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Branchial Cleft Cyst Carcinoma: A Case Reportopen access

Authors
Kim, HyunjiHong, Hyun SookKwak, Jeong JaLee, Seung WonJeong, Sun Hye
Issue Date
Jul-2017
Publisher
Kowsar
Keywords
Head and Neck Neoplasms; Diagnosis Differential Branchioma; Carcinoma; Squamous Cell; Lymphatic Metastasis
Citation
Iranian Journal of Radiology, v.14, no.3
Journal Title
Iranian Journal of Radiology
Volume
14
Number
3
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/7393
DOI
10.5812/iranjradiol.39283
ISSN
1735-1065
2008-2711
Abstract
Branchial cleft cyst carcinoma (BCCC) is an extremely rare malignancy originating from cells within the branchial cleft cyst wall. A 73-year-old man presented with a cystic mass with cellulitis mimicking abscess initially and recurred 3 years later as complex cystic lesion in right neck level II with multiple necrotic ipsilateral lymphadenopathy. The pathological diagnosis of cystic lesion was squamous cell carcinoma, suggesting possibility of originating from branchial cleft cyst. There was no identifiable primary cancer elsewhere by a thorough evaluation; eventually final diagnosis was branchial cleft cyst carcinoma to meet the modified criteria of Khafif et al. Up to the present time, there has been no evidence of recurrence. Although the BCCC is very rare, accurate diagnosis is important to plan proper treatment for patient. This report should help increase awareness of BCCC, which should be included in the differential diagnosis of a cystic neck mass.
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