ABSTRACT Available therapies which can be offered to the patient with clinical \u003cbr\u003e\nstage I nonseminomatous germ cell \u003cb\u003etesticular cancer\u003c/b\u003e (CSI NSGCT) immediately \u003cbr\u003e\nfollowing orchiectomy include retroperitoneal lymph node dissection, systemic ...
Book Title: Testicular Cancer Research Trends
Author:Paulo V. Brantus
Published on 2007 by Nova Publishers
ISBN: 9781600216671 / 1600216676
Total Page: 144
Book Category:Medical
Book is About: Testicular Cancer
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Seminomas account for about 30-40% of all testicular tumours. These are usually is found in men in their 30s and 40s. The condition is usually localised to the testes, although in about 25% of cases it has spread to lymph nodes. Non-seminomas account for 60% of all testicular tumours; subcategories of these tumours are listed below. Non-seminoma tumours often contain more than one of the following cell types: Testicular cancer is an abnormal, rapid, and invasive growth of cancerous (malignant) cells in the testicles. Embryonal carcinoma (about 20% of testicular cancers) occurs in 20-30 year olds and is highly malignant. It grows rapidly and spreads to the lung and liver. Yolk sac tumour (about 60% of all testicular cancers in young boys). Teratomata (about 7% of testicular cancers in adult men and 40% in young boys). Choriocarcinoma is rare. Stromal cell tumours are a kind of tumour that is made of Leydig cells (testosterone-secreting cells), Sertoli cells (cells where sperm matures), and granulose cells. These tumours account for only 3-4% of all testicular tumours. However, they do make up nearly 20% of all childhood testicular tumours. These tumours may secrete a hormone -- estradiol -- that can cause one of the symptoms of testicular cancer, gynecomastia (excessive development of breast tissue). This book presents leading-edge research in the field.
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