Abdominal Lymphangioma and Hemangioma in a Newborn

Abstract

Abdominal hemangiolymphangioma (HLA) in neonates is a rare condition that demands surgical intervention after a complete preoperative diagnostic approach. The differential diagnosis and the establishment of a therapeutic algorithm is a challenge, both for the neonatologists and the pediatric surgeons, because there is no consensus in the management of HLAs in infancy according to the literature. We report a rare case of abdominal HLA in a female newborn that was admitted to our pediatric surgery department with a prenatal diagnosis of an abdominal cystic tumor. After a thorough preoperative diagnostic approach, the neonate underwent an explorative laparotomy and lesion excision with simultaneous splenectomy due to the operative findings. The neonate had an uncomplicated postoperative period and is free of recurrence a year after. Only the pathology examination can reveal the HLA diagnosis. When a total surgical excision is evitable, a close follow-up follows an uncomplicated postoperative hospitalization.

Hemangiolinfangioma mesentérico: reporte de un caso

“…En la literatura se encuentran varios reportes de caso de hemangiolinfangioma en sitios poco comunes como cordón espermático [9], cuerpos vertebrales [8], mucosa oral [2], tracto gastrointestinal, páncreas [11], vejiga [12], extremidades [13], zona paravertebral [14] e incluso en rodilla [5]. El intervalo desde su origen prenatal hasta la presentación clínica es a menudo descrito en décadas [1].…”