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多发性皮肤纤维组织细胞瘤伴系统性红斑狼疮。

Multiple cutaneous fibrous histiocytomas in association with systemic lupus erythematosus.

作者信息

Yamamoto Toshiyuki, Sumi Koji, Yokozeki Hiroo, Nishioka Kiyoshi

机构信息

Department of Dermatology, Tokyo Medical and Dental University, School of Medicine, Yushima, Tokyo, Japan.

出版信息

J Dermatol. 2005 Aug;32(8):645-9. doi: 10.1111/j.1346-8138.2005.tb00815.x.

Abstract

Cutaneous fibrous histiocytomas are usually regarded as superficial lesions and commonly known as dermatofibromas; however, unusual cases histologically showing fibrohistiocytic proliferation extending into the deeper dermis or subcutaneous tissues are occasionally experienced. Some authors propose this type as benign fibrous histiocytoma of the skin, distinct from dermatofibroma. We describe herein a case of systemic lupus erythematosus (SLE) who developed multiple nodules on the face, trunk and extremities. The nodule on the forehead did not present a typical clinical appearance of dermatofibroma, and histopathological examination showed fibrohistiocytic proliferation with a storiform pattern extending into the deep dermis and subcutaneous tissues. By contrast, histology of the nodule on the abdomen showed fibrohistiocytic proliferation confined to the dermis and compatible with dermatofibroma. Although multiple dermatofibromas are occasionally seen in patients with SLE, benign fibrous histiocytoma of the skin showing deeper invasion than dermatofibroma is rarely associated with SLE.

摘要

皮肤纤维组织细胞瘤通常被视为浅表病变,通常称为皮肤纤维瘤;然而,偶尔会遇到组织学上显示纤维组织细胞增生延伸至真皮深层或皮下组织的不寻常病例。一些作者将这种类型定义为皮肤良性纤维组织细胞瘤,与皮肤纤维瘤不同。我们在此描述一例系统性红斑狼疮(SLE)患者,其面部、躯干和四肢出现多个结节。前额的结节没有呈现出皮肤纤维瘤的典型临床表现,组织病理学检查显示纤维组织细胞增生呈漩涡状,延伸至真皮深层和皮下组织。相比之下,腹部结节的组织学显示纤维组织细胞增生局限于真皮,与皮肤纤维瘤相符。虽然SLE患者偶尔会出现多个皮肤纤维瘤,但显示比皮肤纤维瘤更深浸润的皮肤良性纤维组织细胞瘤很少与SLE相关。

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