scholarly journals An Unusual Case of a Dematiaceous Fungus with an Exclusive Cerebral Involvement After ABO-Incompatible Renal Transplantation

2020 ◽  
Vol 21 ◽  
Author(s):  
Arunima Ray ◽  
Kaustuv Mukherjee ◽  
Sharmila Thukral ◽  
Arpita Sarkar ◽  
Deepak Shankar Ray
Nephrology ◽  
2016 ◽  
Vol 21 ◽  
pp. 60-62 ◽  
Author(s):  
Atsushi Sugitani ◽  
Chihiro Takahashi ◽  
Takuji Naka ◽  
Kazunori Hisamitsu ◽  
Osamu Yamamoto ◽  
...  

2010 ◽  
Vol 39 (3) ◽  
pp. 112-114
Author(s):  
M.N. Raza ◽  
Alexander Spiers ◽  
Lucy Smyth

2013 ◽  
Vol 28 (5) ◽  
pp. 317-319
Author(s):  
S. Lombardo Galera ◽  
E. Roldán Romero ◽  
F. Bravo Rodríguez

2019 ◽  
Vol 25 ◽  
pp. 100890
Author(s):  
Gede Wirya Kusuma Duarsa ◽  
Anak Agung Gede Oka ◽  
Kadek Budi Santosa ◽  
I. Wayan Yudiana ◽  
Pande Wisnu Tirtayasa ◽  
...  

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.


2015 ◽  
Vol 47 (4) ◽  
pp. 1042-1044
Author(s):  
J. Guerra ◽  
M.J. Melo ◽  
J.A. Gonçalves ◽  
C. Nascimento ◽  
A. Santana ◽  
...  

2013 ◽  
Vol 42 (11) ◽  
pp. 1623-1626 ◽  
Author(s):  
Sarahn Smith ◽  
Akimichi Inaba ◽  
Joseph Murphy ◽  
Gary Campbell ◽  
Andoni P. Toms

2016 ◽  
Vol 3 (3) ◽  
pp. 57
Author(s):  
Satyanarayana R Vaidya ◽  
Chandana R Bhavanam ◽  
Ananda R Gurram

Dense deposit disease (DDD) is a prototypical form of C3 Glomerulopathy that affects both children and adults at a rate of 2 to 3 people per million. It often progresses to ESRD and recurs after Renal Transplantation. DDD presentation for 10 years or more is known to progress to ESRD in half of patients. We report a rare case of DDD which has been in clinical and histological remission for 14 years after treatment with Glucocorticoid therapy.


1969 ◽  
Vol 100 (6) ◽  
pp. 744-748 ◽  
Author(s):  
F. G. Schellander
Keyword(s):  

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