Yasmeen Nuzhat, Ashraf Shamvil
Oncology Unit, National Institute of Child Health, Karachi, Pakistan.
J Pak Med Assoc. 2009 Mar;59(3):150-3.
To study epidemiology, clinical presentation and laboratory features of childhood Acute Lymphoblastic Leukaemia.
This retrospective review included all newly diagnosed children with acute lymphoblastic Leukaemia less than 15 years of age registered from April 1999 to December 2004 at oncology unit of National Institute of Child Health and Children Cancer Hospital, Karachi. The objective was to look for epidemiological data, the clinical features and laboratory findings at presentation and compare it with reported literature.
Acute lymphoblastic Leukaemia constituted 32% (611 /1890) of all cancers in this study. Majority of patients hailed from Karachi (59%) and interior Sindh (27%) while rest from other parts of country. Patient's referral increased over the years, from 42 in 1999 to 127 in 2004. The age ranged between 3 months to 15 years with a median age of 6.5 years. Male to female ratio was 1.7:1 Family history of cancer was present in 5% of patients. Fever and pallor were the commonest presenting features. Anaemia (86%), lymphadenopathy (75%) hepatomegaly (67%) and splenomegly (58%) were common findings on physical examination. Initial high white cell count (> 50,000) was observed in 34% patients. Haemoglobin < 7gm/dl was seen in 54% and Platelet counts less than 20,000 was observed in 33% cases. CNS disease was present in 5% and HBsAg was positive in 14% patients at diagnosis.
Acute Lymphoblastic Leukaemia accounts for one third of total registered cases. Age distribution in this series shows less prominemt early peak and more significant late peak and a median age of 6 years. Consangunity was found in 47% cases. The fraction with a WBC count above 50,000 mm3 (30%), a higher proportion with lymphadenopathy (75%) and haemoglobin less than 7 gm/dl (54%) suggest that Pakistani children have significantly higher burdens of Leukaemia cells at presentation. These may have prognostic implication resulting in poor outcome of Leukaemia in this part of the world.
研究儿童急性淋巴细胞白血病的流行病学、临床表现及实验室特征。
本回顾性研究纳入了1999年4月至2004年12月在卡拉奇国家儿童健康研究所和儿童癌症医院肿瘤科登记的所有新诊断的15岁以下急性淋巴细胞白血病患儿。目的是寻找流行病学数据、临床表现及实验室检查结果,并与已发表的文献进行比较。
在本研究中,急性淋巴细胞白血病占所有癌症的32%(611/1890)。大多数患者来自卡拉奇(59%)和信德省内陆地区(27%),其余来自该国其他地区。多年来患者转诊人数有所增加,从1999年的42例增至2004年的127例。年龄范围在3个月至15岁之间,中位年龄为6.5岁。男女比例为1.7:1。5%的患者有癌症家族史。发热和面色苍白是最常见的临床表现。体格检查常见贫血(86%)、淋巴结病(75%)、肝肿大(67%)和脾肿大(58%)。34%的患者初诊时白细胞计数高(>50,000)。54%的患者血红蛋白<7g/dl,33%的病例血小板计数低于20,000。诊断时5%的患者有中枢神经系统疾病,14%的患者乙肝表面抗原呈阳性。
急性淋巴细胞白血病占登记病例总数的三分之一。本系列研究中的年龄分布显示早期高峰不明显,晚期高峰更显著,中位年龄为6岁。47%的病例存在近亲结婚。白细胞计数高于50,000/mm³(30%)、淋巴结病比例较高(75%)以及血红蛋白低于7g/dl(54%)表明,巴基斯坦儿童初诊时白血病细胞负担明显更高。这些可能对预后有影响,导致世界这一地区白血病的不良结局。