孤立性胃纤维性肿瘤:诊断缺陷和临床意义。

IF 0.7 Q4 SURGERY
Surgical Case Reports Pub Date : 2025-01-01 Epub Date: 2025-09-04 DOI:10.70352/scrj.cr.25-0314
Tadakazu Ao, Eiji Shinto, Tenma Ichisawa, Koki Ichio, Takafumi Suzuki, Shohei Mori, Hiroki Abe, Tomomi Koiwai, Makoto Nishikawa, Kiyoshi Nishiyama, Kimi Kato, Hiroaki Takeo
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引用次数: 0

摘要

孤立性纤维性肿瘤(SFT)是一种罕见的间质肿瘤,最常起源于胸膜,但也可发生在胸膜外部位,包括腹腔。其中,原发性胃SFT极为罕见。由于重叠的临床、内镜和放射学特征,区分SFT和胃肠道间质瘤(GIST)尤其具有挑战性。误诊可能导致不适当的治疗,如不必要的伊马替尼的管理。因此,准确的术前鉴别对于适当的治疗至关重要。病例介绍:一名74岁男性在例行健康检查时偶然发现胃粘膜下肿瘤,转介至我院接受进一步评估和治疗。上消化道内窥镜显示胃底大弯曲处一30毫米上皮下病变。超声内镜引导下的细针穿刺(EUS-FNA)显示分离和聚集的细胞,细胞核呈卵形至纺锤形。虽然不确定,但内镜和细胞学检查的结果使术前诊断为疑似GIST,随后进行腹腔镜和内镜联合手术(LECS)进行局部切除。切除标本的组织病理学检查显示纺锤形细胞不规则增殖,信号传导和转录激活因子6 (STAT6)核免疫阳性,最终诊断为胃SFT。根据Demicco风险分层模型,将肿瘤归为低危。患者通过LECS进行了完全切除,术后超过2.5年没有复发。结论:该病例强调了术前区分SFT和GIST的困难,并强调了获得足够的组织样本以进行免疫组织化学分析的重要性,特别是STAT6染色。认识到胃SFT作为鉴别诊断的一部分是避免误诊和确保适当的治疗决策的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Solitary Fibrous Tumor of the Stomach: Diagnostic Pitfalls and Clinical Implications.

Introduction: Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm that most commonly originates in the pleura but can also occur at extrapleural sites, including the abdominal cavity. Among these, primary SFT of the stomach is exceptionally rare. Due to overlapping clinical, endoscopic, and radiologic characteristics, distinguishing SFT from gastrointestinal stromal tumor (GIST) can be particularly challenging. Misdiagnosis may result in inappropriate treatment, such as unnecessary administration of imatinib. Therefore, accurate preoperative differentiation is essential for appropriate management.

Case presentation: A 74-year-old man was incidentally found to have a submucosal gastric tumor during a routine health checkup and was referred to our hospital for further evaluation and treatment. Upper gastrointestinal endoscopy revealed a 30-mm subepithelial lesion on the greater curvature of the gastric fundus. Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) demonstrated isolated and clustered cells with ovoid to spindle-shaped nuclei. Although not definitive, the combined endoscopic and cytological findings led to a preoperative diagnosis of suspected GIST, and laparoscopy and endoscopy cooperative surgery (LECS) was subsequently performed for local resection. Histopathological examination of the resected specimen revealed an irregular proliferation of spindle cells and nuclear immunopositivity for signal transducer and activator of transcription 6 (STAT6), leading to a final diagnosis of SFT of the stomach. According to Demicco's risk stratification model, the tumor was classified as low risk. The patient underwent complete resection via LECS and has remained free of recurrence for more than 2.5 years postoperatively.

Conclusions: This case highlights the difficulty in differentiating SFT from GIST preoperatively and underscores the importance of obtaining sufficient tissue samples to allow for immunohistochemical analysis, particularly STAT6 staining. Recognizing gastric SFT as part of the differential diagnosis is critical to avoid misdiagnosis and ensure appropriate therapeutic decision-making.

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