Case Report: Primary Peritonitis as the Onset of Pediatric Ménétrier's Disease

Frontiers in Pediatrics

Carmen Quiñones-Torrelo¹  Anaïs Moscardó-Navarro²  José Rafael Bretón-Martínez³  Cecilia Martínez-Costa³  Elena Crehuá-Gaudiza³  Ana Barrés-Fernández⁴  Andrés Piolatti-Luna⁴  Cristina Fuertes-Latasa⁴ 

[1] Clinic Biochemistry and Molecular Pathology Department, Hospital Clínico Universitario, Valencia, Spain;Department of Pathology, Hospital Clínico Universitario, Valencia, Spain;Department of Pediatrics, University of Valencia, Valencia, Spain;Pediatric Department, Hospital Clínico Universitario, Valencia, Spain;

关键词: Ménétrier's disease;    protein-losing enteropathy;    hypertrophic gastropathy;    case report;    primary peritonitis;   

DOI  :  10.3389/fped.2020.589853

来源: DOAJ

【 摘 要 】

Introduction: 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.Case Presentation: 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.Conclusion: 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.

【 授权许可】

Unknown