Waisberg Daniel Reis, de Mello Evandro Sobroza, Tustumi Francisco, Szor Daniel José, Charruf Amir Zeide, Fuhro Felipe Emanuel, Waisberg Jaques, Dias André Roncon
Department of Surgery, Hospital de Clínicas Municipal José Alencar, Sao Bernardo do Campo, Brazil.
Department of Pathology, Instituto do Câncer do Estado de São Paulo (ICESP), Sao Paulo, Brazil.
Int J Surg Case Rep. 2020;77:498-502. doi: 10.1016/j.ijscr.2020.11.055. Epub 2020 Nov 12.
Ménétrier's disease is a rare condition, frequently associated with Helicobacter pylori infection, hypergastrinemia and hypoalbuminaemia.
A case of a 55 years-old female patient with a previous diagnosis of pernicious anemia complaining of epigastric discomfort, hyporexia, vomiting, and weight loss is reported. Endoscopy showed multiple gastric polyploid formations and Helicobacter pylori infection was detected. Laboratory tests showed elevated gastrin serum levels and presence of antibodies antiparietal cells, as well as microcytic hypochromic anemia compatible with chronic iron deficiency. Albumin serum level was slightly decreased. Full thickness biopsy performed via echoendoscopy reported gastritis cystica/polyposa profunda. Given the association of diffuse involvement of the entire stomach, the possibility of developing malignant disease and the clinical symptoms, the patient underwent laparoscopic total gastrectomy with Roux-en-Y reconstruction. The surgical specimen showed the mucosa hyperemic and swollen, with prominent gastric folds. Hyperplastic elongation of gastric foveolas associated with disappearance of oxyntic glands was compatible with Ménétrier's disease.
The Ménétrier's disease diagnosis may be tricky, especially when an unusual endoscopic presentation is associated with other conditions that may mislead the diagnostic evaluation. The differential diagnoses were gastric malignancies, Zollinger-Ellison syndrome, massive gastric polyposis and gastritis cystica/polyposa profunda.
Clinical, laboratory, endoscopic and histopathological findings are paramount for reaching the diagnosis of Ménétrier's disease, but it should be suspected in all cases of upper gastrointestinal symptoms and hypertrophied gastric mucosa.
梅内特里耶病是一种罕见疾病,常与幽门螺杆菌感染、高胃泌素血症和低白蛋白血症相关。
报告一例55岁女性患者,既往诊断为恶性贫血,现主诉上腹部不适、食欲减退、呕吐和体重减轻。内镜检查显示多个胃息肉样肿物,检测到幽门螺杆菌感染。实验室检查显示血清胃泌素水平升高、存在抗壁细胞抗体,以及与慢性缺铁相符的小细胞低色素性贫血。血清白蛋白水平略有下降。经超声内镜进行的全层活检报告为深部囊性/息肉样胃炎。鉴于整个胃弥漫性受累、发生恶性疾病的可能性以及临床症状,患者接受了腹腔镜全胃切除术并进行Roux-en-Y重建。手术标本显示黏膜充血、肿胀,胃皱襞突出。胃小凹增生延长伴胃底腺消失与梅内特里耶病相符。
梅内特里耶病的诊断可能具有挑战性,尤其是当不寻常的内镜表现与其他可能误导诊断评估的情况相关时。鉴别诊断包括胃恶性肿瘤、佐林格-埃利森综合征、巨大胃息肉病和深部囊性/息肉样胃炎。
临床、实验室、内镜和组织病理学检查结果对于梅内特里耶病的诊断至关重要,但在上消化道症状和胃黏膜肥厚的所有病例中均应怀疑该病。