S144 Mixed ventilatory defects in pulmonary sarcoidosis: prevalence and clinical features

Author(s):  
V Kouranos ◽  
S Ward ◽  
M Kokosi ◽  
D Castillo ◽  
F Chua ◽  
...  
2016 ◽  
Vol 25 (6) ◽  
pp. 785-789 ◽  
Author(s):  
Aleksandra Radosavljević ◽  
Vesna Jakšić ◽  
Lato Pezo ◽  
Dragana Kovačević-Pavićević ◽  
Aleksandra Ilić ◽  
...  

2020 ◽  
Vol 169 ◽  
pp. 105998
Author(s):  
Adriana Iriarte ◽  
Manuel Rubio-Rivas ◽  
Nadia Villalba ◽  
Xavier Corbella ◽  
Juan Mañá

2021 ◽  
Vol 10 (3) ◽  
pp. 3438-3444
Author(s):  
Yun Li ◽  
Zhixin Liang ◽  
Yiqiong Zheng ◽  
Juan Qiao ◽  
Ping Wang

2018 ◽  
Vol 2018 ◽  
pp. 1-6 ◽  
Author(s):  
Seung Yong Choi ◽  
Jae Hoon Lee ◽  
Jae-Yon Won ◽  
Jeong Ah Shin ◽  
Young-Hoon Park

Purpose. To investigate the clinical features and ocular manifestations of biopsy-proven pulmonary sarcoidosis in Korea. Methods. 55 patients diagnosed with pulmonary sarcoidosis by bronchoscopic or excisional biopsy were included. By retrospective clinical chart review, we investigated features of uveitis, ocular and systemic treatments, visual acuity, angiotensin-converting enzyme level, chest radiography, and pulmonary function tests. Clinical features were analyzed by presence of uveitis, site of biopsy, and first manifested sign of sarcoidosis. Results. The group with uveitis (n=39) presented with higher systemic (71.8%) and immunosuppressive treatment rates (35.9%) than the group without uveitis (31.3%, 0%, resp.) (P=0.007, P=0.005, resp.). There were no significant differences in clinical features, including systemic treatment rate, by type of biopsy. Of 39 patients with uveitis, the group with ocular manifestation as a first sign of sarcoidosis showed higher systemic and immunosuppressive treatment rates (88.9%, 55.6%) compared to the group with pulmonary manifestation as a first sign (57.1%, 19.0%) (P=0.037, P=0.018, resp.). Conclusions. In patients with biopsy-proven pulmonary sarcoidosis, the presence of ocular involvement and uveitis as a first sign could be significant factors associated with higher systemic treatment rate, especially with immunosuppressive agents. Biopsy site determined by location and size had no influence on clinical features.


2017 ◽  
Vol 56 (15) ◽  
pp. 1957-1960 ◽  
Author(s):  
Yuki Iijima ◽  
Yukihiko Sugiyama ◽  
Michiru Sawahata ◽  
Masayuki Nakayama ◽  
Masashi Bando

2020 ◽  
Vol 41 (05) ◽  
pp. 607-617
Author(s):  
W. Ennis James

AbstractSarcoidosis is a multisystem inflammatory disease characterized by noncaseating granulomatous inflammation. While pulmonary sarcoidosis is most common, extrapulmonary involvement occurs in 50 to 74% of patients and can be the presenting abnormality in some patients. The diagnosis of sarcoidosis is based on a compatible clinical presentation in combination with granulomas on histology and exclusion of other causes. However, the absence of a diagnostic biomarker for sarcoidosis, in addition to the overlap of granulomatous inflammation and nonspecific clinical findings with other diseases, often results in a delayed diagnosis. Sarcoidosis overlap syndromes are typically described when sarcoidosis is diagnosed in the presence of another disease (concurrently or sequentially) with shared clinical and histologic features, or when sarcoidosis presents with clinical features typically observed in, but not diagnostic of, other diseases. Awareness of overlap syndromes is important for clinicians to avoid diagnostic errors and evaluate for concomitant diagnoses that may impact the management and outcome of sarcoidosis. This article is intended to provide an overview of these presentations and the most commonly associated diseases, with attention to their prevalence, clinical features, and reciprocal impacts on disease outcomes.


Sign in / Sign up

Export Citation Format

Share Document