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Multiple disseminated glomuvenous malformations: do we know enough?

作者信息

Solovan C, Chiticariu Elena, Beinsan Doina, Zurac Sabina, Baderca Flavia

机构信息

Department of Dermatology, Victor Babes University of Medicine and Pharmacy, Timisoara, Romania.

出版信息

Rom J Morphol Embryol. 2012;53(4):1077-80.

Abstract

Multiple glomuvenous malformations (GVMs), also known as glomangiomas, are uncommon entities with histological features of both glomus cells proliferation and venous malformation. A 14-year-old boy was admitted to our clinic with multiple dermal blue nodules, disseminated in different segments of the body. The patient's family history was positive for similar lesions; his mother and maternal grandmother had some asymptomatic blue nodules on their body. Histological examination showed a tumor composed of multiple caveronous vessels surrounded by glomus cells, positive for alpha smooth muscle actin, HHF35 (pan-actin), and h-caldesmon. This is a case of multiple GVMs, a rare disease caused by mutations in glomulin gene, with an autosomal dominant pattern of inheritance. The clinical and histopathological features are briefly discussed.

摘要

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