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An unusual case of rudimentary parotid gland with distended Stensen duct

机译:少见的腮腺发育不全伴扩张管扩张

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摘要

Congenital absence or rudiment major salivary glands, especially of the parotid glands, are a rare entity. Aplasia of parotid glands has been described alone or in association with abnormalities of other salivary glands, first branchial arch developmental disturbances and other congenital anomalies such as lacrimoauriculodentodigital syndrome, mandibulofacial dysostosis and ectodermal dysplasia. Absence is most commonly unilateral, and may be associated with accessory or rudimentary glandular tissue. There are several reported cases of isolated patulous Stensen’s duct causing air insufflations in the glands and recurrent parotid gland enlargement. However, in the literature there is no reported case of association of rudimentary parotid gland with a patulous Stensen’s duct. This paper aims at reporting an interesting and unusual presentation of unilateral imperfectly developed parotid gland with a distended Stensen’s duct in a five year old mentally challenged girl who presented with an unintentional habit of blowing out cheeks several times in a day resulting in air insufflations and recurrent parotid swelling
机译:先天性缺如或少见的主要唾液腺,尤其是腮腺,是罕见的实体。腮腺发育不全已被单独描述或与其他唾液腺异常,第一弓弓发育障碍和其他先天性异常(如泌尿生殖道十二指肠综合征,下颌面发育不良和外胚层发育异常)相关联。缺席最常见于单侧,并可能与附属或原始腺体组织相关。据报道,有几例孤立的延张性Stenten导管引起腺体空气吹入和腮腺复发。但是,在文献中,没有报告称腮腺根部与斯滕森管结节相关。本文旨在报告一个有趣的和不寻常的表现,该表现为一名五岁智障女孩的单侧不完全发育的腮腺和扩张的斯滕森氏管,该女孩每天无意识地习惯两次吹双颊,导致空气吹入和反复发作腮腺肿胀

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