Barrés-Fernández Ana, Piolatti-Luna Andrés, Bretón-Martínez José Rafael, Crehuá-Gaudiza Elena, Quiñones-Torrelo Carmen, Moscardó-Navarro Anaïs, Fuertes-Latasa Cristina, Martínez-Costa Cecilia
Pediatric Department, Hospital Clínico Universitario, Valencia, Spain.
Department of Pediatrics, University of Valencia, Valencia, Spain.
Front Pediatr. 2021 Jan 13;8:589853. doi: 10.3389/fped.2020.589853. eCollection 2020.
Primary peritonitis (PP) and Ménétrier's Disease (MD) are both rare conditions among pediatric population. Although about 150 MD cases have been described in the scientific literature to date, its onset with a PP is an unusual condition. We present a case of an 11-year-old boy who was admitted to our unit because of abdominal pain and distension. Complementary tests showed ascites, bilateral pleural effusion, leukocytosis, increased acute phase reactants and hypoproteinemia with hypoalbuminemia. Laparoscopy ruled out appendicitis or visceral perforations and exposed purulent peritoneal fluid, compatible with PP. Biochemical stool analysis showed increased clearance of alpha-1-antitrypsin, which was consistent with a protein-losing enteropathy. Gastroscopy findings were compatible with MD. The clinical course was favorable and he had no recurrence after 12 months of follow-up. PP can be the first clinical manifestation of pediatric MD. Knowledge of MD and its generally benign nature in children is important in order to avoid excessive testing and unnecessary treatment.
原发性腹膜炎(PP)和门脉高压性胃病(MD)在儿科人群中均属罕见病症。尽管迄今为止科学文献中已描述了约150例MD病例,但其以PP起病实属罕见。我们报告一例11岁男孩,因腹痛和腹胀入住我科。辅助检查显示有腹水、双侧胸腔积液、白细胞增多、急性期反应物升高以及伴有低白蛋白血症的低蛋白血症。腹腔镜检查排除了阑尾炎或内脏穿孔,并发现脓性腹腔积液,符合PP表现。粪便生化分析显示α-1抗胰蛋白酶清除率增加,这与蛋白丢失性肠病相符。胃镜检查结果符合MD表现。临床过程良好,随访12个月后无复发。PP可能是小儿MD的首发临床表现。了解MD及其在儿童中通常为良性的性质对于避免过度检查和不必要的治疗很重要。