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一名成年男性腹膜后神经鞘瘤的罕见病例。

A Rare Case of Retroperitoneal Schwannoma in an Adult Male.

作者信息

Ponirakos Marios, Kalfoutzou Areti, Vrysis Christos, Demetriou Nicole, Mylonakis Adam, Almpanis Zannis, Mostratou Eleni, Papadimitropoulos Konstantinos, Chrysikos Dimosthenis, Troupis Theodore

机构信息

Second Department of Surgery, 251 Hellenic Air Force General Hospital, Athens, Greece; Anatomy, NKUA/ Department of Anatomy, Athens, Greece.

Second Department of Internal Medicine, 251 Air Force General Hospital, Athens, Greece.

出版信息

Acta Med Acad. 2024 Aug;53(2):193-198. doi: 10.5644/ama2006-124.447.

Abstract

OBJECTIVE

This study aims to illustrate a rare case of retroperitoneal schwannoma by presenting the clinical, imaging, and histological parameters.

CASE REPORT

A 36-year-old patient visited the outpatient clinic because of back pain experienced over the previous two months. There were no complaints regarding the nervous system or urinary system. Thorough imaging evaluation, including magnetic resonance for the lumbar spine, abdominal computed tomography, and positron emission tomography was conducted. An encapsulated mass was found in the retroperitoneal area, positioned in front of the O4 vertebra and in close proximity to the left psoas muscle, the left common iliac artery, and the left ureter. The lesion exhibited FDG radioisotope uptake, and a CT-guided biopsy confirmed a benign peripheral nerve tumor. The patient underwent laparotomy surgery, where the tumor was removed. The histological investigation, along with immunohistochemistry, confirmed the presence of a retroperitoneal schwannoma.

CONCLUSION

Schwannoma is a rare type of retroperitoneal tumor, with nonspecific clinical and radiological characteristics that make diagnosis difficult. Surgical resection is the primary treatment for symptomatic patients, with a favorable prognosis. Long-term follow-up is advised to reduce the chance of late recurrence.

摘要

目的

本研究旨在通过展示临床、影像学和组织学参数来说明一例罕见的腹膜后神经鞘瘤病例。

病例报告

一名36岁患者因前两个月出现的背痛前往门诊就诊。无关于神经系统或泌尿系统的主诉。进行了全面的影像学评估,包括腰椎磁共振成像、腹部计算机断层扫描和正电子发射断层扫描。在腹膜后区域发现一个包膜完整的肿块,位于腰4椎体前方,紧邻左腰大肌、左髂总动脉和左输尿管。该病变表现出氟代脱氧葡萄糖(FDG)放射性同位素摄取,CT引导下活检证实为良性周围神经肿瘤。患者接受了剖腹手术,肿瘤被切除。组织学检查及免疫组化证实为腹膜后神经鞘瘤。

结论

神经鞘瘤是一种罕见的腹膜后肿瘤,具有非特异性的临床和放射学特征,诊断困难。手术切除是有症状患者的主要治疗方法,预后良好。建议进行长期随访以降低晚期复发的几率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0ff/11626244/542357393aac/AMA-53-193-g001.jpg

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