Cutaneous manifestations of lymphomatoid granulomatosis. Report of 44 cases and a review of the literature
- 1 April 1981
- journal article
- review article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 117 (4) , 196-202
- https://doi.org/10.1001/archderm.117.4.196
Abstract
A review of records of 44 patients who had lymphomatoid granulomatosis (LYG) with skin lesions showed that cutaneous manifestations are protean and generally transient. S.c. or dermal nodules were present in more than 60% of cases. A maculopapular rash or macular erythema was less common; ulceration was rare. Skin lesions were widely distributed. Frequently, in patients who had early cutaneous involvement with LYG, associated involvement of the nervous system and joints occurred. Findings from laboratory studies were generally inconclusive. Lymphomatoid granulomatosis progressed to lymphoma in 18% of the cases; death from respiratory failure was common. Theories on the possible cause and the pathogenesis of LYG are presented.This publication has 4 references indexed in Scilit:
- Wegener's Granulomatosis, Lymphomatoid Granulomatosis, and Benign Lymphocytic Angiitis and Granulomatosis of LungAnnals of Internal Medicine, 1977
- Granulomatous Vasculitides: Distinct but RelatedAnnals of Internal Medicine, 1977
- Cutaneous manifestations of Wegener granulomatosisArchives of Dermatology, 1977
- Limited forms of angiitis and granulomatosis of Wegener's typeThe American Journal of Medicine, 1966