电邮这篇文章 A case of congenital glaucoma in type I neurofibromatosis
- 作者: Pleskova A.V.1, Lugovkina K.V.1, Panova A.Y.1, Sorokin A.A.1
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隶属关系:
- Helmholtz National Medical Research Center of Eye Diseases
- 期: 卷 16, 编号 3 (2021)
- 页面: 37-42
- 栏目: Case reports
- URL: https://journals.rcsi.science/1993-1859/article/view/79195
- DOI: https://doi.org/10.17816/rpoj79195
- ID: 79195
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详细
BACKGROUND: Recklinghausen’s generalized neurofibromatosis (NF) is a hereditary disease characterized by the formation of benign tumors from the nervous tissue that provokes skin and bone changes of various types. Often, involvement in the pathological process and the organ of vision. The variability of eye lesions in NF-I type is known according to the clinical course, severity, and clinical forms. Gliomas and atrophy of the optic nerves, neurofibromas in the iris, sclera, conjunctiva, eyelids, less often — glaucoma, buphthalmos, orbital osteodystrophy are described.
RESULTS: The article describes a rare case of type I neurofibromatosis, the first clinical manifestation of congenital glaucoma. Modern complex ophthalmological examination made it possible to identify the cause and clarify the nature of the development of glaucoma.
CONCLUSION: The need for an interdisciplinary approach to the diagnosis, dispensary observation, and treatment of NF-I is emphasized.
作者简介
A. Pleskova
Helmholtz National Medical Research Center of Eye Diseases
Email: dho@igb.ru
ORCID iD: 0000-0002-4458-4605
MD, Dr. Med. Sciences
俄罗斯联邦, MoscowK. Lugovkina
Helmholtz National Medical Research Center of Eye Diseases
Email: ksushalyg@mail.ru
ORCID iD: 0000-0002-3531-3846
MD, PhD, Researcher
俄罗斯联邦, MoscowAnna Panova
Helmholtz National Medical Research Center of Eye Diseases
Email: annie_panova18@mail.ru
ORCID iD: 0000-0003-2103-1570
SPIN 代码: 9930-4813
MD, PhD
俄罗斯联邦, MoscowA. Sorokin
Helmholtz National Medical Research Center of Eye Diseases
编辑信件的主要联系方式.
Email: a.a.sorokin@inbox.ru
ORCID iD: 0000-0002-8213-8518
PhD student
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