Husain Parvez, Saxena Shikhar, Ahmed Shaheen Khalil, Tapparwal Anita
Department of ENT, Expert ENT & Diagnostic Centre, Barabanki, India.
41, Indira Market, Barabanki, Uttar Pradesh 225001 India.
Indian J Otolaryngol Head Neck Surg. 2022 Oct;74(Suppl 2):2372-2375. doi: 10.1007/s12070-020-02188-y. Epub 2020 Oct 6.
IJP is a rare, congenital, benign, isolated, sporadically occurring fusiform or saccular dilatation of Internal Jugular Vein (IJV) of unknown aetiology usually presenting as a unilateral neck mass. It is mostly seen in children and young adults. We report a 4 year old male presented to Expert ENT & Diagnostic Centre presenting with history of painless right neck swelling in the right carotid triangle first observed on crying with no history of trauma, facial congestion, chronic cough, difficulty in swallowing or breathing, non febrile, venous humps, heaviness or cessation of normal voice. Diagnosis of right IJP was made. Exploration and wrapping the dilated segment in polytetrafluoroethylene tube graft was done. Because of its rarity, this entity is frequently ignored or misdiagnosed. This case report intends to stress the importance of keeping IJP as differential diagnosis while dealing with such a swelling to avoid invasive investigations and inappropriate treatment.
颈内静脉扩张症(IJP)是一种罕见的、先天性的、良性的、孤立的、偶发的颈内静脉梭形或囊状扩张,病因不明,通常表现为单侧颈部肿块。多见于儿童和青年。我们报告一例4岁男性患儿,就诊于耳鼻喉专家与诊断中心,主诉右侧颈动脉三角区无痛性右颈部肿胀,首次发现于哭闹时,无外伤史、面部充血、慢性咳嗽、吞咽或呼吸困难、无发热、静脉嗡鸣声、声音沉重或声音异常等情况。诊断为右侧颈内静脉扩张症。对扩张段进行了探查,并将其包裹于聚四氟乙烯管移植物中。由于其罕见性,该疾病常被忽视或误诊。本病例报告旨在强调在处理此类肿胀时将颈内静脉扩张症作为鉴别诊断的重要性,以避免进行侵入性检查和不恰当的治疗。