肘部丛状纤维组织细胞瘤:罕见病例报告

S. Usman, Avadh Vihari Lal Sharma, Veena Maheshwari, Murad Ahmad, Zeeshan Nahid
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引用次数: 0

摘要

丛状纤维组织细胞瘤是一种非常罕见的软组织肿瘤,多发于青少年和儿童。在组织病理学检查中,它表现为多个小结节或束状体,呈丛状排列,因此得名。在此,我们将介绍一例双侧肘部发生 PFT 的病例。患者的肿物逐渐增大且无痛,已有 7 年之久。手术切除后,根据组织病理学和免疫组化检查确诊为 PFT。
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Plexiform fibrohistiocytic tumor of elbow: A rare case report
Plexiform fibrohistiocytic tumor is a very rare tumor of soft tissue that affects usually adolescents and children. On histopathological examination it shows multiple small nodules or fascicles that are arranged in plexiform pattern, hence its name. Here we are presenting a case of occurrence of PFT in bilateral elbows. Patient presented with gradually increasing in size and painless swellings for 7 years. Excision was done and on the basis of histopathological and immunohistochemical examination diagnosis of PFT was reached.
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