Waseda Yuko, Johkoh Takeshi, Egashira Ryoko, Sumikawa Hiromitsu, Saeki Keigo, Watanabe Satoshi, Matsunuma Ryo, Takato Hazuki, Ichikawa Yukari, Hamaguchi Yasuhito, Shiraki Akira, Muro Yoshinao, Yasui Masahide, Prosch Helmut, Herold Christian, Kasahara Kazuo
From the Department of Respiratory Medicine, Japan Community Health care Organization Kanazawa Hospital, Ha-15, Oki-machi, Kanazawa, Ishikawa 920-8641, Japan.
From the Department of Respiratory Medicine, Japan Community Health care Organization Kanazawa Hospital, Ha-15, Oki-machi, Kanazawa, Ishikawa 920-8641, Japan.
Eur J Radiol. 2016 Aug;85(8):1421-6. doi: 10.1016/j.ejrad.2016.05.012. Epub 2016 May 24.
To describe the pulmonary CT findings in patients with anti-ARS-antibody-positive interstitial lung disease (anti-ARS-ILD) METHODS: The CT findings of 64 patients with anti-ARS-ILD were retrospectively reviewed. The images were retrospectively reviewed independently by 2 chest radiologists, and the final decision on the CT findings was made by a third chest radiologist.
There were 16 male and 48 female patients, aged 54.2±13.4 years. Sixteen patients had anti Jo-1, 24 had anti-EJ, 9 had anti-PL-7, 7 had anti-PL-12, 5 had anti-KS, and 3 had anti-OJ antibodies. Overall, 63 patients (98.4%) had CT findings predominantly in the lower lobe; 61 patients (95.3%) showed peripheral opacities, and 47 patients (73.4%) showed peribronchovascular opacities. Ground-glass attenuation, consolidation, and reticulation showed similar distribution patterns. Regarding detailed CT findings, 89.1% of patients had lower volume loss, 76.6% had interlobular septal thickening, and 67.2% had thickening of bronchovascular bundles. The final radiologic diagnoses were as follows: inconsistent with usual interstitial pneumonia (UIP) in 63 patients (98.4%), which included nonspecific interstitial pneumonia (NSIP) in 35 patients (55.6%), organizing pneumonia (OP) in 4 patients (6.3%), and OP with fibrosis in 22 patients (34.9%).
The characteristic CT findings of patients with anti-ARS-ILD were areas of ground-glass attenuation and reticulation, predominantly distributed as lower and peribronchovascular lesions, which is compatible with NSIP. One-third of patients showed OP with fibrosis.
描述抗合成酶抗体阳性间质性肺疾病(抗ARS-ILD)患者的肺部CT表现。方法:回顾性分析64例抗ARS-ILD患者的CT表现。图像由2名胸部放射科医生独立进行回顾性分析,最终的CT诊断由第3名胸部放射科医生做出。
患者中男性16例,女性48例,年龄54.2±13.4岁。16例患者抗Jo-1抗体阳性,24例抗EJ抗体阳性,9例抗PL-7抗体阳性,7例抗PL-12抗体阳性,5例抗KS抗体阳性,3例抗OJ抗体阳性。总体而言,63例患者(98.4%)CT表现主要位于下叶;61例患者(95.3%)表现为外周性实变影,47例患者(73.4%)表现为支气管血管周围实变影。磨玻璃影、实变影和网状影分布相似。关于详细的CT表现,89.1%的患者有肺容积减小,76.6%有小叶间隔增厚,67.2%有支气管血管束增粗。最终影像学诊断如下:63例患者(98.4%)不符合普通型间质性肺炎(UIP),其中35例患者(55.6%)为非特异性间质性肺炎(NSIP),4例患者(6.3%)为机化性肺炎(OP),22例患者(34.9%)为伴有纤维化的OP。
抗ARS-ILD患者典型的CT表现为磨玻璃影和网状影,主要分布于下叶及支气管血管周围,符合NSIP表现。三分之一的患者表现为伴有纤维化的OP。