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首页> 外文期刊>Auris, nasus, larynx >Atypical fibroxanthoma of the external ear in a cardiac transplant recipient: case report and the causal role of the immunosuppressive therapy.
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Atypical fibroxanthoma of the external ear in a cardiac transplant recipient: case report and the causal role of the immunosuppressive therapy.

机译:心脏移植受者中外耳的非典型纤维性黄瘤:病例报告和免疫抑制治疗的因果关系。

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摘要

Atypical fibroxanthoma (AF) is an unusual cutaneous fibrohistiocytic tumour that is most commonly found in ENT sun-exposed areas of elderly males. Cardiac transplant patients have an increased incidence of multiple cutaneous neoplasms, but the AF is uncommon. Although this neoplasm is benign, it may mimic spindle cell carcinoma, squamous cell carcinoma, melanoma and soft tissue sarcoma on histologic examination. Immunohistochemical stains for cytokeratin, alpha-1-antichymotrypsin, S100 protein and vimentin may be helpful in differential diagnosis. AF rarely recur or metastasize, if wide excision has been performed. We present a case of a cardiac transplant recipient who developed, after multiple cutaneous squamous tumours, an AF of external ear following the prolonged immunosuppressive treatment with cyclosporin.
机译:非典型纤维性黄瘤(AF)是一种不寻常的皮肤纤维组织细胞性肿瘤,最常见于老年男性的ENT暴露于阳光的区域。心脏移植患者多发皮肤肿瘤的发生率增加,但房颤并不常见。尽管这种肿瘤是良性的,但在组织学检查中可能模仿梭形细胞癌,鳞状细胞癌,黑色素瘤和软组织肉瘤。细胞角蛋白,α-1-抗胰凝乳蛋白酶,S100蛋白和波形蛋白的免疫组织化学染色可能有助于鉴别诊断。如果进行了广泛的切除,则房颤很少复发或转移。我们提出了一个心脏移植受者的案例,该接受者在经过多次皮肤鳞状肿瘤治疗后,用环孢菌素长时间免疫抑制治疗后,外耳出现房颤。

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