Management of invasive juvenile nasopharyngeal angiofibromas:: The role of a multimodality approach

被引:33
|
作者
Roche, Pierre-Hugues
Paris, Jerôme
Régis, Lean
Moulin, Guy
Zanaret, Michel
Thomassin, Jean-Marc
Pellet, William
机构
[1] Saintee Marguerite Univ Hosp, Dept Neurosurg, Marseille, France
[2] Timone Univ Hosp, Fed Ear Nose & Throat Surg, Marseille, France
[3] Timone Univ Hosp, Dept Stereotact & Funct Neurosurg, Marseille, France
[4] Timone Univ Hosp, Dept Radiol, Marseille, France
关键词
angiofibroma; cranial base surgery; neurosurgery; radiosurgery; skull base surgery;
D O I
10.1227/01.NEU.0000298905.71259.BB
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: Juvenile nasopharyngeal angiofibromas involving the cranial base and intracranial compartment are challenging tumors. We reviewed our experience of these tumors and analyzed the efficacy of a multimodality management. METHODS: Between 1981 and 2000, 15 extensive juvenile nasopharyngeal angiofibromas (Fisch Grade III or IV) were treated at our institution. The mean age of the patients was 14.5 years, and the mean interval between the first symptom and diagnosis was 12.9 months. Initial management included preoperative embolization of the external carotid artery feeders, followed by tumor removal. A maxillofacial procedure was performed in eight cases, a combination of maxillofacial and neurosurgical approach was performed in four cases, and a neurosurgical cranial base approach was performed in three cases. RESULTS: Total removal after the initial procedure was obtained in eight patients. Subtotal removal justified additional surgery in one case, gamma knife radiosurgery in two cases, and fractionated irradiation in four cases. True recurrences were observed in four cases at a mean interval of 37 months (range, 24-46 mo) and required tailored multimodality management. No cases of perioperative death were observed. One patient underwent hemiparesis after embolization in the early period of our experience. Permanent facial numbness was reported in four cases, moderate cosmetic problems were reported in three cases, and hyposmia was reported in three cases. Except for one patient who was lost to follow-up at 18 months, 12 patients were free of disease and two patients were free of tumor progression. All patients had normal or near-normal daily life at the last check-up, with a median follow-up period of 108 months (mean, 117 mo; range, 91-2 52 mo). CONCLUSION: Extensive juvenile nasopharyngeal angiofibromas are efficiently managed with a multimodal protocol in which preoperative embolization is followed by optimal surgical removal using various transcranial or transfacial approaches. Adjunctive gamma knife radiosurgery is a valuable option for intracavernous residual tumor. Our protocol offers long-term cure with acceptable morbidity.
引用
收藏
页码:768 / 777
页数:10
相关论文
共 50 条
  • [21] Juvenile nasopharyngeal angiofibromas with unique extrapharyngeal extensions
    Debabrata Biswas
    M. Somnath Saha
    Abdur Rashid
    Tapan Kumar Nandi
    Indian Journal of Otolaryngology and Head and Neck Surgery, 2001, 53 (2): : 176 - 178
  • [22] Transoral "adenoidectomy" excision of juvenile nasopharyngeal angiofibromas
    Solomon, Don
    Isaacson, Glenn
    ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 2007, 116 (04): : 243 - 247
  • [23] HORMONAL RECEPTOR DETERMINATION IN JUVENILE NASOPHARYNGEAL ANGIOFIBROMAS
    LEE, DA
    RAO, BR
    MEYER, JS
    PRIOLEAU, PG
    BAUER, WC
    CANCER, 1980, 46 (03) : 547 - 551
  • [24] Bilateral Vascular Supply in Juvenile Nasopharyngeal Angiofibromas
    Wu, Arthur W.
    Mowry, Sarah E.
    Vinuela, Fernando
    Abemayor, Elliot
    Wang, Marilene B.
    LARYNGOSCOPE, 2011, 121 (03): : 639 - 643
  • [25] PREOPERATIVE EMBOLIZATION OF JUVENILE NASOPHARYNGEAL ANGIOFIBROMAS WITH GELFOAM
    NATVIG, K
    SKALPE, IO
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 1984, 98 (08): : 829 - 833
  • [26] Frequent β-catenin mutations in juvenile nasopharyngeal angiofibromas
    Abraham, SC
    Montgomery, EA
    Giardiello, FM
    Wu, TT
    AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (03): : 1073 - 1078
  • [27] Bilateral Vascular Supply in Juvenile Nasopharyngeal Angiofibromas
    Wu, Arthur
    Mowry, Sarah
    Vinuela, Fernando
    Abemayor, Elliot
    Wang, Marilene
    LARYNGOSCOPE, 2010, 120 : S248 - S248
  • [28] Relaxation of imprinting of IGFII gene in juvenile nasopharyngeal angiofibromas
    Coutinho-Camillo, CM
    Brentani, MM
    Butugan, O
    Torloni, H
    Nagai, MA
    DIAGNOSTIC MOLECULAR PATHOLOGY, 2003, 12 (01) : 57 - 62
  • [29] Spontaneous Involution of Juvenile Nasopharyngeal Angiofibromas: Report of a Case
    Chua, Janice T.
    Choy, Joseph A.
    Sahyouni, Ronald
    Birkenbeuel, Jack L.
    Cheung, Dillon C.
    Kuan, Edward C.
    Bhandarkar, Naveen D.
    LARYNGOSCOPE, 2021, 131 (07): : 1455 - 1457
  • [30] Bilateral synchronous juvenile nasopharyngeal angiofibromas: a rare entity
    Hendriks, Thomas
    Pollaers, Katherine
    Giblett, Neil
    Kadhim, Latif
    Khaleel, Ziyad
    Cooney, Tim
    ANZ JOURNAL OF SURGERY, 2021, 91 (03) : E132 - E134