Gastric inflammatory myofibroblastic tumor: a case report

被引:3
作者
Hattori, Taku [1 ]
Tanizawa, Yutaka [1 ]
Shimoda, Tadakazu [2 ]
Koseki, Yusuke [1 ]
Furukawa, Kenichiro [1 ]
Fujiya, Keiichi [1 ]
Aizawa, Daisuke [2 ]
Sugino, Takashi [2 ]
Terashima, Masanori [1 ]
Bando, Etsuro [1 ]
机构
[1] Shizuoka Canc Ctr, Div Gastr Surg, 1007 Shimonagakubo, Nagaizumi, Shizuoka 4118777, Japan
[2] Shizuoka Canc Ctr, Div Pathol, 1007 Shimonagakubo, Nagaizumi, Shizuoka 4118777, Japan
关键词
Inflammatory myofibroblastic tumor; Stomach; Submucosal tumor; Gastric tumor; GASTROINTESTINAL STROMAL TUMORS; ALK EXPRESSION; ADULT WOMAN; RARE CAUSE; STOMACH; PSEUDOTUMOR; PROLIFERATION; FEVER;
D O I
10.1186/s40792-024-01844-7
中图分类号
R61 [外科手术学];
学科分类号
摘要
BackgroundInflammatory myofibroblastic tumor (IMT) of the stomach is an uncommon mesenchymal neoplasm. We present a case of gastric submucosal tumor (SMT) where the final diagnosis was IMT.Case presentationA 69-year-old man presented with a 24-mm SMT on the posterior wall of the middle third of the stomach that was detected by screening upper gastrointestinal endoscopy. Abdominal contrast-enhanced computed tomography showed that the tumor was well-enhanced. Although endoscopic ultrasonography-guided biopsy was performed, the histological diagnosis was not confirmed preoperatively. Since the tumor was clinically suspected to be a gastrointestinal stromal tumor, we performed gastric wedge resection by laparoscopic-endoscopic cooperative surgery. Pathologically, proliferative spindle cells with a positive reaction for smooth muscle actin, negativity for c-kit, desmin, s-100, CD34, STAT-6, beta-catenin and anaplastic lymphoma kinase 1 were identified. Hence, the tumor was finally diagnosed as an IMT originating from the stomach.ConclusionsWhen an SMT of the stomach is identified, the possibility of gastric IMT should be considered.
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页数:8
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