scholarly journals Management of Leydig cell tumors of the testis-a case report

2020 ◽  
Vol 28 ◽  
pp. 101064
Author(s):  
P.P. Genov ◽  
D.P. Georgieva ◽  
G.V. Koleva ◽  
N.H. Kolev ◽  
V.R. Dunev ◽  
...  
Urology ◽  
2020 ◽  
Vol 142 ◽  
pp. e29-e31
Author(s):  
David Crook ◽  
Clint Cary

2015 ◽  
Vol 2015 ◽  
pp. 1-4
Author(s):  
Julio J. Geminiani ◽  
Stephen D. Marshall ◽  
Tammy S. Ho ◽  
Steven B. Brandes

Leydig cell tumors represent 3% of testicular masses and usually occur in prepubertal boys and men between 30 and 60 years of age. Leydig cell tumors are benign in children but can be malignant in 10% of adults. This case report describes a 41-year-old patient who was diagnosed with a Leydig cell tumor that originated in his right testicle that subsequently metastasized to his liver, lungs, and retroperitoneum. We discuss the patient’s presentation and review the radiographic findings, surgical treatment, surgical pathology, chemotherapeutic treatment, and published literature on this rare pathology.


1991 ◽  
Vol 46 (1) ◽  
pp. 104-106 ◽  
Author(s):  
N. Kondoh ◽  
E. Koh ◽  
M. Nakamura ◽  
M. Namiki ◽  
H. Kiyohara ◽  
...  

2014 ◽  
Vol 7 (1) ◽  
Author(s):  
Ancuta Augustina Gheorghisan-Galateanu

Author(s):  
S. Ahmed Hussain ◽  
Elizabeth A. Dubil ◽  
Javier N. De Luca-Johnson ◽  
Michael Johnston

2020 ◽  
Author(s):  
Fernando Mendonça ◽  
Selma Souto ◽  
Daniela Magalhães ◽  
Ana Sofia Fernandes ◽  
Ana Rita Coelho ◽  
...  

Author(s):  
Maria Shekhovtsova ◽  
Gisela Lage ◽  
Liliana Lima dos Santos ◽  
Ana Pires-Luís

Author(s):  
Bozo Kruslin ◽  
Zoran Gatalica ◽  
Ondrej Hes ◽  
Faruk Skenderi ◽  
Markku Miettinen ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
B. Wormald ◽  
S. Elorbany ◽  
H. Hanson ◽  
J. W. Williams ◽  
S. Heenan ◽  
...  

Sertoli-Leydig cell tumours of the ovary (SLCT) are rare tumours predominantly caused by mutations in the DICER1 gene. We present a patient with a unilateral SLCT who had an underlying germline DICER1 gene mutation. We discuss the underlying pathology, risks, and screening opportunities available to those with a mutation in this gene as SLCT is only one of a multitude of other tumours encompassing DICER1 syndrome. The condition is inherited in an autosomal dominant fashion. As such, genetic counselling is a key component of the management of women with SLCT.


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