POLYBIOPSY FULMINANS: PULMONARY LYMPHOMATOID GRANULOMATOSIS

CHEST Journal ◽  
2019 ◽  
Vol 156 (4) ◽  
pp. A888-A889
Author(s):  
Chase Baxter ◽  
Elliott Yee ◽  
Cristina Perez Chumbiauca ◽  
Gabriel Bosslet
2002 ◽  
Vol 8 (4) ◽  
pp. 280-282 ◽  
Author(s):  
Nil Culhaci ◽  
Edi Levi ◽  
Serdar Sen ◽  
Furuzan Kacar ◽  
İbrahim Meteoglu

2012 ◽  
Vol 14 (5) ◽  
pp. 662-664 ◽  
Author(s):  
W. Bartosik ◽  
A. Raza ◽  
S. Kalimuthu ◽  
A. Fabre

2014 ◽  
Vol 45 (7) ◽  
pp. 1082-1085 ◽  
Author(s):  
Subin Lee ◽  
Mi-Jin Kang ◽  
Hyun-Jung Kim ◽  
Hyo-Bin Kim ◽  
Jihae Lee

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Ghulam Rehman Mohyuddin ◽  
Fatima Sultan ◽  
Ghulam Khaleeq

A 70-year-old female presented with a 4-week history of dry cough and wheezing. Chest radiograph showed a 10.5 cm mass-like density in the anterior mediastinum which had not been previously visualized. Computed tomography scan (CT) of the chest showed a right hilar mass encasing and narrowing right upper lobe bronchus and right mainstem bronchus and secondary atelectatic changes. Biopsy was consistent with a diagnosis of lymphomatoid granulomatosis Grade 3. She responded well clinically and radiologically to therapy. Lymphomatoid granulomatosis is a rare EBV-associated disorder which is considered a lymphoproliferative disease. The most common radiographic feature is multiple lung nodules. An isolated hilar mass is an exceptionally rare presentation of this rare disease.


Chemotherapy ◽  
2009 ◽  
Vol 55 (5) ◽  
pp. 386-390 ◽  
Author(s):  
Ki Hwan Jung ◽  
Hwa Jung Sung ◽  
Ju-Han Lee ◽  
Ki Yeol Lee ◽  
Jae Seung Shin ◽  
...  

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