A case of ichthyosiform sarcoidosis with unusual localization
Author:
Tekin Salim1, Cayir Kerim1, Bilici Mehmet1, Şipal Sare2, Atasoy Mustafa3, Türkeli Mehmet1
Affiliation:
1. 1Division of Medical Oncology, Department of Internal Medicine, 25240, Erzurum, Turkey 2. 3Department of Pathology, Atatürk University, School of Medicine, 25240, Erzurum, Turkey 3. 2Department of Dermatology, 25240, Erzurum, Turkey
Abstract
AbstractSarcoidosis is a systemic granulomatous disease of unknown cause that commonly involves the lungs, lymph nodes, bones, liver, spleen, or skin. Cutaneous findings of sarcoidosis occur in 20% to 35% of patients with systemic disease. The recognition of cutaneous lesions is important, because it gives important clues to diagnosis and also allows for easy biopsy. We report a 71-year-old Turkish woman with erythematous lesions, which included widespread, erythematous macules of various sizes on the chest, abdomen, and back on both sides of her body. Fine white scales covered some of the lesions. Hepatomegaly and bilateral hilar lymphadenopathy were also observed. Biopsy specimens of the skin showed dermal, noncaseating, epitheloid granulomas. The diagnosis, based on correlation of the clinical presentation and histopathological findings, was ichthyosiform sarcoidosis with systemic involvement. The difference between our case and other cases of ichthyosiform sarcoidosis described in the literature is that ours involved only the trunk and not the extremities. We are presenting this case because it is an interesting and rare variant of ichthyosiform sarcoidosis.
Publisher
Walter de Gruyter GmbH
Reference12 articles.
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