{Reference Type}: Case Reports
{Title}: A case report of a blueberry muffin baby caused by congenital self-healing indeterminate cell histiocytosis.
{Author}: Koster SBL;Vinke ME;van den Bos C;van Heel WJM;Kranendonk MEG;Natté R;van Tuyll van Serooskerken AM;
{Journal}: BMC Pediatr
{Volume}: 23
{Issue}: 1
{Year}: 03 2023 8
{Factor}: 2.567
{DOI}: 10.1186/s12887-023-03922-5
{Abstract}: Blueberry muffin is a descriptive term for a neonate with multiple purpuric skin lesions. Many causes are known, amongst them life-threatening diseases like congenital infections or leukemia. Indeterminate cell histiocytosis (ICH) is an exceptionally rare cause of blueberry muffin rash. ICH is a histiocytic disorder which can be limited to the skin or can present with systemic involvement. A mutation that has been described in histiocytic disorders is a MAP2K1 mutation. In ICH, this mutation has previously been described in merely one case.<BR>A term male neonate was admitted to the neonatology ward directly after birth because of a blueberry muffin rash. ICH was diagnosed on skin biopsy. The lesions resolved spontaneously. The patient is currently 3 years old and has had no cutaneous lesions or systemic involvement so far. This disease course is similar to that of the Hashimoto-Pritzker variant of LCH.<BR>ICH can manifest in neonates as resolving skin lesions. It is limited to the skin in most cases, but systemic development is possible. Therefore, it is essential to confirm the diagnosis with a biopsy before the lesions resolve and to monitor these patients closely with routine follow-up.