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Male gynecomastia and risk for malignant tumours--a cohort study

Olsson, H ; Bladstrom, A and Alm, P LU (2002) In BMC Cancer 2. p.26-26
Abstract

BACKGROUND: Men with gynecomastia may suffer from absolute or relative estrogen excess and their risk of different malignancies may be increased. We tested whether men with gynecomastia were at greater risk of developing cancer.

METHODS: A cohort was formed of all the men having a histopathological diagnosis of gynecomastia at the Department of Pathology, University of Lund, following an operation for either uni- or bilateral breast enlargement between 1970-1979. All possible causes of gynecomastia were accepted, such as endogenous or exogenous hormonal exposure as well as cases of unknown etiology. Prior to diagnosis of gynecomastia eight men had a diagnosis of prostate carcinoma, two men a diagnosis of unilateral breast cancer... (More)

BACKGROUND: Men with gynecomastia may suffer from absolute or relative estrogen excess and their risk of different malignancies may be increased. We tested whether men with gynecomastia were at greater risk of developing cancer.

METHODS: A cohort was formed of all the men having a histopathological diagnosis of gynecomastia at the Department of Pathology, University of Lund, following an operation for either uni- or bilateral breast enlargement between 1970-1979. All possible causes of gynecomastia were accepted, such as endogenous or exogenous hormonal exposure as well as cases of unknown etiology. Prior to diagnosis of gynecomastia eight men had a diagnosis of prostate carcinoma, two men a diagnosis of unilateral breast cancer and one had Hodgkin's disease. These patients were included in the analyses. The final cohort of 446 men was matched to the Swedish Cancer Registry, Death Registry and General Population Registry.

RESULTS: At the end of the follow up in December 1999, the cohort constituted 8375.2 person years of follow-up time. A total of 68 malignancies versus 66.07 expected were observed; SIR = 1.03 (95% CI 0.80-1.30). A significantly increased risk for testicular cancer; SIR = 5.82 (95% CI 1.20-17.00) and squamous cell carcinoma of the skin; SIR = 3.21 (95% CI 1.71-5.48) were noted. The increased risk appeared after 2 years of follow-up. A non-significantly increased risk for esophageal cancer was also seen while no new cases of male breast cancer were observed. However, in the prospective cohort, diagnostic operations for gynecomastia may substantially have reduced this risk

CONCLUSIONS: There is a significant increased risk of testicular cancer and squamous cell carcinoma of the skin in men who have been operated on for gynecomastia.

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keywords
Adolescent, Adult, Age Distribution, Aged, Aged, 80 and over, Carcinoma, Squamous Cell, Child, Cohort Studies, Follow-Up Studies, Gynecomastia, Humans, Male, Middle Aged, Neoplasms, Risk Factors, Skin Neoplasms, Sweden, Testicular Neoplasms, Time Factors
in
BMC Cancer
volume
2
pages
26 - 26
publisher
BioMed Central (BMC)
external identifiers
  • wos:000180227900001
  • pmid:12383352
  • scopus:0037121116
  • pmid:12383352
ISSN
1471-2407
DOI
10.1186/1471-2407-2-26
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Cancer Epidemiology (013007100), Pathology, (Lund) (013030000)
id
905d281e-f6b8-4b93-b455-53902a4857b2 (old id 909534)
date added to LUP
2016-04-01 16:30:51
date last changed
2022-02-05 08:43:03
@article{905d281e-f6b8-4b93-b455-53902a4857b2,
  abstract     = {{<p>BACKGROUND: Men with gynecomastia may suffer from absolute or relative estrogen excess and their risk of different malignancies may be increased. We tested whether men with gynecomastia were at greater risk of developing cancer.</p><p>METHODS: A cohort was formed of all the men having a histopathological diagnosis of gynecomastia at the Department of Pathology, University of Lund, following an operation for either uni- or bilateral breast enlargement between 1970-1979. All possible causes of gynecomastia were accepted, such as endogenous or exogenous hormonal exposure as well as cases of unknown etiology. Prior to diagnosis of gynecomastia eight men had a diagnosis of prostate carcinoma, two men a diagnosis of unilateral breast cancer and one had Hodgkin's disease. These patients were included in the analyses. The final cohort of 446 men was matched to the Swedish Cancer Registry, Death Registry and General Population Registry.</p><p>RESULTS: At the end of the follow up in December 1999, the cohort constituted 8375.2 person years of follow-up time. A total of 68 malignancies versus 66.07 expected were observed; SIR = 1.03 (95% CI 0.80-1.30). A significantly increased risk for testicular cancer; SIR = 5.82 (95% CI 1.20-17.00) and squamous cell carcinoma of the skin; SIR = 3.21 (95% CI 1.71-5.48) were noted. The increased risk appeared after 2 years of follow-up. A non-significantly increased risk for esophageal cancer was also seen while no new cases of male breast cancer were observed. However, in the prospective cohort, diagnostic operations for gynecomastia may substantially have reduced this risk</p><p>CONCLUSIONS: There is a significant increased risk of testicular cancer and squamous cell carcinoma of the skin in men who have been operated on for gynecomastia.</p>}},
  author       = {{Olsson, H and Bladstrom, A and Alm, P}},
  issn         = {{1471-2407}},
  keywords     = {{Adolescent; Adult; Age Distribution; Aged; Aged, 80 and over; Carcinoma, Squamous Cell; Child; Cohort Studies; Follow-Up Studies; Gynecomastia; Humans; Male; Middle Aged; Neoplasms; Risk Factors; Skin Neoplasms; Sweden; Testicular Neoplasms; Time Factors}},
  language     = {{eng}},
  month        = {{10}},
  pages        = {{26--26}},
  publisher    = {{BioMed Central (BMC)}},
  series       = {{BMC Cancer}},
  title        = {{Male gynecomastia and risk for malignant tumours--a cohort study}},
  url          = {{http://dx.doi.org/10.1186/1471-2407-2-26}},
  doi          = {{10.1186/1471-2407-2-26}},
  volume       = {{2}},
  year         = {{2002}},
}