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"Yong hoon Cho"

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"Yong hoon Cho"

Original Articles

[English]
Comparative Analysis of Two National Surveys on Esophageal Atresia With or Without Tracheoesophageal Fistula: A Retrospective Study by the Korean Association of Pediatric Surgeons
Jinyoung Park, Dae Yeon Kim, Seong Chul Kim, Hyun-Young Kim, So Hyun Nam, Jeong-Meen Seo, Jung-Tak Oh, Myung-Duk Lee, Suk-Koo Lee, Soo Min Ahn, Hye Kyung Chang, Sung Eun Jung, Yeon Jun Jeong, Eunyoung Jung, Jae Hee Chung, Yong Hoon Cho, Soon Ok Choi, Seung Hoon Choi, Yun Mee Choe, Seok Joo Han, Jeong Hong, Nam-Hyuk Lee
Adv Pediatr Surg 2024;30(1):1-8.   Published online May 31, 2024
DOI: https://doi.org/10.13029/aps.2024.30.1.1
Purpose
The Korean Association of Pediatric Surgeons (KAPS) conducts annual nationwide surveys on various aspects of pediatric surgical diseases, with the results being discussed during KAPS’s annual spring meetings.
Methods
KAPS conducted two national surveys, in 1995 and 2016, to investigate esophageal atresia (EA) with or without tracheoesophageal fistula (TEF). The authors analyzed data from these surveys to identify differences or changes in the annual occurrence, demographic characteristics, clinical presentation, preoperative diagnostic methods, anatomical type, associated anomalies, surgical treatment, and postoperative outcomes among patients with EA/TEF treated by KAPS members.
Results
The first and second national surveys included 148 and 211 patients with EA/TEF, respectively. Excessive salivation was the most prevalent clinical symptom in both surveys. Type C was the most common form of EA/TEF in both surveys. The first survey included 126 patients, all of whom underwent open surgery. In the second survey, 152 (78.4%) of 194 patients underwent open surgery, while 34 (17.5%) underwent thoracoscopic surgery. Primary esophageal repair was performed on 96 (76.2%) of 126 patients in the first survey and on 160 (82.5%) of 194 patients in the second survey. Anastomotic strictures developed in 21.4% and 32.5% of patients, anastomotic leakage in 22.2% and 10.3%, recurrent fistula in 2.4% and 4.2% during the first and second surveys, respectively. The respective survival rates for group A were 90.2% and 98.3% in the first and second surveys. For group B, the rates were 73.9% and 98.1%, and for group C, they were 34.5% and 68.1%, respectively, according to the Waterston classifications.
Conclusion
These nationwide surveys provide comprehensive information on the status, detailed treatment, and outcomes for Korean pediatric patients with EA/TEF. They are anticipated to be an invaluable resource and guide for pediatric surgeons seeking to expand their knowledge on EA/TEF and its treatment options.
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[English]
Sacrococcygeal Teratoma: A Survey by the Korean Association of Pediatric Surgeons in 2018
Jung-Tak Oh, Hye Kyung Chang, Min Jeong Cho, Yong Hoon Cho, Soo Jin Na Choi, Yoon Mi Choi, Jae Hee Chung, Sang Young Chung, Jeong Hong, Seok Joo Han, Yeon Jun Jeong, Eunyoung Jung, Kyuhwan Jung, Dae Youn Kim, Hae-Young Kim, Hyun-Young Kim, Ki Hoon Kim, Sang Youn Kim, Seong Chul Kim, Seong Min Kim, Soo-Hong Kim, Jong-In Lee, Myung-Duk Lee, Nam-Hyuk Lee, Suk-Koo Lee, So Hyun Nam, Jin Young Park, Kwi-Won Park, Tae-Jin Park, Jeong-Meen Seo, Jae Ho Shin, Jiyoung Sul
Adv Pediatr Surg 2019;25(2):35-43.   Published online December 18, 2019
DOI: https://doi.org/10.13029/aps.2019.25.2.35
Purpose

The Korean Association of Pediatric Surgeons (KAPS) performed a nationwide survey on sacrococcygeal teratoma in 2018.

Methods

The authors reviewed and analyzed the clinical data of patients who had been treated for sacrococcygeal teratoma by KAPS members from 2008 to 2017.

Results

A total of 189 patients from 18 institutes were registered for the study, which was the first national survey of this disease dealing with a large number of patients in Korea. The results were discussed at the 34th annual meeting of KAPS, which was held in Jeonju on June 21–22, 2018.

