Clinicopathological guide to malignant bone tumours: A retrospective analysis of the cancer registry at Kilimanjaro Christian Medical Centre in northern Tanzania

Pamela T.K. Samoyo, Gilbert Z Nkya, F. Minja, R. Temu
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Abstract

Background: Primary neoplasms of the skeleton are rare. This study aimed at determining the spectrum of different malignant bone tumours at a tertiary hospital cancer registry in the Northern Zone of Tanzania, along with related symptoms, clinical presentations, and clinical diagnosis accuracy (using histology as the standard). Methods: This retrospective study reviewed bone specimen records in the cancer registry at Kilimanjaro Christian Medical Centre (KCMC) in Tanzania, for the period from 1 January 1998-31 December 2012. Patient information for corresponding cancer registry records was traced from hospital files and x-ray reports. Data were analysed using a mixed quantitative and qualitative approach. Results: Two hundred twenty-five malignant bone tumours were recorded at KCMC Cancer Registry over a period of 14 years. Seventy-five with adequate records were analysed. Forty-seven patients (62.7%) were male. Mean age was 34.1 (standard deviation 20) years. The femur was affected in 26 cases (34.7%). Osteosarcoma (22 cases; 29.3%) was the most common malignant bone tumour. Clinicians correctly preliminarily diagnosed multiple myeloma, osteosarcoma, and ameloblastoma, but had inexperience with carcinomas and other types of sarcomas. Chronic osteomyelitis and metastatic lesions were mentioned frequently by radiologists as the diagnosis of some malignant bone tumours that turned out to be carcinomas or sarcomas on histology. Conclusions: Clinician and radiologist training of other types of malignant bone tumours other than multiple myeloma, osteosarcoma, and ameloblastoma is required. An Orthopaedic Biopsy Form (OBF) was developed to address high loss to follow-up (66.7%). https://dx.doi.org/10.4314/ecajs.v22i2.4   This work is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source (including a link to the formal publication), provide a link to the Creative Commons license, and indicate if changes were made.
恶性骨肿瘤的临床病理指南:坦桑尼亚北部乞力马扎罗山基督教医疗中心癌症登记的回顾性分析
背景:骨骼的原发性肿瘤是罕见的。本研究旨在确定坦桑尼亚北部地区三级医院癌症登记处不同恶性骨肿瘤的频谱,以及相关症状、临床表现和临床诊断准确性(以组织学为标准)。方法:本回顾性研究回顾了1998年1月1日至2012年12月31日期间坦桑尼亚乞力马扎罗山基督教医疗中心(KCMC)癌症登记处的骨标本记录。从医院档案和x光报告中追踪相应癌症登记记录的患者信息。数据分析采用混合定量和定性方法。结果:在14年间,KCMC癌症登记处记录了225例恶性骨肿瘤。分析了75个有充分记录的案例。男性47例(62.7%)。平均年龄34.1岁(标准差20)。股骨受累26例(34.7%)。骨肉瘤22例;29.3%)为最常见的恶性骨肿瘤。临床医生对多发性骨髓瘤、骨肉瘤和成釉细胞瘤的初步诊断是正确的,但对癌和其他类型的肉瘤缺乏经验。慢性骨髓炎和转移性病变经常被放射科医师提及,因为一些恶性骨肿瘤的诊断结果在组织学上是癌或肉瘤。结论:除多发性骨髓瘤、骨肉瘤和成釉细胞瘤外,临床医生和放射科医生需要接受其他类型恶性骨肿瘤的培训。骨科活检表(OBF)是为了解决随访损失高(66.7%)的问题而开发的。https://dx.doi.org/10.4314/ecajs.v22i2.4本作品遵循知识共享署名4.0国际许可协议,允许在任何媒体上不受限制地使用、分发和复制,前提是您要适当注明原作者和来源(包括正式出版物的链接),提供知识共享许可协议的链接,并注明是否进行了更改。
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