Long-Term Follow-Up Using Testicle-Sparing Surgery for Leydig Cell Tumor

2013 ◽  
Vol 11 (3) ◽  
pp. 321-324 ◽  
Author(s):  
Giorgio Bozzini ◽  
Stefano Picozzi ◽  
Franco Gadda ◽  
Renzo Colombo ◽  
Ottavio DeCobelli ◽  
...  
2012 ◽  
Vol 187 (4S) ◽  
Author(s):  
Giorgio Bozzini ◽  
Stefano Picozzi ◽  
Franco Gadda ◽  
Renzo Colombo ◽  
Ottavio De Cobelli ◽  
...  

1998 ◽  
Vol 28 (5) ◽  
pp. 323-328 ◽  
Author(s):  
Y. Oda ◽  
H. Miura ◽  
M. Tsuneyoshi ◽  
Y. Iwamoto

2006 ◽  
Vol 176 (5) ◽  
pp. 2040-2043 ◽  
Author(s):  
Luca Carmignani ◽  
Roberto Salvioni ◽  
Franco Gadda ◽  
Maurizio Colecchia ◽  
Giacomo Gazzano ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-4 ◽  
Author(s):  
Philip Zeuschner ◽  
Christian Veith ◽  
Johannes Linxweiler ◽  
Michael Stöckle ◽  
Julia Heinzelbecker

Gynecomastia is a common incidental finding in males that can be caused by various benign or malignant diseases. In rare cases, it results from Leydig cell tumors, a rare entity accounting for 3% of all testicular neoplasms. Some of them are hormonally active but seldom cause symptomatic endocrine disturbance. Here we report on a 32-year-old male presenting with gynecomastia which he had already been suffering from for two years. Although he had been seen by three other specialists, including a urologist, none of them found the small mass in the upper pole of his right testis. We decided to perform testis-sparing surgery which confirmed the diagnosis of a hormonally active Leydig cell tumor. During follow-up, hormonal status normalized, and gynecomastia began to resolve.


2011 ◽  
Vol 42 (5) ◽  
pp. 727-733 ◽  
Author(s):  
Tsuyoshi Saito ◽  
Hiroyuki Mitomi ◽  
Hiroshi Izumi ◽  
Yoshiyuki Suehara ◽  
Taketo Okubo ◽  
...  

2020 ◽  
Vol 22 (Supplement_3) ◽  
pp. iii335-iii335
Author(s):  
Takahiro Yamamoto ◽  
Keishi Makino ◽  
Hideo Nakamura ◽  
Jun-ichiro Kuroda ◽  
Takashi Itoyama ◽  
...  

Abstract INTRODUCTION Central nervous system germ cell tumor (GCT) is one of the pediatric brain tumors. Although there have been epidemiological studies in the past, long-term prognosis and the late effects remained unclear. In this study, we examined GCT over the past 41 years in Kumamoto prefecture. METHODS Epidemiological features and complications with radiation-induced tumors were searched in patients diagnosed with GCT in the 41-year period from 1977 to 2018. RESULTS There were 93 patients diagnosed with GCT. These cases were divided into 14-year periods before and after incorporation of chemotherapy into the treatment, and the results for germinomas were compared. An improvement in the 10-year survival rate from 12 of 23 cases (52.2%) between 1977 and 1991 to 19 of 28 cases (67.9%) between 1992 and 2006 was observed. The 10-year survival rate for germinoma cases that received medical treatment during a more recent 5-year period between 2004 and 2009 increased to over 90%. However, 10.3% of all long-term survivors of GCT developed radiation-induced glioblastoma. The examination results showed that regardless of the tumor type, patients who received a high dose of radiation during their initial treatment developed the complication of radiation-induced glioblastoma within 10 to 25 years after their initial treatment. CONCLUSION This study suggests that the long-term survival rates for GCT are improving but the rate of radiation-induced glioblastoma in these cases are too high to be ignored. Long-term follow-up of at least 10 years is essential to effectively evaluate the details of treatment for pediatric brain tumors.


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