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梨状窝瘘继发的复发性颈部病变。

Recurrent neck lesions secondary to pyriform sinus fistula.

作者信息

Zhang Peijun, Tian Xiufen

机构信息

Department of Otorhinolaryngology and Head-Neck Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.

出版信息

Eur Arch Otorhinolaryngol. 2016 Mar;273(3):735-9. doi: 10.1007/s00405-015-3572-2. Epub 2015 Feb 24.

Abstract

Recurrent neck lesions associated with third or fourth branchial arch fistula are much less common than those of second arch and usually present with acute suppurative thyroiditis or neck abscess. Our aim is to describe clinical features, management and treatment outcomes of 64 cases of congenital pyriform sinus fistula (PSF). Medical record of these 64 patients (33 males, 31 females) treated at the First Affiliated Hospital of Zhengzhou University from 2011 to 2014 were reviewed. The patients comprised 33 males and 31 females, and their ages ranged from 18 months to 47 years (median 10 years, mean 12.7 years). Neck abscess and recurrent infection was the mode of presentation in 37 cases (57.8 %), 4 patients (6.3 %) presented with acute suppurative thyroiditis, neck mass was the mode of presentation in 17 cases (26.6 %), 2 patients (3.1 %) presented with neck mass with respiratory distress, and cutaneous discharging fistula was the mode of presentation in 1 cases (1.6 %). The remaining 3 patients (4.7 %) presented with cutaneous discharging fistula with neck infection. Investigations performed include barium swallow, CT scan, and ultrasound which were useful in delineating PSF tract preoperatively. Barium swallow was taken as the gold standard for diagnosis. Our patients were treated by fistulectomy with hemithyroidectomy, fistulectomy, fistulectomy with endoscopic electric cauterization, endoscopic electric cauterization or endoscopic coblation cauterization, respectively. Histopathologic examination of the surgical specimens revealed that they were lined with ciliated epithelium, stratified cuboid epithelium with chronic inflammatory cell infiltration and fibrosis. Voice hoarseness occurred after operation in seven patients, but disappeared 1 week later. PSF recurred in 6 patients, 4 of them were cured by a successful re-excision. One patient was cured by successful endoscopic electric cauterization. The other 1 has remained asymptomatic for 5 months. In our series, mean follow-up period was 13.3 months and median follow-up period was 12.5 months (range 2-40 months). Presence of congenital PSF should be suspected when intra-thyroidal abscess formation occurs as the gland is resistant to infection. Strong clinical suspicion, barium swallow study, CT scan and ultrasound are the key to diagnosis. Both fistulectomy with hemithyroidectomy and endoscopic treatment have comparable success rate. Endoscopic coblation cauterization may prove a useful and equally effective method of treatment for PSF in future.

摘要

与第三或第四鳃弓瘘相关的复发性颈部病变比第二鳃弓的病变少见得多,通常表现为急性化脓性甲状腺炎或颈部脓肿。我们的目的是描述64例先天性梨状窝瘘(PSF)的临床特征、治疗方法及治疗效果。回顾了2011年至2014年在郑州大学第一附属医院接受治疗的这64例患者(33例男性,31例女性)的病历。患者包括33例男性和31例女性,年龄范围为18个月至47岁(中位数10岁,平均12.7岁)。37例(57.8%)以颈部脓肿和反复感染为表现形式,4例(6.3%)表现为急性化脓性甲状腺炎,17例(26.6%)以颈部肿块为表现形式,2例(3.1%)表现为伴有呼吸窘迫的颈部肿块,1例(1.6%)以皮肤瘘口溢液为表现形式。其余3例(4.7%)表现为伴有颈部感染的皮肤瘘口溢液。所进行的检查包括食管吞钡、CT扫描和超声,这些检查有助于术前明确PSF的瘘管情况。食管吞钡被视为诊断的金标准。我们的患者分别接受了瘘管切除术加甲状腺半切除术、瘘管切除术、瘘管切除术加内镜电灼术、内镜电灼术或内镜低温等离子消融术治疗。手术标本的组织病理学检查显示,其内衬为纤毛上皮、分层立方上皮,并伴有慢性炎性细胞浸润和纤维化。7例患者术后出现声音嘶哑,但1周后消失。6例患者PSF复发,其中4例经再次成功切除治愈。1例患者经内镜电灼术成功治愈。另1例患者5个月来一直无症状。在我们的系列研究中,平均随访期为13.3个月,中位随访期为12.5个月(范围2 - 40个月)。当甲状腺内出现脓肿形成且甲状腺对感染有抵抗力时,应怀疑先天性PSF的存在。强烈的临床怀疑、食管吞钡检查、CT扫描和超声是诊断的关键。瘘管切除术加甲状腺半切除术和内镜治疗的成功率相当。内镜低温等离子消融术未来可能被证明是一种有用且同样有效的PSF治疗方法。

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