Montgomery Nathan D, Liomba N George, Kampani Coxcilly, Krysiak Robert, Stanley Christopher C, Tomoka Tamiwe, Kamiza Steve, Dhungel Bal M, Gopal Satish, Fedoriw Yuri
From the Department of Pathology and Laboratory Medicine, Division of Hematopathology.
UNC Project-Malawi, Lilongwe, Malawi.
Am J Clin Pathol. 2016 Oct;146(4):423-30. doi: 10.1093/ajcp/aqw118. Epub 2016 Sep 4.
The incidence of lymphoproliferative disorders (LPDs) is increasing in sub-Saharan Africa (SSA) due to population growth, aging, and human immunodeficiency virus (HIV). Despite significant burden, resources for diagnosis and treatment of LPDs are limited, with little infrastructure to deliver modern pathology services. Diagnostic and therapeutic decisions are therefore frequently made without tissue confirmation, leading to high rates of misdiagnosis and inappropriate treatment.
We have established a laboratory in Malawi to support clinical and research efforts at a national teaching hospital. Consensus real-time diagnoses are rendered by local pathologists after weekly clinicopathologic teleconferences involving clinicians and pathologists from the United States and Malawi. Additional ancillary studies are then performed in the United States prior to final diagnosis.
We report our first 2 years' experience and demonstrate high concordance between real-time diagnoses in Malawi and final diagnoses in the United States (5% major discordance rate for formalin-fixed, paraffin-embedded samples). In addition, we describe characteristics of pathologically confirmed LPDs in Malawi, highlighting differences by HIV status.
Our multidisciplinary approach can be a model for strong pathology services that provide direct, real-time support to clinical care and research in SSA.
由于人口增长、老龄化以及人类免疫缺陷病毒(HIV)感染,撒哈拉以南非洲(SSA)地区淋巴增殖性疾病(LPDs)的发病率正在上升。尽管负担沉重,但LPDs的诊断和治疗资源有限,提供现代病理学服务的基础设施很少。因此,诊断和治疗决策常常在没有组织确诊的情况下做出,导致误诊率和不适当治疗率很高。
我们在马拉维建立了一个实验室,以支持一家国家教学医院的临床和研究工作。每周举行一次临床病理电话会议,美国和马拉维的临床医生和病理学家参加,之后由当地病理学家做出实时共识诊断。然后在美国进行额外的辅助研究,再做出最终诊断。
我们报告了最初两年的经验,并证明马拉维的实时诊断与美国的最终诊断高度一致(福尔马林固定、石蜡包埋样本的主要不一致率为5%)。此外,我们描述了马拉维经病理确诊的LPDs的特征,突出了HIV感染状态的差异。
我们的多学科方法可以成为强大病理学服务的典范,为SSA地区的临床护理和研究提供直接、实时的支持。