scholarly journals Post-transplant lymphoproliferative disorder associated with immunosuppressive therapy for renal transplantation in rhesus macaques (Macaca mulatta)

2013 ◽  
Vol 65 (7-8) ◽  
pp. 1019-1024 ◽  
Author(s):  
Eugenia K. Page ◽  
Cynthia L. Courtney ◽  
Prachi Sharma ◽  
Jennifer Cheeseman ◽  
Joe B. Jenkins ◽  
...  
2004 ◽  
Vol 118 (11) ◽  
pp. 906-908 ◽  
Author(s):  
Jonathan D. Clarke ◽  
David Stock ◽  
Vijay Singh

An unusual case of epistaxis resulting from post-transplant lymphoproliferative disorder is described.A 30-year-old woman who had undergone renal transplantation 12 years previously presented with profuse, posterior, unilateral epistaxis. The initial findings, workup and treatment are presented. A post-nasal space (PNS) mass was detected and biopsy showed this to be an Epstein-Barrvirus-positive polymorphous B-cell post-transplant lymphoproliferative disorder. Computed tomography findings showed a polypoid lesion protruding from the sphenoethmoidal recess and filling the left PNS.Post-transplant lymphoproliferative disorder is well known to involve tonsil tissue. Commonly, this is the first presentation of the disease in children. However, until now post-transplant lymphoproliferative disorder has not been described in the PNS or nasal cavity presenting as epistaxis. We conclude that all transplant patients presenting with epistaxis should be followed up for an accurate examination of the PNS and nasal cavity after the acute episode.


2018 ◽  
Vol 97 (12) ◽  
pp. E-15-E-17
Author(s):  
Richard Heyes ◽  
Courtney M Tomblinson ◽  
David G Lott

Post-transplant lymphoproliferative disorder (PTLD) is a unifying term for a spectrum of lymphoid expansion entities brought about by immunosuppression. It can present throughout the head and neck, and tonsillar involvement is not limited to children. We report the case of a 67-year-old woman who developed odynophagia associated with putrid halitosis 4 months after she had undergone renal transplantation. Direct visualization of the oropharynx revealed multiple sites of severe ulceration and erythema, with erosion of both the anterior and posterior right tonsillar pillars and a necrotic ulceration fistulating deeply. Biopsy analysis led to a diagnosis of PTLD. The patient underwent rituximab monotherapy and responded well. However, after the cessation of therapy, she experienced a recurrence that necessitated chemotherapy, which resulted in a lasting remission. At follow-up 5 years later, she remained PTLD-free with stable stage 4 chronic kidney disease.


2009 ◽  
Vol 17 (1) ◽  
pp. 48-54 ◽  
Author(s):  
Toyofumi Abe ◽  
Naotsugu Ichimaru ◽  
Yukito Kokado ◽  
Tetsuo Maeda ◽  
Yoichi Kakuta ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document