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Intranodal Palisaded Myofibroblastoma; a Case Report and Review of the Literature

机译:内睑肌肌成纤维细胞瘤;病例报告及文献复习

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Intranodal palisaded myofibroblastoma (IPM) also called as intranodal hemorrhagic spindle cell tumor with amianthoid fibers is a distinctive and rare mesenchymal neoplasm of lymph nodes. This entity generally misdiagnosed as intranodal Kaposi’s sarcoma or schwannoma in past. In contrast to Kaposi’s sarcoma, it behaves in a benign fashion and does not need any further therapy except total surgical resection of the mass. This neoplasm has a great predilection for the inguinal region. The lesion presents typically as a unilateral, painless, solitary mass. To our knowledge, approximately 53 cases of IPM have been reported in the English-language literature. We present a 43-year-old-male patient with IPM and discuss histological, immunohistochemical features and pathogenesis of this rare benign neoplasm.
机译:内跨节律性肌纤维母细胞瘤(IPM)也被称为淋巴结性纺锤体细胞瘤,其具有阿米色类纤维是淋巴结的一种独特且罕见的间质肿瘤。该实体过去通常被误诊为结节内卡波氏肉瘤或神经鞘瘤。与卡波济氏肉瘤相反,它的表现为良性,除了全部手术切除肿块外,不需要其他任何治疗方法。这种肿瘤对腹股沟区有很大的偏爱。病变通常表现为单侧,无痛,孤立性肿块。据我们所知,英语文献中已经报告了约53例IPM病例。我们介绍了一名43岁的IPM男性患者,并讨论了这种罕见的良性肿瘤的组织学,免疫组化特征和发病机理。

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