scholarly journals Sjögren Syndrome Complicated by Mucosa-Associated Lymphoid Tissue Lymphoma and Lymphocytic Interstitial Pneumonia

2015 ◽  
Vol 5 ◽  
Author(s):  
Fatma Ahmed ◽  
Osama Raslan ◽  
Razi Muzaffar ◽  
Nadeem Parkar ◽  
Nitin Marwaha ◽  
...  
CHEST Journal ◽  
2018 ◽  
Vol 153 (3) ◽  
pp. e41-e43 ◽  
Author(s):  
Grace Thompson ◽  
Andrew Mclean-Tooke ◽  
Jeremy Wrobel ◽  
Melanie Lavender ◽  
Michaela Lucas

2020 ◽  
Vol 53 (5) ◽  
pp. 287-292 ◽  
Author(s):  
Guilherme Felix Louza ◽  
Luiz Felipe Nobre ◽  
Alexandre Dias Mançano ◽  
Bruno Hochhegger ◽  
Arthur Soares Souza Jr. ◽  
...  

Abstract Objective: To analyze the computed tomography (CT) findings of lymphocytic interstitial pneumonia (LIP). Materials and Methods: We retrospectively reviewed the clinical and CT findings of 36 patients with LIP, including 25 women and 11 men, with a mean age of 52.5 years (age range, 22-78 years). Results: The main associated diseases with LIP were Sjögren syndrome (42%), human immunodeficiency virus infection (17%), amyloidosis (17%), Sjögren syndrome associated with secondary amyloidosis (11%), idiopathic (8%), and systemic lupus erythematosus (5%). The predominant CT abnormalities were multiple cystic airspaces (n = 35), small nodules (n = 15), ground-glass opacities (n = 13), bronchiectasis and/or bronchiolectasis (n = 8), and thickening of the bronchovascular bundles (n = 8). Other CT findings included reticular opacities (n = 7), calcified nodules (n = 4), airspace consolidation (n = 4), emphysema (n = 3), honeycombing (n = 3), lymph node enlargement (n = 2), mosaic attenuation pattern (n = 1), and cavitated nodules (n = 1). Conclusion: The main CT findings of LIP were multiple cysts, small nodules, and ground-glass opacities.


2021 ◽  
Vol 182 ◽  
pp. 106405
Author(s):  
Santiago Auteri ◽  
María L. Alberti ◽  
Martin E. Fernández ◽  
Guadalupe Blanco ◽  
Mercedes Rayá ◽  
...  

2006 ◽  
Vol 2 (3) ◽  
pp. 101-104
Author(s):  
Prince James ◽  
D.J. Christopher ◽  
T. Balamugesh ◽  
Rajesh Thomas ◽  
Richa Gupta ◽  
...  

Cureus ◽  
2021 ◽  
Author(s):  
Michael R Povlow ◽  
Mitchell Streiff ◽  
Sunthosh Madireddi ◽  
Couger Jaramillo

2015 ◽  
Vol 35 (3) ◽  
pp. 825-828 ◽  
Author(s):  
Andrés González García ◽  
José Luis Callejas Rubio ◽  
Raquel Ríos Fernández ◽  
Norberto Ortego Centeno

Author(s):  
Luiz Alcino Gueiros ◽  
Isabelle Lemos ◽  
Alessandra Albuqerque Tavares Caravalho ◽  
Jair Carneiro Leão

2020 ◽  
Vol 153 (6) ◽  
pp. 719-724 ◽  
Author(s):  
Antonio Travaglino ◽  
Claudia Giordano ◽  
Mirella Pace ◽  
Silvia Varricchio ◽  
Marco Picardi ◽  
...  

Abstract Objectives Sjögren syndrome (SS) is considered as a major etiologic factor for primary salivary gland lymphoma (SGL). However, the percentage of SGL that is caused by SS (and thus the real impact of SS on SGL epidemiology) is unclear. We aimed to assess the prevalence of SS in patients with SGL through a systematic review and meta-analysis. Methods Electronic databases were searched for studies assessing the presence of SS in patients with SGL. Pooled prevalence of SS in SGL was calculated, with a subgroup analysis based on histotype (mucosa-associated lymphoid tissue [MALT] vs non-MALT). Results Sixteen studies with 665 SGLs were included. Pooled prevalence of SS in SGL was 18.2%, with high heterogeneity among studies. In MALT SGL, the prevalence of SS was 29.5%, with moderate heterogeneity. In non-MALT SGL, the prevalence of SS was 0%, with null heterogeneity. Conclusions SS seems to be responsible for a significant but minor portion of SGLs. SS appears involved in MALT-type SGL but not in other histotypes.


2019 ◽  
Vol 41 (5) ◽  
pp. 413-416 ◽  
Author(s):  
Melissa S. Tesher ◽  
Ysabella Esteban ◽  
Tara O. Henderson ◽  
Gabriela Villanueva ◽  
Karen B. Onel

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