Clinical Features and Surgical Management of Orbitotemporal Neurofibromatosis: A - Retrospective Interventional Case Series

被引:10
作者
Altan-Yaycioglu, Rana
Hintschich, Christoph
机构
[1] Ludwig Maximilians Univ Munchen, Eye Clin, Ophthalm Plast & Reconstruct Surg Unit, Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Eye Clin, Ophthalm Plast & Reconstruct Surg Unit,Ophthalmol, Munich, Germany
来源
ORBIT-AN INTERNATIONAL JOURNAL ON ORBITAL DISORDERS AND FACIAL RECONSTRUCTIVE SURGERY | 2010年 / 29卷 / 05期
关键词
Neurofibromatosis type 1; NF1; Peripheral neurofibromatosis; Von Recklinghausen disease;
D O I
10.3109/01676831003660689
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To evaluate the clinical features and surgical preferences of patients with neurofibromatosis. Methods: Histologically confirmed neurofibromatosis cases that underwent surgery during a 15-year period were retrospectively evaluated. The patients' demographics, severity of periorbital involvement, aim of surgery, surgery types, postoperative outcome, and complications were recorded. Results Nineteen patients with a mean age of 24.7 +/- 21.2 years were included in the study. Nine were younger and 10 were older than 16 years. Seventeen patients had unilateral and two had bilateral involvement. Patients were followed for a mean of 5.8 +/- 5.7 years. A total of 35 surgeries were performed. In 22 times the surgery was performed to improve vision, and in others to get a cosmetically acceptable appearance. Although there was an improvement in visual acuity, the difference was not significant (P = 0.085). Debulking of the tumor was performed in 100%, ptosis surgery in 90%, and lateral canthal fixation in 50% of surgeries. All patients showed improvement: at the last examination, six eyes had no ptosis, in 13 eyes ptosis not covering the pupil in primary gaze was observed on the involved side, and in only one eye the pupil was half covered. Conclusion In neurofibromatosis the treatment should be customized to each patient. As confirmed in our study, an open visual axis is the main goal in surgery, followed by cosmetic appearance. The authors believe that, with possibly multiple surgeries an acceptable result can be achieved.
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收藏
页码:232 / 238
页数:7
相关论文
共 11 条
[1]   NEUROFIBROMATOSIS OF THE HEAD AND NECK - CLINICAL PRESENTATION AND TREATMENT [J].
ADEKEYE, EO ;
ABIOSE, A ;
ORD, RA .
JOURNAL OF MAXILLOFACIAL SURGERY, 1984, 12 (02) :78-85
[2]   Tarsal infiltration in orbitotemporal neurofibromatosis [J].
deSousa, Jean-Louis ;
Malhotra, Raman .
JOURNAL OF PLASTIC RECONSTRUCTIVE AND AESTHETIC SURGERY, 2006, 59 (07) :780-781
[3]   FACIAL HAMARTOMAS IN CHILDREN - NEUROFIBROMA, LYMPHANGIOMA, AND HEMANGIOMA [J].
GRABB, WC ;
DINGMAN, RO ;
ONEAL, RM ;
DEMPSEY, PD .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1980, 66 (04) :509-527
[4]  
JACKSON IT, 1993, PLAST RECONSTR SURG, V92, P1
[5]   THE SURGICAL-MANAGEMENT OF ORBITAL NEUROFIBROMATOSIS [J].
JACKSON, IT ;
LAWS, ER ;
MARTIN, RD .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1983, 71 (06) :751-758
[6]  
JACKSON IT, 1995, CLIN PLAST SURG, V22, P513
[7]   Orbitotemporal neurofibromatosis - Clinical features and surgical management [J].
Lee, V ;
Ragge, NK ;
Collin, JRO .
OPHTHALMOLOGY, 2004, 111 (02) :382-388
[8]   The surgical management of childhood orbito-temporal neurofibromatosis [J].
Lee, V ;
Ragge, NK ;
Collin, JRO .
BRITISH JOURNAL OF PLASTIC SURGERY, 2003, 56 (04) :380-387
[9]   A novel approach to the management of severe facial disfigurement in neurofibromatosis type 1 [J].
Madill, Karen E. ;
Brammar, Robin ;
Leatherbarrow, Brian .
OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY, 2007, 23 (03) :227-228
[10]   Remodelling the upper eyelid in the management of orbitopalpebral neurofibromatosis [J].
Marchac, D ;
Britto, JA .
BRITISH JOURNAL OF PLASTIC SURGERY, 2005, 58 (07) :944-956