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鳃裂畸形:一项五年回顾性研究

Branchial cleft anomalies: a five-year retrospective review.

作者信息

Kenealy J F, Torsiglieri A J, Tom L W

机构信息

Department of Pediatric Otorhinolaryngology, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Pennsylvania.

出版信息

Trans Pa Acad Ophthalmol Otolaryngol. 1990;42:1022-5.

PMID:2084977
Abstract

Branchial cleft cysts, sinuses and fistulas are among the most commonly encountered congenital anomalies in pediatric otolaryngic practice. They can present difficulties in differential diagnosis and surgical management. In order to study the clinical presentation and surgical management of branchial cleft anomalies, the operative records of the Children's Hospital of Philadelphia (CHOP) were reviewed for a five year period, January 1, 1982 through December 31, 1986. All patients with a pathologically-confirmed post-operative diagnosis of a branchial cleft anomaly were included in a retrospective chart review. Their case histories were studied to determine symptoms upon presentation, presence or absence of drainage, type of lesion, site of lesion, characteristics of the lesion, accuracy of pre-operative diagnosis, recurrence and complications. A total of 71 patients, 39 males and 32 females, underwent surgical excision of a branchial cleft cyst, sinus or fistula during the study period. There were 23 branchial cleft cysts, 50 sinuses and 3 fistulas. A correct pre-operative diagnosis was established in 60 (85%) of the patients, being highest for patients with branchial cleft fistulas. Incorrect pre-operative diagnoses included thyroglossal duct cyst, cervical lymphadenitis, dermoid, dermal inclusion cyst, lymphangioma and malignant neoplasm. The clinical presentation, pre-operative evaluation, pitfalls in diagnosis, surgical management and post-operative complications are discussed and strategies for the management of branchial cleft anomalies are presented.

摘要

鳃裂囊肿、鳃裂窦道和鳃裂瘘管是小儿耳鼻咽喉科临床最常见的先天性畸形。它们在鉴别诊断和手术治疗方面可能存在困难。为了研究鳃裂畸形的临床表现和手术治疗,回顾了费城儿童医院(CHOP)1982年1月1日至1986年12月31日这五年期间的手术记录。所有术后病理确诊为鳃裂畸形的患者均纳入回顾性病历审查。研究他们的病史,以确定就诊时的症状、有无引流、病变类型、病变部位、病变特征、术前诊断的准确性、复发情况及并发症。在研究期间,共有71例患者(39例男性和32例女性)接受了鳃裂囊肿、鳃裂窦道或鳃裂瘘管的手术切除。其中有23例鳃裂囊肿、50例鳃裂窦道和3例鳃裂瘘管。60例(85%)患者术前诊断正确,其中鳃裂瘘管患者的诊断正确率最高。术前误诊包括甲状舌管囊肿、颈淋巴结炎、皮样囊肿、皮肤包涵体囊肿、淋巴管瘤和恶性肿瘤。本文讨论了鳃裂畸形的临床表现、术前评估、诊断陷阱、手术治疗和术后并发症,并提出了鳃裂畸形的治疗策略。

