@Article{Kaleta2022,
journal="Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii",
issn="1642-395X",
volume="39",
number="2",
year="2022",
title="Blueberry muffin baby syndrome. A critical primary sign
of systemic disease",
abstract="Blueberry muffin baby syndrome is a rare and non-specific clinical presentation in newborns, characterized by the presence of widespread, maculopapular lesions of blue-red or violaceous colour and cohesive consistency [1]. The term “blueberry muffin baby” was initially coined to describe the skin manifestations of congenital rubella during the American epidemic in the 1960s [2, 3]. The presence of skin lesions is secondary to extramedullary hematopoiesis, which can result from intrauterine viral infections (TORCH syndrome), hematologic dyscrasias (twin-to-twin transfusion syndrome, hereditary spherocytosis, haemolytic disease of the newborn) or neoplasms (mastocytosis, histiocytosis, neuroblastoma, rhabdomyosarcoma, leukaemia) [1, 3].",
author="Kaleta, Katarzyna
and Kłosowicz, Agata
and Juśko, Natalia
and Kapińska-Mrowiecka, Monika",
pages="418--420",
doi="10.5114/ada.2022.115895",
url="http://dx.doi.org/10.5114/ada.2022.115895"
}