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Stromal tumor; Gonadal stromal tumor; Sex cord tumor; Androblastoma
See also: Sertoli-Leydig cell tumor
This is a rare tumor. It accounts for less than 0.5% of all ovarian tumors.
These tumors are found in women of all age groups, but are most common in young women.
This tumor releases male hormones, which causes the following symptoms in women:
Surgery is the main treatment. If the cancer has spread, chemotherapy or radiation therapy should be considered.
The outcome of this disease depends on whether it has spread, and whether surgery can completely remove the tumor. The overall 5-year survival rate is 70 - 90%.
Arrhenoblastoma has a low chance of spreading. If the tumor is found early, the cure rate can be very good.
Call your health care provider if you are a woman experiencing masculine symptoms, or you feel a lump near your ovaries.
There is no good screening test. Getting a gynecological exam each year and recognizing masculine symptoms can help detect the disease.
Bulun SE, Adashi EY. The physiology and pathology of the female reproductive axis. In: Kronenberg HM, Melmed S, Polonsky KS, Larsen PR, eds. Williams Textbook of Endocrinology. 11th ed. Philadelphia, Pa: Saunders Elsevier; 2008:chap 16.
Coleman RL, Gershenson DM. Neoplastic diseases of the ovary: screening, benign and malignant epithelial and germ cell neoplasms, sex-cord stromal tumors. In: Katz VL, Lentz GM, Lobo RA, Gershenson DM, eds. Comprehensive Gynecology. 5th ed. Philadelphia, Pa: Mosby Elsevier; 2007:chap 33.
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