Literature DB >> 25691417

Hepatoblastoma in a patient with methylmalonic aciduria.

Randall Chan1, Leo Mascarenhas, Richard G Boles, Nanda Kerkar, Yuri Genyk, Rajkumar Venkatramani.   

Abstract

Childhood malignant tumors and their treatment are not well described in the natural history of methylmalonic aciduria (MMA). Here we present a case of hepatoblastoma occurring in the native liver of a 19-month-old male with MMA. His tumor was unresectable at diagnosis and he received neoadjuvant chemotherapy with cisplatin, 5-fluorouracil and vincristine. He developed metabolic acidosis and hyperglycemia during chemotherapy. In addition, he developed anemia, thrombocytopenia and febrile neutropenia. He underwent a combined liver-kidney transplant for local control of his tumor and to treat MMA. He remains in remission more than five years after his transplant. In addition, his transplant has cured his MMA and he is able to tolerate a regular diet without developing metabolic crises.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  chemotherapy; hepatoblastoma; kidney transplantation; liver transplantation; methylmalonic aciduria

Mesh:

Year:  2015        PMID: 25691417     DOI: 10.1002/ajmg.a.36925

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

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Review 2.  Toxic Metabolites and Inborn Errors of Amino Acid Metabolism: What One Informs about the Other.

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5.  Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemia.

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Review 6.  Combined liver-kidney transplantation for rare diseases.

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