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肾脏炎性恶性纤维组织细胞瘤:一例报告

Inflammatory malignant fibrous histiocytoma of kidney: a case report.

作者信息

Ghosh Amrita, Dwivedi U S, Kumar Abhay

机构信息

Department of Pathology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.

出版信息

Pathol Res Pract. 2008;204(11):857-61. doi: 10.1016/j.prp.2008.03.012. Epub 2008 Aug 3.

Abstract

Among the renal sarcomas, inflammatory malignant fibrous histiocytoma (MFH) is an extremely rare presentation. A 45-year-old woman presented with acute retention urine following an episode of gross hematuria. Computerized tomography showed a solid mass at the lower pole of the left kidney. The patient underwent left nephrectomy. Histologically and immunohistochemically, the tumor was diagnosed as an inflammatory subtype of MFH. Histological appearances of inflammatory MFH vary widely and frequently overlap with benign reactive conditions such as Xanthogranulomatous pyelonephritis (XGPN) and malignant lesions, e.g. malignant lymphoma and, less frequently, a sarcomatoid variant of renal cell carcinoma. It is important, though difficult, to differentiate inflammatory MFH from these lesions. Careful morphological examination and immunohistochemical findings of the lesion are of great value, in particular in excluding it from its mimics. We discuss the pathological features and challenges involved in differentiating inflammatory MFH from its masquerader.

摘要

在肾肉瘤中,炎性恶性纤维组织细胞瘤(MFH)是一种极其罕见的表现形式。一名45岁女性在一次肉眼血尿发作后出现急性尿潴留。计算机断层扫描显示左肾下极有一个实性肿块。该患者接受了左肾切除术。经组织学和免疫组织化学检查,肿瘤被诊断为MFH的炎性亚型。炎性MFH的组织学表现差异很大,且常与良性反应性疾病如黄色肉芽肿性肾盂肾炎(XGPN)以及恶性病变(如恶性淋巴瘤,较少见的是肾细胞癌的肉瘤样变体)重叠。将炎性MFH与这些病变区分开来虽然困难,但很重要。仔细的形态学检查和病变的免疫组织化学结果具有重要价值,特别是在将其与模仿病变区分开来方面。我们讨论了区分炎性MFH与其伪装病变所涉及的病理特征和挑战。

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