eMedicine Specialties > Endocrinology > Gonads

Gynecomastia: Treatment & Medication

Author: Mark R Allee, MD, Associate Professor, Department of Medicine, University of Oklahoma Health Sciences Center
Coauthor(s): Mary Zoe Baker, MD, Professor, Department of Medicine, Section of Endocrinology, Metabolism and Hypertension, University of Oklahoma; Medical Director, University of Oklahoma Physicians, Medicine Specialty Clinic, General Medicine Clinic and Medicine Residents' Clinic
Contributor Information and Disclosures

Updated: Sep 23, 2009

Treatment

Medical Care

  • Generally, no treatment is required for physiologic gynecomastia.
  • A major factor that should influence the initial choice of therapy is the duration of gynecomastia. It is unlikely that any medical therapy will result in significant regression in the late fibrotic stage (a duration of 12 mo or longer). As a result, medical therapies, if used, should be tried early in the condition's course.
  • Pubertal gynecomastia resolves spontaneously within several weeks to 3 years in approximately 90% of patients. Breasts greater than 4 cm in diameter may not completely regress.
  • Identifying and managing an underlying primary disorder often alleviates breast enlargement.
  • If hypogonadism (primary or secondary) is the cause of gynecomastia, parenteral or transdermal testosterone replacement therapy is instituted. However, testosterone does have the potential to exacerbate gynecomastia through the aromatization of the exogenous hormone into estradiol.
  • For patients with idiopathic gynecomastia or with residual gynecomastia after treatment of the primary cause, medical or surgical treatment may be considered.
  • Clomiphene,10 an antiestrogen, can be administered on a trial basis at a dose of 50-100 mg per day for up to 6 months. Approximately 50% of patients achieve partial reduction in breast size, and approximately 20% of patients note complete resolution. Adverse effects, while rare, include visual problems, rash, and nausea.
  • Tamoxifen, an estrogen antagonist, is effective for recent-onset and tender gynecomastia when used in doses of 10-20 mg twice a day.11 Up to 80% of patients report partial to complete resolution. Tamoxifen is typically used for 3 months before referral to a surgeon. Nausea and epigastric discomfort are the main adverse effects.12
  • Other drugs used less frequently include danazol and testolactone13 :

    • Danazol, a synthetic derivative of testosterone, inhibits pituitary secretion of LH and follicle-stimulating hormone (FSH), which decreases estrogen synthesis from the testicles. The dose used for gynecomastia is 200 mg twice a day. Complete resolution of breast enlargement has been reported in 23% of cases. Adverse effects include weight gain, acne, muscle cramps, fluid retention, nausea, and abnormal liver function test results.
    • Testolactone, a peripheral aromatase inhibitor, has been used with varying success rates in doses of 150 mg 3 times per day for 6 months. Nausea, vomiting, edema, and worsening of hypertension have been reported with its use.

Surgical Care

  • Reduction mammoplasty is considered for patients with macromastia or long-standing gynecomastia or in persons in whom medical therapy has failed.1 It is also considered for cosmetic reasons (and for accompanying psychosocial reasons).14,15,16,17,18
  • If surgery is necessary for patients with pseudogynecomastia, liposuction may be warranted.
  • More extensive plastic surgery may be required in patients with marked gynecomastia or who have developed excessive sagging of the breast tissue due to weight loss.
  • Complications of surgery include sloughing of tissue due to a compromised blood supply, contour irregularity, hematoma or seroma formation, and permanent numbness in the nipple-areolar area.
  • A Chinese study indicated that endoscopic subcutaneous mastectomy, without skin excision, could be an effective treatment for gynecomastia.19 In a report on the procedure's use in 65 patients (125 breasts) with gynecomastia, grade IIB or III, the authors stated that only a few operative complications occurred, including 2 cases of partial nipple necrosis and 1 case of subcutaneous hydrops. They also reported that postsurgical chest contour was satisfactory in all patients, and that no recurrences were seen during the 3- to 36-month follow-up period.

