Abstract
We describe the first known case of hepatoblastoma associated with bilateral autosomal recessive polycystic kidney disease in a preterm twin boy. The diagnostic and therapeutic considerations are addressed. The patient survived after primary hepatectomy operation and administration of modified adjuvant chemotherapy.
Copyright © 2010 Elsevier Inc. All rights reserved.
MeSH terms
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Antineoplastic Agents / therapeutic use
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Birth Weight
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Chemotherapy, Adjuvant
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Diagnosis, Differential
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Follow-Up Studies
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Hepatectomy
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Hepatoblastoma / diagnosis
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Hepatoblastoma / etiology*
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Hepatoblastoma / therapy
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Humans
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Infant, Newborn
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Infant, Premature
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Liver Neoplasms / diagnosis
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Liver Neoplasms / etiology*
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Liver Neoplasms / therapy
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Magnetic Resonance Imaging
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Male
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Polycystic Kidney, Autosomal Recessive / complications*
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Polycystic Kidney, Autosomal Recessive / diagnosis