摘要
We report a patient with generalized recessive dystrophic epidermolysis bullosa (RDEB) who developed 3 squamous cell carcinomas. The tumours appeared simultaneously at acral sites on both upper limbs and were poorly differentiated. Despite surgery and radiotherapy the patient died from metastatic disease within 6 months of presentation. This case highlights many of the typical features of this complication of RDEB, including the overall poor prognosis. Of particular interest was the histology of one of the tumours which caused diagnostic difficulties: haematoxylin and eosin staining suggested an angiosarcomatous pathology, but the use of immunocytochemistry proved that the tumour was a squamous cell carcinoma in origin.
| 原文 | English |
|---|---|
| 頁(從 - 到) | 235-238 |
| 頁數 | 4 |
| 期刊 | Dermatology |
| 卷 | 182 |
| 發行號 | 4 |
| DOIs | |
| 出版狀態 | Published - 1991 |
UN SDG
此研究成果有助於以下永續發展目標
-
SDG 3 良好的健康和福祉
All Science Journal Classification (ASJC) codes
- 皮膚科
指紋
深入研究「Metastatic squamous cell carcinoma resembling angiosarcoma complicating dystrophic epidermolysis bullosa」主題。共同形成了獨特的指紋。引用此
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