Endoscopic ultrasound-guided fine-needle aspiration for diagnosing a rare extraluminal duodenal gastrointestinal tumor

Duodenal gastrointestinal stromal tumors(GISTs) are extremely rare disease entities, and the extraluminal type is difficult to diagnose. These tumors have been misdiagnosed as pancreatic tumors; hence, pancreaticoduodenectomy has been performed, although partial duodenectomy can be performed if accu...

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Veröffentlicht in:World journal of gastrointestinal endoscopy 2017-12, Vol.9 (12), p.583-589
Hauptverfasser: Hayashi, Kazunao, Kamimura, Kenya, Hosaka, Kazunori, Ikarashi, Satoshi, Kohisa, Junji, Takahashi, Kazuya, Tominaga, Kentaro, Mizuno, Kenichi, Hashimoto, Satoru, Yokoyama, Junji, Yamagiwa, Satoshi, Takizawa, Kazuyasu, Wakai, Toshifumi, Umezu, Hajime, Terai, Shuji
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Sprache:eng
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Zusammenfassung:Duodenal gastrointestinal stromal tumors(GISTs) are extremely rare disease entities, and the extraluminal type is difficult to diagnose. These tumors have been misdiagnosed as pancreatic tumors; hence, pancreaticoduodenectomy has been performed, although partial duodenectomy can be performed if accurately diagnosed. Developing a diagnostic methodology including endoscopic ultrasonography(EUS) and fine-needle aspiration(FNA) has allowed us to diagnose the tumor directly through the duodenum. Here, we present a case of a 50-year-old woman with a 27-mm diameter tumor in the pancreatic uncus on computed tomography scan. EUS showed a well-defined hypoechoic mass in the pancreatic uncus that connected to the duodenal proper muscular layer and was followed by endoscopic ultrasoundguided fine-needle aspiration(EUS-FNA). Histological examination showed spindle-shaped tumor cells positively stained for c-kit. Based on these findings, the tumor was finally diagnosed as a duodenal GIST of the extraluminal type, and the patient underwent successful mass resection with partial resection of the duodenum. This case suggests that EUS and EUS-FNA are effective for diagnosing the extraluminal type of duodenal GISTs, which is difficult to differentiate from pancreatic head tumor, and for performing the correct surgical procedure.
ISSN:1948-5190
1948-5190
DOI:10.4253/wjge.v9.i12.583