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先天性颈部中线裂的治疗

Management of congenital midline cervical cleft.

作者信息

McInnes Colin W, Benson Alex D, Verchere Cynthia G, Ludemann Jeffrey P, Arneja Jugpal S

机构信息

Faculty of Medicine, University of British Columbia, and Division of Plastic Surgery, British Columbia Children's Hospital, Vancouver, British Columbia, Canada.

出版信息

J Craniofac Surg. 2012 Jan;23(1):e36-8. doi: 10.1097/SCS.0b013e318241db99.

Abstract

Congenital midline cervical cleft (CMCC) is a rare developmental defect of the anterior neck normally characterized by an atrophic mucosal plaque with a cranial nipple-like skin tag, a short caudal sinus, and may be attached to a subcutaneous fibrous cord of variable length. Clinically, patients present at an early age with, white females being the most commonly affected population. In addition to aesthetic concerns, CMCC can prevent full extension of the neck, result in micrognathia and torticollis, predispose patients to infection, and can coexist with other clefting defects or cysts. Fewer than 50 cases have been published in the English-language literature. Herein, we report a case of CMCC that also presented with a mild contracture of the right sternohyoid muscle. The embryopathogenesis, histopathology, diagnosis, and treatment of this rare condition are also discussed.

摘要

先天性颈部中线裂(CMCC)是一种罕见的前颈部发育缺陷,通常表现为萎缩性黏膜斑块,伴有头侧乳头样皮肤赘生物、短尾侧窦,且可能附着于长度可变的皮下纤维索。临床上,患者发病年龄较早,白人女性是最常受累人群。除了美观问题外,CMCC可妨碍颈部完全伸展,导致小颌畸形和斜颈,使患者易发生感染,还可与其他裂缺陷或囊肿并存。英文文献报道的病例少于50例。在此,我们报告1例CMCC患者,其还伴有右侧胸骨舌骨肌轻度挛缩。本文还讨论了这种罕见疾病的胚胎发病机制、组织病理学、诊断及治疗。

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