scholarly journals S2104 Acquired Tracheoesophageal Fistula in Diffuse B Cell Lymphoma Associated With Persistent COVID-19

2021 ◽  
Vol 116 (1) ◽  
pp. S906-S907
Author(s):  
Eugene C. Nwankwo ◽  
Jennifer M. Ray ◽  
Antonio R. Cheesman
2020 ◽  
Vol 21 ◽  
Author(s):  
Waleed K. Al-Darzi ◽  
Aeman Hana ◽  
Marc K. Lahiri ◽  
Carina Dagher ◽  
Joshua C. Greenberg ◽  
...  

2019 ◽  
Vol 64 (4) ◽  
pp. 338
Author(s):  
AngooriGnaneshwar Rao ◽  
SyedaSaba Farheen ◽  
Kolli Amit ◽  
UdayDeshmukh Reddy ◽  
Karanam Aparna ◽  
...  

CHEST Journal ◽  
2013 ◽  
Vol 144 (4) ◽  
pp. 503A
Author(s):  
Elif Sen ◽  
Ugur Gonullu ◽  
Koray Ceyhan ◽  
Hatice Taslak

2019 ◽  
Vol 12 (7) ◽  
pp. e229327
Author(s):  
John Mayo ◽  
Kenneth Bogenberger ◽  
Thomas Raj ◽  
Jeffrey Reha

Diffuse large B-cell lymphoma (DLBCL) can present in a number of different ways, including as a primary cutaneous lesion or at various other extranodal sites. However, it is rare for a DLBCL to present as a clinically subcutaneous mass without visible skin changes or nodal involvement. A 36-year-old man presented with a 4×4×1 cm subcutaneous mass to his shoulder with normal overlying skin which had been enlarging over 6 months. Physical exam and imaging together made a strong case for sarcoma, and the patient underwent a radical resection. The final pathological diagnosis returned as a diffuse B-cell lymphoma (germinal centre type). The patient subsequently healed and tolerated chemotherapy well. DLBCL can masquerade as a soft tissue mass at initial presentation. If the diagnosis is not clear, a biopsy should be pursued.


2013 ◽  
Vol 31 (3) ◽  
pp. 253-257 ◽  
Author(s):  
H.M. Eissa ◽  
C.E. Allen ◽  
K. Kamdar ◽  
S. Simko ◽  
P. Goradia ◽  
...  

2013 ◽  
Vol 5 (1) ◽  
pp. e2013019 ◽  
Author(s):  
Sujith V Cherian ◽  
Subhraleena Das ◽  
Bandita Das Basu ◽  
Robert E Hutchison

Intravascular large B cell lymphoma (IVLBCL) is a rare, aggressive extranodal B cell lymphoma, classified as a subset of diffuse B cell lymphoma. IVLBCL typically occurs in elderly persons, and the clinical heterogeneity of the condition makes the diagnosis elusive in most cases. Most of the reported cases have been in the asian population with the majority of the cases being diagnosed postmortem. We present a unique case of IVLBCL in a 65-year-old Caucasian male who presented with fever of unknown origin.


CHEST Journal ◽  
2016 ◽  
Vol 150 (4) ◽  
pp. 752A ◽  
Author(s):  
Laura Barnes ◽  
Eric Scholten ◽  
Anas Khalil ◽  
Samir Makani ◽  
Rebecca Sell

2020 ◽  
Vol 115 (1) ◽  
pp. S1545-S1546
Author(s):  
David J. Truscello ◽  
Neethi R. Dasu ◽  
Matthew Everwine ◽  
Lucy M. Joo ◽  
Richard Gordon

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