相似文献

1
Branchial cleft anomalies: a five-year retrospective review.鳃裂畸形:一项五年回顾性研究
Trans Pa Acad Ophthalmol Otolaryngol. 1990;42:1022-5.
2
Branchial cleft anomalies: accuracy of pre-operative diagnosis, clinical presentation and management.鳃裂畸形:术前诊断的准确性、临床表现及治疗
J Laryngol Otol. 2012 Jun;126(6):598-604. doi: 10.1017/S0022215112000473. Epub 2012 Apr 12.
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Branchial anomalies in the pediatric population.儿科人群中的鳃裂畸形
Otolaryngol Head Neck Surg. 2007 Aug;137(2):289-95. doi: 10.1016/j.otohns.2007.03.009.
4
Congenital cervical cysts, sinuses, and fistulae in pediatric surgery.小儿外科学中的先天性颈部囊肿、窦道和瘘管。
Surg Clin North Am. 2012 Jun;92(3):583-97, viii. doi: 10.1016/j.suc.2012.03.015.
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Branchial cleft and arch anomalies in children.儿童鳃裂及鳃弓畸形
Semin Pediatr Surg. 2006 May;15(2):64-9. doi: 10.1053/j.sempedsurg.2006.02.002.
6
[First branchial cleft anomaly].[第一鳃裂畸形]
Ugeskr Laeger. 1993 Jun 21;155(25):1971-2.
7
Management of second branchial cleft anomalies.第二鳃裂畸形的管理
Rom J Morphol Embryol. 2008;49(1):69-74.
8
Current management of congenital branchial cleft cysts, sinuses, and fistulae.先天性鳃裂囊肿、窦道及瘘管的当前治疗方法
Curr Opin Otolaryngol Head Neck Surg. 2012 Dec;20(6):533-9. doi: 10.1097/MOO.0b013e32835873fb.
9
Bilateral first and second branchial cleft fistulas: a case report.双侧第一和第二鳃裂瘘管:一例报告
Ear Nose Throat J. 2008 May;87(5):291-3.
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Thyroglossal duct and other congenital midline cervical anomalies.甲状舌管及其他先天性颈部中线异常。
Semin Pediatr Surg. 2006 May;15(2):70-5. doi: 10.1053/j.sempedsurg.2006.02.003.

引用本文的文献

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Coexistence of Bilateral First and Second Branchial Cleft Anomalies: A Rare Case Report.双侧第一和第二鳃裂畸形并存:一例罕见病例报告
Indian J Otolaryngol Head Neck Surg. 2022 Oct;74(Suppl 2):2252-2255. doi: 10.1007/s12070-020-02115-1. Epub 2020 Sep 2.
2
[Diagnosis and treatment of the fourth branchial fissure: a clinical report of 1 case and literature review].[第四鳃裂的诊断与治疗:1例临床报告并文献复习]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Jul;35(7):648-650. doi: 10.13201/j.issn.2096-7993.2021.07.016.
3
Branchial cleft anomalies: hybrid "Branchial Inclusion" theory.
鳃裂畸形:杂交“鳃裂包含”理论。
Eur Arch Otorhinolaryngol. 2021 Jul;278(7):2593-2601. doi: 10.1007/s00405-020-06551-1. Epub 2021 Jan 11.
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Branchial Cysts in Quito, Ecuador.厄瓜多尔基多的鳃裂囊肿
Int Arch Otorhinolaryngol. 2020 Jul;24(3):e347-e350. doi: 10.1055/s-0039-1695023. Epub 2020 Jan 9.
5
A fatal case of severe neck abscess due to a third branchial cleft fistula: morphologic and immunohistochemical analyses.一例因第三鳃裂瘘管导致的严重颈部脓肿致死病例:形态学和免疫组织化学分析
Diagn Pathol. 2016 Sep 15;11(1):87. doi: 10.1186/s13000-016-0540-0.
6
Neonatal Presentation of an Air-Filled Neck Mass that Enlarges with Valsalva: A Case Report.新生儿期出现瓦尔萨尔瓦动作时增大的颈部气性肿块:病例报告
AJP Rep. 2015 Oct;5(2):e207-11. doi: 10.1055/s-0035-1563388. Epub 2015 Sep 7.
7
Distribution of branchial anomalies in a paediatric Asian population.亚洲儿科人群鳃裂畸形的分布情况。
Singapore Med J. 2015 Apr;56(4):203-7. doi: 10.11622/smedj.2015060.
8
Branchial anomalies: diagnosis and management.鳃裂畸形:诊断与治疗
Int J Otolaryngol. 2014;2014:237015. doi: 10.1155/2014/237015. Epub 2014 Mar 4.
9
Coexistence of bilateral first and second branchial arch anomalies.双侧第一和第二鳃弓异常并存。
BMJ Case Rep. 2013 Apr 10;2013:bcr2013008698. doi: 10.1136/bcr-2013-008698.
10
Diagnosis and treatment of branchial cleft anomalies in UKMMC: a 10-year retrospective study.马来西亚国民大学医药中心鳃裂畸形的诊断和治疗:一项 10 年回顾性研究。
Eur Arch Otorhinolaryngol. 2013 Mar;270(4):1501-6. doi: 10.1007/s00405-012-2200-7. Epub 2012 Oct 7.