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血管样恶性纤维组织细胞瘤:1例临床病程高度侵袭性的罕见病例报告。

Angiomatoid malignant fibrous histiocytoma: report of an unusual case with highly aggressive clinical course.

作者信息

Chow L T, Allen P W, Kumta S M, Griffith J, Li C K, Leung P C

机构信息

Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, Hong Kong.

出版信息

J Foot Ankle Surg. 1998 May-Jun;37(3):235-8. doi: 10.1016/s1067-2516(98)80117-8.

Abstract

The authors report a case of angiomatoid malignant fibrous histiocytoma (AMFH), affecting a 9-year-old girl, with a highly aggressive clinical course. The tumor, noticed by the patient as a painless nodule in the dorsum of her left foot for 12 months, recurred 8 months after initial excision, and despite wide local reexcision, metastasized 4 months later to the liver and lung, where it grew at an alarming rate, to the extent of occupying the entire left hemithorax in a period of 10 weeks and killed the patient 14 months after initial excision. Review of the literature showed that the culminated rates of recurrence, metastasis, and mortality for AMFH were 23.2%, 8.7%, and 4.3%, respectively, indicating that it is definitely a malignant neoplasm with a potentially fatal outcome.

摘要

作者报告了一例血管样恶性纤维组织细胞瘤(AMFH),患者为一名9岁女孩,临床病程极具侵袭性。该肿瘤最初被患者发现为左脚背一个无痛性结节,持续12个月。初次切除8个月后复发,尽管进行了广泛的局部再次切除,但4个月后转移至肝脏和肺部,在那里肿瘤以惊人的速度生长,在10周内占据了整个左半胸,并在初次切除14个月后导致患者死亡。文献回顾显示,AMFH的复发率、转移率和死亡率分别为23.2%、8.7%和4.3%,表明它绝对是一种具有潜在致命后果的恶性肿瘤。

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