Sahu Sanjay Kumar, Agrawal Aman, Das Palash
Pediatrics, Kalinga Institute of Medical Sciences, Bhubaneswar, IND.
Pediatrics, Kalinga Institute of Medical Sciences, Bhubaneshwar, IND.
Cureus. 2020 Dec 24;12(12):e12255. doi: 10.7759/cureus.12255.
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder due to uncontrolled activation of macrophage and cytokine release, which can be due to either genetic causes (familial) or secondary to infections malignancy and other less common cause. Parvovirus B19 rarely causes HLH. Diagnosing HLH in sickle cell disease, which inherently has high ferritin levels and pancytopenia, is particularly challenging. We are reporting HLH as a complication with parvovirus B19 infection in the background of sickle beta-thalassemia. Based on our search of available medical literature, this is the first case of HLH complicating parvovirus B19 infection in a pediatric age group with sickle beta-thalassemia.
噬血细胞性淋巴组织细胞增生症(HLH)是一种危及生命的疾病,由于巨噬细胞不受控制的激活和细胞因子释放所致,其病因可能是遗传因素(家族性),也可能继发于感染、恶性肿瘤和其他不太常见的原因。细小病毒B19很少引起HLH。在镰状细胞病中诊断HLH尤其具有挑战性,因为镰状细胞病本身就有高铁蛋白水平和全血细胞减少。我们报告了在镰状β地中海贫血背景下,细小病毒B19感染并发HLH的病例。根据我们对现有医学文献的检索,这是小儿镰状β地中海贫血年龄组中首例细小病毒B19感染并发HLH的病例。