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Cheun, Han, Youn, Yang, Oh, Kim, and Jung: Early Experience of Pediatric Thoracoscopic Surgery Performed by a Pediatric Surgeon
Original Article

Journal of the Korean Association of Pediatric Surgeons 2017; 23(2): 29-36.

Published online: 20 December 2017

DOI: https://doi.org/10.13029/jkaps.2017.23.2.29

Early Experience of Pediatric Thoracoscopic Surgery Performed by a Pediatric Surgeon

Jong-Ho Cheun1, Ji-Won Han1, Joong Kee Youn1, Hee-Beom Yang1, Chaeyoun Oh1, Hyun-Young Kim1, 2, Sung-Eun Jung1, 2

1Department of Pediatric Surgery, Seoul National University Children's Hospital, Seoul, Korea.

2Department of Pediatric Surgery, Seoul National University College of Medicine, Seoul, Korea.

Correspondence: Hyun-Young Kim, Department of Pediatric Surgery, Seoul National University College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul 03080, Korea. Tel: +82-2-2072-2478, Fax: +82-2-747-5130, spkhy02@snu.ac.kr

Received 13 October 2017       Revised 25 October 2017       Accepted 25 October 2017

Copyright © 2017 Korean Association of Pediatric Surgeons

Korean Association of Pediatric Surgeons

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

Minimally invasive surgery (MIS) in abdomen and thorax has been widely accepted for pediatric diseases. Thoracoscopic surgery has the advantage of less pain, better cosmetic outcomes and less musculoskeletal sequelae in comparison to open surgery. We would like to share our initial experience with thoracoscopic surgery performed by one pediatric surgeon.

Methods

We performed a retrospective review of patients who underwent thoracoscopic surgery by one pediatric surgeon between April 2010 and August 2017 in Department of Pediatric Surgery, Seoul National University Children's Hospital.

Results

There were totally 18 cases; 8 cases for esophageal atresia, 3 cases for congenital diaphragm hernia, 2 cases for diaphragm eventration, 2 cases for esophageal duplication cyst, 2 cases for pleural mass and 1 case for esophageal bronchus. At the operation, median age was 9.5 months (range, 0-259 months) and median body weight was 9.4 kg (range, 1.9-49.4 kg). Median operative time was 157.5 minutes (range, 45-335 minutes). There was no case of open conversion and 2 cases of minor leakage at anastomosis site in case of esophageal atresia. Median follow-up month was 5 months (range, 0-87 months). During follow-up, 4 cases of esophageal atresia showed anastomosis site narrowing and average 2.5 times (range, 1-5 times) of esophageal balloon dilatation was done.

Conclusion

We performed thoracoscopic surgery in case of esophageal, diaphragm disease and pleural mass. Thoracoscopic surgery can be an effective and feasible option of treatment for well-selected pediatric patients of intra-thoracic disease including esophagus, diaphragm and mediastinum disease.

Keywords: Thoracoscopy, Pediatrics, Minimally invasive surgical procedures

Figures and Tables

Fig. 1

Esophageal atresia (EA) with tracheoesophageal fistula. (A) Position of patient for operation of EA (white dots, working port; black dot, camera port). (B) After ligating azygos vein, fistula was also ligated with simple suture, and end-to-end anastomosis of esophagus was done with interrupted suture. Arrow, end-to-end anastomosis site.

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Fig. 2

Esophageal atresia, Gross type A. (A) After 7 months, he underwent thoracoscopy and laparoscopy surgery simultaneously by gastric tube interposition. (B) Stomach was incised along great curvature with endo GIA, and gastric tube was made. (C) Gastric tube with distal esophagus was interpositioned to thorax, and esophagoesophagostomy was done by thoracoscopy. Arrows: a, gastric tube-distal part of esophagus; b, proximal part of esophagus. Arrowheads, resected with Endo GIA (Covidien, USA).

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Fig. 3

Esophageal duplication cyst located at posterior mediastinum. (A) The mass was abutting with anterior wall of esophagus on chest CT (2.5×1.9×2.5-cm-sized mass). (B) Mass was connected to muscle layer of esophagus. Arrows: a, mass; b, esophagus.

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Fig. 4

Esophageal duplication cyst of superior mediastinum. (A) There was a mass situated at just front of upper esophagus on neck MRI (2.5×2.2×4.5-cm-sized mass). (B) There was a mass at the front and right of the esophagus. Arrows: a, esophageal duplication cyst; b, true esophagus.

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Fig. 5

Esophageal bronchus. (A) Upper gastrointestinal series showed a community between esophagus and trachea. The contrast also showed that bronchus and bronchioles are risen from esophagus. (B) Intraoperative photo. There was fistula tract between bronchus and esophagus, so it was ligated with simple suture. Patient underwent thoracoscopic right upper lobectomy and fistula division. Arrows: a, fistula tract; b, esophagus.

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Fig. 6

Congenital diaphragm hernia. (A) There was hernia sac on right diaphragmatic defect. (B) Hernia sac was excised and primary repair was performed. Arrows: a, hernia sac; b, primary closure.

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Fig. 7

Venous malformation. (A) There was mass at cardoiphrenic angle and it was suspected an inflammatory pseudo-tumor or congenital lung lesion like cystic lymphangioma on chest CT (3.0×3.6×2.3-cm-sized mass). (B) It was being originated from right pleura and was resected clearly. Arrows: a, mass; b, lung; c, diaphragm.

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Table 1

Demographics and Perioperative Findings

jkaps-23-29-i001

Values are presented as n (%) or median (range).

EA, esophageal atresia; CDH, congenital diaphragmatic hernia; CDE, congenital diaphragmatic eventration.

Notes

CONFLICTS OF INTEREST No potential conflict of interest relevant to this article was reported.

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