Testosterone therapy and breast histopathological features in transgender individuals
Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long-term effect of exogenous testosterone on breast tissues remains unclear. Our study evaluated the modulation of breast morphology by TT in transgender individuals with special attention to durati...
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Published in | Modern pathology Vol. 34; no. 1; pp. 85 - 94 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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New York
Elsevier Inc
01.01.2021
Nature Publishing Group US Elsevier Limited |
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Abstract | Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long-term effect of exogenous testosterone on breast tissues remains unclear. Our study evaluated the modulation of breast morphology by TT in transgender individuals with special attention to duration of TT. We reviewed 447 breast surgical specimens from gender affirming chest-contouring surgery, and compared histopathological findings including degree of lobular atrophy, and atypical and non-atypical proliferations between subjects who did (n = 367) and did not (n = 79) receive TT. TT for one patient was unknown. TT for >12 months was associated with seven histopathological features. Longer duration of TT was significantly associated with higher degrees of lobular atrophy (p < 0.001). This relationship remained significant after accounting for age at surgery, ethnicity, body mass index, and presurgical oophorectomy (adjusted p < 0.001). Four types of lesions were more likely to be absent in breast tissues exposed to longer durations of TT: cysts (median = 16.2 months; p < 0.01; adjusted p = 0.01), fibroadenoma (median = 14.8 months; p = 0.02; adjusted p = 0.07), pseudoangiomatous stromal hyperplasia (median = 17.0 months; p < 0.001; adjusted p < 0.001), and papillomas (median = 14.7 months; p = 0.04; adjusted p = 0.20). Columnar cell change and mild inflammation were also less likely to occur in subjects receiving TT (p < 0.05), but were not linked to the duration of TT. Atypia and ductal carcinoma in situ were detected in 11 subjects (2.5%) all of whom received TT ranging from 10.1 to 64.1 months. The incidental findings of high-risk lesions and carcinoma as well as the risk of cancer in residual breast tissue after chest-contouring surgery warrant the consideration of culturally sensitive routine breast cancer screening protocols for transgender men and masculine-centered gender nonconforming individuals. Long-term follow-up studies and molecular investigations are needed to understand the breast cancer risk of transgender individuals who receive TT. |
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AbstractList | Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long-term effect of exogenous testosterone on breast tissues remains unclear. Our study evaluated the modulation of breast morphology by TT in transgender individuals with special attention to duration of TT. We reviewed 447 breast surgical specimens from gender affirming chest-contouring surgery, and compared histopathological findings including degree of lobular atrophy, and atypical and non-atypical proliferations between subjects who did (n = 367) and did not (n = 79) receive TT. TT for one patient was unknown. TT for >12 months was associated with seven histopathological features. Longer duration of TT was significantly associated with higher degrees of lobular atrophy (p < 0.001). This relationship remained significant after accounting for age at surgery, ethnicity, body mass index, and presurgical oophorectomy (adjusted p < 0.001). Four types of lesions were more likely to be absent in breast tissues exposed to longer durations of TT: cysts (median = 16.2 months; p < 0.01; adjusted p = 0.01), fibroadenoma (median = 14.8 months; p = 0.02; adjusted p = 0.07), pseudoangiomatous stromal hyperplasia (median = 17.0 months; p < 0.001; adjusted p < 0.001), and papillomas (median = 14.7 months; p = 0.04; adjusted p = 0.20). Columnar cell change and mild inflammation were also less likely to occur in subjects receiving TT (p < 0.05), but were not linked to the duration of TT. Atypia and ductal carcinoma in situ were detected in 11 subjects (2.5%) all of whom received TT ranging from 10.1 to 64.1 months. The incidental findings of high-risk lesions and carcinoma as well as the risk of cancer in residual breast tissue after chest-contouring surgery warrant the consideration of culturally sensitive routine breast cancer screening protocols for transgender men and masculine-centered gender nonconforming individuals. Long-term follow-up studies and molecular investigations are needed to understand the breast cancer risk of transgender individuals who receive TT.Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long-term effect of exogenous testosterone on breast tissues remains unclear. Our study evaluated the modulation of breast morphology by TT in transgender individuals with special attention to duration of TT. We reviewed 447 breast surgical specimens from gender affirming chest-contouring surgery, and compared histopathological findings including degree of lobular atrophy, and atypical and non-atypical proliferations between subjects who did (n = 367) and did not (n = 79) receive TT. TT for one patient was unknown. TT for >12 months was associated with seven histopathological features. Longer duration of TT was significantly associated with higher degrees of lobular atrophy (p < 0.001). This relationship remained significant after accounting for age at surgery, ethnicity, body mass index, and presurgical