Tumori, 90: 410-415, 2004 GYNECOMASTIA DUE TO HORMONE THERAPY FOR ADVANCED PROSTATE CANCER: A REPORT OF TEN SURGICALLY TREATED CASES AND A REVIEW OF TREATMENT OPTIONS Domenico Prezioso, Giuseppe Piccirillo, Raffaele Galasso, Vincenzo Altieri, Vincenzo Mirone, and Tullio Lotti Department of Urology, University of Naples “Federico II”, Italy Aims and background: Gynecomastia is an abnormal increase in the volume of the male breast that is generally considered to be due to an increased estrogen/androgen ratio. Pathological causes of gynecomastia include organic diseases and therapy, such as the administration of estrogens and antiandrogens, which alter the ratio of circulating hormones. Hormone therapy for prostate cancer is generally well tolerated but often accompanied by the occurrence of gynecomastia and breast pain or tenderness. The increased use of antiandrogens as monotherapy is leading to an increase in the number of patients affected by gynecomastia. Treatments are available to alleviate or prevent the development of gynecomastia, including medical treatment with antiestrogens and aromatase inhibitors. Alternatively, mastectomy with excision of the gland, liposuction or an association of the two techniques have proved to be effective. Radiation therapy may provide effective relief from the breast pain associated with gynecomastia. In this paper we show the good results of mastectomy performed with a lower semicircular periareolar incision in men suffering from gynecomastia due to antiandrogen therapy for inoperable prostate cancer. In addition, we present a review of the various techniques used for the treatment of gynecomastia. Methods and study design: During the period from September 1998 to May 2001, 10 patients receiving hormone treatment for metastatic or inoperable prostatic cancer were selected for the study if they had breast pain and bilateral gynecomastia. Five of these patients had been offered prophylactic radiotherapy before treatment but refused, while the remaining five patients had refused radiotherapy after hormone treatment. These patients were therefore given the option of surgical treatment. Before surgery all patients underwent clinical and ultrasound examination of the breast. All surgical samples were examinated histopathologically. During follow-up clinical examinations were carried out one week, one month, six months, one year and two years after surgery. Results: The results were satisfactory in all patients especially from an aesthetic point of view. Moreover, breast pain disappeared about one week after surgery. After a follow-up of 6-36 months (average, 22.8 months) no recurrences were observed. Only a few immediate postoperative complications were recorded (hematoma in one case and seroma in another). Histological examination of the excised glands showed fibrosclerotic tissue and a small amount of fat. Conclusion: Surgical liposuction can be considered an effective treatment for gynecomastia, in particular in the very early stages because the breast becomes irreversibly fibrous as the disease progresses. This surgical technique is simple and effective and is therefore to be considered favorable, especially because of the very short hospitalization and the absence of complications. Key words: gynecomastia, gynecomastia and prostate cancer, gynecomastia and hormone therapy, gynecomastia and antiandrogens, gynecomastia and mastectomy, gynecomastia and radiation therapy, gynecomastia and antiestrogens, gynecomastia and aromatase inhibitors, mastodynia and prostate cancer. Introduction Gynecomastia is an abnormal increase in the volume of the male breast, characterized by a tender discoid enlargement 2-4 cm in diameter beneath the areola, with hypertrophy of the gland and the surrounding fatty tissue. This pathological change may occur unilaterally or bilaterally and, according to most authors, it is generally considered to be due to an increased estrogen/androgen ratio. Physiological gynecomastia associated with a change in hormone levels has been reported in newborns, boys at the time of puberty and older men1,2. Pathological causes of gynecomastia include organic diseases and therapy, such as the administration of estrogens and antiandrogens3, which alter the ratio of circulating hormones. Orchiectomy, administration of luteinizing hormonereleasing factor (LH-RH) agonists, or the use of antiandrogens alone or in combination represent the standard care for patients with metastatic or inoperable prostate cancer. Nonsteroidal antiandrogen monotherapy gives no difference in