Long-standing retroperitoneal schwannoma in a 36-year-old female: A case report.

IF 0.6 Q4 SURGERY
Abhishek Kumar Shah, Sasmit Ghimire, Balkrishna Gyawali, Bishal Karki, Narayan Prasad Neupane
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引用次数: 0

Abstract

Introduction: Schwannomas are encapsulated nerve sheath tumors derived from Schwann cells, primarily found in the head, neck, and extremities. Retroperitoneal schwannomas are rare and typically asymptomatic.

Case presentation: A 36-year-old female presented with a long-standing, asymptomatic right lower abdominal mass. Imaging revealed a retroperitoneal cystic mass displacing adjacent structures. The tumor was surgically excised, and histopathology confirmed the diagnosis of schwannoma. The patient had an uneventful postoperative recovery and remains symptom-free with no signs of recurrence.

Discussion: Schwannomas are benign nerve tumors primarily affecting women aged 30 to 50. This case involved an asymptomatic retroperitoneal schwannoma displacing the inferior vena cava without neurological symptoms. Imaging methods like ultrasound and CT are useful but often lack definitive results, and preoperative biopsy is not recommended due to risks of vascular injury. While conservative management may be suitable for asymptomatic cases, complete surgical excision is crucial to prevent recurrence. Although some suggest partial excision, most literature supports curative resection with negative margins, as incomplete removal can lead to a 10-20 % recurrence rate. The patient underwent successful complete resection.

Conclusion: Retroperitoneal schwannomas are rare tumors that are difficult to diagnose preoperatively. Radiologic findings are usually nondiagnostic. The treatment of choice is complete surgical excision.

一名 36 岁女性的长期腹膜后分裂瘤:病例报告。
简介:许旺瘤是由许旺细胞衍生的包裹性神经鞘瘤,主要发生在头部、颈部和四肢。腹膜后的许旺瘤非常罕见,通常没有症状:一名 36 岁女性因长期无症状的右下腹肿块就诊。影像学检查发现腹膜后囊性肿块移位邻近结构。手术切除了肿瘤,组织病理学确诊为分裂瘤。患者术后恢复顺利,目前仍无症状,无复发迹象:讨论:裂间神经瘤是一种良性神经肿瘤,主要影响30至50岁的女性。本病例中,无症状的腹膜后神经分裂瘤使下腔静脉移位,但无神经症状。超声波和 CT 等影像学方法很有用,但往往缺乏明确的结果,而且由于存在血管损伤的风险,不建议进行术前活检。虽然保守治疗可能适合无症状的病例,但彻底的手术切除对于防止复发至关重要。尽管有人建议进行部分切除,但大多数文献都支持阴性边缘的根治性切除,因为不完全切除会导致10%-20%的复发率。该患者成功接受了完全切除术:结论:腹膜后分裂瘤是一种罕见的肿瘤,术前很难诊断。结论:腹膜后分裂瘤是一种罕见肿瘤,术前诊断困难,放射学检查结果通常无法确诊。治疗首选完全手术切除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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