Anandpara Karan Manoj, Aswani Yashant, Hira Priya
Seth G S Medical College and KEM Hospital, Mumbai, Maharashtra, India.
BMJ Case Rep. 2015 Feb 16;2015:bcr2014207087. doi: 10.1136/bcr-2014-207087.
Ménétrier's disease is a rare protein-losing hypertrophic gastroenteropathy. While it still remains a medical curiosity, infection with Cytomegalovirus and Helicobacter pylori, and hormonal, congenital, dietary and neurogenic factors have been postulated as causative factors. We describe a case of a 14-year boy who presented with epigastric discomfort, vomiting, inability to gain weight and pedal oedema. Investigations revealed hypoproteinaemia without proteinuria and elevated faecal α-1-antitrypsin levels suggestive of protein-losing enteropathy. Imaging and endoscopic features demonstrated cerebriform gastric folds indicative of Ménétrier's disease. Infective, hormonal and neurogenic causes were ruled out in our patient. Surprisingly, the patient had a history of pica and an associated large gastric bezoar, which was ultimately removed surgically. An association of Ménétrier's disease with a bezoar has been reported only once previously. We thus add to the existing literature and highlight the plausible role of a bezoar as a causative factor in the pathogenesis of Ménétrier's disease due to its irritant nature.
梅内特里耶病是一种罕见的失蛋白性肥厚性胃肠病。尽管它仍是医学上的一个奇症,但巨细胞病毒和幽门螺杆菌感染以及激素、先天性、饮食和神经源性因素已被假定为致病因素。我们描述了一名14岁男孩的病例,他出现上腹部不适、呕吐、体重不增和足部水肿。检查发现低蛋白血症但无蛋白尿,粪便α-1抗胰蛋白酶水平升高提示失蛋白性肠病。影像学和内镜特征显示脑回样胃皱襞,提示梅内特里耶病。我们的患者排除了感染、激素和神经源性病因。令人惊讶的是,该患者有异食癖病史及相关的巨大胃石,最终通过手术切除。梅内特里耶病与胃石的关联此前仅报道过一次。因此,我们补充了现有文献,并强调胃石因其刺激性本质在梅内特里耶病发病机制中作为致病因素的可能作用。