Treating a Rare Angiomyomatous Hamartomas of Head and Neck Region, Our Experience: Case Repor

Author:

Papikyan Artur1,Papikyan Hayk2,Eghiazaryan Nahapet2,Hakobyan Gagik1

Affiliation:

1. Yerevan State Medical University

2. Mikayelyan University Hospital, Yerevan, Armenia

Abstract

Angiomyomatous hamartoma of head and neck region is very are disease, of unknown etiology and more often than not it can be misdiagnosed preoperatively. Materials and Methods: In a study we present a case of angiomyomatous hamartoma in the carotid triangle, a site where a tumor has an invasion to external carotid artery, treatment carried out by surgical excision, after histological examination, the final diagnosis was made. The patient was under observation for 3 years, there were no relapses. Conclusion: The diagnosis of angiomyomatous hamartoma is based on histologic examination. Although this entity is rare, we believe that head and neck surgeons should include it in the differential diagnosis of head and neck masses

Publisher

"Akra" LLC

Reference16 articles.

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2. Ober WB. Selected items from the history of pathology: Eugen Albrecht, MD (1872-1908): hamartoma and choristoma. Am J Pathol. 1978;91:606.

3. Owens D, Alderson D, Garrido C. Nasopharyngeal hamartoma: importance of routine complete nasal examination. J Laryngol Otol. 2004;118(7):558–560.

4. Ghosh P, Saha K, Gosh AK. Vascular transformation of bilateral cervical lymph node sinuses: a rare entity masquerading as tumor recurrence. J Maxillofacial Oral Surgery. 2015;14:397–400.

5. Samuel J, Fernandes CC. Hamartomas of the head and neck. Areportof4 cases. SAfr Med J. 1985;68(4):265–267.

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