Ganesan Prasanth, Thulkar Sanjay, Gupta Ritu, Bakhshi Sameer
Department of Medical Oncology, Dr. B. R. A. Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi, India.
J Pediatr Endocrinol Metab. 2009 May;22(5):463-7. doi: 10.1515/jpem.2009.22.5.463.
A 16 year-old boy presented with severe hypercalcemia, diffuse osteolytic lesions and vertebral fractures. He was initially diagnosed with metabolic bone disease, and the hypercalcemia responded to treatment with intravenous hydration and bisphosphonates. However, the intact parathormone level was normal. He had no lymphadenopathy or organomegaly. The only hematological abnormality was moderate anemia, which prompted bone marrow studies leading to a diagnosis of acute lymphoblastic leukemia (ALL). He was treated with standard chemotherapy and achieved remission as well as resolution of his skeletal symptoms. We discuss the diagnostic challenges of this rare entity of aleukemic leukemia with hypercalcemia and lytic bone lesions, and review all the previously reported pediatric literature.
一名16岁男孩出现严重高钙血症、弥漫性溶骨性病变和椎体骨折。他最初被诊断为代谢性骨病,高钙血症经静脉补液和双膦酸盐治疗后有反应。然而,完整甲状旁腺激素水平正常。他没有淋巴结病或器官肿大。唯一的血液学异常是中度贫血,这促使进行骨髓检查,结果诊断为急性淋巴细胞白血病(ALL)。他接受了标准化化疗,病情缓解,骨骼症状也得到缓解。我们讨论了这种伴有高钙血症和溶骨性病变的无白血病性白血病这一罕见实体的诊断挑战,并回顾了所有先前报道的儿科文献。