Affiliation:
1. U.O.S. Maxillofacial Surgery, S. Andrea Hospital, Rome, Italy
Abstract
Abstract
Cystic lymphangioma (CL) in adult is a very rare pathology. Its etiology remains unclear, but it is supposed to be congenital or to be a result of obstruction and lymph fluid retention of developing lymphatic vessels. It generally occurs in the head and neck region, probably because of the rich lymphatics in this area. It can be easily misdiagnosed with other cervicofacial masses. We present the case of a 56-year-old-female presented with a right-sided painless cervical swelling. Ultrasonography and magnetic resonance imaging were performed and a surgical complete removal was carried out. Histological examination revealed that the mass was composed by a variety of dilated lymph vessels involved in a fibrovascular stroma. Diagnose of CL was done. With this article, we want to highlight the features of CL and its role in the differential diagnoses of adults’ cervicofacial masses.
Publisher
Oxford University Press (OUP)
Reference10 articles.
1. Sudden onset, rapidly expansile, cervical cystic hygroma in an adult: a rare case with unusual presentation and extensive review of the literature;Dokania;Case Rep Otolaryngol,2017
2. Adult-onset cystic hygroma: a case report and review of management;Gow;Grand Rounds,2011
3. Cystic hygroma of the neck: single center experience and literature review;Damaskos;Eur Rev Med Pharmacol Sci.,2017
4. Treatment guidelines of lymphatic malformations of the HN;Zhou;Oral Oncol,2011
5. Adult-onset giant cervical cystic hygroma with pressure manifestations on aerodigestive tract, managed surgically: reporting of a rare case;Elshaar;Ann R Coll Surg Engl,2019
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