Galanis Ilias, Floros Georgios
Department of Surgery, Evangelismos General Hospital, Athens, GRC.
Cureus. 2022 Mar 18;14(3):e23296. doi: 10.7759/cureus.23296. eCollection 2022 Mar.
Adrenal schwannomas are extremely uncommon tumors. We report the case of a 39-year-old male with a right adrenal mass. Laboratory tests were normal and radiological exams revealed the adrenal tumor. Open surgical adrenalectomy was performed. The postoperative course was uneventful. Microscopy and immunohistochemistry revealed a cellular schwannoma. Adrenal schwannomas are rare tumors, very difficult to diagnose in preoperative evaluation. Surgical excision of the tumor, histological and immunohistochemical examination of the specimen provide a definitive diagnosis. Prognosis is generally very good. Recurrence rates are related to positive surgical margins.
肾上腺神经鞘瘤是极为罕见的肿瘤。我们报告一例39岁男性右肾上腺肿块病例。实验室检查正常，影像学检查发现肾上腺肿瘤。实施了开放性肾上腺切除术。术后病程顺利。显微镜检查和免疫组织化学检查显示为细胞型神经鞘瘤。肾上腺神经鞘瘤是罕见肿瘤，在术前评估中很难诊断。肿瘤的手术切除、标本的组织学和免疫组织化学检查可提供明确诊断。总体预后通常非常好。复发率与手术切缘阳性有关。
