A unique intraluminal growth of juvenile nasopharyngeal angiofibroma: A case report

被引:1
|
作者
Ardehali, Mojtaba Mohammadi [1 ]
Irani, Shirin [1 ]
Firouzifar, Mohammadreza [1 ]
机构
[1] Univ Tehran Med Sci, Amir Alam Hosp, Otorhinolaryngol Res Ctr, Tehran, Iran
来源
BIOMEDICINE-TAIWAN | 2020年 / 10卷 / 03期
关键词
Angiofibroma; sinus endoscopy; intraluminal growth;
D O I
10.37796/2211-8039.1019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Juvenile nasopharyngeal angiofibroma (JNA) is a rare, hypervascular, benign tumor which is mainly seen among male adolescents. The tumor typically originates from the sphenopalatine fossa, but could spread through natural foramens and fissures. There are some reports of atypical growth of this tumor in literature but the intraluminal growth, which could be seen in paraganglioma and glomus tumors, has not reported yet in angiofibroma. In this article we present a case of extensive angiofoibroma with intraluminal involvement of the ophthalmic vein. Our patient was a 19-year-old boy with a complaint of nasal obstruction and occasional epistaxis since a year ago, without any visual or neurologic complaints. The patient underwent an endoscopic resection of the tumor after embolization via the nasal cavity. The intraoperative findings revealed the tumor extension to the orbit, intracranial space and cavernous sinus via inferior orbital fissure. The intracranial extension of the tumor was extradural and was successfully excised without CSF leakage. An interesting finding in this patient, was an intraluminal extension of the tumor in to the ophthalmic vein, which was completely excised endoscopically. (pre and post operation pictures are available in the full text). The definitive treatment of angiofibroma is surgical excision. Different surgical approaches are used but nowadays endoscopic resection with or without pre-operative embolization is the first choice of treatment. The intraluminal growth of the tumor was also excised as a pedunculated mass separately.
引用
收藏
页码:41 / 44
页数:4
相关论文
共 50 条
  • [1] JUVENILE NASOPHARYNGEAL ANGIOFIBROMA - REPORT OF CASE
    SCHOELZEL, EP
    ANNALS OF ALLERGY, 1971, 29 (03): : 148 - +
  • [2] Juvenile Nasopharyngeal Angiofibroma: An Aberrant Case Report
    Jadhav, Swaragandha
    Khandaitkar, Sandeep
    Mitra, Kajal
    Chaudhari, Shyam
    Dhok, Avinash P.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2022, 14 (04)
  • [3] Bilateral juvenile nasopharyngeal angiofibroma: Report of a case
    Wu, Edward C.
    Chark, Davin W.
    Bhandarkar, Naveen D.
    INTERNATIONAL FORUM OF ALLERGY & RHINOLOGY, 2014, 4 (07) : 603 - 606
  • [4] JUVENILE NASOPHARYNGEAL ANGIOFIBROMA IN A FEMALE - REPORT OF A CASE
    OSBORN, DA
    SOKOLOVSKI, A
    ARCHIVES OF OTOLARYNGOLOGY, 1965, 82 (06): : 629 - +
  • [5] Bilateral, independent juvenile nasopharyngeal angiofibroma: case report
    Morkenborg, M-L
    Frendo, M.
    Stavngaard, T.
    Von Buchwald, C.
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2015, 129 (10): : 1032 - 1035
  • [6] Bilateral juvenile nasopharyngeal angiofibroma: A rare case report
    Adham, Marlinda
    Hajarani, Kartika
    Rachmadi, Lisnawati
    Suroyo, Indrati
    ACTA OTO-LARYNGOLOGICA CASE REPORTS, 2021, 6 (01): : 45 - 52
  • [7] Application of cyberknife for the treatment of juvenile nasopharyngeal angiofibroma: a case report
    Deguchi, K
    Fukuiwa, T
    Saito, K
    Kurono, Y
    AURIS NASUS LARYNX, 2002, 29 (04) : 395 - 400
  • [8] JUVENILE NASOPHARYNGEAL ANGIOFIBROMA WITH LATERAL EXTENSION INTO THE CHEEK - REPORT OF CASE
    MCDANIEL, RK
    HOUSTON, GD
    JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1995, 53 (04) : 473 - 476
  • [9] JUVENILE NASOPHARYNGEAL ANGIOFIBROMA - REPORT OF A CASE WITH ELECTRON-MICROSCOPY
    WEBBER, BL
    SOUTH AFRICAN MEDICAL JOURNAL, 1974, 48 (28): : 1225 - 1225
  • [10] INVOLUTION OF RESIDUAL JUVENILE NASOPHARYNGEAL ANGIOFIBROMA (A CASE-REPORT)
    STANSBIE, JM
    PHELPS, PD
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 1986, 100 (05): : 599 - 603