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患有纤维肉瘤和消耗性凝血病的新生儿。

Neonate with a fibrosarcoma and consumptive coagulopathy.

作者信息

Asgari Maryam, Rubin Brian P, Hornung Robin L

机构信息

Division of Dermatology, Department of Pediatrics, University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, USA.

出版信息

J Am Acad Dermatol. 2004 Feb;50(2 Suppl):S23-5. doi: 10.1016/s0190-9622(03)01486-5.

Abstract

We report a case of a neonate with a congenital tumor on the left palm. The patient had a grapefruit-sized tumor and coagulopathy at birth and was presumed to have a hemangioendothelioma with associated Kasabach-Merritt phenomenon. When the tumor failed to respond to systemic steroids, a biopsy specimen was taken, revealing a fibrosarcoma. We describe this case to highlight the importance of including rare tumors, such as fibrosarcomas, in the clinical differential when evaluating a congenital tumor with associated coagulopathy. We discuss subtle differences in clinical presentations that might aid in differentiating vascular tumors from fibrosarcomas.

摘要

我们报告一例左掌先天性肿瘤的新生儿病例。该患者出生时患有柚子大小的肿瘤及凝血功能障碍,推测患有伴有卡萨巴赫-梅里特现象的血管内皮瘤。当肿瘤对全身类固醇治疗无反应时,取活检标本,结果显示为纤维肉瘤。我们描述此病例以强调在评估伴有凝血功能障碍的先天性肿瘤时,将罕见肿瘤(如纤维肉瘤)纳入临床鉴别诊断的重要性。我们讨论了可能有助于区分血管肿瘤和纤维肉瘤的临床表现细微差异。

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