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Case Reports
. 2018 Jan;22(Suppl 1):S73-S76.
doi: 10.4103/jomfp.JOMFP_43_17.

Juvenile primary extranasopharyngeal angiofibroma, presenting as cheek swelling

Affiliations
Case Reports

Juvenile primary extranasopharyngeal angiofibroma, presenting as cheek swelling

J Nandhini et al. J Oral Maxillofac Pathol. 2018 Jan.

Abstract

Angiofibroma is a locally advancing immensely vascular tumor that essentially arises from the nasopharynx. The clinical characteristics of extranasopharyngeal angiofibroma (ENA) do not accord to that of nasopharyngeal angiofibroma and can present a diagnostic confront. We describe a case of primary juvenile ENA in a 19-year-old patient who presented with a rapidly enlarging mass of the cheek region. The case is unusual because of its anatomic location. The diagnostic and management particulars are sketched.

Keywords: Cheek swelling; extranasopharyngeal angiofibroma; masticator space; vascular tumor.

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Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
Clinical photograph of the patient showing swelling of the left cheek
Figure 2
Figure 2
(a) Ultrasonogram shows 4 cm hypoechoic foci. (b) Computed tomography shows soft-tissue mass with positive Holman–Miller sign in the lateral wall of the left maxillary sinus. (c) Magnetic resonance imaging shows isointense soft-tissue mass in T1-weighted images in the left masticator space
Figure 3
Figure 3
(a) Preoperative patient preparation. (b) Extraoral incision and exposure of the mass. (c) Soft-tissue mass after excision. (d) Cut section of the excised mass. (e) Postoperative profile after 2 months
Figure 4
Figure 4
(a and b) Histopathological picture showing fibrous tissues along with scattered vascular channels ×50 and ×100, respectively
Figure 5
Figure 5
(a) Immunohistochemical stain of angiofibroma showing vimentin-positive fibroblastic stroma ×100. (b) Immunohistochemical stain of angiofibroma showing CD 34 shows positive for vascular channels ×100

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References

    1. Witt TR, Shah JP, Sternberg SS. Juvenile nasopharyngeal angiofibroma. A 30 year clinical review. Am J Surg. 1983;146:521–5. - PubMed
    1. Windfuhr JP, Remmert S. Extranasopharyngeal angiofibroma: Etiology, incidence and management. Acta Otolaryngol. 2004;124:880–9. - PubMed
    1. Chauveau UC. Juvenile nasopharyngeal angiofibroma. Arch Int Laryng. 1906;21:889.
    1. McDaniel RK, Houston GD. Juvenile nasopharyngeal angiofibroma with lateral extension into the cheek: Report of case. J Oral Maxillofac Surg. 1995;53:473–6. - PubMed
    1. Neel HB 3rd, Whicker JH, Devine KD, Weiland LH. Juvenile angiofibroma. Review of 120 cases. Am J Surg. 1973;126:547–56. - PubMed

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