An unusual presentation of branchial cleft fistula penetrating the submandibular gland

Toshihiko Watanabe , Takahiro Shimizu , Michinobu Ohno , Yasushi Fuchimoto , Kunio Mizutari , Noriko Morimoto , Takako Yoshioka , Yutaka Kanamori
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引用次数: 2

Abstract

First branchial cleft anomalies constitute a rare entity with variable clinical presentations and anatomic findings. We describe a 14-month-old girl with a congenital cutaneous fistula running from a cutaneous opening in the left submandibular triangle through the submandibular gland and ending in the pharyngeal cavity. These features suggested type II first branchial cleft fistula with an extremely unusual path. Complete excision resulted in successful treatment without recurrence. Since the first branchial cleft fistula can originate anywhere along the salivary gland and can extend from this area, surgeons should maintain a high index of suspicion for anatomic variants of this rare condition.

罕见的鳃裂瘘管穿透下颌下腺
首先,鳃裂畸形是一种罕见的临床表现和解剖结果多变的疾病。我们描述了一个14个月大的女孩先天性皮瘘从左下颌下三角的皮肤开口穿过下颌下腺,并在咽腔结束。这些特征提示II型第一鳃裂瘘,其路径极不寻常。完全切除治疗成功,无复发。由于第一鳃裂瘘管可以沿唾液腺的任何地方起源,并可以从该区域延伸,外科医生应该对这种罕见疾病的解剖变异保持高度的怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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