梅内特里尔病。临床病例

Ludmila Martínez Leyva, Carla Oliveira, Gerusa Tanoeiro, Maria de Sousa, Neusa Leite, Georgina de Fátima Almeida
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引用次数: 0

摘要

Ménétrier病是一种罕见的临床疾病,包括继发于小凹粘膜细胞增生的胃折叠增厚,并且经常与肠道蛋白质损失和低白蛋白血症有关。其病因尚不清楚。目前,它被认为是恶性前期。该病例为一名27岁患者,因腹痛、体重减轻和呕吐入院。这种疾病是通过内窥镜检查和胃组织活检来诊断的。治疗方法的最新进展尚未明确定义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enfermedad de Ménétrier. Caso clínico

Ménétrier's disease is an infrequent clinical condition consisting of thickening of the gastric folds secondary to hyperplasia of the foveolar mucosa cells, and is frequently associated with loss of enteric proteins and hypoalbuminaemia. Its aetiology is unknown. At present it is considered to be pre-malignant. The case is presented of a 27-year-old patient who was admitted for abdominal pain, loss of weight, and vomiting. This disease is diagnosed using endoscopy and biopsy of stomach tissue. An update is presented on the therapeutic approach, which has not yet been clearly defined.

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