Biphasic Synovial Sarcoma in the Abdominal Cavity

iRadiology Pub Date : 2025-02-16 DOI:10.1002/ird3.118
Yubo Wang, Jiageng Li, Yang Fu, Bin Yang
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Abstract

A 63-year-old man was admitted to the hospital with a > 1-year history of repeated acid reflux and belching and a 1-month history of an abdominal mass. On admission, the patient was in good condition, and his vital signs were stable. Laboratory examinations revealed no significant abnormalities. Abdominal computed tomography (CT) revealed a soft tissue mass with uneven density, measuring approximately 13.3 cm × 9.0 cm and extending from the right abdomen into the pelvic cavity. Enhanced CT showed mild uneven enhancement of the mass during the arterial phase, with significant wall enhancement and visible septa. Significant enhancement of the solid components within the mass was observed during the venous and delayed phases with a CT value of approximately 50.3 HU, indicating “progressive enhancement.” Curved blood vessels were visible around the mass, and the surrounding structures were compressed and displaced (Figure 1). During the operation, a tumor measuring approximately 15 cm × 10 cm was observed in the lower right retroperitoneum. It was tightly adhered to the small intestine, ascending colon, and greater omentum, and showed invasive growth. No metastasis was found in the liver, gallbladder, or stomach during the surgical exploration. The pathological diagnosis was synovial sarcoma (SS) with extensive necrosis. Immunohistochemistry revealed epithelial–mesenchymal biphasic differentiation of the tumor cells.

SS is a rare malignant soft tissue tumor originating from primitive mesenchymal cells. It most commonly affects the limb joints, particularly those of the lower limbs. Cases of SS arising from the abdominal cavity, especially involving the ascending colon and small intestine, are rare and prone to preoperative misdiagnosis. This case exhibited unique imaging features, including significant arterial phase enhancement of the tumor wall, consistent with progressive enhancement. Magnetic resonance imaging further revealed characteristic signs, such as the “triple signal sign,” “liquid–liquid plane,” and “grape bowl sign,” which can help differentiate SS from other abdominal tumors.

Yubo Wang: writing–original draft (lead), resources (equal). Jiageng Li: writing–original draft (equal). Yang Fu: writing–original draft (equal). Bin Yang: resources (equal), writing–review and editing (lead).

The authors have nothing to report.

The patient provided written informed consent at the time of entering this study.

The authors declare no conflicts of interest.

Abstract Image

腹腔双相滑膜肉瘤
一名63岁的男子因心脏病入院。1年反复胃酸反流和打嗝史,1个月腹部肿块史。入院时,患者情况良好,生命体征稳定。实验室检查未见明显异常。腹部计算机断层扫描(CT)显示一软组织肿块,密度不均匀,大小约13.3 cm × 9.0 cm,从右腹部延伸至盆腔。增强CT显示动脉期肿块轻度不均匀强化,明显壁强化,可见间隔。在静脉期和延迟期观察到肿块内固体成分明显增强,CT值约为50.3 HU,表明“进行性增强”。肿块周围可见弯曲血管,周围结构受压移位(图1)。术中右下腹膜后见约15 cm × 10 cm的肿瘤。与小肠、升结肠、大网膜紧密粘连,呈侵袭性生长。手术探查期间未发现肝、胆囊或胃转移。病理诊断为滑膜肉瘤伴大面积坏死。免疫组化显示肿瘤细胞呈上皮-间质双期分化。SS是一种罕见的起源于原始间充质细胞的软组织恶性肿瘤。它最常影响肢体关节,特别是下肢关节。发生于腹腔的SS,尤其是累及升结肠和小肠的病例非常罕见,且术前容易误诊。该病例表现出独特的影像学特征,包括明显的动脉期肿瘤壁强化,与进行性强化一致。磁共振成像进一步显示特征性征象,如“三重信号征”、“液-液面征”、“葡萄碗征”,有助于区分SS与其他腹部肿瘤。王玉波:写作——原稿(主导),资源(对等)。李家庚:写作-原稿(相等)。杨复:原稿(相等)。杨斌:资源(平等),撰稿编辑(主导)。作者没有什么可报告的。患者在进入本研究时提供了书面知情同意书。作者声明无利益冲突。
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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