Lipoblastoma in children: Review of 12 cases

• DOI: 10.1111/ped.13239
• Publication Date: 2017-01-13T15:20:29Z
• Authors: Hilal Susam‐Sen; Bilgehan Yalcin; Tezer Kutluk; Feridun Cahit Tanyel; Mithat Haliloglu; Diclehan Orhan; Burca Aydin; Nilgun Kurucu; Ali Varan; Canan Akyuz
• Keywords: Male; Infant; 3. Good health; Diagnosis, Differential; 03 medical and health sciences; Treatment Outcome; 0302 clinical medicine; Child, Preschool; Humans; Female; Child; Follow-Up Studies; Lipoblastoma; Retrospective Studies

AbstractBackgroundLipoblastoma is a rare benign mesenchymal tumor of infancy and early childhood. Symptoms vary depending on localization, and signs of compression of adjacent organs may be seen.MethodsA total of 12 children with pathologically proven lipoblastoma from 2000 to 2014 were reviewed retrospectively for their clinical features, treatment and follow up.ResultsThere were seven boys and five girls between 7.5 months and 7.5 years of age. The most common symptom was painless rapid‐growing mass. The tumors were located in the neck, the abdomen, the groin, pelvis, axilla, glutea, labium majus, thigh and trunk. The largest tumor was in a retroperitoneal location and was 13 × 10 cm in size. Complete resection was performed in 10 patients. All of these patients were followed without any evidence of recurrence. Subtotal excision was performed in two patients. At a median follow up of 38 months (range, 1.8 months–10 years), all patients were disease free.ConclusionsLipoblastoma should be considered in the differential diagnosis of rapidly growing mass in patients <3 years of age. Total excision is the treatment of choice with preservation of vital organs. The prognosis is excellent despite large tumor size and local invasion. Recurrence rate is high in incompletely resected tumors. Regular follow up is important for early detection of recurrence.