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1.
Indian J Cancer ; 2009 Oct-Dec; 46(4): 311-317
Article in English | IMSEAR | ID: sea-144267

ABSTRACT

Background : Cisplatin-induced ototoxicity shows high interindividual variability and is often accompanied by transient or permanent tinnitus. It is not possible to identify the susceptible individuals before commencement of the treatment. We conducted a prospective, randomized and observational study in a tertiary care centre and evaluated the effects of different doses of cisplatin on hearing. Materials and Methods : Fifty-seven patients scheduled for cisplatin-based chemotherapy were included in the study. All patients were divided into three groups depending on the dose of cisplatin infused in 3 weeks. Results : The subjective hearing loss was found in seven patients, while six patients had tinnitus during the chemotherapy. The hearing loss was sensorineural, dose dependent, symmetrical, bilateral and irreversible. Higher frequencies were first to be affected in cisplatin chemotherapy. Conclusion : As use of high-frequency audiometry is still limited in research work only, we need a strict protocol of adding high-frequency audiometry in the cisplatin-based chemotherapy regimen.


Subject(s)
Adult , Aged , Antineoplastic Agents/administration & dosage , Audiometry , Cisplatin/administration & dosage , Dose-Response Relationship, Drug , Female , Hearing Loss/chemically induced , Humans , Male , Middle Aged , Neoplasms/drug therapy , Tinnitus/chemically induced , Young Adult
2.
Indian J Cancer ; 2005 Oct-Dec; 42(4): 208-10
Article in English | IMSEAR | ID: sea-50882

ABSTRACT

Testicular tumors account for 1% of all cancers in men and it occurs in 1 in 500 men. Incidence of familial testicular tumours is rare. Total number of cases till the year 1992 in identical twins is 21, in brothers 82 and father-son both affected in 31 pairs. We report a case of two brothers presenting simultaneously with testicular tumours. Both were subjected to retrograde orchidectomy. Histopathologic examination of one revealed embryonal cell carcinoma and other mature teratoma of the testis. Patient with embryonal carcinoma was given adjuvant chemotherapy based on Bleomycin, Etoposide and cisplatinum (BEP) and one with mature teratoma was put on a follow up.


Subject(s)
Adult , Follow-Up Studies , Genetic Predisposition to Disease , Germinoma/genetics , Humans , Male , Orchiectomy , Pedigree , Risk Assessment , Siblings , Testicular Neoplasms/genetics , Treatment Outcome
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