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  • A clinical case of Neurofibromatosis type 1 (NF1), also known as von Recklinghausen’s disease

    Редактор | 2019, Clinical case, Practical medicine part 17 №6 (2) 2019 | 20 октября, 2019

    R.Yu. ILINA1, E.V. URAKOVA1, O.V. NESTEROV1, R.V. LEKSIN2

     1Kazan State Medical Academy — Branch Campus of  RMACPE MH Russia, Kazan

    2Republican Clinical Hospital of the Ministry of Healthcare of the Republic of Tatarstan, Kazan

      Contact details:

    Ilina R.Yu. — PhD (medicine), Associate Professor of the Department of Maxillofacial Surgery and Surgical Dentistry

    Address: 36 Butlerova St., Kazan, Russian Federation, 420012, ​​tel. +7-917-255-43-87, e-mail: ilroza@yandex.ru

     This article describes a clinical case of Neurofibromatosis type 1 (NF1) (von Recklinghausen’s disease) in a patient with localization of formations in the maxillofacial region. Neurofibromatous nodes were located along the course of the second trigeminal branch — infraorbital; and the regional branch of the facial nerve. The patient was disturbed by radiating pain in the maxillofacial region. During surgical intervention, large nodes were removed, the diagnosis of neurofibromatosis was confirmed, and the pain syndrome was stopped.

    Neurofibromatosis 1 (NF1) is a rare pathology encountered by maxillofacial surgeons, which causes difficulties in the initial diagnosis when visiting a dentist. 

    Key words: Neurofibromatosis type 1 (NF1), von Recklinghausen’s disease, maxillofacial region.

    (For citation: Ilina R.Yu., Urakova E.V., Nesterov O.V., Leksin R.V. A clinical case of Neurofibromatosis type 1 (NF1), also known as von Recklinghausen’s disease. Practical medicine. 2019, Vol. 17, № 6 (part 2), P. 64-66)

    REFERENCES

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    7. Tateishi A., Okada M., Nakai M., Yokota Y., Miyamoto Y. Spontaneous ascending aortic rupture in a pregnant woman with neurofibromatosis type 1. Gen Thorac Cardiovasc Surg, 2018, no. 17, pp. 122-128.
    8. Leppävirta J., Kallionpää RA., Uusitalo E., Vahlberg T. Congenital anomalies in neurofibromatosis 1: a retrospective register-based total population study. Orphanet J Rare Dis, 2018, no. 13(1), pp. 5-16.

    Метки: 2019, E.V. URAKOVА, maxillofacial region, Neurofibromatosis type 1 (NF1), O.V. NESTEROV, Practical medicine part 17 №6 (2) 2019, R.V. LEKSIN, R.Yu. ILINA, von Recklinghausen's disease

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