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原发性皮肤恶性纤维组织细胞瘤:一例报告。

Primary cutaneous malignant fibrous histiocytoma: a case report.

作者信息

Bose Ashitha C, Kate Vikram, Ananthakrishnan Nilakantan, Srinivasan Sowmya

机构信息

Department of Surgery and Pathology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.

出版信息

Med Sci Monit. 2006 Jul;12(7):CS61-3. Epub 2006 Jun 28.

Abstract

BACKGROUND

Malignant fibrous histiocytoma (MFH) is one of the commonest soft tissue sarcomas to occur in the extremities, but presentation as a primary cutaneous lesion is rare. MFH can present as a cutaneous lesion in the form of a primary tumor or as metastasis from MFH at other sites, such as primary MFH of the breast; however, both presentations are very rare.

CASE REPORT

We report here a 55-year-old male patient with cutaneous MFH on the right thigh region. The patient presented with two swellings on the outer aspect of the thigh of three months' duration, which ulcerated following the first month. The swellings were non-tender, soft, compressible, and not fixed to underlying structures. Histopathologic examination of the excised tumor revealed highly pleomorphic spindle-shaped cells arranged in sheets and irregular fascicles with a focal storiform pattern. Many thin-walled blood vessels and focal inflammatory cell infiltration with occasional focus of myxoid change was seen. Storiform-pleomorphic type of MFH grade II was diagnosed. Wide local excision was done. The patient made an uneventful recovery.

CONCLUSIONS

Although MFH is one of the commonest soft tissue sarcomas, cutaneous presentation is very rare. A high index of suspicion is necessary to keep this possibility in mind, as it can present in different forms, including the pedunculated types, which can be compressible. MFH variants such as atypical fibrous histiocytoma or atypical fibroxanthoma can occur sometimes as cutaneous MFH. Wide local excision is commonly possible in most of the cases for therapy.

摘要

背景

恶性纤维组织细胞瘤(MFH)是最常见于四肢的软组织肉瘤之一,但表现为原发性皮肤病变的情况罕见。MFH可表现为原发性肿瘤形式的皮肤病变,或作为MFH在其他部位转移而来的病变,如乳腺原发性MFH;然而,这两种表现形式都非常罕见。

病例报告

我们在此报告一名55岁男性患者,其右大腿区域患有皮肤MFH。患者大腿外侧出现两个肿物,持续三个月,第一个月后出现溃疡。肿物无压痛,质地柔软,可压缩,未与下方结构固定。对切除肿瘤的组织病理学检查显示,高度多形性的梭形细胞呈片状和不规则束状排列,具有局灶性车轮状结构。可见许多薄壁血管和局灶性炎性细胞浸润,偶尔有黏液样变区域。诊断为II级车轮状-多形性MFH。进行了广泛局部切除。患者恢复顺利。

结论

尽管MFH是最常见的软组织肉瘤之一,但皮肤表现非常罕见。必须保持高度怀疑指数,以牢记这种可能性,因为它可以以不同形式出现,包括带蒂类型,后者可压缩。MFH的变异型,如非典型纤维组织细胞瘤或非典型纤维黄色瘤,有时可能以皮肤MFH的形式出现。在大多数病例中,广泛局部切除通常可作为治疗方法。

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