Transbronchial Cryobiopsy for the Diagnosis of Culture Negative Miliary Tuberculosis

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL Clinical Case Reports Pub Date : 2024-11-19 DOI:10.1002/ccr3.9595
Atif Saleem Siddiqui
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BAL and tracheal aspirates were negative for <i>Mycobacterium tuberculosis</i> (MTB) polymerase chain reaction (PCR), acid-fast bacilli (AFB), bacterial, and fungal cultures. He remained on mechanical ventilation for 1 week, and all his cultures were negative. A second bronchoscopy with transbronchial cryobiopsy (TBLC) was performed to obtain a tissue diagnosis. TBLC revealed caseating granulomas and multinucleated giant cells (Figure 1B). Grocott's methenamine silver stain was negative. Tissue AFB cultures and MTB PCR obtained via TBLC came back positive for tuberculosis within 1 week. The patient was started on rifampin, isoniazid, pyrazinamide, and ethambutol for a 6-month course. He required a tracheostomy 16 days after mechanical ventilation and was able to wean off mechanical ventilation, being successfully decannulated 2 weeks after the tracheostomy.</p><p>Miliary tuberculosis is a life-threatening hematogenous dissemination of <i>Mycobacterium tuberculosis</i> bacilli. The diagnosis of pulmonary tuberculosis is determined by symptoms, risk factors, sputum smear microscopy, and chest radiography. In miliary TB, acid-fast bacilli (AFB) smears are positive in only 20%–25% of cases, and cultures of sputum are positive in 30%–65% of patients [<span>1</span>]. Transbronchial biopsy diagnostic yields are 62.5%–76% [<span>2</span>]. TBLC has been widely used for the diagnosis of interstitial lung disease. However, the role of TBLC in the diagnosis of culture-negative miliary TB remains unclear. There is limited data on the use of TBLC in culture-negative miliary TB. A case report by Nasu et al. [<span>3</span>] demonstrated the utility of TBLC in diagnosing miliary tuberculosis that initially mimicked hypersensitivity pneumonitis. In this case, cryobiopsy specimens revealed necrotic granulomas, which led to a re-examination of sputum and subsequent identification of <i>Mycobacterium tuberculosis</i>. 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Abstract

A 19-year-old male with no known medical comorbidities presented to the emergency department with a dry cough and shortness of breath for 3 months. His heart rate was 114/min, respiratory rate was 32/min, blood pressure was 110/80 mmHg, temperature was 101.5 °F, and oxygen saturation was 86% on room air. Initial laboratory data were normal, and a serum Quantiferon test was positive. Computed tomography (CT) of the chest showed bilateral diffuse miliary infiltrates and ground-glass opacities (GGO), with mild bronchiectasis in the left upper lobe (Figure 1A). He required heated high-flow oxygen in the emergency department; however, he was intubated due to worsening respiratory failure and increased work of breathing. Bronchoscopy with bronchoalveolar lavage (BAL) was performed. BAL and tracheal aspirates were negative for Mycobacterium tuberculosis (MTB) polymerase chain reaction (PCR), acid-fast bacilli (AFB), bacterial, and fungal cultures. He remained on mechanical ventilation for 1 week, and all his cultures were negative. A second bronchoscopy with transbronchial cryobiopsy (TBLC) was performed to obtain a tissue diagnosis. TBLC revealed caseating granulomas and multinucleated giant cells (Figure 1B). Grocott's methenamine silver stain was negative. Tissue AFB cultures and MTB PCR obtained via TBLC came back positive for tuberculosis within 1 week. The patient was started on rifampin, isoniazid, pyrazinamide, and ethambutol for a 6-month course. He required a tracheostomy 16 days after mechanical ventilation and was able to wean off mechanical ventilation, being successfully decannulated 2 weeks after the tracheostomy.

Miliary tuberculosis is a life-threatening hematogenous dissemination of Mycobacterium tuberculosis bacilli. The diagnosis of pulmonary tuberculosis is determined by symptoms, risk factors, sputum smear microscopy, and chest radiography. In miliary TB, acid-fast bacilli (AFB) smears are positive in only 20%–25% of cases, and cultures of sputum are positive in 30%–65% of patients [1]. Transbronchial biopsy diagnostic yields are 62.5%–76% [2]. TBLC has been widely used for the diagnosis of interstitial lung disease. However, the role of TBLC in the diagnosis of culture-negative miliary TB remains unclear. There is limited data on the use of TBLC in culture-negative miliary TB. A case report by Nasu et al. [3] demonstrated the utility of TBLC in diagnosing miliary tuberculosis that initially mimicked hypersensitivity pneumonitis. In this case, cryobiopsy specimens revealed necrotic granulomas, which led to a re-examination of sputum and subsequent identification of Mycobacterium tuberculosis. The patient described in our case had ground-glass opacities (GGO), a rare presentation of miliary TB. Furthermore, sputum and BAL AFB cultures, as well as MTB PCR, were negative. Additionally, Sánchez-Cabral et al. highlighted the diagnostic value of TBLC in non-interstitial lung diseases, including infectious diseases like TB. The study reported a high diagnostic yield when TBLC was combined with bronchoalveolar lavage (BAL), suggesting that TBLC can be a robust diagnostic tool in cases where traditional methods are inconclusive. This case contributes to the limited pool of literature, highlighting the use of TBLC in miliary TB in patients with negative BAL and tracheal aspirates. Furthermore, GGO is an uncommon CT chest characteristic of disseminated TB and can be associated with serious complications. In conclusion, further studies are needed to determine the utility and diagnostic yield of TBLC in this patient population.

