Report on 8 Cases of Testicular Tumors in Childhood.

1974 ◽  
Vol 60 (2) ◽  
pp. 157-162 ◽  
Author(s):  
Giorgio Pizzocaro ◽  
Fulvio Zanoni

Since 1944, 8 patients under 15 years of age have been hospitalized at the National Cancer Institute in Milano for testicular neoplasms, that is 2 % of all cases. Four were embryonal carcinomas (pure or with associated teratoma and choriocarcinoma), and two were rhabdomyosarcomas. Only one case of seminoma and one case of benign mesothelioma of the tunica vaginalis propria of testis were described. Embryonal carcinoma and rhabdomyosarcoma in infants and children should be managed by radical orchiectomy and bilateral retroperitoneal lymphadenectomy. Inoperable cases have a very poor prognosis and adequate chemotherapy may prolong survival. Pure seminoma should be treated by radical orchiectomy and radiotherapy on the lymph-nodes as indicated by the extent of the disease. In advanced cases, alkylating agents are very useful. Mesotheliomas are not true testicular tumors, as they arise from the tunica vaginalis propria of testis. They may be benign or malignant. In benign cases orchiectomy alone is sufficient for cure, whereas in malignant instances bilateral retroperitoneal lymph-node dissection in mandatory.

Cancer ◽  
2003 ◽  
Vol 98 (4) ◽  
pp. 753-757 ◽  
Author(s):  
Ashraf A. Mosharafa ◽  
Richard S. Foster ◽  
Richard Bihrle ◽  
Michael O. Koch ◽  
Thomas M. Ulbright ◽  
...  

2014 ◽  
Vol 8 (3-4) ◽  
pp. 245
Author(s):  
Jae Heon Kim ◽  
Tae Il Noh ◽  
Ji Sung Shim ◽  
Byeong Kuk Ham ◽  
Jae Hyun Bae ◽  
...  

We report a case of primary testicular carcinoid tumour with mature teratoma metastatic to the para-aortic lymph node and the lymph node around the left gonadal vein, which was treated with radical orchiectomy, bleomycin, etoposide, and cisplatin chemotherapy, and modified retroperitoneal lymph node dissection. Three days after modified retroperitoneal lymph node dissection, bleomycin-induced pneumonitis occurred, which was resolved with steroid administration. The patient is alive without recurrence 31 months after radical orchiectomy.


2014 ◽  
Vol 192 (5) ◽  
pp. 1397-1402 ◽  
Author(s):  
Kevin R. Rice ◽  
Stephen D.W. Beck ◽  
Richard Bihrle ◽  
K. Clint Cary ◽  
Lawrence H. Einhorn ◽  
...  

Author(s):  
Mihai Domnutiu Suciu ◽  
Nucu Alexandru Marica ◽  
Traian Oniu ◽  
Andrei Ionut Tomuta ◽  
Radu Badea

Cryptorchidism, as a singular pathology or associated with other dysgenesis syndromes, is one of the main factors of risk for the development of the testicular tumors. Although there are a great number of cases of undescended testicles that are diagnosed and treated during the first 6-12 months of life, there are rare cases of adults who are undiagnosed and untreated from this anomaly, which can present a high risk of malignancy . In this study we present the case of a 36-year-old patient, diagnosed at puberty with left cryptorchidism, untreated, who also hadevidenced a large intraabdominal tumoral mass associated with it. The tumoral mass had its origin in the undescended left testicle. Surgical excision of the tumor and retroperitoneal lymphadenectomy was performed. The histological result revealed embryonal carcinoma, without lymphnode metastasis. Adult patients with untreated cryptorchidism should be thoroughly investigated, as they have a high risk of developing testicular cancer.


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