scholarly journals A RARE CASE OF ISOLATED PULMONARY INVOLVEMENT IN LYMPHOID VARIANT HYPEREOSINOPHILIC SYNDROME

CHEST Journal ◽  
2020 ◽  
Vol 158 (4) ◽  
pp. A2025
Author(s):  
Jason Lofters ◽  
Matthew Tavares ◽  
Ahmad Alkhatatneh ◽  
Fausto Lisung
2011 ◽  
Vol 149 (1) ◽  
pp. e30-e32 ◽  
Author(s):  
Tilo Kleinfeldt ◽  
Hueseyin Ince ◽  
Christoph A. Nienaber

2018 ◽  
Vol 66 (10) ◽  
pp. 1508
Author(s):  
JayantaK Das ◽  
Krati Gupta ◽  
Saurabh Deshmukh ◽  
Richa Shrivastava

Cureus ◽  
2020 ◽  
Author(s):  
Elise Lambird ◽  
Dharti Patel ◽  
Arun Amble ◽  
Elizabeth Henderson ◽  
Salman Muddassir

CHEST Journal ◽  
2016 ◽  
Vol 150 (4) ◽  
pp. 794A
Author(s):  
Enambir Josan ◽  
Jason Green ◽  
April Lambert-Drwiega ◽  
Emilie Cook ◽  
Jayantilal Mehta

Author(s):  
Makoto Yoshiji ◽  
Kensuke Matsumoto ◽  
Hiroshi Fujita ◽  
Keisuke Miwa ◽  
Hidekazu Tanaka ◽  
...  

2015 ◽  
Vol 27 (5) ◽  
pp. 629 ◽  
Author(s):  
Joon Min Jung ◽  
Mi Hye Lee ◽  
Chong Hyun Won ◽  
Sung Eun Chang ◽  
Mi Woo Lee ◽  
...  

CHEST Journal ◽  
1994 ◽  
Vol 105 (3) ◽  
pp. 656-660 ◽  
Author(s):  
Richard E. Winn ◽  
Marin H. Kollef ◽  
James I. Meyer

2014 ◽  
Vol 18 (6) ◽  
pp. 424-429 ◽  
Author(s):  
Joshua M. Mercer ◽  
Paul Kuzel ◽  
Muhammad N. Mahmood ◽  
Alain Brassard

Introduction: We report a case of a 61-year-old woman with locally destructive vulvar pyoderma gangrenosum (PG) with pulmonary involvement who was refractory to numerous systemic therapies and developed complications resulting in her demise. Objective: To report a rare case of treatment-resistant vulvar PG with pulmonary involvement that proved to be fatal. Methods: PubMed was used to search for other reports that discuss PG, or more specifically perigenital PG, with pulmonary involvement. Results and Conclusion: A thorough review of the literature revealed 33 cases of PG with pulmonary involvement, with only 4 involving the perigenital region. We report the second case of a female with vulvar PG and pulmonary involvement. In contrast to the first case described, our patient did not respond to systemic therapy, and, ultimately, her disease was fatal. It is hoped that with continued documentation of this rare and potentially lethal presentation of PG, physicians will determine more effective treatments.


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