survival compared to combined androgen blockade or castration in patients with nonmetastatic locally advanced cancer, while there are significant quality-of-life benefits in terms of sexual interest and physical capacity4,5. Hormone therapy for prostate cancer seems to be generally well tolerated but is often accompanied by the occurrence of gynecomastia and pain or tenderness in the breast (mastodynia). The results of recent studies report an incidence of gynecomastia and breast pain from 3% to 12.7% with the use of the LHRH agonist leuprolide6,7. The increased use of antiandrogens as monotherapy is leading to an increase in the number of patients affected by gynecomastia6. Studies with bicalutamide8,9 and nilutamide 10,11 have reported gynecomastia and breast pain in approximately 50% and 24-76% of patients, respectively. This condition was observed in 3079% of patients treated with flutamide12,13. Correspondence to: Domenico Prezioso, MD, Department of Urology, University of Naples “Federico II”, Via Manzoni 71, 80123, Naples, Italy. Tel +39-081-5465803 or +39-081-7462504; fax +39-081-5452959 or +39-081-7466154; e-mail [email protected] Received September 4, 2003; accepted December 3, 2003. SURGICAL TREATMENT OF GYNECOMASTIA BY HORMONE THERAPY Although gynecomastia is not directly harmful, in an adult male the enlargement of the breast and the associated pain and tenderness may cause psychological and social problems, often severe enough to lead to discontinuation of the therapy. It is therefore often necessary and sometimes essential to find a solution to this – not only cosmetic – problem. There are treatments available to alleviate or prevent the development of gynecomastia, including medical treatment with antiestrogens and aromatase inhibitors14,15. Several studies of the antiestrogen tamoxifen in prostate cancer patients with gynecomastia have demonstrated a reduction in breast pain and size16-21. Aromatase inhibitors should alleviate gynecomastia by preventing the peripheral aromatization of circulating androgens to estrogens. However, publications to date refer only to two prototype compounds, testolactone and anastrozole22,23. An alternative option is surgery, which has proved to be effective. The three most frequently used procedures are mastectomy with excision of the gland, liposuction, and combination of the two techniques24. Radiation therapy may provide effective relief from the breast pain associated with gynecomastia. There are also several reports indicating that the development of breast pain and gynecomastia may be prevented by prophylactic irradiation of the breast tissue25-27. In this paper we show the good results of mastectomy performed with a lower semicircular periareolar incision in men suffering from gynecomastia due to antiandrogen therapy for inoperable prostate cancer. In addition, we present a review of the various techniques used for the treatment of this disease which, although less important than the prostate cancer itself, often leads to psychological problems that considerably worsen the patient’s quality of life. Materials and methods During the period from September 1998 to May 2001, patients aged 58-70 years receiving hormone treatment for disease or inoperable prostatic cancer were selected for the study if they had breast pain and bilateral gynecomastia. In 10 patients there was marked enlargement of the breast accounting for a visible pathological change. Gynecomastia was of grade 2-3 according to Simon and Hoffman’s classification28 and was not well tolerated because of the associated psychological problems. Five of the patients had been offered prophylactic radiotherapy before treatment but refused. The remaining five patients had refused therapeutic radiotherapy after hormone treatment. They were therefore given the option of a surgical procedure. This was accepted and surgery was performed in all ten patients. An example of the preoperative appearance of the affected breasts of a patient treated with bicalutamide 150 mg/day is shown in Figure 1. Before surgery all patients underwent clinical and ultrasound examination of the breast. 