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10.14309/crj.2015.78

http://scihub22266oqcxt.onion/10.14309/crj.2015.78
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suck abstract from ncbi


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pmid26203458      ACG+Case+Rep+J 2015 ; 2 (4): 258-60
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  • Mesenchymal Hamartoma of the Liver in an Infant With Beckwith-Wiedemann Syndrome: A Rare Condition Mimicking Hepatoblastoma #MMPMID26203458
  • Abrahao-Machado LF; de Macedo FC; Dalence C; Stambo G; Abrahao-Machado EF; Abrahao-Machado EC; Bahrami A; Nascimento AG
  • ACG Case Rep J 2015[Jul]; 2 (4): 258-60 PMID26203458show ga
  • Patients with Beckwith-Wiedemann syndrome (BWS) are known to be at an increased risk for childhood malignancies, particularly Wilms tumor and hepatoblastoma. We report a case of genetically confirmed BWS in a 5-month-old girl who presented with a 9.5-cm abdominal mass associated with elevated alpha-fetoprotein levels. The clinical impression was strongly suggestive of hepatoblastoma. Histologic examination of the surgically excised mass revealed mesenchymal hamartoma of the liver (MHL), a benign hepatic neoplasm.
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