Wilson–Jones头皮血管肉瘤伴脱发和胸部水肿一例报告

IF 0.3 Q4 DERMATOLOGY

Journal of the Egyptian Women's Dermatologic Society Pub Date : 2022-01-01 DOI:10.4103/jewd.jewd_46_21

G. El Enany, N. Nagui, H. Nada, M. Fawzy, Iman Sany, S. Shalaby, Omar El Ghanam

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引用次数: 0

摘要

Wilson–Jones血管肉瘤是皮肤血管肉瘤之一，是一种罕见的侵袭性皮肤血管肿瘤。在本病例报告中，我们介绍了一名72岁的女性，她出现了持续2年的多发性面部水肿，并伴有头皮部分脱发。包括皮肤活检在内的调查诊断为头皮血管肉瘤。

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Wilson–Jones angiosarcoma of the scalp associated with alopecia and chest edema: a case report

Wilson–Jones angiosarcoma is one of cutaneous angiosarcomas, which is a rare aggressive tumor of blood vessels of the skin. In this case report, we present a 72-year-old female who developed multiple episodes of facial edema of 2-year duration along with partial hair loss of the scalp. Investigations, including a skin biopsy, were diagnostic of scalp angiosarcoma.

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来源期刊

Journal of the Egyptian Women's Dermatologic Society Medicine-Dermatology

CiteScore

0.50

自引率

0.00%

发文量

审稿时长

17 weeks

期刊介绍： The Journal of The Egyptian Women''s Dermatologic Society (JEWDS) was founded by Professor Zenab M.G. El-Gothamy. JEWDS is published three times per year in January, May and September. Original articles, case reports, correspondence and review articles submitted for publication must be original and must not have been published previously or considered for publication elsewhere. Their subject should pertain to dermatology or a related scientific and technical subject within the field of dermatology.