全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

An Unusual Location of Juvenile Angiofibroma: A Case Report and Review of the Literature

DOI: 10.1155/2013/175326

Full-Text   Cite this paper   Add to My Lib

Abstract:

A 10-year-old boy presented with left-sided nasal obstruction and epistaxis. Endoscopic evaluation revealed a polypoid mass in the vestibule arising from the lateral wall of the nasal cavity anteroinferior to the left inferior turbinate. Computed tomography (CT) scan showed a soft tissue opacity in the vestibule of the left nasal cavity. After the endoscopic excision of the mass, postoperative and histopathological analyses confirmed the diagnosis of an angiofibroma. 1. Introduction Angiofibromas are highly vascular, nonencapsulated, and histologically benign but locally aggressive tumors which most commonly arise in the nasopharynx of adolescent males. It is a unique fibrovascular tumor with the specific histopathological finding of irregularly configured endothelial-lined vascular spaces embedded in a fibrous stroma. They usually arise from the posterolateral wall of the nasal cavity, where the sphenoidal process of the palatine bone meets the horizontal ala of the vomer and the pterygoid process. Angiofibromas constitute about 0.5% of all head and neck neoplasms [1]. These tumors may rarely localize in extranasopharyngeal sites. We report a case of angiofibroma in the left vestibule arising from the lateral wall of nasal cavity anteroinferior to the inferior turbinate. 2. Case Report A 10-year-old boy came to the outpatient department with a four month history of progressive left-sided nasal obstruction and intermittent epistaxis. He had history of fever 5 days back. The patient had no other health problems. The coagulation status was normal. Anterior rhinoscopy revealed a fragile, lobular, red-grayish-colored, smooth, and polypoidal mass, arising anteroinferiorly to the left inferior turbinate filling the vestibule (Figure 1). Posterior rhinoscopy was normal in appearance. Figure 1: Reddish-gray-colored polypoidal mass in the left vestibule. Computed tomography (CT) scan of the nose and paranasal sinuses demonstrated a soft tissue opacity that filled the vestibule of the left nasal cavity, without any sinus invasion and bony destruction. On postcontrast study, the soft tissue is showing intense enhancement (Figures 2(a), 2(b), and 2(c)). Figure 2: Axial, sagittal, and coronal CT images showing an intensely enhancing homogenous mass lesion in the left vestibule. The mass was later excised under general anaesthesia. It was lobular, smooth, red-grayish, about 12?mm long tumour, and with the diameter up to 8?mm. This was followed by profuse bleeding which was controlled with anterior intranasal packing. The mass was sent for histopathological analysis.

References

[1]  J. P. Windfuhr and S. Remmert, “Extranasopharyngeal angiofibroma: etiology, incidence and management,” Acta Oto-Laryngologica, vol. 124, no. 8, pp. 880–889, 2004.
[2]  A. Peri?, N. Baleti?, S. Cerovi?, et al., “Middle turbinate angiofibroma in an elderly woman,” Vojnosanitetski Pregled, vol. 66, no. 7, pp. 583–586, 2009.
[3]  L. U. Sennes, F. S. G. Fortes, O. Butugan, P. H. Saldiva, and F. C. Bernardi, “Tissue maturation correlating to clinical manifestations in juvenile angiofibroma,” Annals of Otology, Rhinology and Laryngology, vol. 114, no. 9, pp. 705–708, 2005.
[4]  V. Starlinger, O. Wendler, M. Gramann, and B. Schick, “Laminin expression in juvenile angiofibroma indicates vessel's early developmental stage,” Acta Oto-Laryngologica, vol. 127, no. 12, pp. 1310–1315, 2007.
[5]  B. Celik, L. Erisen, O. Saraydaroglu, and H. Coskun, “Atypical angiofibromas: a report of four cases,” International Journal of Pediatric Otorhinolaryngology, vol. 69, no. 3, pp. 415–421, 2005.
[6]  I. Tasca and G. C. Compadretti, “Extranasopharyngeal angiofibroma of nasal septum. A controversial entity,” Acta Otorhinolaryngologica Italica, vol. 28, no. 6, pp. 312–314, 2008.
[7]  D. Taggarshe, M. S. Quraishi, and J. M. Dugar, “Inferior turbinate angiofibroma: an atypical preservation,” Rhinology, vol. 42, no. 1, pp. 45–47, 2004.
[8]  G. Lloyd, D. Howard, V. J. Lund, and L. Savy, “Imaging for juvenile angiofibroma,” Journal of Laryngology and Otology, vol. 114, no. 9, pp. 727–730, 2000.
[9]  T. Hofmann, M. Bernal-Sprekelsen, W. Koele, P. Reittner, E. Klein, and H. Stammberger, “Endoscopic resection of juvenile angiofibromas—long term results,” Rhinology, vol. 43, no. 4, pp. 282–289, 2005.
[10]  K. Nomura, A. Shimomura, T. Awataguchi, K. Murakami, and T. Kobayashi, “A case of angiofibroma originating from the inferior nasal turbinate,” Auris Nasus Larynx, vol. 33, no. 2, pp. 191–193, 2006.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133