Boos Markus D, Wine Lee Lara, Freedman Jason L, Novoa Roberto A, Chu Emily Y, Perman Marissa J
Section of Dermatology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Pediatr Dermatol. 2015 Sep-Oct;32(5):e204-7. doi: 10.1111/pde.12643. Epub 2015 Jul 23.
Children with trisomy 21 are prone to developing hematologic disorders, including transient myeloproliferative disorder (TMD) and acute megakaryoblastic leukemia (AMKL). The papulovesicular eruption of TMD provides an important clue to the diagnosis. In contrast, AMKL rarely has associated cutaneous findings. We report the case of a 22-month-old child with trisomy 21 who presented with the acute onset of diffusely scattered and crusted papules, plaques, and vesicles. A thorough infectious evaluation was negative and the patient was unresponsive to empiric antibiotic and antiinflammatory therapies. Complete blood count (CBC) was notable for mild pancytopenia, with a normal peripheral smear. Two weeks later he was reassessed and found to have a population of blasts on repeat CBC. Subsequent evaluation ultimately led to a diagnosis of AMKL. This is the first reported case of a cutaneous eruption in a young child with Down syndrome and transformed AMKL. When children with trisomy 21 present with the acute onset of crusted papules and vesicles that cannot be accounted for by an infectious etiology, a diagnosis of AMKL should be considered even in the absence of a history of TMD.
21三体综合征患儿易患血液系统疾病,包括短暂性骨髓增殖性疾病(TMD)和急性巨核细胞白血病(AMKL)。TMD的丘疹水疱性皮疹为诊断提供了重要线索。相比之下,AMKL很少有相关的皮肤表现。我们报告一例22个月大的21三体综合征患儿,其急性起病,出现弥漫性散在的结痂丘疹、斑块和水疱。全面的感染评估结果为阴性,患者对经验性抗生素和抗炎治疗无反应。全血细胞计数(CBC)显示轻度全血细胞减少,外周血涂片正常。两周后对他进行复查,发现复查CBC时有一群原始细胞。后续评估最终确诊为AMKL。这是第一例报道的患有唐氏综合征且转化为AMKL的幼儿出现皮肤疹的病例。当21三体综合征患儿急性起病出现结痂丘疹和水疱且不能用感染病因解释时,即使没有TMD病史,也应考虑诊断为AMKL。