Conclusions

We believe that this study could be utilized as a guideline for the treatment of sacrococcygeal teratoma to diminish pediatric surgeons' difficulties in treating this disease and thus lead to better outcomes.

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Case Report

[English]
Mature Cystic Gastric Teratoma in an Infant: A Case Presenting with a Gastrointestinal Bleeding
Soo-Hong Kim, Yong Hoon Cho, Hae Young Kim, Yeoun Joo Lee, Jae-Hong Park
J Korean Assoc Pediatr Surg 2015;21(2):42-45.   Published online December 22, 2015
DOI: https://doi.org/10.13029/jkaps.2015.21.2.42

Gastric teratoma is an extremely rare tumor that accounts for less than 1% of all teratomas. Gastric teratoma is mostly presented as a palpable abdominal mass, and is rarely accompanied with gastrointestinal bleeding such as melena or hematemesis. A 5-month-old male infant was brought with a history of pale facial color and dark-colored stool. The hemoglobin level was at 6.1 g/dL, with melena having begun 1 month previous. Upper gastrointestinal endoscopy revealed a polypoid mass with bleeding at the upper body and lesser curvature of the stomach. Wedge resection of the stomach was performed and histopathological analysis confirmed the mass to be a mature cystic teratoma. There was no recurrence after the operation during follow-up.

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Original Articles

[English]
Cystic Enteric Duplication: Prenatally and Postnatally Diagnostic Group
Tae Beom Lee, Yong Hoon Cho, Soo-Hong Kim, Hae-Young Kim
J Korean Assoc Pediatr Surg 2015;21(2):24-27.   Published online December 22, 2015
DOI: https://doi.org/10.13029/jkaps.2015.21.2.24
Purpose

The duplication of gastrointestinal tract has been known to be a rare condition and two different forms, cystic and tubular type. This study was conducted to examine its clinical characteristics, especially cystic enteric duplication which was detected antenatally or postnatally.

Methods

There were 13 patients, who confirmed as cystic enteric duplication after operation between July 1996 and June 2015. Clinical data, including a gender, age at operation, presenting symptoms, diagnostic modalities, locations of lesion, and results of surgical treatment, were reviewed retrospectively according to cases detected antenatally and postnatally.

Results

Five cases were included in antenatal diagnosis group and 8 cases in postnatal diagnosis group. Both groups show slightly common in female and the lesion most common in ileum. Antenatal diagnosis group shows 2 males and 3 females and the mean age at operation was 12±52 days (range, 5 to 90 days). They received operation regardless of symptom. Postnatal group shows 3 males and 5 females and the mean age at operation was 462.5±777.0 days (range, 4 days to 6 years). Moreover, 6 patients (75.0%) were age before 2 years. They usually presented abdominal pain with vomiting.

Conclusion

Cystic enteric duplication could present symptoms at any time during childhood, mainly before 2 years old, and so a proper management should be considered when suspect it. Although it is uncommon, surgical management including a minimal invasive procedure could be attempted despite the neonatal period.

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[English]
Clinical Study of Congenital Diaphragmatic Diseases in Neonates and Infants
Soo hong Kim, Yong hoon Cho, Je ho Ryu
J Korean Assoc Pediatr Surg 2010;16(2):143-153.   Published online December 31, 2010
DOI: https://doi.org/10.13029/jkaps.2010.16.2.143

Congenital diaphragmatic disease is one of the common major congenital anomalies, and its mortality remained still high despite recent medical advances. The aim of this study is to examine the clinical characteristics of congenital diaphragmatic diseases. A total of 39 patients with congenital diaphragmatic disease that underwent surgery from January, 1997 to December, 2009 at Pusan National University Hospital were included in this study. Medical records were retrospectively reviewed. The male to female ratio was 30:9. Six out of 39 cases died (NS) before surgery, 17 patients had Bochdalek's hernia (BH), 11 patients hiatus hernia (HH), 4 diaphragmatic eventration (DE), and 1 Morgagni hernia (MH). There were no differences in mean birth weight and mean gestational age. NS (83.3%). BH (35.3%) was diagnosed more frequently than other diseases in the prenatal period. Three patients (17.6%) of BH expired due to pulmonary hypoplasia and 1 patient had co-existing congenital heart disease. BH was diagnosed more frequently in the prenatal stage and had a higher motality rate than other conditions. Therefore, BH needs to be concentrated more than other anomalies.

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