Renal failure after high-dose methotrexate in a child homozygous for MTHFR C677T polymorphism


Autoria(s): Turello, R.; Rentsch, K.; Di Paolo, E.; Popovic, M.B.
Data(s)

2008

Resumo

We report the case of an 11-year-old female treated for mediastinal T-cell lymphoma who presented renal failure following the second cycle of high-dose methotrexate (HDMTX). Because of life threatening plasma methotrexate (MTX) levels, carboxypeptidase G2 (CPDG2) was administered resulting in a dramatic decrease within 1 hr. The patient recovered from renal failure and no other side effects were observed. Homozygosity for the methylentetrahydrofolate reductase (MTHFR) C677T polymorphism diagnosed by molecular genetic analysis was the only explanation for this toxicity.

Identificador

https://serval.unil.ch/notice/serval:BIB_5F148A65F68F

info:pmid:17387702

pmid:17387702

doi:10.1002/pbc.21176

isiid:000251410400034

Idioma(s)

eng

Fonte

Pediatric Blood & Cancer501154-156

Palavras-Chave #Antimetabolites, Antineoplastic; Child; Female; Homozygote; Humans; Kidney Failure, Acute; Lymphoma, T-Cell; Methotrexate; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Genetic
Tipo

info:eu-repo/semantics/article

article