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Juvenile xanthogranuloma in a child with previously unsuspected neurofibromatosis type 1 and juvenile myelomonocytic leukemia
Pediatric Blood & Cancer, 10/06/09
Raygada M et al. – 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 cafe–au–lait and JXG lesions should be evaluated and monitored closely for the possible development of JMML.
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Today in Pediatric Heme/Oncology...keeping you current
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