Conti Clara Benedetta, Baccarin Alessandra, Conte Dario, Fraquelli Mirella
Gastroenterology and Endoscopy Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.
Intern Emerg Med. 2015 Oct;10(7):839-42. doi: 10.1007/s11739-015-1284-7. Epub 2015 Jul 26.
Present case report refers to a 48-year-old man with genetic haemochromatosis (C282Y mut/mut) diagnosed at the age of 26. After aggressive iron depleting regimen carried out up to normalization of iron-related indexes, he received a maintenance regimen based on regular phlebotomies for about 20 years. In 2014, a marked reduction of both serum ferritin and transferrin saturation percent, without concomitant anaemia, was noted on two different occasions at 5-month interval. An obscure occult GI bleeding was suspected, but both upper and lower GI tract endoscopy were negative for abnormal findings, as also was a detailed abdominal US scan. The persistence of low iron-related indexes prompted the physicians to perform a videocapsule endoscopy, which showed an ulcerative bleeding lesion in the small bowel, not confirmed however by both anterograde and retrograde double-balloon enteroscopy. Further MRI and PET allowed the identification of a 3.5 cm large lesion, located outside the small bowel wall, suspected to be a gastrointestinal stromal tumour (GIST). A further laparoscopic procedure allowed the resection of 10 cm of midileum, which included the mass, fully consistent with GIST at pathology.
本病例报告涉及一名48岁男性,其在26岁时被诊断为遗传性血色素沉着症(C282Y突变/突变型)。在进行积极的铁消耗治疗直至铁相关指标恢复正常后,他接受了基于定期放血的维持治疗约20年。2014年,在间隔5个月的两次不同时间,发现血清铁蛋白和转铁蛋白饱和度百分比均显著降低,且无伴随贫血。怀疑存在隐匿性消化道出血,但上消化道和下消化道内镜检查均未发现异常,详细的腹部超声扫描也未发现异常。铁相关指标持续偏低促使医生进行了胶囊内镜检查,结果显示小肠有溃疡性出血病变,但经顺行和逆行双气囊小肠镜检查均未证实。进一步的MRI和PET检查发现一个3.5厘米大的病变,位于小肠壁外,怀疑是胃肠道间质瘤(GIST)。进一步的腹腔镜手术切除了10厘米的空肠中段,其中包括肿块,病理检查完全符合GIST。