411 Figure 1 - Presurgical appearance of the breasts of a patient with prostate cancer treated with bicalutamide 150 mg/day. All surgical samples were examinated histopathologically. During follow-up clinical examinations were carried out one week, one month, six months, one year and two years after surgery. Surgical technique The surgical procedure was performed under general anesthesia and involved a lower semicircular periareolar skin incision from a three o’clock to nine o’clock position along the edge of the pigmented area (Figure 2). The incision was extended to the subcutaneous tissue until the whitish, firm disk of the mammary gland was exposed. The glandular tissue was dissected laterally from the subcutaneous fat until its edge was reached and its deeper surface was dissected medially for some centimeters from the pectoralis fascia. Then the same dissection procedure was repeated medially and subcutaneously until the subareolar ductal tissue was identified and freed from the areola around the attachment to the nipple. It is very important to cut the ductal tissue leaving a 3 to 4-mm-thick piece attached to the nipple. Figure 2 - Surgical incision performed during mastectomy. 412 Figure 3 - Postsurgical appearance of the breasts of a patient with prostate cancer treated with bicalutamide 150 mg/day. After removal of the disk and careful control of bleeding, the wound was closed by approximating the margins using 3/0 Vicryl Rapide sutures and a compressive dressing was applied. The dressing was removed after 48 hours and the sutures were removed after seven days. Results The median operating time was 60 minutes (±15) for bilateral mastectomy. All patients were discharged the day after surgery. The results were satisfactory in all patients, especially from an aesthetic point of view (Figure 3). Moreover, breast pain disappeared about one week after surgery. After a follow-up of 6-36 months (average, 22.8 months) no recurrences were observed. Immediate postoperative complications were hematoma in one case and seroma in another. No delayed complications such as nipple necrosis or abnormal scar retraction with areolar deformity were observed except for the loss of areolar tactile sensation in one case. Histological examination of the excised glands showed a large proportion of fibrosclerotic tissue and a small amount of fat. Discussion and conclusion Gynecomastia is a troublesome complication of hormone therapy for advanced prostate cancer because of the associated breast pain and the psychological problems arising from the cosmetic appearance. With the increasing use of hormone therapy for early prostate cancer, the incidence of gynecomastia also needs to be investigated in this population. Studies on antiandrogen therapy, either as immediate hormonal treatment or as adjuvant to therapy with curative intent, in patients with localized or locally advanced prostate cancer should provide this information. D PREZIOSO, G PICCIRILLO, R GALASSO ET AL Gynecomastia is most common in the first nine months of antiandrogen therapy, with new cases rarely occurring subsequently. Treatment should be performed very early because gynecomastia of more than one year’s duration is more likely to show a poor response to therapy due to the irreversible accumulation of fibrous glandular tissue. In this report a simple technique is described that is very easy to perform. In our patients there were few postoperative complications and the aesthetic results were good, with negligible scarring or other complications in the areolar area. No drain was placed to avoid further cosmetic defects, even though postoperative bleeding and hematomas have been reported in many studies. In the present study there were two cases with local accumulation of fluid, which spontaneously resolved with no further consequences Histopathological examination of the excised glands from the patients who underwent hormone treatment for prostate cancer showed decreased ductal proliferation and progressive increase in fibrosclerotic tissue. In spite of the reports in the literature that emphasize the good efficacy and limited side effects of prophylactic irradiation of the male breast, we could not use this treatment in our patients because of poor compliance. All our patients were very afraid to undergo radiation treatment and, in spite of our reassurance, categorically refused this therapeutic option, considering it at very high risk of sequelae and therefore too “dangerous” to treat a benign condition. Surgical removal of the mammary gland can be considered a very effective way to treat this type of gynecomastia, especially after the first year of antiandrogen treatment. Numerous methods to treat gynecomastia have been reported, indicating that there is no generally accepted satisfactory approach. A large number of surgical procedures have been described in the literature, including various types of techniques and incisions. Surgeons aim to reduce the breast size to normal contours, to