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一例罕见的无症状腹膜后及大腿股神经鞘瘤。

A rare case of asymptomatic retroperitoneal and thigh femoral nerve schwannoma.

作者信息

Novoselac Jurjana, Simetić Luka, Jemendžić Damir, Mužinić Darija, Jurca Ivana

机构信息

Department for Transfusion Medicine and Transplantation Biology, Clinical Hospital Centre Zagreb, Croatia.

Department for Oncology, Clinical Hospital Centre Zagreb, Croatia.

出版信息

Radiol Case Rep. 2025 Jan 20;20(4):1915-1919. doi: 10.1016/j.radcr.2025.01.024. eCollection 2025 Apr.

Abstract

We present a rare case of an asymptomatic extensive tumor in the retroperitoneum and thigh, which has not been published in the scientific literature so far. During the preventive examination, in an otherwise healthy 29-years old man, a tumor mass in the lower left abdominal quadrant was observed on ultrasound. A computed tomography scan and magnetic resonance imaging revealed a large, lobulated, multiseptated retroperitoneal mass stretching from the level of the lower left kidney pole to the distal third of the left thigh. Positron emission tomography/ computed tomography showed weak metabolically active mass with low probability of malignancy, and radiological differential diagnosis included lymphangioma, less likely lymphoma and as least likely sarcoma. Due to the assumed liquid content of the tumor, no preoperative biopsy was performed. A demanding and long-lasting operation was performed on Department of abdominal surgery at Clinical Hospital Merkur. The tumor was removed completely along with most part of the femoral nerve. Pathohistological analysis showed a benign tumor of the nerve sheath- schwannoma A novel aspect in the presentation of this clinical entity is the extensiveness of the neoplasm to multiple regions without symptoms. According to the available literature, only 2 similar case reports are described, which were symptomatic.

摘要

我们报告一例罕见的无症状性腹膜后及大腿广泛肿瘤病例,该病例迄今尚未在科学文献中发表。在预防性检查中,超声发现一名29岁身体健康男性左下腹部象限有一肿瘤肿块。计算机断层扫描和磁共振成像显示,一个大的、分叶状、多分隔的腹膜后肿块,从左肾下极水平延伸至左大腿远侧三分之一处。正电子发射断层扫描/计算机断层扫描显示代谢活性较弱的肿块,恶性可能性较低,放射学鉴别诊断包括淋巴管瘤,淋巴瘤可能性较小,肉瘤可能性最小。由于假定肿瘤为液体成分,未进行术前活检。在梅尔库尔临床医院腹部外科进行了一场要求高且耗时久的手术。肿瘤连同大部分股神经被完整切除。病理组织学分析显示为神经鞘良性肿瘤——施万细胞瘤。该临床实体表现的一个新特点是肿瘤广泛累及多个区域却无症状。根据现有文献,仅描述了2例类似的有症状病例报告。

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