Chimona T S, Tamiolakis D, Proimos E, Perogamvrakis G, Korres S G, Papadakis C E
ENT Department, Chania General Hospital, Chania, Crete, Greece.
B-ENT. 2007;3(1):39-43.
Branchial cleft anomalies are developmental disorders of the neck. Our aim is to report the diagnostic and treatment procedure followed in three cases of second branchial cleft abnormalities in adults.
A patient aged over 40 underwent surgical excision of a well-encapsulated cystic neck structure and two further patients of a branchial sinus and branchial fistula respectively. Prior to surgery the patients were assessed by means of imaging techniques, FNA cytology and cytometric DNA analysis.
Neutrophils, debris, mature squamous epithelial cells including degenerate forms and lymphoid cells were the key features in the cytological diagnosis. DNA analysis of the pre-operative cytological material in two cases revealed euploidy, thus indicating no malignancy. Histological examination of the lesions after excision established the diagnosis in all cases. No recurrences were reported.
Although congenital lesions, the second branchial cleft abnormalities usually present in adulthood and have to be distinguished from benign and malignant lateral neck swellings. FNA cytology as well as DNA ploidy determination contributes to the establishment of the diagnosis of branchial cleft abnormalities and their differential diagnosis.
鳃裂畸形是颈部的发育性疾病。我们的目的是报告三例成人第二鳃裂异常的诊断和治疗过程。
一名40多岁的患者接受了对一个包膜完整的颈部囊性结构的手术切除,另外两名患者分别接受了鳃裂窦和鳃裂瘘的手术。术前通过影像学技术、细针穿刺抽吸活检(FNA)细胞学检查和细胞计量DNA分析对患者进行评估。
中性粒细胞、碎屑、包括退变形式的成熟鳞状上皮细胞和淋巴细胞是细胞学诊断的关键特征。两例术前细胞学材料的DNA分析显示为整倍体,因此表明无恶性病变。切除术后病变的组织学检查确诊了所有病例。未报告复发情况。
虽然是先天性病变,但第二鳃裂异常通常在成年期出现,必须与颈部外侧的良性和恶性肿胀相鉴别。FNA细胞学检查以及DNA倍性测定有助于鳃裂异常的诊断及其鉴别诊断。