Profile of polycythaemia vera in South Western Nigeria

P. Osho, M. Ojo, E. Osho
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引用次数: 0

Abstract

Background: Polycythaemia vera (PV) is the most common myeloproliferative neoplasms (MPNs), others include essential thrombocytosis and primary myelofibrosis. PV is a Philadelphia chromosome-negative MPN, it is a rare haematologic disorder seen primarily in adults aged 60 years and older, with a higher prevalence in men. Aim: The aim of this study is to record the prevalence and explain the epidemiological, clinical, and biological PV in teaching hospital in South Western Nigeria. Materials and Methods: Case notes of all patients with a diagnosis of polycythaemia vera managed at the University of Medical Sciences Teaching Hospital, Ondo state, over a 3-year period between January 2018 and November 2021 were reviewed. The clinical and laboratory findings were extracted from the case records. SPSS-16 (SPSS Inc., USA) and Microsoft Excel statistical software packages were used for statistical calculations. Results: A total of 26 cases of PV were managed at University of Medical Sciences, Ondo state, during the period of the review. There were 20 male and 6 female, with the mean age for males 41.61 ± 18.1 and 32.33 ± 0.52 for females. Majority of the patients in the study (53.8%) had headache and fatigue, 54.5% of the patients experienced dizziness, itching and visual disturbance, hypertension, weight loss, and subconjunctival haemorrhage were found in 6 (23.08%), 5 (19.20%), and 4 (15.40%), respectively, night sweat, dyspepsia, and splenomegaly accounted for (1) 3.85%. None of the patients experienced thrombosis and bleeding. Six of the patients were able to pay for Janus Kinase 2 (JAK2) mutation in which 4 of the results were positive for JAK2 mutation while 2 patients were able to afford to pay for serum erythropoietin; the results were below the normal value. All the patients were able to pay for full blood count, peripheral blood film, and bone marrow aspirations. The average packed cell volume for males was 59.7 ± 2.3 and 55.22 ± 4.9 for females while the mean blood and platelets count in our study was 11.19 ± 1.23 and 486 ± 122.3 × 109/l. Conclusion: The study showed a low prevalence of PV in Nigeria although most cases of PV were seen among the young adults < 60 years of age affecting their life expectancy because it has a detrimental effect on their work productivity, family life, and social life.
尼日利亚西南部真性红细胞增多症概况
背景:真性红细胞增多症(PV)是最常见的骨髓增生性肿瘤(MPNs),其他包括原发性血小板增多症和原发性骨髓纤维化。PV是一种费城染色体阴性MPN,是一种罕见的血液病,主要见于60岁及以上的成年人,在男性中患病率更高。目的:本研究的目的是记录尼日利亚西南部教学医院的流行情况,并解释流行病学、临床和生物学PV。材料和方法:回顾了2018年1月至2021年11月在翁多州医学科学大学教学医院治疗的所有诊断为真性红细胞增多症的患者的病例记录。临床和实验室检查结果摘自病例记录。使用SPSS-16(SPSS股份有限公司,USA)和Microsoft Excel统计软件包进行统计计算。结果:在审查期间,翁多州医学科学大学共处理了26例PV病例。男20例,女6例,男平均年龄41.61±18.1,女平均年龄32.33±0.52。研究中的大多数患者(53.8%)有头痛和疲劳,54.5%的患者有头晕、瘙痒和视觉障碍,高血压、体重减轻和结膜下出血分别发生在6例(23.08%)、5例(19.20%)和4例(15.40%),盗汗、消化不良,脾肿大占3.85%,无血栓形成和出血。其中6名患者能够支付Janus激酶2(JAK2)突变的费用,其中4名患者的JAK2突变结果呈阳性,而2名患者能够负担血清促红细胞生成素的费用;结果低于正常值。所有患者都能支付全血细胞计数、外周血片和骨髓检查的费用。男性的平均堆积细胞体积为59.7±2.3,女性为55.22±4.9,而我们研究中的平均血液和血小板计数分别为11.19±1.23和486±122.3×109/l。结论:研究表明,尽管大多数PV病例发生在60岁以下的年轻人中,但尼日利亚的PV发病率较低,这影响了他们的预期寿命,因为这对他们的工作效率、家庭生活和社会生活有不利影响。
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来源期刊
自引率
0.00%
发文量
65
审稿时长
20 weeks
期刊介绍: The Nigerian Journal of Medicine publishes articles on socio-economic, political and legal matters related to medical practice; conference and workshop reports and medical news.
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