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• W2034247238 abstract "The association of neurofibromatosis 1 (NF1), juvenile xanthogranulomas (JXG), and juvenile myelomonocytic leukemia (JMML) has been previously reported. We describe herein this triad in a Caucasian male infant with a pathogenic mutation in the NF1 gene (neurofibromin). The clinical course from initial presentation to final diagnosis is detailed; the physical features and hematologic characteristics are discussed. The patient underwent bone marrow transplantation and is currently in remission. Children with concurrent cutaneous café-au-lait and JXG lesions should be evaluated and monitored closely for the possible development of JMML." @default.
• W2034247238 created "2016-06-24" @default.
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• W2034247238 date "2009-09-25" @default.
• W2034247238 modified "2023-10-02" @default.
• W2034247238 title "Juvenile xanthogranuloma in a child with previously unsuspected neurofibromatosis type 1 and juvenile myelomonocytic leukemia" @default.
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• W2034247238 doi "https://doi.org/10.1002/pbc.22297" @default.
• W2034247238 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2783853" @default.
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