eliminate painful tissue and to restore the patient’s chest to an acceptable cosmetic shape. In 1946 Webster described a subcutaneous mastectomy through an areolar or periareolar incision that could be inferior or lateral29, in 1969 Letterman placed the incision in the upper half of the areola, which did not lead to hypertrophic scarring in his experience30, and in 1984 Saad and Kay described a circumareolar incision31. Colombo-Benkmann32 performed surgical treatment in 100 patients and obtained satisfactory results in 86%, while minor complications such as skin retraction, hypertrophic scars, hypesthesia and skin redundancy occurred in 53% of cases, significantly more often in grade III and II gynecomastia. In 81% of the breasts (grade I and II gynecomastia) a lower periareolar incision was performed and hematomas occurred in 11.4% of these cases. In order to reduce the incidence of complications such as hypesthesia, Pitanguy suggested a transareolar incision33. In a study involving 24 cases he performed the new technique in 53.3% with satisfactory SURGICAL TREATMENT OF GYNECOMASTIA BY HORMONE THERAPY results in all patients, except for one case where a hypertrophic scar occurred. Liposuction34 is a surgical technique that corrects abnormal and excessive collections of adipose tissue and is considered by many authors as one of the most effective treatments for gynecomastia, especially because of the low incidence of sequelae. As liposuction removes fatty tissue only, gynecomastia mainly due to glandular hypertrophy requires more strenuous work and diligence, and additional sharp dissection to remove the parenchyma is often needed. In a report by Samdal35, among 62 patients who were treated with a combined approach 37 (60%) were very satisfied with the results and 19 (31%) were satisfied. However, despite these good results, liposuction is not likely to be effective in gynecomastia of patients with hormone-treated prostate cancer, due to the increase in glandular tissue and the lack of fatty tissue. Webster classified gynecomastia into three types: glandular, fatty-glandular and simple fatty, according to the most frequent tissue type. The glandular type can be characterized by different levels of fibrotic tissue30. Patients with a glandular component require surgical removal of the gland, while in case of simple fatty gynecomastia liposuction alone seems to be appropriate; wherever there is a fatty glandular form, surgery combined with liposuction gives good results. In 1973 Simon described another classification where patients were grouped into categories according to the size of the gynecomastia: I) minor but visible breast enlargement without skin redundancy; II) moderate breast enlargement without skin redundancy; III) moderate breast enlargement with minor skin redundancy; IV) gross breast enlargement with skin redundancy simulating a pendulous female breast. Patients of group I and II require minimal solutions and rarely a skin incision, but in group III and IV the marked excess skin should be removed and a mastopexy-type procedure is required. The overall aim of surgery is to provide a normal breast and chest contour with minimal signs of surgery. Incisions outside the areola should be avoided, as should removal of the nipple, because these procedures often result in hypertrophic scarring. Most authors suggest a hemi-circumareolar or periareolar incision and preservation of the nipple. There is general agreement that the operation is cosmetic and should be performed by surgeons with appropriate experience because the development of unaesthetic scarring may result in a worse problem than the original condition. With regard to other treatment options, there are many reports in the literature on therapeutic and especially prophylactic irradiation of the male breast. In a study by Gangai36 10 patients were treated by radiation therapy with a dose of 300 rads to each nipple and areo- 413 la on alternative days for a total dose of 900 rads in air. Hormonal treatment was started two days following the completion of radiation. After a one-year follow-up no patient had symptoms related to the breasts, and only in three cases was minimal hypertrophy noted. In all patients there was a complete lack of nipple sensitivity, localized tenderness or pain, but none of them showed any skin changes secondary to radiation. In a similar study, Malis37 divided the patients into two groups: the 18 patients in group A received bilateral breast irradiation prior to starting estrogen therapy while the 10 patients in group B were