• Skip to content

TriStar Centennial

  • Home
  • Need A Doctor?
  • Maps & Directions
  • Phone Directory
  • Contact Us
ER Wait Time

Wait times are an average and provided for informational purposes only. What does this mean?

Search TriStar Centennial
GO
  • About
    • Awards and Honors
    • Contact Us
    • CEO Message
    • Mission and Values
    • Phone Directory
    • Hospital Overview
    • Maps & Directions
    • News
    • TriStar Health
  • Services
  • Careers
    • Volunteers
    • Find a Career
    • Benefits
    • For Physicians
    • Pharmacy Residency
    • Need Help?
    • TriStar Centennial Store
  • News & Media
    • Newsroom
    • Media & Vendor Resources
    • HealthBreaks
  • Your Health
    • Health Videos
    • Virtual Body
    • Health Tools
    • Kids Health
  • Quality & Patient Safety
    • Patient Safety
    • Awards & Recognition
    • Quality & Safety Measures
    • Electronic Health Record
    • Resources & References
    • HIPAA Notice of Privacy Practices
    • Policies & Procedures
    • Joint Commission Public Notice
prescription
  • For Physicians
  • For Visitors
  • For Patients

Arrhenoblastoma

  • Homect_img
  • Your Health
Back
DefinitionCausesRisk FactorsSymptomsDiagnosisTreatmentPreventionrevision

Definition

An arrhenoblastoma is a rare type of ovarian tumor. This tumor primarily secretes the male sex hormone, testosterone, and rarely the female sex hormone, estrogen. It accounts for less than 0.5% of all ovarian tumors.

Arrhenoblastomas are generally benign, meaning they do not normally spread beyond the ovary. However, they may cause male physical characteristics to develop in women, such as facial hair and a deepening voice. If you suspect you have this condition, contact your doctor immediately.

Arrhenoblastoma
Ovarian Cancer
Copyright © Nucleus Medical Media, Inc.

Causes

The cause of arrhenoblastoma is unknown.

Risk Factors

A risk factor is something that increases your chance of getting a disease or condition. The following factors increase your chance of developing arrhenoblastoma. If you have any of these risk factors, tell your doctor:

  • Being female
  • Young age—arrhenoblastomas most commonly occur among young women (ages 20-30), however they may occur at any age, including toddlers, young girls, and postmenopausal women
  • Very rarely, arrhenoblastoma is a complication of pregnancy

Symptoms

If you experience any of these symptoms, do not assume it is due to an arrhenoblastoma. These symptoms may be caused by other, less serious health conditions. If you experience any one of them, see your physician.

  • In many cases, infrequent menstrual periods or cessation of menstrual periods is the only symptom
  • In up to one in three patients, arrhenoblastoma is accompanied by masculinization, including any of the following:
    • Acne
    • Deepening voice
    • Hirsutism (increased facial hair)
    • Enlarged clitoris

Diagnosis

Your doctor will ask about your symptoms and medical history, and perform a physical exam. He or she will also test your levels of male hormones (such as testosterone and androsterone) to see if they are excessive.

Tests may include the following:

  • Blood tests of hormone levels (including testosterone, DHEA, CD56, and progesterone levels)—to detect if male hormones are high
  • Ultrasound —to identify the location, size, and shape of the tumor

Pelvic Ultrasound
Pelvic Ultrasound
Copyright © Nucleus Medical Media, Inc.

Treatment

Treatment involves surgery to remove one or both ovaries. This procedure is usually successful in returning normal menstruation (in premenopausal women) and ceasing masculinization. If the tumor is late stage and particularly aggressive (which is rare), radiation therapy , chemotherapy , or both, in addition to surgery, may be needed.

Prevention

There are no known ways to prevent ovarian cancer of any kind, as the cause is unknown. To learn more about risk factors for ovarian cancers in general, see the fact sheet on ovarian cancer for more information.

Revision Information

  • Reviewer: Ganson Purcell Jr., MD, FACOG, FACPE
  • Review Date: 12/2011 -
  • Update Date: 12/30/2011 -

This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.

Copyright © EBSCO Publishing
All rights reserved.

Health Library Home

Related Health Content

  • Arrhenoblastoma
  • Ovarian Cancer
  • Chemotherapy for Ovarian Cancer
  • Diagnosis of Ovarian Cancer
  • Conditions InDepth: Ovarian Cancer
  • Lifestyle Changes to Manage Ovarian Cancer
  • Medications for Ovarian Cancer
  • Other Treatments for Ovarian Cancer
  • Radiation Therapy for Ovarian Cancer
  • Reducing Your Risk of Ovarian Cancer
Show All

RESOURCES

  • The Endocrine Society

    http://www.endo-society.org

  • Ovarian Cancer National Alliance

    http://www.ovariancancer.org

CANADIAN RESOURCES

  • National Ovarian Cancer Association

    http://www.ovariancanada.org

  • Ovarian Cancer Canada

    http://www.ovariancancercanada.ca

References

  • Chen F, Sheu B, Lin M, Chow S, Lin H. Sertoli-leydig cell tumor of the ovary. J Formos Med Assoc . Available at: http://cat.inist.fr/?aModele=afficheN&cpsidt=17460145 . Accessed November 30, 2006.

  • Choong S, Fuller P, Chu S, et al. Sertoli-Leydig cell tumor of the ovary, a rare cause of precocious puberty in a 12-month-old infant. J Clin Endocrinol Metab . 2002;87:49-56.

  • Colombo N, Parma G, Zanagnolo V, Insinga A. Management of ovarian stromal cell tumors. J Clin Oncol . 2007;20:2944-51.

  • DynaMed Editorial Team. Sertoli-Leydig cell tumor. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed/what.php . Accessed November 27, 2006.

  • McCluggage WG, McKenna M, McBride HA. CD56 is a sensitive and diagnostically useful immunohistochemical marker of ovarian sex cord stromal tumor. Int J Gyn Pathol. 2007;26:322-327.

  • Sachdeva P, Arora R, Dubey C, et al. Cell tumor: a rare ovarian neoplasm. Gynecologic Endocrinology. 2008;24(4):230-234.

  • Sex cord-stromal tumors. Johns Hopkins Pathology website. Available at: http://ovariancancer.jhmi.edu/stromal.cfm . Accessed November 27, 2006.

  • Patients & Visitors
    • Admissions
    • View / Pay Bill
    • Need A Doctor?
    • Events & Classes
    • Visitor Information
    • Maps & Directions
    • Insurance Plans Accepted
  • Services
    • Emergency Services
    • Radiology
    • Orthopaedics
    • Neurosciences
    • Cardiac
    • Sleep Disorders Center
    • Physical Therapy
  • Our Community
    • Events & Classes
    • Local News
    • Facebook
    • YouTube
HIPAA Privacy  |  Patient Satisfaction  |  Policy & Procedures  |  Site Map  |  Disaster Preparedness

TriStar Centennial
2300 Patterson St
Nashville, TN 37203
(615) 342-1000
You May Also Visit Us At
TriStarHealth.com.

Copyright 1999-2013 ehc.com ; All rights reserved. Terms & Conditions of Use | Privacy Notice