Department of Pathology and Graduate Institute of Pathology, College of Medicine, National Taiwan University, Taipei, Taiwan; Department of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
Tuberculosis Research Center, Taiwan Centers for Disease Control, Taipei, Taiwan, ROC; Reference Laboratory of Mycobacteriology, Taiwan Centers for Disease Control, Taipei, Taiwan, ROC.
J Microbiol Immunol Infect. 2024 Oct;57(5):749-759. doi: 10.1016/j.jmii.2024.05.007. Epub 2024 May 24.
Granulomatous lymphadenitis, a histopathological diagnosis, often indicates infections, such as those caused by mycobacterial and fungal agents.
We conducted an analysis of 1098 granulomatous lymphadenitis cases, examining age distribution, lymph node locations, and laterality. Molecular detection of Bacillus Calmette-Guérin (BCG) was performed on archived formalin-fixed paraffin-embedded tissue specimens.
Our analysis revealed a bimodal age distribution, notably with a minor peak in infants. These infantile cases predominantly featured axillary involvement, frequently occurring on the left side. Positive rates of BCG identification decreased with age: <1 year, 71%; 1-2 year, 33%; 2-3 year, 13%; 3-4 year, 0%. Remarkably, only one of the 14 cases with molecularly confirmed BCG lymphadenitis had comments regarding BCG in the pathological report. Compared with patients born after 2016 (BCG at 5-8 months), those born before 2016 (BCG at birth) developed BCG lymphadenitis at a wider age range with right skewness (before 2016, 13 ± 11 months [range, 3-33 months] vs. after 2016, 10 ± 2 months [range, 8-13 months]). Four of the 14 BCG-positive cases had congenital heart disease. Seven patients received anti-tuberculosis drugs following surgical excision. No surgical complications were reported.
BCG lymphadenitis constitutes a distinctive minor peak within the spectrum of granulomatous lymphadenitis in Taiwan. Pathologists should consider the possibility of BCG infection, especially in cases of infantile axillary, supraclavicular, neck lymphadenopathies on the left side. Moreover, BCG administration at 5-8 months may reduce delayed-onset BCG lymphadenitis.
肉芽肿性淋巴结炎是一种组织病理学诊断,常提示感染,如分枝杆菌和真菌引起的感染。
我们分析了 1098 例肉芽肿性淋巴结炎病例,观察年龄分布、淋巴结位置和侧别。对存档的福尔马林固定石蜡包埋组织标本进行卡介苗(BCG)的分子检测。
我们的分析显示出双峰年龄分布,婴儿期有一个小高峰。这些婴儿期病例主要表现为腋窝受累,常发生在左侧。BCG 鉴定的阳性率随年龄降低:<1 岁,71%;1-2 岁,33%;2-3 岁,13%;3-4 岁,0%。值得注意的是,在分子上确认的 14 例 BCG 淋巴结炎中,只有 1 例病理报告中有关于 BCG 的评论。与 2016 年后出生的患者(BCG 在 5-8 个月时接种)相比,2016 年前出生的患者(BCG 在出生时接种)发生 BCG 淋巴结炎的年龄范围更广,呈右偏态(2016 年前,13±11 个月[范围,3-33 个月] vs. 2016 年后,10±2 个月[范围,8-13 个月])。14 例 BCG 阳性病例中有 4 例患有先天性心脏病。7 例患者在手术切除后接受抗结核药物治疗。无手术并发症报告。
BCG 淋巴结炎是台湾肉芽肿性淋巴结炎谱中的一个独特的小高峰。病理学家应考虑 BCG 感染的可能性,特别是在左侧婴儿期、锁骨上、颈部淋巴结病的情况下。此外,在 5-8 个月时给予 BCG 可能会减少迟发性 BCG 淋巴结炎的发生。