Belgian Journal of Paediatrics
Neonatal acute myeloid leukemia with KMT2A/MLLT3 rearrangement revealed by a Blueberry Muffin syndrome

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Keywords

blueberry Muffin syndrome
neonatal leukemia
leukemia cutis
KMT2A rearrangement
case report

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How to Cite

Koutny, C., Legros, L., Mostaert, A., Truant, A.-S., Vatcheva, T., Florkin, B., Longton, J., Gatineau, S., & Henrion, E. (2023). Neonatal acute myeloid leukemia with KMT2A/MLLT3 rearrangement revealed by a Blueberry Muffin syndrome. Belgian Journal of Paediatrics, 24(3), 205–208. Retrieved from https://belgjpaediatrics.com/index.php/bjp/article/view/38 (Original work published December 12, 2022)

Abstract

Blueberry Muffin syndrome is a rare skin manifestation of extramedullary hematopoiesis in neonates. The differential diagnosis  includes congenital infections, intrauterine anemias and, more rarely, neoplastic pathologies.

We report the case of a newborn showing birth lesions suggestive of this syndrome. In the absence of associated clinical signs and abnormalities in the blood count, diagnostic investigations were completed by a skin biopsy and a bone marrow aspiration which led to the diagnosis of acute myeloid leukemia with a KMT2A/MLLT3 rearrangement. As leukemic burden was low, a watch-and-wait approach was chosen, until chemotherapy needed to be initiated at eight weeks of life.

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