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 8 条
[1]   Endoscopic approach for excision of juvenile nasopharyngeal angiofibroma: complications and outcomes [J].
Ardehali, Mojtaba Mohammadi ;
Ardestani, Seyed-Hadyi Samimi ;
Yazdani, Nasrin ;
Goodarzi, Hassan ;
Bastaninejad, Shahin .
AMERICAN JOURNAL OF OTOLARYNGOLOGY, 2010, 31 (05) :343-349
[2]   Atypical angiofibromas: a report of four cases [J].
Celik, B ;
Erisen, L ;
Saraydaroglu, O ;
Coskun, H .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2005, 69 (03) :415-421
[3]  
Husband AD, 2000, J LARYNGOL OTOL, V114, P389
[4]   Endoscopic graduated multiangle, multicorridor resection of juvenile nasopharyngeal angiofibroma: an individualized, tailored, multicorridor skull base approach [J].
Liu, James K. ;
Husain, Qasim ;
Kanumuri, Vivek ;
Khan, Mohemmed N. ;
Mendelson, Zachary S. ;
Eloy, Jean Anderson .
JOURNAL OF NEUROSURGERY, 2016, 124 (05) :1328-1338
[5]   Bilateral, independent juvenile nasopharyngeal angiofibroma: case report [J].
Morkenborg, M-L ;
Frendo, M. ;
Stavngaard, T. ;
Von Buchwald, C. .
JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2015, 129 (10) :1032-1035
[6]   Rare Infratentorial and Supratentorial Localization of Juvenile Angiofibroma: A Case Report [J].
Pasalic, Ivan ;
Trninic, Ines ;
Nemir, Jakob ;
Jednacak, Hrvoje ;
Zarkovic, Kamelija ;
Mrak, Goran .
PEDIATRIC NEUROSURGERY, 2016, 51 (06) :313-317
[7]   Invasive growth patterns of juvenile nasopharyngeal angiofibroma: radiological imaging and clinical implications [J].
Szymanska, Anna ;
Szymanski, Marcin ;
Czekajska-Chehab, Elzbieta ;
Szczerbo-Trojanowska, Malgorzata .
ACTA RADIOLOGICA, 2014, 55 (06) :725-731
[8]   Atypical angiofibroma in a patient with compromised general health: A case report [J].
Vasconcelos, Artur Cunha ;
Juvencio de Freitas Filho, Silas Antonio ;
de Almeida, Vinicius Lima ;
Caetano, Rafael da Silva ;
Tramujas, Julia ;
Paranhos, Luiz Renato .
ANNALS OF MEDICINE AND SURGERY, 2018, 35 :133-136