Endoscopic treatment of juvenile nasopharyngeal angiofibromas: our experience and review of the literature

被引:26
作者
Fyrmpas, G. [1 ]
Konstantinidis, I. [1 ]
Constantinidis, J. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Acad Dept Otorhinolaryngol Head & Neck Surg 2, Papageorgiou Hosp, Thessaloniki 56429, Greece
关键词
Juvenile nasal angiofibroma; Endoscopic approach; Minimally invasive surgery; Surgical treatment; Outcome; SURGICAL-MANAGEMENT; INFRATEMPORAL FOSSA; FOLLOW-UP; RESECTION; SURGERY; EMBOLIZATION; TRANSNASAL; REMOVAL; TUMORS;
D O I
10.1007/s00405-011-1708-6
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
The endoscopic resection of juvenile nasopharyngeal angiofibroma (JNA) emerges as an alternative approach to open procedures due to reduced morbidity and comparable recurrence rates. The purpose of this study was to present our experience with the endoscopic management of JNA using retrospective chart review of ten male patients (mean age 15.7 years) with JNA who were treated endoscopically at our institution between the years 2003 and 2010. According to the Radkowski's system, one patient was at stage Ia, two at stage Ib, one at stage IIa, two at stage IIb, two at stage IIc (infratemporal fossa invasion) and two at stage IIIa (clivus erosion). Six patients underwent preoperative embolization. The endoscopic treatment involved total ethmoidectomy, middle meatal antrostomy, sphenoidotomy, clipping of the sphenopalatine artery and its branches and drilling of the pterygoid basis. All patients underwent magnetic resonance imaging 3 months postoperatively and then if indicated clinically. Mean follow-up was 23.7 months (range 3-70). All but one patient were free of macroscopic disease. A patient with stage IIb JNA developed a recurrence after 9 months. The residual tumor was resected endoscopically and the sphenopalatine foramen widened by drilling. The patient is free of disease 25 months postoperatively. The intra-operative blood loss was not excessive (200-800 ml, mean: 444 ml) and no patient required a blood transfusion. Patients were discharged after 4-8 days (mean 5 days). One patient developed postoperative infraorbital nerve hypoesthesia. Results showed that endoscopic treatment of stage I and IIa/b JNA is a valid alternative to external approaches. For select tumors with limited infratemporal fossa invasion and skull base erosion, the endoscopic approach may also be indicated. It is a safe and effective treatment modality due to the lack of external scars, minimal bone resection and blood loss and low recurrence rate.
引用
收藏
页码:523 / 529
页数:7
相关论文
共 40 条
[1]   Exclusively endoscopic surgery for juvenile nasopharyngeal angiofibroma [J].
Andrade, Nilvano A. ;
Pinto, Jose Antonio ;
Nobrega, Monica de Oliveira ;
Aguiar, Jose Estelita P. ;
Aguiar, Tamara Ferraro A. P. ;
Vinhaes, Eriko S. A. .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2007, 137 (03) :492-496
[2]   THE SURGICAL-MANAGEMENT OF EXTENSIVE NASOPHARYNGEAL ANGIOFIBROMAS WITH THE INFRATEMPORAL FOSSA APPROACH [J].
ANDREWS, JC ;
FISCH, U ;
VALAVANIS, A ;
AEPPLI, U ;
MAKEK, MS .
LARYNGOSCOPE, 1989, 99 (04) :429-437
[3]  
Banhiran Wish, 2005, Curr Opin Otolaryngol Head Neck Surg, V13, P50, DOI 10.1097/00020840-200502000-00012
[4]   Endoscopic resections of juvenile nasopharyngeal angiofibromas [J].
Bernal-Sprekelsen, M ;
Vazquez, AA ;
Pueyo, J ;
Casasus, JC .
HNO, 1998, 46 (02) :172-174
[5]  
Borghei Peyman, 2006, Ear Nose Throat J, V85, P740
[6]   Long-term outcome of facial growth after functional encloscopic sinus surgery [J].
Bothwell, MR ;
Piccirillo, JF ;
Lusk, RP ;
Ridenour, BD .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2002, 126 (06) :628-634
[7]  
Budzynowska K, 2008, Otolaryngol Pol, V62, P408, DOI 10.1016/S0030-6657(08)70281-6
[8]   Juvenile nasopharyngeal angiofibroma: Evaluation and surgical management of advanced. disease [J].
Danesi, Giovanni ;
Panciera, Davide T. ;
Harvey, Richard J. ;
Agostinis, Cristina .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2008, 138 (05) :581-586
[9]  
El Sharkawy AA, 2011, INT J PEDIAT OTORHIN
[10]   Endoscopic-assisted midfacial degloving approach for type III juvenile angiofibroma [J].
El-Banhawy, OA ;
El-Dien, AEHS ;
Amer, T .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2004, 68 (01) :21-28