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Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia
Testicular adrenal rest tumours (TART) are found in patients with congenital adrenal hyperplasia (CAH) with the severity of testicular infiltration linearly related to the degree of enzymatic defect and subsequent compliance with treatment. We report a highly unusual case of TART in an adult patient...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The British Institute of Radiology.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809912/ https://www.ncbi.nlm.nih.gov/pubmed/36632556 http://dx.doi.org/10.1259/bjrcr.20220072 |
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author | Forster, Danielle Andrea Marzouk, Sherief Chakraborti, Indrani Berney, Daniel Wolfe, Konrad Liyanage, Sidath H |
author_facet | Forster, Danielle Andrea Marzouk, Sherief Chakraborti, Indrani Berney, Daniel Wolfe, Konrad Liyanage, Sidath H |
author_sort | Forster, Danielle Andrea |
collection | PubMed |
description | Testicular adrenal rest tumours (TART) are found in patients with congenital adrenal hyperplasia (CAH) with the severity of testicular infiltration linearly related to the degree of enzymatic defect and subsequent compliance with treatment. We report a highly unusual case of TART in an adult patient with CAH caused by 21-hydroxylase deficiency who had not engaged with health services over a 3-year period. Typical imaging features of TART include bilateral well-defined lesions adjacent to the rete testes. However, in this rare case, the follow-up imaging found that the entirety of the testicular parenchyma had been replaced with TART and the patient had gone on to develop an adrenal nodule. As these testicular tumours are commonly misdiagnosed as primary germ tumours and tend respond well to treatment with circadian or reverse glucocorticoids, it is essential for the radiologist to be aware of both the common and more unusual imaging features appearances of TART in patients with CAH in order to facilitate early diagnosis and thus timely initiation of treatment. |
format | Online Article Text |
id | pubmed-9809912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The British Institute of Radiology. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98099122023-01-10 Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia Forster, Danielle Andrea Marzouk, Sherief Chakraborti, Indrani Berney, Daniel Wolfe, Konrad Liyanage, Sidath H BJR Case Rep Case Report Testicular adrenal rest tumours (TART) are found in patients with congenital adrenal hyperplasia (CAH) with the severity of testicular infiltration linearly related to the degree of enzymatic defect and subsequent compliance with treatment. We report a highly unusual case of TART in an adult patient with CAH caused by 21-hydroxylase deficiency who had not engaged with health services over a 3-year period. Typical imaging features of TART include bilateral well-defined lesions adjacent to the rete testes. However, in this rare case, the follow-up imaging found that the entirety of the testicular parenchyma had been replaced with TART and the patient had gone on to develop an adrenal nodule. As these testicular tumours are commonly misdiagnosed as primary germ tumours and tend respond well to treatment with circadian or reverse glucocorticoids, it is essential for the radiologist to be aware of both the common and more unusual imaging features appearances of TART in patients with CAH in order to facilitate early diagnosis and thus timely initiation of treatment. The British Institute of Radiology. 2022-11-01 /pmc/articles/PMC9809912/ /pubmed/36632556 http://dx.doi.org/10.1259/bjrcr.20220072 Text en © 2022 The Authors. Published by the British Institute of Radiology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Forster, Danielle Andrea Marzouk, Sherief Chakraborti, Indrani Berney, Daniel Wolfe, Konrad Liyanage, Sidath H Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia |
title | Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia |
title_full | Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia |
title_fullStr | Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia |
title_full_unstemmed | Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia |
title_short | Testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia |
title_sort | testicular adrenal rest tumours in an adult patient with congenital adrenal hyperplasia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809912/ https://www.ncbi.nlm.nih.gov/pubmed/36632556 http://dx.doi.org/10.1259/bjrcr.20220072 |
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