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表现为胰头肿块的十二指肠胃肠道间质瘤——病例报告

Duodenal gastrointestinal stromal tumor presenting as pancreatic head mass - a case report.

作者信息

Vasile DănuŢ, Iancu George, Iancu Raluca Claudia, Simion George, Ciuluvică Radu Constantin

机构信息

Department of Obstetrics and Gynecology, "Carol Davila" University of Medicine and Pharmacy, "Filantropia" Clinical Hospital, Bucharest, Romania;

出版信息

Rom J Morphol Embryol. 2017;58(1):255-259.

PMID:28523328
Abstract

Duodenal gastrointestinal stromal tumors (GISTs) are uncommon. Tumors arising from the first and the second part of the duodenum (DI and DII, respectively) can be wrongly diagnosed as pancreatic mass. We present a case of a 59-year-old woman who came with abdominal pain and severe upper gastrointestinal bleeding (hemoglobin 3.5 g÷dL). A solid, heterogeneously enhancing neoplasm in the head of the pancreas was revealed preoperatively by an abdominal computed tomography scan. A diagnosis of GIST was suggested. On exploratory laparotomy, there was a large mass which appeared to be originating from duodenum or from head of pancreas. Intraoperative histopathological diagnosis was GIST. Histopathology showed spindle cell tumor with cytoplasmic eosinophilia and foci of necrosis. The mitotic count was less than 5÷50 high power fields (HPFs). Tumor was involving duodenal muscularis propria, with no infiltration in the duodenal epithelial layer and the pancreas. Immunohistochemical study revealed positive staining for CD117. The tumor was finally diagnosed as GIST arising from the duodenal wall, growing exophytically and attached to the common bile duct and pancreas, without infiltrating the pancreas. Duodenal gastrointestinal stromal tumors can grow exophytically into a large mass and involve the pancreas without infiltrating microscopically and present as pancreatic head mass.

摘要

十二指肠胃肠道间质瘤(GISTs)并不常见。起源于十二指肠第一部分和第二部分(分别为D1和D2)的肿瘤可能会被误诊为胰腺肿块。我们报告一例59岁女性患者,因腹痛和严重上消化道出血(血红蛋白3.5 g÷dL)前来就诊。术前腹部计算机断层扫描显示胰腺头部有一个实性、不均匀强化的肿瘤。提示诊断为GIST。在剖腹探查术中,发现一个大肿块,似乎起源于十二指肠或胰腺头部。术中组织病理学诊断为GIST。组织病理学显示为梭形细胞瘤,胞质嗜酸性,有坏死灶。有丝分裂计数小于5÷50个高倍视野(HPFs)。肿瘤累及十二指肠固有肌层,未浸润十二指肠上皮层和胰腺。免疫组织化学研究显示CD117染色阳性。该肿瘤最终被诊断为起源于十二指肠壁的GIST,呈外生性生长,附着于胆总管和胰腺,未浸润胰腺。十二指肠胃肠道间质瘤可呈外生性生长形成大肿块,并累及胰腺,但无微观浸润,表现为胰腺头部肿块。

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引用本文的文献

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A duodenal gastrointestinal stromal tumor mimicking a pancreatic neuroendocrine tumor: a case report.十二指肠胃肠道间质瘤酷似胰腺神经内分泌肿瘤:一例报告。
J Med Case Rep. 2022 Aug 16;16(1):308. doi: 10.1186/s13256-022-03468-7.
2
Duodenal gastrointestinal stromal tumour imitating as pancreatic head tumour.十二指肠胃肠道间质瘤,类似胰头肿瘤。
BMJ Case Rep. 2022 Mar 1;15(3):e248828. doi: 10.1136/bcr-2022-248828.
3
Duodenal Teratoma: A Rare Diagnostic and Therapeutic Challenge.十二指肠畸胎瘤:一项罕见的诊断与治疗挑战。
J Indian Assoc Pediatr Surg. 2019 Oct-Dec;24(4):313-314. doi: 10.4103/jiaps.JIAPS_226_18.
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Duodenal gastrointestinal stromal tumors appear similar to pancreatic neuroendocrine tumors: A case report.十二指肠胃肠道间质瘤表现类似胰腺神经内分泌肿瘤:一例报告。
Int J Surg Case Rep. 2018;53:358-361. doi: 10.1016/j.ijscr.2018.11.011. Epub 2018 Nov 15.
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Surgical treatment of gastrointestinal stromal tumors of the duodenum: a literature review.十二指肠胃肠道间质瘤的外科治疗:文献综述
Transl Gastroenterol Hepatol. 2018 Sep 21;3:71. doi: 10.21037/tgh.2018.09.04. eCollection 2018.
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Endoscopic ultrasound-guided fine-needle aspiration for diagnosing a rare extraluminal duodenal gastrointestinal tumor.内镜超声引导下细针穿刺活检用于诊断罕见的十二指肠腔外胃肠道肿瘤。
World J Gastrointest Endosc. 2017 Dec 16;9(12):583-589. doi: 10.4253/wjge.v9.i12.583.