Frontiers in Pediatrics (Oct 2017)

Mucinous Cystadenoma: A Rare Hepatic Tumor in a Child

  • Danielle A. Ferraguti,
  • Molly McGetrick,
  • Ivan Zendejas,
  • Ivan Zendejas,
  • David Hernandez-Gonzalo,
  • Regino Gonzalez-Peralta

DOI
https://doi.org/10.3389/fped.2017.00215
Journal volume & issue
Vol. 5

Abstract

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Mucinous cystadenomas (MCAs) of the liver (also called hepatic biliary cystadenomas) are rare tumors that comprise about 5% of cystic masses of the liver in adults. These slow-growing lesions most commonly occur in middle-aged individuals, with a female sex predominance. Herein, we present a MCA in a 6-year-old male, one of only very few such cases described in the pediatric literature to date. Although MCAs are generally considered benign lesions, malignant transformation rarely occurs. The recurrence rate is high when partial cyst excision is performed. Therefore, complete surgical cyst resection with clinical follow-up, including imaging, is warranted.

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