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黏液样恶性纤维组织细胞瘤酷似丘疹性黏蛋白病。

Myxoid malignant fibrous histiocytoma mimicking papular mucinosis.

作者信息

Stephen M R, Morton R

机构信息

Department of Pathology, Western Infirmary, Glasgow, Scotland, UK.

出版信息

Am J Dermatopathol. 1998 Jun;20(3):290-5. doi: 10.1097/00000372-199806000-00013.

Abstract

Malignant fibrous histiocytoma is the most common type of soft tissue sarcoma in late adulthood. The myxoid variant of malignant fibrous histiocytoma, also known as myxofibrosarcoma, can develop in subcutaneous rather than deep soft tissue, and the true extent of these superficial tumors is often underestimated. Patients with these low-grade myxoid malignant fibrous histiocytomas have an excellent 5-year survival rate, and it is therefore important to recognize them. We present a case with a superficial cutaneous accumulation of mucin that was diagnosed clinically and histologically as papular mucinosis. In retrospect, a subcutaneous presentation of myxofibrosarcoma should have been considered.

摘要

恶性纤维组织细胞瘤是成年晚期最常见的软组织肉瘤类型。恶性纤维组织细胞瘤的黏液样变型,也称为黏液纤维肉瘤,可发生于皮下而非深部软组织,这些浅表肿瘤的实际范围常常被低估。患有这些低级别黏液样恶性纤维组织细胞瘤的患者5年生存率很高,因此识别它们很重要。我们报告一例临床上和组织学上诊断为丘疹性黏蛋白沉积症的皮肤浅表黏液积聚病例。回顾来看,本应考虑黏液纤维肉瘤的皮下表现。

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引用本文的文献

1
Myxofibrosarcoma: a diagnostic pitfall.黏液纤维肉瘤:一个诊断陷阱。
Rare Tumors. 2013 May 31;5(2):60-1. doi: 10.4081/rt.2013.e15. Print 2013 Apr 15.

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