Finasteride-induced gynecomastia (male breasts)

ncbi.nlm.nih.gov/entrez/quer … t=Abstract

Am J Med Sci. 1995 Jun;309(6):322-5.
Case report: finasteride-induced gynecomastia in a 62-year-old man.
Volpi R, Maccarini PA, Boni S, Chiodera P, Coiro V.
Department of Medicine, University of Parma, Italy.

The authors describe a case of bilateral (with left prevalence) gynecomastia in a 62-year-old man after finasteride treatment because of benign prostatic hypertrophy.

Finasteride is an inhibitor of 5 alpha-reductase, the enzyme responsible for testosterone metabolism to dihydrotestosterone. In this patient, nonspecific endocrine alterations were found, except for a significant decrease in dihydrotestosterone levels.

In addition, there were no pathologic conditions affecting other organs or pharmacologic treatments that could be responsible for gynecomastia. Drug withdrawal started a progressive reduction of the lumps until complete their disappearance.

It is possible that gynecomastia was caused by alterations of estrogen/androgen ratio because of a finasteride-induced decrease in circulating dihydrotestosterone levels.

In this article, the authors confirm finasteride antiandrogenic activity and recommend a close follow-up of long-term treatments with finasteride to find out other possible side effects.

PMID: 7539584 [PubMed - indexed for MEDLINE]

Cytologic Atypia in a 53-Year-Old Man With Finasteride-Induced Gynecomastia

arpa.allenpress.com/arpaonline/? … -9985(2000124%3C0625:CAIAYO%3E2.0.CO%3B2


Note: The patient was taking this drug for alopecia (hairloss) and was himself a physician.

Microscopic photos included.

Anyone want to summarize in plain English? I couldn’t tell if the study was saying that the gyno was cancerous or not.

No, it wasn’t cancerous (yet), but it was still gyno.

Selected bits:

Gynecomastia is a known complication of a variety of conditions characterized by hormonal imbalance. Several drugs, including chemotherapeutic agents used to treat prostate and other cancers, have been associated with gynecomastia.

The drug finasteride (Proscar), used to treat benign prostatic hypertrophy and alopecia, has also been documented to cause gynecomastia.4

Typically, the gynecomastia resolves after the drug is discontinued.5 Rarely, ductal or lobular carcinomas of the male breast have been documented to arise in these cases.5

The cytology of these cancers is similar to that seen in females. However, to date there has been no description of any cytologic changes of gynecomastia induced by finasteride.

We present the case of a 53-year-old man who developed unilateral gynecomastia while taking finasteride for alopecia.

A fine-needle aspiration biopsy of the mass was initially diagnosed as adenocarcinoma. Subsequent excisional biopsy revealed gynecomastia without evidence of carcinoma. This case represents a potential pitfall when evaluating a male breast mass in the setting of finasteride therapy.

We believe this case report also represents the first description of the cytologic changes associated with finasteride therapy.

Finasteride was approved in 1992 for the treatment of benign prostatic hypertrophy under the trade name Proscar. The same drug was approved in 1997 for the treatment of alopecia under the trade name Propecia.

The Food and Drug Administration and case reports in the literature have documented an association between finasteride and gynecomastia.4

… While male breast carcinoma is exceedingly unusual, we found 2 documented instances of adenocarcinoma, including a lobular carcinoma, arising in association with finasteride therapy.5

We recommend that vacuolated cells on aspirate smears not be considered evidence of malignancy in a patient with a history of therapy with finasteride or other newly developed medications. Rather, we suggest a diagnosis of epithelial atypia and recommend an excisional biopsy.

Two Cases of Reversible Bilateral Painful Gynecomastia Induced by 1mg Oral Finasteride(Propecia®).

koreamed.org/SearchBasic.php?DT=1&RID=224193

Kim BJ, Kim YJ, Ro BI.

Department of Dermatology, College of Medicine, Chung-Ang University, Seoul, Korea.


Oral finasteride(Propecia®), 1mg/day, has been widely used as an effective treatment for male androgenetic alopecia since it had been approved by the Food and Drug Administration(FDA) of U.S. in December 1997.

Gynecomastia has been one of the most common adverse effects in the patients who were taking 5mg of oral finasteride(Proscar®). Recently, several cases of unilateral or bilateral finasteride induced gynecomastia have also been reported in 1mg of oral finasteride(Propecia®).

We report two cases of finasteride(Propecia®) induced painful bilateral gynecomastia, which are the first published documentations in Korea.

Anyone have access to full article?

Unilateral Gynecomastia Induced by Treatment With 1 mg of Oral Finasteride

Archives of Dermatology
Vol. 138 No. 4, April 2002

Oral finasteride (Propecia; Merck & Co, Inc, Whitehouse Station, NJ), 1 mg/d, has been widely used as an effective treatment for male androgenic alopecia (MAGA).1

In 5 clinical trials submitted by Merck to the US Food and Drug Administration, the company only quoted once "breast enlargement and sensitivity occasionally reported."2

In their review of some of these protocols (087 and 092), McClellan and Markham3 state that the incidence of breast tenderness or enlargement reported with a 1-mg/d dosage was the same as that with placebo (0.4%) and that “there is no evidence that finasteride 1 mg/day causes breast tenderness or enlargement.”

[b]Recently, Wade and Sinclair4 reported a case of reversible painful gynecomastia induced by finasteride use.

