| Literature DB >> 17584327 |
Mehmet Salih Gurel1, Mehmet Kamil Mulayim, Ilyas Ozardali, Muharrem Bitiren.
Abstract
Two siblings presented with clinical and histopathological findings of familial cutaneous collagenoma which is a rare connective tissue nevus, inherited in an autosomal-dominant pattern. A 13-year-old girl had oval-round, soft, painless papules, 5-10 mm in size and a total of 9-10 on her abdomen and flanks. Skin biopsy demonstrated dense, coarse collagen fibers in the dermis and a decrease in elastic fibers. Doppler echocardiography indicated an atrioseptal defect of the secundum type. Her 9-year-old brother was also examined; four lesions were discovered on his back but he was otherwise normal. Our cases comprise the sixth affected family to be reported in the medical published work and all lesions had appeared prepubertally.Entities:
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Year: 2007 PMID: 17584327 DOI: 10.1111/j.1346-8138.2007.00314.x
Source DB: PubMed Journal: J Dermatol ISSN: 0385-2407 Impact factor: 4.005