罕见的肺外结核病:隐匿症状与诊断难题。

Guddi Rani Singh, Anila Sinha, Anushweta, Richa Sharma, Kumar Saurabh, Debaditya Haldar
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引用次数: 0

摘要

背景:肺结核如果未能及早发现,或处于免疫功能低下状态,可能会导致血行和淋巴管扩展,从而引发肺外结核。肺外结核的罕见部位包括胃肠道、肌肉骨骼系统、生殖道、中耳和心包。组织病理学发现大融合性肉芽肿伴或不伴有干酪样坏死,同时在齐氏-奈尔森(ZN)染色法中检测到酸性无菌杆菌(AFB),以及检测结核分枝杆菌 DNA 的 GeneXpert 是确诊肺结核的关键:本研究纳入了经活检证实的肺外肉芽肿病变。对送往病理科的所有肺外活检标本进行组织病理学评估,以确定是否存在肉芽肿和坏死,并对所有存在或不存在坏死的肉芽肿病变病例进行 AFB ZN 染色。同样的病例,其活组织切片标本在正常生理盐水中送检,并在分子实验室借助 GeneXpert MTB 检测结核分枝杆菌 DNA 的帮助下进行了重新评估。所有送往病理科的肺外部位活检标本均用于提取 DNA:结果:在 10 例肺外肉芽肿病变中,8 例显微镜下显示病例性坏死,7 例齐氏-奈尔森染色显示存在耐酸杆菌。基因检测仪在 9 例病例中检测到结核分枝杆菌 DNA:结论:肺外结核很少是原发性的,大多是从肺实质经血行播散而来。胃肠道、腹膜、淋巴结和实体内脏结核统称为腹腔结核。心包结核和耳结核等实体病极为罕见。在诊断困难的慢性无应答病例中,肺外结核应作为鉴别诊断依据。为避免诊断延误,在高度怀疑的病例中,应进行活组织切片检查,同时进行 ZN 染色以确诊,因为这样做成本效益高;在高度怀疑的病例中,如果没有病理坏死且 ZN 染色阴性,则应进行基因Xpert 检测结核分枝杆菌。
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Rare Extrapulmonary Tuberculosis: Covert symptoms and Diagnostic Dilemma.

Background: Pulmonary tuberculosis may result in haematogenous and lymphatic extension in case of failure of early detection, or immunocompromised status, leading to extrapulmonary tuberculosis. Rare sites of extrapulmonary tuberculosis include the gastrointestinal tract, musculoskeletal system, genital tract, middle ear and pericardium. Histopathological findings of macro-confluent granuloma with or without caseous necrosis, along with detection of acid-fast bacilli (AFB) on Ziehl-Neelsen (ZN) staining, and GeneXpert for detection of Mycobacterium tuberculosis DNA, are key in establishing a diagnosis of tuberculosis.

Methodology: Biopsy-proven extrapulmonary granulomatous lesions were included in this study. Histopathological evaluation of all extrapulmonary biopsy specimens sent to the Department of Pathology were done for the presence of granuloma and necrosis, and ZN staining for AFB was done in all the cases of granulomatous lesions with or without the presence of necrosis. The same cases, with biopsy specimens sent in normal saline, were re-evaluated in a molecular laboratory with the help of GeneXpert MTB to detect the DNA of Mycobacterium tuberculosis. All biopsy specimens from extrapulmonary sites which were sent to the Department of Pathology were used for DNA extraction.

Results: Out of the 10 cases of extrapulmonary granulomatous lesions, 8 showed caseous necrosis on microscopy, and 7 showed the presence of acid-fast bacilli on Ziehl-Neelsen staining. GeneXpert detected DNA of Mycobacterium tuberculosis in 9 cases.

Conclusion: Extrapulmonary tuberculosis rarely occurs as primary, and mostly spreads from lung parenchyma via a haematogenous route. Tuberculosis of the gastrointestinal tract, peritoneum, lymph nodes, and solid viscera are together termed abdominal tuberculosis. Entities like tuberculosis of the pericardium and ear are extremely rare. Extrapulmonary tuberculosis should be a differential in cases of chronic non-responding cases with diagnostic dilemmas. To avoid diagnostic delay, in cases of high suspicion, one should go for biopsy along with ZN staining for diagnostic confirmation as this is cost-effective, followed by GeneXpert for Mycobacterium tuberculosis in highly suspected cases with absent caseous necrosis and negative ZN staining.

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