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1
Anaesthesia concerns and perioperative management in a child with DiGeorge syndrome with corrected tetralogy of Fallot with pulmonary atresia posted for laparoscopic orchidopexy: Case report.患有法洛四联症合并肺动脉闭锁且已矫正的迪乔治综合征患儿拟行腹腔镜睾丸固定术的麻醉问题及围手术期管理：病例报告
Indian J Anaesth. 2020 Apr;64(4):322-324. doi: 10.4103/ija.IJA_770_19. Epub 2020 Mar 28.
2
Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.法洛四联症合并肺动脉闭锁伴22q11染色体缺失
J Am Coll Cardiol. 1996 Jan;27(1):198-202. doi: 10.1016/0735-1097(95)00415-7.
3
Echocardiographic identification of thymic hypoplasia in tetralogy of fallot/tetralogy pulmonary atresia.
Am J Cardiol. 1999 Nov 15;84(10):1268-71, A9. doi: 10.1016/s0002-9149(99)00547-0.
4
[Cardiac surgery of tetralogy of Fallot associated with DiGeorge syndrome: a case report].[法洛四联症合并迪格奥尔格综合征的心脏手术：一例报告]
Kokyu To Junkan. 1989 Nov;37(11):1243-6.
5
[A case of tetralogy of Fallot associated with isolation of a subclavian artery and partial DiGeorge syndrome].[一例法洛四联症合并锁骨下动脉离断及部分迪格奥尔格综合征]
Kyobu Geka. 1993 Sep;46(10):870-5.
6
Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot.家族性22q11.2缺失：一名患有主动脉弓中断和迪格奥尔格综合征的婴儿，其母亲患有法洛四联症。
Eur J Pediatr. 2002 Mar;161(3):173-4. doi: 10.1007/s00431-001-0890-8.
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Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly.11例DiGeorge综合征患者中降钙素细胞减少及其他先天性异常分析
Am J Med Genet. 1993 Jul 1;46(6):641-6. doi: 10.1002/ajmg.1320460608.
8
Association Between Tetralogy of Fallot and Tracheobronchial Branching Abnormalities: A New Clue for Pathogenesis?法洛四联症与气管支气管分支异常的相关性：发病机制的新线索？
J Am Heart Assoc. 2017 Dec 29;7(1):e006921. doi: 10.1161/JAHA.117.006921.
9
Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival.伴有法洛四联症且生存期延长的家族性迪格奥尔格综合征
Eur J Pediatr. 1984 Jan;141(3):171-2. doi: 10.1007/BF00443218.
10
Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.迪乔治综合征中的心血管异常以及神经嵴作为可能致病因素的重要性。
Am J Cardiol. 1986 Jul 1;58(1):133-7. doi: 10.1016/0002-9149(86)90256-0.

本文引用的文献

1
Undescended Testes and Laparoscopy: Experience from the Developing World.隐睾与腹腔镜检查：来自发展中世界的经验
Adv Urol. 2018 Oct 24;2018:1620470. doi: 10.1155/2018/1620470. eCollection 2018.
2
Practical guidelines for managing adults with 22q11.2 deletion syndrome.22q11.2缺失综合征成年患者管理实用指南。
Genet Med. 2015 Aug;17(8):599-609. doi: 10.1038/gim.2014.175. Epub 2015 Jan 8.
3
Challenges in paediatric laparoscopic surgeries.小儿腹腔镜手术中的挑战。
Indian J Anaesth. 2009 Oct;53(5):560-6.
4
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.22q11.2缺失综合征的心脏缺陷及心脏手术结果
Dev Disabil Res Rev. 2008;14(1):35-42. doi: 10.1002/ddrr.6.
5
Laparoscopic surgery in the pediatric patient post Fontan procedure.法洛四联症修复术后小儿患者的腹腔镜手术
Paediatr Anaesth. 2006 May;16(5):591-5. doi: 10.1111/j.1460-9592.2005.01826.x.
6
Laparoscopic orchiopexy: report of 203 cases with review of diagnosis, operative technique, and lessons learned.腹腔镜睾丸固定术：203例报告并对诊断、手术技术及经验教训进行回顾
J Endourol. 2003 Aug;17(6):365-8. doi: 10.1089/089277903767923128.
7
New treatments for pulmonary arterial hypertension.
Am J Respir Crit Care Med. 2002 May 1;165(9):1209-16. doi: 10.1164/rccm.200110-028PP.
8
A population study of chromosome 22q11 deletions in infancy.一项关于婴儿期22q11染色体缺失的群体研究。
Arch Dis Child. 1998 Oct;79(4):348-51. doi: 10.1136/adc.79.4.348.

患有法洛四联症合并肺动脉闭锁且已矫正的迪乔治综合征患儿拟行腹腔镜睾丸固定术的麻醉问题及围手术期管理：病例报告

Anaesthesia concerns and perioperative management in a child with DiGeorge syndrome with corrected tetralogy of Fallot with pulmonary atresia posted for laparoscopic orchidopexy: Case report.

作者信息

Kale Natasha, Katkade Sandip, Mehta Hemant, Krishnanaik Shivaprakash

机构信息

Department of Anaesthesiology and Paediatric Cardiac Sciences, Sir H. N. Reliance Hospital, Mumbai, Maharashtra, India.

出版信息

Indian J Anaesth. 2020 Apr;64(4):322-324. doi: 10.4103/ija.IJA_770_19. Epub 2020 Mar 28.

DOI:10.4103/ija.IJA_770_19
PMID:32489208
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7259404/
Abstract

DiGeorge syndrome is afflicted with multiple congenital anomalies such as conotruncal and craniofacial anomaly, immune system dysfunction and hypoplasia/aplasia of parathyroid glands. Laparoscopy is a preferred surgical approach over open orchidopexy due to better visualisation of impalpable testis avoiding long incision, minimal tissue damage and a faster recovery. We report a case of DiGeorge syndrome with corrected tetralogy of Fallot with pulmonary atresia in a 1-year-old male child posted for laparoscopic orchidopexy. The anaesthesiologists face unique challenges due to the multisystem involvement and the effects of laparoscopic surgery on multiple organs. Thorough understanding of DiGeorge syndrome is essential for a good perioperative outcome.

摘要

迪乔治综合征伴有多种先天性异常，如圆锥干和颅面异常、免疫系统功能障碍以及甲状旁腺发育不全/发育不良。由于腹腔镜手术能更好地观察无法触及的睾丸，避免长切口，减少组织损伤并加快恢复，因此相较于开放睾丸固定术，它是一种更可取的手术方法。我们报告了一例1岁男性迪乔治综合征患儿，合并法洛四联症伴肺动脉闭锁，拟行腹腔镜睾丸固定术。由于多系统受累以及腹腔镜手术对多个器官的影响，麻醉医生面临着独特的挑战。全面了解迪乔治综合征对于实现良好的围手术期结果至关重要。