Kuczkowski Jerzy, Brzoznowski Wojciech, Kobierska-Gulida Grazyna, Czaczkowski Jarosław
Katedra i Klinika Otolaryngologii Gdańskiego Uniwersytetu Medycznego.
Otolaryngol Pol. 2011 May-Jun;65(3):194-8. doi: 10.1016/S0030-6657(11)70674-6.
Preauricular fistulas are not uncommon congenital disorders in children. They are associated with imperfect auricle formation as a consequence of incomplete fusion of the auditory hillocks of the first and second branchial arches.
The aim of this study was to present diagnostic methods with evaluation of treatment results of preauricular fistulas in children.
We analysed retrospectively clinical and epidemiological features, diagnostic methods and treatment results of the patients with preauricular fistula attended in the Otolaryngology Department of Medical University in Gdańsk.
Between 1995 and 2009 in the Department of Otolaryngology MGUed 23 children (13 girls and 10 boys) were treated for preauricular fistulas. The age of the children ranged between 2 to 16 years (median 7.7). The fistula was recognized on the left side in 14 children, in 6 on the right and bilaterally in 3 children. The diagnosis was based on the presence of a cutaneous fistula in the region of the helix's anterior crus with inflamed surrounding and purulent discharged in physical examination and in radiological imaging (MRI). Patients were treated surgically in the classical way and using Prasada's method including resection of the cutaneous fistula and cyst with a part of the helix. Squamous epithelium in the resected fistulas was found in 91.3% of the children. No recurrence was observed, good cosmetic outcome was achieved in all children.
Each patient with bilateral preauricular fistula needs to be diagnosed for congenital disorders of the middle ear and kidneys. MRI may be useful in establishing the location of the fistula. Surgical treatment is not necessary in preauricular, blind-ended sinuses. In the postoperative material of the sinus squamous epithelium is found.
耳前瘘管是儿童中并不罕见的先天性疾病。它们与第一和第二鳃弓的听结节不完全融合导致的耳廓形成不完善有关。
本研究的目的是介绍儿童耳前瘘管的诊断方法并评估其治疗结果。
我们回顾性分析了格但斯克医科大学耳鼻喉科收治的耳前瘘管患者的临床和流行病学特征、诊断方法及治疗结果。
1995年至2009年期间,格但斯克医科大学耳鼻喉科为23名儿童(13名女孩和10名男孩)治疗耳前瘘管。儿童年龄在2至16岁之间(中位数7.7岁)。14名儿童的瘘管位于左侧,6名位于右侧,3名儿童为双侧。诊断依据是体格检查和放射影像学检查(MRI)显示耳轮前脚区域存在皮肤瘘管,周围有炎症且有脓性分泌物。患者采用经典手术方法及普拉萨达法进行治疗,包括切除皮肤瘘管和囊肿以及部分耳轮。91.3%的儿童切除的瘘管中发现鳞状上皮。未观察到复发情况,所有儿童均获得了良好的美容效果。
每例双侧耳前瘘管患者均需诊断是否存在中耳和肾脏的先天性疾病。MRI可能有助于确定瘘管的位置。耳前盲端窦无需手术治疗。在窦的术后标本中发现鳞状上皮。