placed on therapeutic maintenance doses of estrogens for 2 to 12 weeks before radiation was started. Each patient received a total orthovoltage dose of 900 rads given in increments of 300 rads, alternating the breasts daily. After a follow-up of 12 to 21 months, 11 patients of group A had no gynecomastia and the remaining seven had only mild breast hypertrophy, while in group B breast enlargement was mild in two patients, moderate in five patients and severe in three patients. In order to determine the side effects of irradiation, Wolf38 conducted a double-blind study of 12 patients followed for more than 18 months (the longest followup being 27 months). All patients received a total dose of 1000 rads to the nipple area in one sitting. At the end of the treatment, all patients showed varying degrees of redness of the irradiated area with subsequent scaling, which disappeared two to three months after irradiation, while half of the patients had transient slight tenderness of the irradiated nipple. No other side effects were observed. In a study of 1986 Fass26 performed a retrospective analysis of 87 patients referred for radiation treatment before receiving DES for prostate cancer from 1972 to 1982. All patients were treated with 4 MV 60 Co superficial X-rays at doses ranging from 1200 to 1500 cGy in three fractions. After an average follow-up of four years, gynecomastia was absent in 67 patients, mild in nine, moderate in eleven and severe in one patient. Radiation was also very effective in preventing mammalgia. Complications occurred in only two patients and consisted of allergic reactions to the dye used in marking the treatment fields. In a Scandinavian trial of 1999 the incidence of gynecomastia was 28% of 283 patients with locally advanced prostate cancer taking flutamide following single-dose radiotherapy to the breast (12-15 Gy), compared with 67% in non-irradiated patients27. In a recent study Tyrrell investigated the efficacy and tolerability of a single 10 Gy dose of radiation before bicalutamide monotherapy in more than 100 patients with localized or locally advanced prostate cancer and found that over a period of 12 months the incidence of gynecomastia in the radiotherapy group was reduced by 33% (P <0.001) compared with the non-irradiated group14. Radiation for the prophylaxis of gynecomastia is usually administered as a single dual low dose to the breast 414 area, which is surrounded by a protective disk. Electron irradiation is most suitable because the dose can be limited to a few centimeters so that deeper organs such as the lungs or heart have minimal exposure. Low-dose irradiation is generally well tolerated, causing only reversible adverse effects such as skin erythema, tenderness and discomfort, without any evidence of long-term complications. Nevertheless, many studies have shown that irradiation is less effective if started one or more months after the beginning of hormone treatment, while the best results are obtained on tissues in active proliferation; we therefore consider radiotherapy after hormone treatment poorly effective in hormone-induced gynecomastia with a large proportion of fibrosclerotic tissue. As regards the radiotherapeutic prophylaxis of gynecomastia, poor patient compliance may represent a major problem. Patients often refuse irradiation for a benign disease that affects only an average of 50% of patients treated with antiandrogens, as reported in many statistical analyses9-12. However, as radiotherapy seems to be highly effective on the immature breast, such prophylaxis is more indicated in younger patients. The risk of severe adverse events such as a second malignancy needs careful consideration, although patients very rarely survive long enough to manifest such sequelae. Medical treatment aims to restore the estrogen-to-androgen balance but is still experimental. Many drugs have been used, including antiestrogens and aromatase inhibitors, but the literature published to date is scarce. Improvement of signs and symptoms of gynecomastia has been reported in several case studies, but only few reports, for example the small study by Serels and Melman involving three cases20, included patients with gynecomastia from treatment for prostate cancer. Most studies reported good results of antiestrogens and aromatase inhibitors, especially in pubertal gynecomastia39. This treatment option therefore seems to be particularly effective in actively proliferating tissue and could have less effect on the fibrotic tissue of hormone-induced gynecomastia. Finally, there is some concern