oophorectomy (adjusted p < 0.001). Four types of lesions were more likely to be absent in breast tissues exposed to longer durations of TT: cysts (median = 16.2 months; p < 0.01; adjusted p = 0.01), fibroadenoma (median = 14.8 months; p = 0.02; adjusted p = 0.07), pseudoangiomatous stromal hyperplasia (median = 17.0 months; p < 0.001; adjusted p < 0.001), and papillomas (median = 14.7 months; p = 0.04; adjusted p = 0.20). Columnar cell change and mild inflammation were also less likely to occur in subjects receiving TT (p < 0.05), but were not linked to the duration of TT. Atypia and ductal carcinoma in situ were detected in 11 subjects (2.5%) all of whom received TT ranging from 10.1 to 64.1 months. The incidental findings of high-risk lesions and carcinoma as well as the risk of cancer in residual breast tissue after chest-contouring surgery warrant the consideration of culturally sensitive routine breast cancer screening protocols for transgender men and masculine-centered gender nonconforming individuals. Long-term follow-up studies and molecular investigations are needed to understand the breast cancer risk of transgender individuals who receive TT. Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long-term effect of exogenous testosterone on breast tissues remains unclear. Our study evaluated the modulation of breast morphology by TT in transgender individuals with special attention to duration of TT. We reviewed 447 breast surgical specimens from gender affirming chest-contouring surgery, and compared histopathological findings including degree of lobular atrophy, and atypical and non-atypical proliferations between subjects who did (n = 367) and did not (n = 79) receive TT. TT for one patient was unknown. TT for >12 months was associated with seven histopathological features. Longer duration of TT was significantly associated with higher degrees of lobular atrophy (p < 0.001). This relationship remained significant after accounting for age at surgery, ethnicity, body mass index, and presurgical oophorectomy (adjusted p < 0.001). Four types of lesions were more likely to be absent in breast tissues exposed to longer durations of TT: cysts (median = 16.2 months; p < 0.01; adjusted p = 0.01), fibroadenoma (median = 14.8 months; p = 0.02; adjusted p = 0.07), pseudoangiomatous stromal hyperplasia (median = 17.0 months; p < 0.001; adjusted p < 0.001), and papillomas (median = 14.7 months; p = 0.04; adjusted p = 0.20). Columnar cell change and mild inflammation were also less likely to occur in subjects receiving TT (p < 0.05), but were not linked to the duration of TT. Atypia and ductal carcinoma in situ were detected in 11 subjects (2.5%) all of whom received TT ranging from 10.1 to 64.1 months. The incidental findings of high-risk lesions and carcinoma as well as the risk of cancer in residual breast tissue after chest-contouring surgery warrant the consideration of culturally sensitive routine breast cancer screening protocols for transgender men and masculine-centered gender nonconforming individuals. Long-term follow-up studies and molecular investigations are needed to understand the breast cancer risk of transgender individuals who receive TT. Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long-term effect of exogenous testosterone on breast tissues remains unclear. Our study evaluated the modulation of breast morphology by TT in transgender individuals with special attention to duration of TT. We reviewed 447 breast surgical specimens from gender affirming chest-contouring surgery, and compared histopathological findings including degree of lobular atrophy, and atypical and non-atypical proliferations between subjects who did ( n = 367) and did not ( n = 79) receive TT. TT for one patient was unknown. TT for >12 months was associated with seven histopathological features. Longer duration of TT was significantly associated with higher degrees of lobular atrophy ( p < 0.001). This relationship remained significant after accounting for age at surgery, ethnicity, body mass index, and presurgical oophorectomy (adjusted p < 0.001). Four types of lesions were more likely to be absent in breast tissues exposed to longer durations of TT: cysts (median = 16.2 months; p < 0.01; adjusted p = 0.01), fibroadenoma (median = 14.8 months; p = 0.02; adjusted p = 0.07), pseudoangiomatous stromal hyperplasia (median = 17.0 months; p < 0.001; adjusted p < 0.001), and papillomas (median = 14.7 months; p = 0.04; adjusted p = 0.20). Columnar cell change and mild inflammation were also less likely to occur in subjects receiving TT ( p < 0.05), but were not linked to the duration of TT. Atypia and ductal carcinoma in situ were detected in 11 subjects (2.5%) all of whom received TT ranging from 10.1 to 64.1 months. The incidental findings of high-risk lesions and carcinoma as well as the risk of cancer in residual breast tissue after chest-contouring surgery warrant the consideration of culturally sensitive routine breast cancer screening protocols for transgender men and masculine-centered gender nonconforming individuals. Long-term follow-up studies and molecular investigations are needed to understand the breast cancer risk of transgender individuals who receive TT. Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long term effect of exogenous testosterone on breast tissues remains unclear. Our study evaluated the modulation of breast morphology by TT in transgender individuals with special attention to duration of TT. We reviewed 447 breast surgical specimens from gender affirming chest-contouring surgery, and compared histopathological findings including degree of lobular atrophy, and atypical and non-atypical proliferations between subjects who did ( n =367) and did not ( n =79) receive TT. TT for one patient was unknown. TT for >12 months was associated with seven histopathological features. Longer duration of TT was significantly associated with higher degrees of lobular atrophy ( p <0.001). This relationship remained significant after accounting for age at surgery, ethnicity, body mass index, and pre-surgical oophorectomy (adjusted p <0.001). Four types of lesions were more likely to be absent in breast tissues exposed to longer durations of TT: cysts (median=16.2 months; p <0.01; adjusted p =0.01), fibroadenoma (median=14.8 months; p =0.02; adjusted p =0.07), pseudoangiomatous stromal hyperplasia (median=17.0 months; p <0.001; adjusted p <0.001), and papillomas (median=14.7 months; p =0.04; adjusted p =0.20). Columnar cell change and mild inflammation were also less likely to occur in subjects receiving TT ( p <0.05), but were not linked to the duration of TT. Atypia and ductal carcinoma in situ (DCIS) were detected in 11 subjects (2.5%) all of whom received TT ranging from 10.1 to 64.1 months. The incidental findings of high-risk lesions and carcinoma as well as the risk of cancer in residual breast tissue after chest-contouring surgery warrant the consideration of culturally sensitive routine breast cancer screening protocols for transgender men and masculine-centered gender non-conforming individuals. Long-term follow-up studies and molecular investigations are needed to understand the breast cancer risk of transgender individuals who receive TT. |
Author | Torous, Vanda F. Collins, Laura C. Schnitt, Stuart J. Wulf, Gerburg M. Fein-Zachary, Valerie J. Tobias, Adam M. Guzman-Arocho, Yaileen D. Bret-Mounet, Vanessa C. Bartlett, Richard A. Heng, Yujing J. Baker, Gabrielle M. |
AuthorAffiliation | 2. Department of Pathology, Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA 1. Department of Pathology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA 3. Dana-Farber/Brigham and Women’s Cancer Center, Harvard Medical School, Dana-Farber Cancer Institute-Brigham and Women’s Hospital, Boston, MA, USA 4. Department of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA 5. Department of Radiology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA 6. Department of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA |
AuthorAffiliation_xml | – name: 3. Dana-Farber/Brigham and Women’s Cancer Center, Harvard Medical School, Dana-Farber Cancer Institute-Brigham and Women’s Hospital, Boston, MA, USA – name: 6. Department of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA – name: 2. Department of Pathology, Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA – name: 1. Department of Pathology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA – name: 4. Department of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA – name: 5. Department of Radiology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA, USA |
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10.1210/er.2018-00011 – ident: 10.1038/s41379-020-00675-9_bib29 doi: 10.5858/arpa.2016-0492-OA – volume: 4 start-page: 326 year: 2019 ident: 10.1038/s41379-020-00675-9_bib15 article-title: Establishing a cohort of transgender men and gender non-conforming individuals to understand the molecular impact of testosterone on breast physiology publication-title: Transgender Health. doi: 10.1089/trgh.2019.0040 – volume: 26 start-page: 1007 year: 2020 ident: 10.1038/s41379-020-00675-9_bib23 article-title: Breast cancer in transgender female-to-male individuals: a case report of androgen receptor-positive breast cancer publication-title: Breast J. doi: 10.1111/tbj.13655 – volume: 149 start-page: 191 year: 2015 ident: 10.1038/s41379-020-00675-9_bib27 article-title: Incidence of breast cancer in a cohort of 5,135 transgender veterans publication-title: Breast Cancer Res Treat. doi: 10.1007/s10549-014-3213-2 – volume: 19 start-page: e271 year: 2019 ident: 10.1038/s41379-020-00675-9_bib24 article-title: Testosterone and breast cancer in transmen: case reports, review of the literature, and clinical observation publication-title: Clin Breast Cancer. doi: 10.1016/j.clbc.2018.12.006 – volume: 2 start-page: 77 year: 2015 ident: 10.1038/s41379-020-00675-9_bib28 article-title: Breast cancer in transgender veterans: a ten-case series publication-title: LGBT Health. doi: 10.1089/lgbt.2014.0123 – volume: 38 start-page: 1067 year: 2008 ident: 10.1038/s41379-020-00675-9_bib12 article-title: Clinicopathological study of breast tissue in female-to-male transsexuals publication-title: Surg Today. doi: 10.1007/s00595-007-3758-3 |
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Snippet | Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long-term effect of exogenous testosterone on breast... Testosterone therapy (TT) is administered to enhance masculinization in transgender individuals. The long term effect of exogenous testosterone on breast... |
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SubjectTerms | 14/63 692/308/575 692/699/67/1347 692/700/139/422 Adult Androgens - adverse effects Atrophy Body mass index Breast - drug effects Breast cancer Breast Diseases - chemically induced Cancer screening Chest Cysts Endocrine therapy Female Fibroadenoma Gender Gender nonconforming Humans Hyperplasia Laboratory Medicine Male Medical screening Medicine Medicine & Public Health Ovariectomy Pathology Retrospective Studies Sex Reassignment Surgery Surgery Testosterone Testosterone - adverse effects Transgender Persons |
Title | Testosterone therapy and breast histopathological features in transgender individuals |
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