Transcriptome analysis of human Leydig cell tumours reveals potential mechanisms underlying its development

Andrologia ◽  
2021 ◽  
Author(s):  
Malgorzata Kotula‐Balak ◽  
Michal Duliban ◽  
Artur Gurgul ◽  
Izabela Krakowska ◽  
Pawel Grzmil ◽  
...  
1960 ◽  
Vol XXXV (IV) ◽  
pp. 513-517
Author(s):  
W. P. Plate

ABSTRACT The hormone-producing mesenchymomas of the ovaries can be divided into androblastomas and gynaecoblastomas. The former are derived from »male« elements, and consist of Sertoli-cell tumours and Leydig-cell tumours. The latter arise from »female« elements and consist of granulosacell tumours and theca-cell tumours. Sertoli-cell tumours and granulosacell tumours produce oestrogens, while Leydig-cell tumours and theca-cell tumours produce oestrogens or androgens. Histologically, androblastomas and gynaecoblastomas are often difficult to distinguish. Since no »female« elements occur in a testicle, a granulosa-cell tumour in a testicle is improbable. Gynandroblastomas, therefore, can only be found in an ovary.


Reproduction ◽  
2000 ◽  
pp. 443-452 ◽  
Author(s):  
MA Peters ◽  
DG de Rooij ◽  
KJ Teerds ◽  
I van Der Gaag ◽  
FJ van Sluijs

Spermatogenesis was examined in testes from 74 dogs of various breeds without clinically detected testicular disease. A modified Johnsen score system was used to determine whether spermatogenesis deteriorates with ageing. The diameter of seminiferous tubules was measured in dogs without testicular disease to examine other possible effects of ageing on tubular performance. There appeared to be no relation between age and these variables. The influence of testicular tumours on spermatogenesis was also investigated in both affected and unaffected testes. The testes of 28 dogs with clinically palpable tumours and 21 dogs with clinically non-palpable tumours were investigated. In cases of unilateral occurrence of a tumour, impairment of spermatogenesis was observed only in the affected testis of dogs with clinically detected tumours. Bilateral occurrence of tumours, whether detected clinically or non-clinically, was associated with severe impairment of spermatogenesis. The prevalence of tumours increased during ageing. Eighty-six per cent of the clinically detected and 57% of the non-clinically detected tumours were found in old dogs. Multiple types of tumour and bilateral occurrence were very common. Seminomas and Leydig cell tumours were more frequent than Sertoli cell tumours. It was concluded that spermatogenesis per se did not decrease during ageing in dogs but the occurrence of testicular tumours increased with ageing and affected spermatogenesis significantly, as reflected by a lower Johnsen score.


Author(s):  
Hailey K. Carroll ◽  
Tom Nolis ◽  
Waseem Darwish ◽  
Michele Harrison ◽  
John A. McCaffrey

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.


2018 ◽  
Vol 39 (3) ◽  
pp. 359-364
Author(s):  
M. Fanta ◽  
D. Fischerová ◽  
T. Indrielle-Kelly ◽  
P. Koliba ◽  
A. Zdeňková ◽  
...  

2001 ◽  
Vol 54 (5) ◽  
pp. 693-697 ◽  
Author(s):  
S. Pekic ◽  
S. Vujovic ◽  
S. Spremovic-Radjenovic ◽  
M. Petakov ◽  
M. Djurovic ◽  
...  

2018 ◽  
Vol 91 ◽  
pp. 125-135 ◽  
Author(s):  
Adriana María Belén Abiuso ◽  
María Luisa Varela ◽  
Luis Haro Durand ◽  
Marcos Besio Moreno ◽  
Alejandra Marcos ◽  
...  

2008 ◽  
Vol 31 (3) ◽  
pp. 331-336 ◽  
Author(s):  
M. M. Cajaiba ◽  
M. Reyes-Múgica ◽  
J. C. S. Rios ◽  
M. Nistal

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