Song Minji, Kim Sung Jin, Yoo Jin Young
Department of Radiology, Chungbuk National University Hospital.
Department of Radiology, Chungbuk National University College of Medicine, Cheongju, Korea.
Medicine (Baltimore). 2020 Nov 13;99(46):e23204. doi: 10.1097/MD.0000000000023204.
Steroid is known to cause generalized immunosuppression, thereby increasing the risk of new infection or recurrence of tuberculosis. However, corticosteroid as a culprit for exacerbation of miliary tuberculosis-from a cryptic to an overt form-has rarely been described in the literature. Moreover, miliary tuberculosis is hardly diagnosed in a living patient as a primary cause of ARDS even in TB-endemic regions. To the best of our knowledge, this is the first case of a steroid-induced progression of cryptic miliary tuberculosis to ARDS, provided with clear depiction of its radiologic evolution.
A 36-year-old male was treated with corticosteroid under suspicion of adult onset still's disease for six-week history of fever. Within 2 weeks since the initiation of corticosteroid therapy, the patient experienced acute exacerbation of cryptic miliary tuberculosis, which evolved to an overt form, appearing as miliary nodules on both chest radiograph and HRCT. Then, his condition suddenly deteriorated to severe acute respiratory distress syndrome in less than a day.
The final diagnosis was miliary tuberculosis complicated by severe acute respiratory distress syndrome.
The patient was placed on classic quadruple anti-TB treatment (isoniazide, ethambutol, rifampin, and pyrazinamide).
His fever subsided in about 6 weeks and 3 consecutive sputum AFB smears collected on different days were confirmed negative. Diffuse infiltrates on his chest x-ray were completely resolved.
The case described here draws a clinical and radiological picture of how an occult form of miliary TB evolved to an overt form with use of steroid, and then suddenly progressed to acute respiratory distress syndrome in an immunocompetent young male. This raises awareness on the potential risk of using corticosteroid in patients with cryptic miliary TB. There is formidable challenge in the diagnosis of miliary TB, especially in the early stages. Atypical or even normal outcomes of clinical, microbiochemical, and radiologic evaluation should not be overlooked and dedicated diagnostic work-up should be performed. For equivocal cases, active surveillance with serial radiographs can be helpful.
已知类固醇会导致全身免疫抑制,从而增加新感染或结核病复发的风险。然而,皮质类固醇作为粟粒性结核病从隐匿型恶化为显性形式的罪魁祸首,在文献中很少被描述。此外,即使在结核病流行地区,粟粒性结核病作为急性呼吸窘迫综合征(ARDS)的主要病因在活体患者中也很难被诊断出来。据我们所知,这是第一例类固醇诱导隐匿性粟粒性结核病进展为ARDS的病例,并对其影像学演变进行了清晰描述。
一名36岁男性因发热6周被怀疑患有成人斯蒂尔病而接受皮质类固醇治疗。在开始皮质类固醇治疗后的2周内,患者隐匿性粟粒性结核病急性加重,发展为显性形式,胸部X线片和高分辨率CT(HRCT)上均出现粟粒结节。然后,他的病情在不到一天的时间里突然恶化为严重急性呼吸窘迫综合征。
最终诊断为粟粒性结核病并发严重急性呼吸窘迫综合征。
患者接受了经典的四联抗结核治疗(异烟肼、乙胺丁醇、利福平、吡嗪酰胺)。
他的发热在约6周后消退,连续3天采集的痰涂片抗酸杆菌检查均证实为阴性。胸部X线片上的弥漫性浸润完全消失。
此处描述的病例展现了隐匿型粟粒性结核病如何在使用类固醇后演变为显性形式,然后在一名免疫功能正常的年轻男性中突然进展为急性呼吸窘迫综合征的临床和影像学表现。这提高了对隐匿性粟粒性结核病患者使用皮质类固醇潜在风险的认识。粟粒性结核病的诊断存在巨大挑战,尤其是在早期阶段。不应忽视临床、微生物学和影像学评估的非典型甚至正常结果,应进行专门的诊断检查。对于可疑病例,连续进行胸部X线片的主动监测可能会有所帮助。