scholarly journals Resection of a late retroperitoneal metastatic Leydig-Sertoli cell sex cord-stromal tumor with concomitant aortocaval reconstruction

Author(s):  
Carlos A. Hinojosa ◽  
Rene Lizola ◽  
Adriana Torres-Machorro ◽  
Hugo Laparra-Escareno ◽  
Javier E. Anaya-Ayala

Leydig-Sertoli cell tumors are rare, with only few cases reported in the literature. We herein present a 41-year-old male who underwent a right orchiectomy for a testicular tumor at the age of 34. Seven years later, he presented at our institution with a large retroperitoneal mass encasing the abdominal great vessels. The patient underwent en-bloc resection of the mass and concomitant infrarrenal aorta and inferior vena cava reconstruction. Pathology report revealed a Leydig-Sertoli cell sex cord-stromal tumor. The patient recovered well from the surgery and he was discharged home in stable condition. To our knowledge this is the first report of a Leydig-Sertoli cell sex cord-stromal tumor with late retroperitoneal metastasis treated by en-bloc resection and vascular reconstruction of the abdominal great vessels.

2016 ◽  
Vol 24 (2) ◽  
pp. 556-557 ◽  
Author(s):  
Matteo Ravaioli ◽  
Matteo Serenari ◽  
Matteo Cescon ◽  
Carlo Savini ◽  
Alessandro Cucchetti ◽  
...  

Chirurgia ◽  
2018 ◽  
Vol 31 (2) ◽  
Author(s):  
Joyce W. Chan ◽  
Peter S. Yu ◽  
Ki K. Li ◽  
Jacky Y. Ho ◽  
Simon C. Chow ◽  
...  

2014 ◽  
Vol 30 (7) ◽  
pp. 492-495
Author(s):  
Giuseppe Massimiliano De Luca ◽  
Angela Gurrado ◽  
Andrea Marzullo ◽  
Giuseppe Piccinni ◽  
Riccardo Memeo ◽  
...  

Objectives Primary tumors of the inferior vena cava are rare, with leiomyosarcoma representing the vast majority. Method A 60-year-old man was admitted in emergency for fainting and mild anemia. A whole-body computed tomography revealed a retroperitoneal mass of approximately 8 cm in diameter, invading the lumen of the inferior vena cava, extending to the renal vein confluence. An en bloc resection of the solid mass was performed. Macroscopically the tumor did not seem to insist on the resection margin. Results Histopathological examination confirmed the diagnosis of leiomyosarcoma of the inferior vena cava. Postoperative recovery was uneventful and the patient was discharged after eight days, starting adjuvant chemotherapy. During the follow-up, the patient did not show other fainting episode, and at 24 months he is disease free. Conclusions: Unusually, fainting could even be the isolated sign of a large leiomyosarcoma of the inferior vena cava, also when it affects its middle portion.


2018 ◽  
Vol 20 ◽  
pp. 94-97
Author(s):  
Ido Orlin ◽  
Yoram Dekel ◽  
Boris Friedman ◽  
Rani Zreik ◽  
Leonid Boyarsky ◽  
...  

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