Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report
A case is described of a three-day-old female with salt wasting type of 21-hydroxylase deficient congenital adrenal hyperplasia who presented with acanthosis nigricans of both axillae. Following corticosteroid and mineralocorticoid therapy for disease, the acanthosis nigricans resolved. It is...
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| Format: | Article |
| Language: | English |
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Hacettepe University Institute of Child Health
2005-04-01
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| Series: | The Turkish Journal of Pediatrics |
| Online Access: | https://turkjpediatr.org/article/view/2711 |
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| _version_ | 1850236686889385984 |
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| author | Selim Kurtoğlu M Emre Atabek Mehmet Keskin Ozlem Canöz |
| author_facet | Selim Kurtoğlu M Emre Atabek Mehmet Keskin Ozlem Canöz |
| author_sort | Selim Kurtoğlu |
| collection | DOAJ |
| description |
A case is described of a three-day-old female with salt wasting type of 21-hydroxylase deficient congenital adrenal hyperplasia who presented with acanthosis nigricans of both axillae. Following corticosteroid and mineralocorticoid therapy for disease, the acanthosis nigricans resolved. It is believed that this is the first reported case of acanthosis nigricans occurring in association with congenital adrenal hyperplasia, a phenomenon that resolved after treatment. We speculate that the acanthosis nigricans resulted from hyperandrogenemia or other unknown factors in our patient.
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| format | Article |
| id | doaj-art-7e9b514faeee4e3f942ccb3db7d61e57 |
| institution | OA Journals |
| issn | 0041-4301 2791-6421 |
| language | English |
| publishDate | 2005-04-01 |
| publisher | Hacettepe University Institute of Child Health |
| record_format | Article |
| series | The Turkish Journal of Pediatrics |
| spelling | doaj-art-7e9b514faeee4e3f942ccb3db7d61e572025-08-20T02:01:54ZengHacettepe University Institute of Child HealthThe Turkish Journal of Pediatrics0041-43012791-64212005-04-01472Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case reportSelim Kurtoğlu0M Emre AtabekMehmet KeskinOzlem CanözDepartment of Pediatric Endocrinology, Erciyes University Faculty of Medicine, Kayseri, Turkey. A case is described of a three-day-old female with salt wasting type of 21-hydroxylase deficient congenital adrenal hyperplasia who presented with acanthosis nigricans of both axillae. Following corticosteroid and mineralocorticoid therapy for disease, the acanthosis nigricans resolved. It is believed that this is the first reported case of acanthosis nigricans occurring in association with congenital adrenal hyperplasia, a phenomenon that resolved after treatment. We speculate that the acanthosis nigricans resulted from hyperandrogenemia or other unknown factors in our patient. https://turkjpediatr.org/article/view/2711 |
| spellingShingle | Selim Kurtoğlu M Emre Atabek Mehmet Keskin Ozlem Canöz Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report The Turkish Journal of Pediatrics |
| title | Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report |
| title_full | Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report |
| title_fullStr | Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report |
| title_full_unstemmed | Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report |
| title_short | Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report |
| title_sort | acanthosis nigricans in association with congenital adrenal hyperplasia resolution after treatment case report |
| url | https://turkjpediatr.org/article/view/2711 |
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