Medication

The goals of pharmacotherapy are to reduce morbidity and prevent complications.

Steroid hormones

These agents are used to inhibit the effects of estrogen.1,10,11,12,13,20


Testosterone (Androderm, Andropository)

Predominant male sex hormone used for replacement therapy in male hypogonadism.

Adult

200-300 mg (testosterone enanthate) IM q2-4wk
4-6 mg (scrotal patch) transdermally qd
5 mg (nonscrotal skin patch) transdermally qd

Pediatric

10-25 mg testosterone propionate 2-3 times/wk

May increase cyclosporine levels and cause toxicity; may increase PT and risk of bleeding in patients receiving oral anticoagulants

Documented hypersensitivity, breast cancer, prostate cancer, severe cardiac dysfunction, hepatic or renal disease

Pregnancy

X - Contraindicated; benefit does not outweigh risk

Precautions

Prostate hypertrophy or cancer; oligospermia (with prolonged use or excessive dosage); may accelerate bone maturation


Clomiphene (Clomid, Milophene, Serophene)

Stimulates release of pituitary gonadotropins.

Adult

50-100 mg PO qd; not to exceed 6 mo

Pediatric

Not established

Documented hypersensitivity, liver disease, abnormal uterine bleeding, uncontrolled thyroid or adrenal dysfunction, pituitary tumor and risk of hemorrhage into tumor

Pregnancy

X - Contraindicated; benefit does not outweigh risk

Precautions

Perform ophthalmic evaluation if patient develops visual symptoms


Tamoxifen (Nolvadex)

Competitively binds to estrogen receptor, producing a nuclear complex that decreases DNA synthesis and inhibits estrogen effects.

Adult

10-20 mg PO bid

Pediatric

Not established

May exacerbate hepatotoxic effects of allopurinol; may increase cyclosporine serum levels; increases anticoagulant effects of warfarin; aminoglutethimide reduces serum concentration; cyclophosphamide, methotrexate, and 5-FU increase thrombotic risk

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in leukopenia, thrombocytopenia, and hyperlipidemia; decreased visual acuity, corneal changes, and retinopathy may occur with >1 y of use; may induce ovulation


Danazol (Danocrine)

Synthetic steroid analog with strong antigonadotropic activity (inhibits LH and FSH) and weak androgenic action.

Adult

200 mg PO bid for 3 mo

Pediatric

Not established

May increase risk of carbamazepine and cyclosporine toxicity; may increase PT in patients receiving oral anticoagulants; inhibits response to clomiphene

Documented hypersensitivity, seizure disorders, renal or hepatic insufficiency, lactation, conditions influenced by edema

Pregnancy

X - Contraindicated; benefit does not outweigh risk

Precautions

Increased risk of bleeding in hemophilic patients; risk of fluid retention, especially with overt CHF or renal failure; caution in seizure disorders


Testolactone (Teslac)

Synthetic peripheral aromatase inhibitor that blocks production of estradiol and estrone from testosterone and androstenedione.

Adult

150 mg PO tid for up to 6 mo

Pediatric

Not established

May alter PT in patients taking oral anticoagulants

Documented hypersensitivity, males with breast cancer

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Monitor liver function; edema may develop in patients with CHF or liver or renal insufficiency; may worsen hypertension; may exacerbate epilepsy and migraine; monitor INR closely in patients taking warfarin (possibly adjust dose)

More on Gynecomastia

Overview: Gynecomastia
Differential Diagnoses & Workup: Gynecomastia
Treatment & Medication: Gynecomastia
Follow-up: Gynecomastia
References
Further Reading

References

  1. Glass AR. Gynecomastia. Endocrinol Metab Clin North Am. Dec 1994;23(4):825-37. [Medline].

  2. Braunstein GD. Gynecomastia. N Engl J Med. Feb 18 1993;328(7):490-5. [Medline].

  3. Mahoney CP. Adolescent gynecomastia. Differential diagnosis and management. Pediatr Clin North Am. Dec 1990;37(6):1389-404. [Medline].