Atif Saleem Siddiqui: conceptualization, data curation, formal analysis, investigation, methodology, project administration, resources, software, validation, visualization, writing – original draft, writing – review and editing.

Written informed consent was obtained from the patient to publish this report in accordance with the journal's patient consent policy.

The author declares no conflicts of interest.

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经支气管冷冻活组织检查诊断培养阴性纤毛膜结核病
一名 19 岁的男性因干咳和气短 3 个月来到急诊科就诊。他的心率为 114 次/分,呼吸频率为 32 次/分,血压为 110/80 mmHg,体温为 101.5 °F,室内空气中的血氧饱和度为 86%。初步实验室数据正常,血清定量因子检测呈阳性。胸部计算机断层扫描(CT)显示双侧弥漫性粟粒状浸润和磨玻璃不透明(GGO),左上叶有轻度支气管扩张(图 1A)。他在急诊科需要加热高流量氧气,但由于呼吸衰竭恶化和呼吸功增加,他被插管。进行了支气管镜检查和支气管肺泡灌洗(BAL)。BAL 和气管抽吸物的结核分枝杆菌(MTB)聚合酶链反应(PCR)、耐酸杆菌(AFB)、细菌和真菌培养结果均为阴性。他接受了一周的机械通气,所有培养结果均为阴性。为了获得组织诊断,医生为他进行了第二次支气管镜检查和经支气管冷冻活检(TBLC)。经支气管镜检查发现了酪状肉芽肿和多核巨细胞(图 1B)。格罗戈特甲氧那明银染色呈阴性。通过 TBLC 获得的组织 AFB 培养和 MTB PCR 检测结果在 1 周内呈结核病阳性。患者开始接受利福平、异烟肼、吡嗪酰胺和乙胺丁醇治疗,疗程为 6 个月。机械通气后 16 天,他需要进行气管造口术,并在气管造口术 2 周后成功脱离机械通气。肺结核的诊断取决于症状、危险因素、痰涂片镜检和胸片检查。在粟粒性肺结核中,仅有 20%-25% 的病例酸性耐药杆菌(AFB)涂片呈阳性,30%-65% 的患者痰培养呈阳性[1]。经支气管活检的诊断率为 62.5%-76% [2]。TBLC 已被广泛用于间质性肺病的诊断。然而,TBLC 在培养阴性的粟粒性肺结核诊断中的作用仍不明确。关于 TBLC 在培养阴性的粟粒性肺结核中应用的数据很有限。Nasu 等人的一份病例报告[3]证明了 TBLC 在诊断最初模仿超敏性肺炎的淤胆型肺结核中的作用。在该病例中,冷冻活组织切片标本发现了坏死性肉芽肿,这导致了对痰液的再次检查,随后确定了结核分枝杆菌。我们病例中描述的患者出现了磨玻璃不透明(GGO),这是一种罕见的粟粒性肺结核表现。此外,痰和 BAL AFB 培养以及 MTB PCR 均为阴性。此外,Sánchez-Cabral 等人强调了 TBLC 对非间质性肺部疾病(包括肺结核等传染性疾病)的诊断价值。该研究报告称,当 TBLC 与支气管肺泡灌洗(BAL)结合使用时,诊断率很高,这表明在传统方法无法得出结论的情况下,TBLC 可以成为一种强有力的诊断工具。本病例为有限的文献库做出了贡献,强调了 TBLC 在 BAL 和气管抽吸物阴性的粟粒性肺结核患者中的应用。此外,GGO 是播散性肺结核不常见的 CT 胸部特征,可能与严重的并发症有关。Atif Saleem Siddiqui:构思、数据整理、正式分析、调查、方法学、项目管理、资源、软件、验证、可视化、撰写-原稿、撰写-审阅和编辑。根据期刊的患者同意政策,发表本报告已获得患者的书面知情同意。
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Clinical Case Reports
Clinical Case Reports MEDICINE, GENERAL & INTERNAL-
自引率
14.30%
发文量
1268
审稿时长
13 weeks
期刊介绍: Clinical Case Reports is different from other case report journals. Our aim is to directly improve global health and increase clinical understanding using case reports to convey important best practice information. We welcome case reports from all areas of Medicine, Nursing, Dentistry, and Veterinary Science and may include: -Any clinical case or procedure which illustrates an important best practice teaching message -Any clinical case or procedure which illustrates the appropriate use of an important clinical guideline or systematic review. As well as: -The management of novel or very uncommon diseases -A common disease presenting in an uncommon way -An uncommon disease masquerading as something more common -Cases which expand understanding of disease pathogenesis -Cases where the teaching point is based on an error -Cases which allow us to re-think established medical lore -Unreported adverse effects of interventions (drug, procedural, or other).
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