We also had the opportunity to observe the same adverse effect in 4 patients receiving 1-mg/d oral finasteride. [/b]

Report of Cases

Case 1

An 18-year-old man affected by MAGA received treatment with Proscar (finasteride, 5 mg; Merck & Co, . . . [Full Text of this Article]

Case 2

Case 3

Case 4

Anyone have access to full article?


Gynecomastia and Breast Cancer during Finasteride Therapy

content.nejm.org/cgi/content/short/335/11/823

To the Editor: From June 1992, when finasteride (Proscar) was approved for the treatment of prostatic hyperplasia, to February 1995, the Food and Drug Administration (FDA) received reports of gynecomastia in 214 men (ages, 47 to 90 years; median, 71) in the United States who were taking the drug.

Gynecomastia has been the most frequently reported adverse effect of this drug, with an onset ranging from 14 days to 2 1/2 years (median, 180 days) after the initiation of therapy. Most of the men were taking the recommended daily dose of 5 mg. About 30 percent had unilateral gynecomastia, and . . .

1998 – Prescription-event monitoring: Recent events and future horizons

blackwell-synergy.com/doi/pd … 98.00774.x

Screenshot from page 5, attached.

Finasteride induced gynecomastia: Case report and review of the literature

HTML: ijtrichology.com/article.asp … last=Ramot

PDF: ijtrichology.com/temp/IntJTr … 174644.pdf

Introduction

Finasteride, 1 mg/day (Propecia®; MSD), a type-II 5α-reductase (5α-R) inhibitor, is the only approved treatment prescribed at present for androgenetic alopecia.[1] Finasteride 5 mg is another alternative, but usually sold off-label, and recently dutasteride, a dual 5α-R inhibitor, was reported as a potential and more effective alternative. [2] [Size=4]Propecia® is marketed internationally as a drug with almost no side effects, and physicians routinely avoid discussion of its uncommon potential side effects.[/size] Here, we report two cases that developed gynecomastia while treated with Propecia® and want to shed light on this side effect that seems more common and meaningful than previously reported.

Case Report

A 21-year-old male, with androgenetic alopecia, generally healthy except for hypothyroidism treated with µg/d Eltroxin, developed bilateral gynecomastia four months after finasteride 1 mg/day initiation. Ten months after cessation of treatment, the patient still had enlarged breasts with no apparent improvement [Figure 1]. The second patient is a 65-year-old healthy male with androgenetic alopecia who developed unilateral left gynecomastia after two months of treatment. Stopping the treatment led to major improvement within two months, but at follow-up six years after this treatment, there is still slight residual swelling.

Discussion

Finasteride is a 4-aza-steroid that specifically inhibits the type II isoform of 5α-R, thereby decreasing the conversion of testosterone to its active metabolite dihydrotestosterone by 75-80%.[3] This inhibition leads to increased conversion of testosterone to estradiol and androstenediol in peripheral tissues (e.g., liver, testes, and peripheral blood). The increased estrogen levels may lead to sexually adverse events as was indeed shown in the largest trial reported on the use of finasteride 1 mg/day for men with androgenetic alopecia, where the only disturbances observed were decreased libido, difficulty in achieving erection, and decrease in semen’s amount. [4] [Size=4]Most of these side effects were claimed to be no more common than in control group[/size].

Gynecomastia is a recognized side effect of a variety of conditions that lead to hormonal imbalance. [5] Among these drugs play a major cause, and exogenous estrogens, digoxin, phenothiazide, or propranolol have been commonly associated with this condition. [6] Finasteride use in the dose of 5 mg/day [usually used for the treatment of benign prostatic hyperplasia, (BPH)] has been associated to this condition [Table 1]. In addition, dutasteride, a new dual 5α-R inhibitor for the treatment of BPH and androgenetic alopecia, has also been associated with this condition [Table 2].

[Size=4]Gynecomastia, however, was not reported originally as a side effect in the large trial of finasteride 1 mg/day as a treatment for androgenetic alopecia[/size], [4] and it was averred that there is no evidence that this dose causes breast tenderness or enlargement. [7] Nevertheless, several reports have described gynecomastia as a side effect of finasteride even in the lower doses [Table 3]. The time of onset (2-4 months) observed in our patients is generally in agreement with the reported literature, which shows a delay in onset of gynecomastia relative to other sexual-related adverse events. [8]

Interestingly, however, when reviewing the reported cases, there is a striking prevalence of unilateral gynecomastia in the lower doses (in contrast to a similar distribution of cases between unilateral and bilateral gynecomastia with the higher doses). [9] Actually, patient 1 is the first reported case of bilateral gynecomastia after treatment with low dose finasteride. Also of importance is the fact that the breast enlargement persisted in patient 1, 10 months following finasteride withdrawal, and in the second patient residual enlargement was observed even six years following drug cessation.

Although a benign condition, gynecomastia may cause substantial embarrassment as well as anxiety and discomfort in the affected patient. [6] [Size=4]Breast tenderness and enlargement are mentioned in the drug’s leaflet, but gain no attention among practicing dermatologists who usually don’t discuss this side effect with their patients[/size].

Therefore, we believe that this side effect should be emphasized when administering this drug for the treatment of androgenetic alopecia. In addition, we share Ferrando et al.'s [10] opinion that this side effect is often overlooked, and that new studies are warranted in order to assess the real incidence of this side effect.[18]
Finasteride induced gynecomastia - Case report and review of the literature.pdf (545 KB)