坦桑尼亚达累斯萨拉姆Muhimbili国家医院卡波西肉瘤的临床和组织病理学诊断评估。

The East African health research journal Pub Date : 2024-01-01 Epub Date: 2025-01-30 DOI:10.24248/eahrj.v8i3.809
Edrick M Elias, Amos Rodger Mwakigonja
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引用次数: 0

摘要

背景:卡波西肉瘤(KS)的治疗和预后取决于正确的组织病理学诊断,然而,发展中国家的大多数KS病例在临床诊断时没有组织病理学证实,这导致过度诊断或诊断不足。此外,由于在KS的不同阶段(包括良性到致死性疾病)存在大量的组织病理学模拟物,因此KS的组织病理学诊断并不总是正确的。然而,HHV-8-LANA-1免疫组织化学(IHC)染色在几乎所有KS病变中都呈阳性,被认为是区分KS与其组织学模拟物的重要诊断工具。本研究旨在确定卡波西肉瘤在MNH的诊断质量,以及是否可以通过常规的HHV-8-LANA-1免疫组化染色来提高卡波西肉瘤的诊断质量。方法:这是一项基于医院的回顾性横断面研究,对2018年通过临床、组织病理学或两者诊断的所有KS病例进行了研究。根据H&E形态学诊断KS,并通过HHV-8-LANA-1免疫组织化学证实KS。比较HHV-8-LANA-1免疫组化对临床和组织病理学的诊断价值。结果:对KS的初步诊断与复查组织病理学几乎完全一致(Kappa值= 0.892,p值= 0.000)。临床诊断符合率为61%,无一致性(Kappa值-0.123,p值=0.102)。临床鉴别诊断包括范围广泛的病理条件,从不太严重的炎症到致命的恶性条件。初始组织病理学与HHV-8-LANA-1免疫组化对KS的诊断有很大的一致性(Kappa=0.70, p值0.000),组织病理学一致性率为88%。结论:本研究表明,MNH对KS的组织病理误诊不太可能是人为失误,因此需要对所有临床KS疑似病例进行组织病理学检查并进行HHV-8-LANA-1免疫组化证实。我们建议在每一个临床疑似KS病例中,都应进行充分的组织活检,进行组织病理学分析和HHV8-LANA-1免疫染色,以避免不适当的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Clinical and Histopathological Diagnosis of Kaposi's Sarcoma at Muhimbili National Hospital, Dar es Salaam, Tanzania.

Background: Treatment and outcome of Kaposi's sarcoma (KS) depend on a correct histopathological diagnosis, however, most KS cases in developing countries are diagnosed clinically without histopathological confirmation, which results in either over or under-diagnosis. Also, due to the number of histopathological mimickers in different stages of KS which include benign to fatal conditions, the histopathological diagnosis of KS is not always correct. However, the HHV-8-LANA-1 Immunohistochemical (IHC) stain is positive in nearly all KS lesions and is considered to be an important diagnostic tool to differentiate KS from its histological mimickers. This study aimed to determine the quality of Kaposi's sarcoma diagnosis at MNH and whether it can be improved by the routine of HHV-8-LANA-1 immunohistochemical stain.

Methodology: This was a retrospective cross-sectional hospital-based study of all KS cases diagnosed either by clinical, histopathological, or both in 2018. KS was diagnosed based on H&E morphology and confirmed by HHV-8-LANA-1 immunohistochemistry. The diagnosis utility of clinical and histopathology was compared with HHV-8-LANA-1 immunohistochemistry.

Results: There was almost perfect agreement between initial and reviewed histopathology for KS diagnosis (Kappa value= 0.892, p-value=.000). The clinical diagnosis concordance rate was 61% with no agreement (Kappa value -0.123, p-value=0.102). Clinical differential diagnosis included a wide range of pathological conditions ranging from less severe inflammatory to fatal malignant conditions. There was a substantial agreement between initial histopathology and HHV-8-LANA-1 IHC for KS diagnosis (Kappa=0.70, p-value .000) with a histopathology concordance rate of 88%.

Conclusion: Histopathological examination of all clinical KS suspicions and HHV-8-LANA-1 immunohistochemistry confirmation is required since the study showed that the histopathology misdiagnosis of KS at MNH was unlikely to be the result of human error. We recommend that in every clinically suspected KS case, an adequate tissue biopsy should be taken for histopathology analysis and HHV8-LANA-1 immunostaining to avoid inappropriate treatment.

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