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Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences
OBJECTIVE: To report a case of untreated classic 21 hydroxylase (OH) deficiency congenital adrenal hyperplasia (CAH) in a transgender patient resulting in pulmonary embolisms (PEs) and bilateral adrenal masses. METHODS: A 36-year-old male (birth sex: female) presenting with bilateral PEs in the sett...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SMC Media Srl
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668005/ https://www.ncbi.nlm.nih.gov/pubmed/34912752 http://dx.doi.org/10.12890/2021_003048 |
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author | Lin, Jack Khoo, Teck K Voelschow, Erin R Viets, Zachary J |
author_facet | Lin, Jack Khoo, Teck K Voelschow, Erin R Viets, Zachary J |
author_sort | Lin, Jack |
collection | PubMed |
description | OBJECTIVE: To report a case of untreated classic 21 hydroxylase (OH) deficiency congenital adrenal hyperplasia (CAH) in a transgender patient resulting in pulmonary embolisms (PEs) and bilateral adrenal masses. METHODS: A 36-year-old male (birth sex: female) presenting with bilateral PEs in the setting of long-standing, untreated classic 21OH CAH was also found to have bilateral adrenal masses (unconfirmed myelolipomas). RESULTS: Further history revealed a known diagnosis of CAH. The patient had been treated with glucocorticoid and mineralocorticoid replacement in childhood but stopped taking these medications against medical advice. During his hospital admission, he was noted to have elevated 17-hydroxyprogesterone, low cortisol with elevated ACTH levels, and male-level testosterone measurements. CT of the abdomen/pelvis revealed a 23 cm mass in the left renal fossa and a 2.5 cm mass in the right renal fossa consistent with bilateral adrenal myelolipomas. The patient attended follow-up in clinic, but declined any further hormonal treatment as he identified as male and felt further treatment was unnecessary. CONCLUSION: This case demonstrated the unique long-term effects of untreated classic CAH due to 21OH deficiency, including bilateral adrenal myelolipoma, adrenal compensation to the point of producing male-level androgens, and possibly PEs. Treatment with hydrocortisone was recommended to suppress ACTH and it was planned that the patient would eventually start on testosterone (although this would have been complicated by his bilateral PEs). Potential aetiologies for the PEs included vascular compression of the renal artery (which could explain the elevated EPO/erythrocytosis contributing to hypercoagulability) or the renal vein by the adrenal mass. LEARNING POINTS: Gender dysphoria in patients with congenital adrenal hyperplasia (CAH) is not uncommon. Adrenal enlargement can allow untreated CAH patients to compensate. Pulmonary embolisms can be a consequence of treating as well as untreated CAH. |
format | Online Article Text |
id | pubmed-8668005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SMC Media Srl |
record_format | MEDLINE/PubMed |
spelling | pubmed-86680052021-12-14 Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences Lin, Jack Khoo, Teck K Voelschow, Erin R Viets, Zachary J Eur J Case Rep Intern Med Articles OBJECTIVE: To report a case of untreated classic 21 hydroxylase (OH) deficiency congenital adrenal hyperplasia (CAH) in a transgender patient resulting in pulmonary embolisms (PEs) and bilateral adrenal masses. METHODS: A 36-year-old male (birth sex: female) presenting with bilateral PEs in the setting of long-standing, untreated classic 21OH CAH was also found to have bilateral adrenal masses (unconfirmed myelolipomas). RESULTS: Further history revealed a known diagnosis of CAH. The patient had been treated with glucocorticoid and mineralocorticoid replacement in childhood but stopped taking these medications against medical advice. During his hospital admission, he was noted to have elevated 17-hydroxyprogesterone, low cortisol with elevated ACTH levels, and male-level testosterone measurements. CT of the abdomen/pelvis revealed a 23 cm mass in the left renal fossa and a 2.5 cm mass in the right renal fossa consistent with bilateral adrenal myelolipomas. The patient attended follow-up in clinic, but declined any further hormonal treatment as he identified as male and felt further treatment was unnecessary. CONCLUSION: This case demonstrated the unique long-term effects of untreated classic CAH due to 21OH deficiency, including bilateral adrenal myelolipoma, adrenal compensation to the point of producing male-level androgens, and possibly PEs. Treatment with hydrocortisone was recommended to suppress ACTH and it was planned that the patient would eventually start on testosterone (although this would have been complicated by his bilateral PEs). Potential aetiologies for the PEs included vascular compression of the renal artery (which could explain the elevated EPO/erythrocytosis contributing to hypercoagulability) or the renal vein by the adrenal mass. LEARNING POINTS: Gender dysphoria in patients with congenital adrenal hyperplasia (CAH) is not uncommon. Adrenal enlargement can allow untreated CAH patients to compensate. Pulmonary embolisms can be a consequence of treating as well as untreated CAH. SMC Media Srl 2021-11-30 /pmc/articles/PMC8668005/ /pubmed/34912752 http://dx.doi.org/10.12890/2021_003048 Text en © EFIM 2021 This article is licensed under a Commons Attribution Non-Commercial 4.0 License |
spellingShingle | Articles Lin, Jack Khoo, Teck K Voelschow, Erin R Viets, Zachary J Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences |
title | Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences |
title_full | Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences |
title_fullStr | Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences |
title_full_unstemmed | Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences |
title_short | Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences |
title_sort | compliance issues in managing 21 hydroxylase deficiency and their short/long-term consequences |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668005/ https://www.ncbi.nlm.nih.gov/pubmed/34912752 http://dx.doi.org/10.12890/2021_003048 |
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