regarding the safety of this type of drugs in men with prostate cancer, and few data in this regard are currently available. D PREZIOSO, G PICCIRILLO, R GALASSO ET AL A recent paper described an interesting randomized, double-blind, placebo-controlled, three-arm multicenter trial on the prophylactic use of the antiestrogen tamoxifen and the aromatase inhibitor anastrozole in gynecomastia. This study evaluated the role of the two agents in the prevention of gynecomastia and breast pain in patients receiving bicalutamide monotherapy (150 mg). The authors demonstrated that the prophylactic role of tamoxifen is significant (P <0.0001) at three months. Prophylactic anastrozole does not reduce the incidence of gynecomastia and breast pain at three months or thereafter. The study demonstrated that prophylactic tamoxifen 20 mg daily initiated at the same time as bicalutamide 150 mg significantly reduces the incidence of gynecomastia and breast pain, but further studies are needed to assess the impact of the combination on prostate cancer control. In fact, tamoxifen seems to increase serum testosterone levels at three months16. Another study on the preventive role of tamoxifen and anastrozole in patients with prostate cancer induced by bicalutamide was conducted more recently and seems to confirm the positive data about tamoxifen, which appears to be safe and not to influence the PSA response17. In conclusion, due to the increased use of antiandrogen monotherapy for prostate cancer the incidence of gynecomastia and mastodynia is destined to rise. Physicians and patients have a number of options for its management, but the supporting data are relevant only for prophylactic low-dose irradiation, whose tolerability and efficacy are good, especially if electrons are used to irradiate tissue to a limited depth. However, long-term follow-up data for this treatment are not available and the exact risk of the development of a malignancy is unknown. Consequently, a considerable number of patients find the potential risk unacceptable and therefore refuse this treatment option. With regard to the surgical options, liposuction can be considered effective only in the very early stages because, with the progression of gynecomastia, the breast becomes irreversibly fibrous. On the basis of the previous reports the authors favor this surgical technique because it is simple and effective, requires only short hospitalization and has very few complications. References 1. Pirke KM, Doerr P: Age related changes in free plasma testosterone, dihydrotestosterone and oestradiol. Acta Endocrinol, 80: 171-178, 1975. 2. Nuttal FQ: Gynecomastia as a physical finding in normal men. J Clin Endocrinol Metab, 48: 338-340, 1979. 3. Braunstein GD: Gynecomastia. N Engl J Med, 328: 490-495, 1993. 4. Boccardo F, Rubagotti A, Barichello M: Bicalutamide monotherapy versus flutamide plus goserelin in prostate cancer patients: results of an Italian Prostate Cancer Project study. J Clin Oncol, 17: 2027-2038, 1999. 5. Fourcade RO, Auxerre CC, Poterre M: An open multicentre randomised study to compare the effect and safety of Ca- sodex (bicalutamide) monotherapy with castration plus nilutamide in metastatic prostate cancer (abst 349). Eur Urol, 33 (Suppl 1): 88, 1998. 6. Anonymous: Leuprolide versus diethylstilbestrol for metastatic prostate cancer. The Leuprolide Study Group. N Engl J Med, 311: 1281-1286, 1984. 7. Crawford ED, Eisenberger MA, McLeod DG, Spaulding JT, Benson R, Dorr FA, Blumenstein BA, Davis MA, Goodman PJ: A controlled trial of leuprolide with and without flutamide in prostatic carcinoma. N Engl J Med, 321: 419-424, 1989. 8. Tyrrell CJ: Tolerability and quality of life aspects with the anti-androgen Casodex (ICI 176,334) as monotherapy for SURGICAL TREATMENT OF GYNECOMASTIA BY HORMONE THERAPY 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20. 21. 22. prostate cancer. International Casodex Investigators. Eur Urol 26 (Suppl 1): 15-19, 1994. Verhelst J, Denis L, Van Vliet P, Van Poppel H, Braeckman J, Van Cangh P, Mattelaer J, D’Hulster D, Mahler C: Endocrine profiles during administration of the new non-steroidal antiandrogen Casodex in prostate cancer. Clin Endocrinol (Oxf), 41: 525-530, 1994. Iversen P, Tyrrell CJ, Kaisary AV, Anderson JB, Van Poppel H, Tammela TL, Chamberlain M, Carroll K, Melezinek I: Bicalutamide monotherapy compared with castration in patients with nonmetastatic locally advanced prostate cancer: 6.3 years of follow-up. J Urol, 164: 1579-1582, 2000. Decensi AU, Boccardo F, Guameri D, Positano N, Paoletti MC, Costantini