  4. Mauras N. Treatment of adolescents with gynecomastia. J Pediatr. Apr 2005;146(4):576; author reply 576-7. [Medline].

  5. Thompson DF, Carter JR. Drug-induced gynecomastia. Pharmacotherapy. Jan-Feb 1993;13(1):37-45. [Medline].

  6. Eckman A, Dobs A. Drug-induced gynecomastia. Expert Opin Drug Saf. Nov 2008;7(6):691-702. [Medline].

  7. Mathew J, Perkins GH, Stephens T, et al. Primary breast cancer in men: clinical, imaging, and pathologic findings in 57 patients. AJR Am J Roentgenol. Dec 2008;191(6):1631-9. [Medline].

  8. Volpe CM, Raffetto JD, Collure DW, et al. Unilateral male breast masses: cancer risk and their evaluation and management. Am Surg. Mar 1999;65(3):250-3. [Medline].

  9. MacIntosh RF, Merrimen JL, Barnes PJ. Application of the probabilistic approach to reporting breast fine needle aspiration in males. Acta Cytol. Sep-Oct 2008;52(5):530-4. [Medline].

  10. Plourde PV, Kulin HE, Santner SJ. Clomiphene in the treatment of adolescent gynecomastia. Clinical and endocrine studies. Am J Dis Child. Nov 1983;137(11):1080-2. [Medline].

  11. Bedognetti D, Rubagotti A, Conti G, et al. An open, randomised, multicentre, phase 3 trial comparing the efficacy of two tamoxifen schedules in preventing gynaecomastia induced by bicalutamide monotherapy in prostate cancer patients. Eur Urol. May 19 2009;[Medline].

  12. Boccardo F, Rubagotti A, Battaglia M, et al. Evaluation of tamoxifen and anastrozole in the prevention of gynecomastia and breast pain induced by bicalutamide monotherapy of prostate cancer. J Clin Oncol. Feb 1 2005;23(4):808-15. [Medline].

  13. Jones DJ, Holt SD, Surtees P, et al. A comparison of danazol and placebo in the treatment of adult idiopathic gynaecomastia: results of a prospective study in 55 patients. Ann R Coll Surg Engl. Sep 1990;72(5):296-8. [Medline][Full Text].

  14. Colombo-Benkmann M, Buse B, Stern J, et al. Indications for and results of surgical therapy for male gynecomastia. Am J Surg. Jul 1999;178(1):60-3. [Medline].

  15. Davanco RA, Sabino Neto M, Garcia EB, et al. Quality of life in the surgical treatment of gynecomastia. Aesthetic Plast Surg. Oct 25 2008;[Medline].

  16. Ridha H, Colville RJ, Vesely MJ. How happy are patients with their gynaecomastia reduction surgery?. J Plast Reconstr Aesthet Surg. Aug 28 2008;[Medline].

  17. Benito-Ruiz J, Raigosa M, Manzano M, et al. Assessment of a suction-assisted cartilage shaver plus liposuction for the treatment of gynecomastia. Aesthet Surg J. Jul-Aug 2009;29(4):302-9. [Medline].

  18. Hammond DC. Surgical correction of gynecomastia. Plast Reconstr Surg. Jul 2009;124(1 Suppl):61e-68e. [Medline].

  19. Fan L, Yang X, Zhang Y, et al. Endoscopic subcutaneous mastectomy for the treatment of gynecomastia: a report of 65 cases. Surg Laparosc Endosc Percutan Tech. Jun 2009;19(3):e85-90. [Medline].

