Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands. The phenotype of MEN1 is broad, and over 20 different combinations of endocrine and non-endocrine metabolic manifestations...
| Format: | Article |
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| Language: | English |
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Endocrinology Research Centre
2012-12-01
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| Series: | Ожирение и метаболизм |
| Subjects: | |
| Online Access: | https://www.omet-endojournals.ru/jour/article/view/5129 |
| _version_ | 1797204670874124288 |
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| collection | DOAJ |
| description | Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands. The phenotype of MEN1 is broad, and over 20 different combinations of endocrine and non-endocrine metabolic manifestations have been described. This case demonstrates multiple formations of endocrine organs, starting non-classical with macroprolactonoma resistant to dopamine agonists therapy, other endocrine disorders developed gradually eventually: hyperparathyreoidism and hypoglycemia caused by pancreas lesions, produced proinsulin in high levels. |
| first_indexed | 2024-03-08T09:14:15Z |
| format | Article |
| id | doaj.art-6a39601c34e147fdb5657d9bf386f60c |
| institution | Directory Open Access Journal |
| issn | 2071-8713 2306-5524 |
| language | English |
| last_indexed | 2024-04-24T08:38:55Z |
| publishDate | 2012-12-01 |
| publisher | Endocrinology Research Centre |
| record_format | Article |
| series | Ожирение и метаболизм |
| spelling | doaj.art-6a39601c34e147fdb5657d9bf386f60c2024-04-16T16:16:07ZengEndocrinology Research CentreОжирение и метаболизм2071-87132306-55242012-12-0194444710.14341/2071-8713-51295087Clinical case: multiple endocrine neoplasia type 1 (MEN 1)Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands. The phenotype of MEN1 is broad, and over 20 different combinations of endocrine and non-endocrine metabolic manifestations have been described. This case demonstrates multiple formations of endocrine organs, starting non-classical with macroprolactonoma resistant to dopamine agonists therapy, other endocrine disorders developed gradually eventually: hyperparathyreoidism and hypoglycemia caused by pancreas lesions, produced proinsulin in high levels.https://www.omet-endojournals.ru/jour/article/view/5129wermer syndromemen 1prolactinomaprolactinhyperparathyroidisminsulinomaproinsulin |
| spellingShingle | Clinical case: multiple endocrine neoplasia type 1 (MEN 1) Ожирение и метаболизм wermer syndrome men 1 prolactinoma prolactin hyperparathyroidism insulinoma proinsulin |
| title | Clinical case: multiple endocrine neoplasia type 1 (MEN 1) |
| title_full | Clinical case: multiple endocrine neoplasia type 1 (MEN 1) |
| title_fullStr | Clinical case: multiple endocrine neoplasia type 1 (MEN 1) |
| title_full_unstemmed | Clinical case: multiple endocrine neoplasia type 1 (MEN 1) |
| title_short | Clinical case: multiple endocrine neoplasia type 1 (MEN 1) |
| title_sort | clinical case multiple endocrine neoplasia type 1 men 1 |
| topic | wermer syndrome men 1 prolactinoma prolactin hyperparathyroidism insulinoma proinsulin |
| url | https://www.omet-endojournals.ru/jour/article/view/5129 |