Bates Sara V, Lakshmanan Ashwini, Green Adam L, Terry Jefferson, Badalian-Very Gayane, Rollins Barrett J, Fleck Patricia, Aslam Muhammad, Degar Barbara A
Division of Neonatology and Newborn Medicine, Department of Pediatrics, Massachusetts General Hospital for Children, Harvard Medical School, Boston, Massachusetts ; These authors contributed equally as primary authors (co-first authors).
AJP Rep. 2013 Oct;3(2):63-6. doi: 10.1055/s-0033-1338168. Epub 2013 Mar 18.
Hemorrhagic pustules with a "blueberry muffin" appearance accompanied by respiratory failure in a neonate present a challenging differential diagnosis that includes infections and neoplasms. We present a case of multiorgan, multisite Langerhans cell histiocytosis (LCH), positive for the oncogenic BRAF V600E mutation, in a preterm neonate. Infants with LCH pose a diagnostic challenge due to their heterogeneous presentations. This case is unusual in that the newborn presented with severe multiorgan involvement. Due to the rare incidence, wide spectrum of clinical manifestations, and high mortality rate, clinicians must maintain a high index of suspicion for LCH.
新生儿出现具有“蓝莓松饼”外观的出血性脓疱并伴有呼吸衰竭,这是一个具有挑战性的鉴别诊断,包括感染和肿瘤。我们报告一例早产新生儿多器官、多部位朗格汉斯细胞组织细胞增多症(LCH),其致癌性BRAF V600E突变呈阳性。患有LCH的婴儿因其表现异质性而带来诊断挑战。该病例不同寻常之处在于新生儿出现了严重的多器官受累。由于发病率低、临床表现谱广且死亡率高,临床医生必须对LCH保持高度的怀疑指数。