Soni P N
Department of Medicine, University of Natal and King Edward VIII Hospital, Congella, Durban, Republic of South Africa.
Postgrad Med J. 1993 Jun;69(812):483-5. doi: 10.1136/pgmj.69.812.483.
A 12 year old boy presenting with hypercalcaemia (calcium 3.25 mmol/l) and osteopaenia with multiple osteolytic lesions was found to have acute lymphoblastic leukaemia without lymph-adenopathy or organomegaly. Hypercalcaemia is a rare feature of acute leukaemia, but the patients previously described all show very similar characteristics, which were highlighted in this patient. These include age (10-20 years), severe osteolytic bone lesions, lymphoblastic leukaemia, and normal white cell count with absent or rare circulating blasts. Parathyroid hormone levels were normal in this patient, and response to induction therapy was good. This case demonstrates that acute lymphoblastic leukaemia may present in an atypical form without peripheral blasts but with hypercalcaemia and gross skeletal changes.
一名12岁男孩因高钙血症(血钙3.25 mmol/L)和骨质减少伴多发溶骨性病变就诊,被诊断为急性淋巴细胞白血病,无淋巴结肿大或器官肿大。高钙血症是急性白血病的罕见特征,但先前描述的患者均表现出非常相似的特征,本患者也突出显示了这些特征。这些特征包括年龄(10 - 20岁)、严重的溶骨性骨病变、淋巴细胞白血病、白细胞计数正常且循环原始细胞缺失或罕见。该患者甲状旁腺激素水平正常,对诱导治疗反应良好。本病例表明,急性淋巴细胞白血病可能以非典型形式出现,无外周原始细胞,但伴有高钙血症和明显的骨骼改变。