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Intestinal perforation secondary to abdominal angiostrongyliasis in an older infant with suspected extraintestinal involvement.

Source: PubMed, NCBI / U.S. National Library of Medicine

Oxford medical case reportsCherif Hugo-Malik, Suazo Nadia, Fontecha Gustavo, et al.Published 6/1/2026Last synced 6/11/2026Status: syncedPMID: 42267205DOI: 10.1093/omcr/omag088

Angiostrongyliasis is a parasitic disease caused bys (Latin America) and(Asia/Pacific). Abdominal angiostrongyliasis often mimics appendicitis, challenging clinical diagnosis and requiring histopathological confirmation. We report a severely malnourished infant in Honduras presenting with 10 days of severe abdominal pain and vomiting, complicated by respiratory insufficiency and seizures. Brain CT revealed cortical atrophy, suggesting a chronic underlying neurologic condition. Laboratory tests showed leukocytosis, lymphocytosis, and massive eosinophilia. Exploratory laparotomy for suspected appendicitis identified an ileal perforation, requiring intestinal resection. Histopathology confirmed non-caseating granulomas containinglarvae within the mesenteric arteriovenous plexus, alongside scattered eggs. This is the first confirmed human case of abdominal angiostrongyliasis with suspected, unconfirmed extraintestinal involvement in the Olancho Department of Honduras. These findings emphasize the critical need for increased clinical awareness and public health measures against this overlooked parasitic infection.

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