VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW
The steadily growing interest in studying of endocrine genetics is driven not only by the search for new pathologies but also by the most pressing need to develop methods for early diagnosis, treatment and management of patients. Though 20% of all the patients with von Hippel-Lindau syndrome do not...
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| Format: | Article |
| Language: | Russian |
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SINAPS LLC
2019-05-01
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| Series: | Архивъ внутренней медицины |
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| Online Access: | https://www.medarhive.ru/jour/article/view/924 |
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| author | I. I. Larina N. M. Platonova E. A. Troshina A. A. Roslyakova D. G. Belzevich L. S. Selivanova M. Yu. Ukina L. V. Nikankina N. M. Malysheva A. N. Tyulpakov L. D. Kovalevich |
| author_facet | I. I. Larina N. M. Platonova E. A. Troshina A. A. Roslyakova D. G. Belzevich L. S. Selivanova M. Yu. Ukina L. V. Nikankina N. M. Malysheva A. N. Tyulpakov L. D. Kovalevich |
| author_sort | I. I. Larina |
| collection | DOAJ |
| description | The steadily growing interest in studying of endocrine genetics is driven not only by the search for new pathologies but also by the most pressing need to develop methods for early diagnosis, treatment and management of patients. Though 20% of all the patients with von Hippel-Lindau syndrome do not have a family history of the disease; a genetic basis is a natural characteristic of the disease and determinates a phenotype. Despite the nonaggressive course, in general, a relative unpredictability of the syndrome signs onset and the lack of regular monitoring can increase the risk of surgery complications and cause a disability at a young age. The presented clinical case shows the need for a multidisciplinary approach to management of the patients with von Hippel-Lindau syndrome. |
| format | Article |
| id | doaj-art-e962004f23b54a6084f19400f8fddd28 |
| institution | DOAJ |
| issn | 2226-6704 2411-6564 |
| language | Russian |
| publishDate | 2019-05-01 |
| publisher | SINAPS LLC |
| record_format | Article |
| series | Архивъ внутренней медицины |
| spelling | doaj-art-e962004f23b54a6084f19400f8fddd282025-08-20T03:00:39ZrusSINAPS LLCАрхивъ внутренней медицины2226-67042411-65642019-05-019316517110.20514/2226-6704-2019-9-3-165-171731VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEWI. I. Larina0N. M. Platonova1E. A. Troshina2A. A. Roslyakova3D. G. Belzevich4L. S. Selivanova5M. Yu. Ukina6L. V. Nikankina7N. M. Malysheva8A. N. Tyulpakov9L. D. Kovalevich10Endocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreEndocrinology research centreThe steadily growing interest in studying of endocrine genetics is driven not only by the search for new pathologies but also by the most pressing need to develop methods for early diagnosis, treatment and management of patients. Though 20% of all the patients with von Hippel-Lindau syndrome do not have a family history of the disease; a genetic basis is a natural characteristic of the disease and determinates a phenotype. Despite the nonaggressive course, in general, a relative unpredictability of the syndrome signs onset and the lack of regular monitoring can increase the risk of surgery complications and cause a disability at a young age. The presented clinical case shows the need for a multidisciplinary approach to management of the patients with von Hippel-Lindau syndrome.https://www.medarhive.ru/jour/article/view/924facomatosisvon hippel-lindau syndromepheochromocytomahemangioblastomavhl |
| spellingShingle | I. I. Larina N. M. Platonova E. A. Troshina A. A. Roslyakova D. G. Belzevich L. S. Selivanova M. Yu. Ukina L. V. Nikankina N. M. Malysheva A. N. Tyulpakov L. D. Kovalevich VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW Архивъ внутренней медицины facomatosis von hippel-lindau syndrome pheochromocytoma hemangioblastoma vhl |
| title | VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW |
| title_full | VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW |
| title_fullStr | VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW |
| title_full_unstemmed | VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW |
| title_short | VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW |
| title_sort | von hippel lindau syndrome aspects of treatment and management case report and literature review |
| topic | facomatosis von hippel-lindau syndrome pheochromocytoma hemangioblastoma vhl |
| url | https://www.medarhive.ru/jour/article/view/924 |
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