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一位 68 岁女性因反复发作的腹痛就诊,盆腔磁共振成像诊断为骶前腹膜后良性 Schwann 瘤,类似于卵巢肿瘤。

A 68-Year-Old Woman Presenting with Recurrent Abdominal Pain and a Diagnosis of a Presacral Retroperitoneal Benign Schwannoma that Mimicked an Ovarian Tumor on Pelvic Magnetic Resonance Imagining.

机构信息

Department of General Surgery, Tondela-Viseu Hospital Center, Viseu, Portugal.

出版信息

Am J Case Rep. 2022 Jul 20;23:e935985. doi: 10.12659/AJCR.935985.

DOI:10.12659/AJCR.935985
PMID:35854634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9309983/
Abstract

BACKGROUND Schwannomas are benign tumors and their appearance in the pelvic region is rare and poses a major diagnostic problem. They can be sporadic or associated with genetical syndromes. They have a slow growth rate and may be asymptomatic for many years. Symptoms are usually nonspecific and due to compression of adjacent structures. Abdominal imaging modalities may not be able to differentiate a benign schwannoma from a malignant retroperitoneal tumor. This report is of a case of a 68-year-old woman presenting with recurrent abdominal pain and a diagnosis of a presacral retroperitoneal benign schwannoma that mimicked an ovarian tumor on pelvic magnetic resonance imaging. CASE REPORT The patient had a history of a femoral hernia repair and recurrent lower abdominal pain. Pelvic imaging raised the suspicion of a primary ovarian tumor. The mass appeared to have clear cleavage planes with the surrounding structures, so the patient was proposed for an exploratory laparotomy. Prior to the surgery, an additional pelvic computed tomography (CT) was performed (10 months after the first one), which did not show progression of the disease. The histological examination result was compatible with a benign retroperitoneal schwannoma and not an ovarian tumor. CONCLUSIONS This report highlights that the diagnosis of retroperitoneal and pelvic masses can be challenging. In women, a primary ovarian tumor should be excluded on imaging and the diagnosis of a benign tumor, such as schwannoma, must be confirmed by histopathology, either preoperatively or following tumor resection.

摘要

背景

神经鞘瘤是良性肿瘤,其在盆腔区域的出现较为罕见,且构成重大诊断难题。它们可以是散发性的,也可以与遗传综合征相关。它们生长缓慢,可能多年无症状。症状通常无特异性,是由于邻近结构受压所致。腹部影像学检查可能无法将良性神经鞘瘤与恶性腹膜后肿瘤区分开来。本报告介绍了一例 68 岁女性病例,其表现为复发性腹痛,并诊断为骶前腹膜后良性神经鞘瘤,在盆腔磁共振成像上类似于卵巢肿瘤。病例报告:患者有股疝修补术和复发性下腹痛病史。盆腔影像学检查提示原发性卵巢肿瘤。该肿块与周围结构似乎有明确的分离平面,因此建议行剖腹探查术。在手术前,进行了额外的盆腔计算机断层扫描(CT)检查(第一次检查后 10 个月),未显示疾病进展。组织学检查结果符合良性腹膜后神经鞘瘤,而非卵巢肿瘤。结论:本报告强调了腹膜后和盆腔肿块的诊断具有挑战性。在女性中,影像学检查应排除原发性卵巢肿瘤,良性肿瘤(如神经鞘瘤)的诊断必须通过组织病理学证实,无论是在术前还是在肿瘤切除术后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/ccff46fe3bc7/amjcaserep-23-e935985-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/cf91c541a269/amjcaserep-23-e935985-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/649d3003a24d/amjcaserep-23-e935985-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/779f09e3ede6/amjcaserep-23-e935985-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/ccff46fe3bc7/amjcaserep-23-e935985-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/cf91c541a269/amjcaserep-23-e935985-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/649d3003a24d/amjcaserep-23-e935985-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/779f09e3ede6/amjcaserep-23-e935985-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcc/9309983/ccff46fe3bc7/amjcaserep-23-e935985-g004.jpg

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