Elferjani Belqis, Liaqat Adnan, Zaman Mohammed, Sexton Marvin
Internal Medicine, Southeast Health Medical Center, Dothan, USA.
Pulmonology, Dothan Pulmonary Associates, Dothan, USA.
Cureus. 2021 Jan 27;13(1):e12936. doi: 10.7759/cureus.12936.
Anti-synthetase syndrome usually comprises interstitial lung disease, myositis, arthralgias, and Raynaud phenomenon. The anti-PL-12 antibody is directed against the enzyme alanyl-tRNA synthetase and has been associated with interstitial lung disease in the absence of inflammatory myositis. We report the case of a 33-year-old woman with complaints of progressive dyspnea, a persistent dry cough, along with intermittent low-grade fever for a few months. A computed tomography (CT) scan of the chest showed the presence of patchy bilateral airspace opacities and infiltrates. It also showed significant mediastinal and hilar lymphadenopathy. Bronchoscopy with transbronchial biopsy was performed, and histopathology changes were consistent with connective tissue disease related to interstitial lung disease. Further workup revealed the presence of anti-PL-12 antibodies. This case illustrates a rare association of interstitial lung disease with the anti-PL-12 antibody.
抗合成酶综合征通常包括间质性肺病、肌炎、关节痛和雷诺现象。抗PL-12抗体针对丙氨酰-tRNA合成酶,与无炎性肌炎的间质性肺病相关。我们报告一例33岁女性病例,患者主诉进行性呼吸困难、持续性干咳,并伴有数月间歇性低热。胸部计算机断层扫描(CT)显示双侧散在的气腔混浊和浸润。还显示有明显的纵隔和肺门淋巴结肿大。进行了支气管镜检查及经支气管活检,组织病理学改变与间质性肺病相关的结缔组织病一致。进一步检查发现存在抗PL-12抗体。该病例说明了间质性肺病与抗PL-12抗体的罕见关联。