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.