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新生儿双侧甲状腺内鳃裂囊肿 1 例。

A case of bilateral intrathyroidal branchial cleft cyst in a newborn.

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Korea University College of Medicine, Seoul 136-705, South Korea.

出版信息

J Pediatr Surg. 2010 Jan;45(1):E1-4. doi: 10.1016/j.jpedsurg.2009.09.038.

Abstract

We describe an extremely rare case of bilateral intrathyroidal branchial cleft cysts. A 2-day-old male neonate presented with intermittent tachypnea, dyspnea, and a palpable neck mass. Cervical ultrasonography and computerized tomography scan demonstrated a right-sided 3 x 3-cm cystic mass and a left sided 4.5 x 4-cm cystic mass, thought to be originating in the thyroid gland. The right-sided cyst decreased in size after OK-432 sclerotherapy. The left-sided cyst showed little response to 2 attempts of OK-432 sclerotherapy. Surgical removal of the left-sided cyst was done because of intermittent airway problems. The cystic mass was thought to be an intrathyroidal lesion. Microscopically, the cyst was lined by nonkeratinized squamous epithelium and respiratory epithelium. Lymphocyte infiltration was found in the subepithelial layer. The patient is currently doing well 12 months later with no evidence of recurrence.

摘要

我们描述了一例极其罕见的双侧甲状腺内鳃裂囊肿。一名 2 天龄男性新生儿出现间歇性呼吸急促、呼吸困难和可触及的颈部肿块。颈部超声和计算机断层扫描显示右侧 3 x 3 厘米囊性肿块和左侧 4.5 x 4 厘米囊性肿块,考虑起源于甲状腺。右侧囊肿在 OK-432 硬化治疗后体积缩小。左侧囊肿在 2 次 OK-432 硬化治疗后反应不大。由于间歇性气道问题,对左侧囊肿进行了手术切除。囊性肿块被认为是甲状腺内病变。镜下可见囊肿内衬非角化鳞状上皮和呼吸上皮。在黏膜下层发现淋巴细胞浸润。患者目前情况良好,12 个月后无复发迹象。

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