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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...

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Autores principales: Lin, Jack, Khoo, Teck K, Voelschow, Erin R, Viets, Zachary J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2021
Materias:
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.
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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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