Infantile Abdominal and Pelvic Lipoblastomas: A Case Series

Author:

Guanà Riccardo1,Garofalo Salvatore2,Ferrero Luisa2,Cortese Maria Grazia3,Lonati Luca2,Teruzzi Elisabetta2,Basso Eleonora4,Morra Isabella5,Lemini Riccardo6,Sardi Nicola7,Gennari Fabrizio1

Affiliation:

1. Division of Pediatric Surgery, Regina Margherita Children's Hospital, Turin, Italy

2. Department of Pediatric Surgery, Ospedale Infantile Regina Margherita, Turin, Piemonte, Italy

3. Department of Pediatric Surgery, Regina Margherita Children's Hospital, Piazza Polonia, Turin, Italy

4. Department of Paediatric Haematology-Oncology, Ospedale Infantile Regina Margherita, Turin, Piemonte, Italy

5. Department of Anatomo-Pathology, Ospedale Infantile Regina Margherita, Turin, Piemonte, Italy

6. Surgery, Section of Colon and Rectal Surgery, Mayo Clinic Hospital Jacksonville, Jacksonville, Florida, United States

7. Department of Paediatrics, Ospedale SS Annunziata di Savigliano, Savigliano, Piemonte, Italy

Abstract

Lipoblastomas are rare benign mesenchymal tumors that arise from embryonal fat cells.They are usually discovered in infants and children under 3 years of age, and mostly occur in the trunk (from 10 to 60%, depending on the study) and extremities (from 40 to 45%), while head and neck localizations are rare, with only five cases described to date.We report on three cases of lipoblastomas in infants younger than 4 years, with unusual localizations: one intra-abdominal, discovered during a laparotomy for an intussusception; one pelvic, misdiagnosed as an ovarian mass; and one gluteal with a pelvic extension.All children underwent magnetic resonance imaging as preoperative workup. All tumors were completely resected with free surgical margins and ultrasonographic follow-up was uneventful for all patients.

Publisher

Georg Thieme Verlag KG

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