巨大腹膜后滑膜肉瘤的 CT 和 MR 成像：病例报告

Q4 Medicine

Radiology Case Reports Pub Date : 2024-10-23 DOI:10.1016/j.radcr.2024.09.151

Adam Sqalli Houssaini MD, Rachida Saouab PhD, Sara Essetti MD, Hassan En-nouali PhD, Jamal El Fenni PhD, Meriem Boui MD

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引用次数: 0

摘要

腹膜后滑膜肉瘤极为罕见，文献中仅有几例报道。由于解剖学上的考虑，诊断往往较晚，常见症状包括腰背痛和体重减轻。影像学检查对诊断至关重要，通常会发现带有 "三联征 "和钙化的异质肿块。主要的鉴别诊断包括脂肪肉瘤、未分化多形性肉瘤和亮肌肉瘤。手术切除仍是首选治疗方法，但并非总是可行，这也是导致预后不良的原因之一。本病例是一名 29 岁男子的腹膜后滑膜肉瘤，超声波、计算机断层扫描和磁共振成像均有发现。

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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CT and MR imaging of a huge retroperitoneal synovial sarcoma: A case report

Retroperitoneal synovial sarcoma is extremely rare, with only a few cases reported in the literature. The diagnosis is often made late, due to anatomical considerations, with common symptoms including low back pain and weight loss. Imaging is critical for diagnosis, often revealing a heterogenous mass with the “triple sign” and calcifications. The main differential diagnoses include liposarcoma, undifferentiated pleomorphic sarcoma and leiomyosarcoma. Surgical resection remains the treatment of choice, though it is not always feasible, which contributes to the poor prognosis. The presented case is a retroperitoneal synovial sarcoma in a 29 years old man with findings from ultrasound, computed tomography and magnetic resonance imaging.

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来源期刊

Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging

CiteScore

1.10

自引率

0.00%

发文量

1074

审稿时长

30 days

期刊介绍： The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.