  20. Gruntmanis U, Braunstein GD. Treatment of gynecomastia. Curr Opin Investig Drugs. May 2001;2(5):643-9. [Medline].

  21. Braunstein GD, Glassman HA. Gynecomastia. Curr Ther Endocrinol Metab. 1997;6:401-4. [Medline].

  22. Neuman JF. Evaluation and treatment of gynecomastia. Am Fam Physician. Apr 1997;55(5):1835-44, 1849-50. [Medline].

Further Reading

Related eMedicine topics:
Breast Embryology
Breast Reduction, Liposuction Only
Disorders of the Breast
Gynecomastia [Plastic Surgery]
Klinefelter Syndrome
Prepubertal Testicular and Paratesticular Tumors

Clinical guidelines:
Practice advisory on liposuction. American Society of Plastic Surgeons - Medical Specialty Society. 2004 Apr. 13 pages. NGC:004125

Clinical trials:
Adaptation Among Adolescents and Adults With Klinefelter Syndrome

Keywords

gynecomastia, male breast, male breasts, gynecomastia surgery, male breast reduction, male breast cancer, gynecomastia treatment, gynecomastia cure, gynaecomastia, pseudogynecomastia, enlargement of the male breast, male breast surgery, male breast reduction surgery, breast lump, physiologic gynecomastia, pathologic gynecomastia, testicular neoplasm, lipomastia, macromastia, pubertal gynecomastia, florid gynecomastia, fibrous gynecomastia, feminization, granular glandular tissue, breast cancer, hypogonadism, Kallmann syndrome, Klinefelter syndrome, congenital anorchia, testicular trauma, testicular torsion, viralorchitis, pituitary tumor, hypopituitarism, renal failure, kidney failure, androgen insensitivity syndrome, 5-alpha-reductase deficiency syndrome, altered estrogen-androgen balance, mumps, sexual dysfunction, infertility, chronic liver disease, thyroid disease, renal disease, eunuchoid habitus, testicular tumors, extragonadal germ cell tumors, malnutrition, hyperthyroidism, adrenal tumors, familial gynecomastia

Contributor Information and Disclosures

Author

Mark R Allee, MD, Associate Professor, Department of Medicine, University of Oklahoma Health Sciences Center
Mark R Allee, MD is a member of the following medical societies: American College of Physicians
Disclosure: Nothing to disclose.

Coauthor(s)

Mary Zoe Baker, MD, Professor, Department of Medicine, Section of Endocrinology, Metabolism and Hypertension, University of Oklahoma; Medical Director, University of Oklahoma Physicians, Medicine Specialty Clinic, General Medicine Clinic and Medicine Residents' Clinic
Mary Zoe Baker, MD is a member of the following medical societies: American Association of Clinical Endocrinologists, American Chemical Society, and American College of Physicians-American Society of Internal Medicine
Disclosure: Nothing to disclose.

Medical Editor

Barry J Goldstein, MD, PhD, Director, Division of Endocrinology, Diabetes and Metabolic Diseases, Professor, Department of Internal Medicine, Thomas Jefferson University
Barry J Goldstein, MD, PhD is a member of the following medical societies: Alpha Omega Alpha, American College of Clinical Endocrinologists, American College of Physicians-American Society of Internal Medicine, American Diabetes Association, and Endocrine Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Yoram Shenker, MD, Chief of Endocrinology Section, Veterans Affairs Medical Center of Madison; Interim Chief, Associate Professor, Department of Internal Medicine, Section of Endocrinology, Diabetes and Metabolism, University of Wisconsin at Madison
Yoram Shenker, MD is a member of the following medical societies: American Heart Association, Central Society for Clinical Research, and Endocrine Society
Disclosure: Nothing to disclose.

CME Editor

Mark Cooper, MBBS, PhD, FRACP, Head, Diabetes & Metabolism Division, Baker Heart Research Institute, Professor of Medicine, Monash University
Disclosure: Nothing to disclose.

Chief Editor

George T Griffing, MD, Professor of Medicine, St Louis University School of Medicine
George T Griffing, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Medical Practice Executives, American College of Physician Executives, American College of Physicians, American Diabetes Association, American Federation for Medical Research, American Heart Association, Central Society for Clinical Research, Endocrine Society, International Society for Clinical Densitometry, and Southern Society for Clinical Investigation
Disclosure: Nothing to disclose.

 
 
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