An infant with a diagnostically challenging hepatic teratoma, hypofibrinogenemia, and adrenal neuroblastoma: Case report

Iris Fried, Eitan Rom-Gross, Milton Finegold, Natalia Simanovsky, Shoshana Revel-Vilk, Ziva Ben-Neriah, Michael Weintraub, Orit Pappo, Karen Meir*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Teratomas of the liver are exceedingly rare. Neuroblastoma is the most common, extracranial solid tumor of infancy. We describe the case of a 2-month-old, female infant who presented with an abdominal mass arising in the right lobe of the liver, and a severe coagulopathy, which necessitated cryoprecipitate infusion. Biopsy was interpreted as hepatoblastoma. Following resection, difficulty classifying the mass led to several consultations, and an eventual diagnosis of teratoma. During follow-up, the patient was diagnosed with right adrenal neuroblastoma, which, in retrospect, had been present before the hepatic resection. To our knowledge, these 2 tumors have never been reported together, or in combination with isolated hypofibrinogenemia.

Original languageEnglish
Pages (from-to)251-256
Number of pages6
JournalPediatric and Developmental Pathology
Volume18
Issue number3
DOIs
StatePublished - 1 May 2015
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2015 Society for Pediatric Pathology.

Keywords

  • Hepatoblastoma
  • Hypofibrinogenemia
  • Liver tumor
  • Neuroblastoma
  • Teratoma

Fingerprint

Dive into the research topics of 'An infant with a diagnostically challenging hepatic teratoma, hypofibrinogenemia, and adrenal neuroblastoma: Case report'. Together they form a unique fingerprint.

Cite this