El Ouardi Walid, Bouchabou Bochra, Regragui Asmaa, Benazzouz Mustapha
Department of Gastroenterology, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco.
Department of Hepatogastroenterology, Mongi Slim Hospital, Tunis, Tunisia.
Pan Afr Med J. 2024 Aug 14;48:178. doi: 10.11604/pamj.2024.48.178.43852. eCollection 2024.
Foveolar-type adenomas are very rare lesions, representing approximately 2.7% of duodenal adenomas with gastric phenotype, histologically characterized by tall columnar cells resembling gastric foveolar epithelium and a tubulovillous structure with various degrees of dysplasia. Their risk of progression to adenocarcinoma is related to the size of the polyp and the presence of high-grade dysplasia. The recommended therapeutic approach is the endoscopic resection. our clinical case reports a rare case of a patient in whom gastric foveolar adenoma was incidentally discovered as an 8 mm sessile polyp in the duodenal bulb resected entirely by en-bloc mucosectomy technique. Through this case, we draw attention to the existence of bulbar adenomas, which carry a risk of dysplasia and progression to adenocarcinoma.
胃小凹型腺瘤是非常罕见的病变,约占具有胃表型的十二指肠腺瘤的2.7%,组织学特征为类似胃小凹上皮的高柱状细胞以及具有不同程度发育异常的管状绒毛结构。它们进展为腺癌的风险与息肉大小和高级别发育异常的存在有关。推荐的治疗方法是内镜下切除。我们的临床病例报告了1例罕见病例,1例患者在十二指肠球部偶然发现1个8mm的无蒂息肉状胃小凹腺瘤,通过整块黏膜切除术技术将其完整切除。通过该病例,我们提醒大家注意十二指肠球部腺瘤的存在,其有发育异常和进展为腺癌的风险。