M, Martorana G, Giullani L: Monotherapy with nilutamide, a pure non-steroidal antiandrogen, in untreated patients with metastatic carcinoma of the prostate. The Italian Prostatic Cancer Project. J Urol, 146: 377-381, 1991. Chang A, Yeap B, Davis T, Blum R, Hahn R, Khanna O, Fisher H, Rosenthal J, Witte R, Schinella R, Trump D: Double-blind, randomised study of primary hormonal treatment of stage D2 prostate carcinoma: flutamide versus diethylstilbestrol. J Clin Oncol, 14: 2250-2257, 1996. Boccon-Gibod L, Foumier G, Bottet P, Marechal JM, Guiter J, Rischman P, Hubert J, Soret JY, Mangin P, Mallo C, Fraysse CE: Flutamide versus orchidectomy in the treatment of metastatic prostate carcinoma. Eur Urol, 32: 391-396, 1997. Tyrrell CJ: Gynaecomastia: aetiology and treatment options. Prost Cancer Prost Dis, 2: 167-171, 1999. McLeod DG, Iversen P: Gynecomastia in patients with prostate cancer: a review of treatment options. Urology, 56: 713-720, 2000. Saltzstein D, Cantwell A, Steber P, Ross JR, Silvay-Mandeau O, Gallo J: Prophylactic tamoxifen significantly reduces the incidence of Bicalutamide-induced gynaecomastia and breast pain. Br J Urol, 90: 120-121, abstract PD-4.07, 2002. Alagaratnam TT: Idiopathic gynecomastia treated with tamoxifen: a preliminary report. Clin Ther, 9: 483-487, 1987. McDermott MT, Hofeldt FD, Kidd GS: Tamoxifen therapy for painful idiopathic gynaecomastia. South Med J, 83: 12831285, 1990. Parker LN, Gray DR, Lai MK, Levin ER: Treatment of gynaecomastia with tamoxifen: a double-blind crossover study. Metabolism, 35: 705-708, 1986. Serels S, Melman A: Tamoxifen as treatment for gynecomastia and mastodynia resulting from hormonal deprivation. J Urol, 159: 1309, 1998. Staiman VR, Lowe FC: Tamoxifen for flutamide/finasterideinduced gynecomastia. Urology, 50: 929-933, 1997. Bocerdo F, Rubagotti A, Garofalo L, Di Tonno P, Conti G, Bertaccini A, De Antoni P, Galassi P: Tamoxifen is more effective than anastrazole in preventing gynaecomastia induced 23. 24. 25. 26. 27. 28. 29. 30. 31. 32. 33. 34. 35. 36. 37. 38. 39. 415 by bicalutamide monotherapy in prostate cancer patients. Proc ASCO, 22: 400 (abst 1608), 2003. Braunstein GD: Aromatase and gynecomastia. Endocr Relat Cancer, 6: 315-324, 1999. Donati L, Grappolini G, Ponzielli M, Colonna M, Capretti A: Surgical treatment of gynaecomastia. Indications and methods (in Italian). Minerva Chir, 48: 743-747, 1993. Chou JL, Easley JD, Feldmeier JJ, Rauth VA, Pomeroy TC: Effective radiotherapy in palliating mammalgia associated with gyecomastia after DES therapy. Int J Radiat Oncol Biol Phys, 15: 749-751, 1988. Fass D, Steinfeld A, Brown J, Tessler A: Radiotherapeutic prophylaxis of estrogen-induced gynecomastia: a study of late sequela. Int J Radiat Oncol Biol Phys, 12: 407-408, 1986. Widmark AJ, Damber L, Fossa SD, Lundmo P, Damber JE, Klepp O: Does prophylactic radiotherapy prevent antiandrogen induced gynaecomastia? Evaluation of patients in the randomised Scandinavian trial SPCG7/SFUO-3. Int J Rad Oncol Biol Phys, 45 (Suppl): 262-263 (abst 1010), 1999. Simon BE, Hoffman S, Kahn S: Classification and surgical correction of gynecomastia. Plast Reconstr Surg, 51: 48-52, 1973. Webster JP: Mastectomy for gynaecomastia through a semicircular intra-areolar incision. Ann Surg, 124: 557-575, 1946. Letterman G, Schurter M: The surgical correction of gynecomastia. Am Surg, 35: 322-325, 1969. Saad MN, Kay S: The circumareolar incision: a useful incision for gynaecomastia. Ann R Coll Surg Engl, 66: 121-122, 1984. Colombo-Benkmann M, Buse B, Stern J, Herfarth C: Indications for and results of surgical therapy for male gynaecomastia. Am J Surg, 178: 60-63, 1999. Pitanguy I: Transareolar incision for gynaecomastia. Plast Reconstr Surg, 38: 414-419, 1966. Rosenberg GJ: Gynecomastia: suction lipectomy as a contemporary solution. Plast Reconstr Surg , 80: 379-386, 1987. Samdal F, Kleppe G, Amland PF: Surgical treatment of gynaecomastia. Five years experience with liposuction. Scand J Reconstr Surg Hand Surg, 28: 123-130, 1994. Gangai MP, Shown TE, Sieber PE, Moore CA: External irradiation: a successful modality in preventing hormonally induced gynaecomastia. J Urol, 97: 338-339, 1967. Malis I, Cooper F, Wolever THS: Breast irradiation in patients with carcinoma of the prostate. J Urol, 102: 336-337, 1969. Wolf H, Madsen PO, Vermund H: Prevention of estrogen-induced gynaecomastia by external irradiation. J Urol, 102: 607-609, 1969. Zachmann M, Eiholzer U, Muritano M: Treatment of pubertal gynaecomastia with testolactone. Acta Endocrinol, 279: 218-226, 1986.
© Copyright 2024