 1971; 2: 14–19.

4. Metha R, Gahlot GP, Das P et al. Sclerosing mesenteric panniculitis in a young patient: common cause of diagnostic dilemma and treatment refractoriness. Acta Gastroenterol Belg 2016; 79 (2): 254–256.

5. Diaz Cascajo C, Borghi S, Weyers W. Panniculitis: definition of terms and diagnostic strategy. Am. J. Dermat 2000; 22: 530–49.

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