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首页> 外文期刊>International Journal of Health Sciences >Inflammatory Myofibroblastic Tumor Arising in the External Ear: Unexpected Location (Case Report and Review of Literature)
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Inflammatory Myofibroblastic Tumor Arising in the External Ear: Unexpected Location (Case Report and Review of Literature)

机译:外耳出现炎症性肌纤维母细胞瘤:位置异常(病例报告和文献复习)

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We present an unexpected extremely rare case of an inflammatory myofibroblastic tumor (IMT) of the external ear. A 3-year-old boy presented with a mass arising on the posterior aspect of the left ear lobule and extending to the external auditory canal. This mass grew slowly and showed no skin changes. Radiologically, it was diagnosed as a vascular tumor. Surgical excision and primary closure was performed for the patient. Histopathologic examination demonstrated a circumscribed noncapsulated mass formed by a proliferation of spindle cells in deep dermis and subcutaneous tissue. The spindle cells were mixedwith lymphoplasmacytic infiltration compatible with the IMT. Because it is very rare to arise in this location, we present this case as a case report with details histopathological examinationand reviewed the English literature for similar cases.
机译:我们提出了外耳炎性肌纤维母细胞瘤(IMT)的意外的极其罕见的情况。一个3岁男孩,左耳小叶后侧出现肿块,并延伸到外耳道。该肿块生长缓慢,没有皮肤变化。在放射学上,它被诊断为血管肿瘤。对患者进行手术切除和一次闭合。组织病理学检查显示由深层真皮和皮下组织中梭形细胞的增殖形成的边界未包囊肿块。将梭形细胞与与IMT相容的淋巴浆细胞浸润混合。由于在此地点很少发生这种情况,因此我们将本病例作为病例报告进行详细的组织病理学检查,并回顾了类似病例的英语文献。

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