Ayoung Kang

Dr. Ayoung Kang

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2020 in Annals of Surgical Treatment and Research
Verified
Journal Article
Open access
PDF file
SJSangtae Jang
Sangtae Jang
AKAyoung Kang
Ayoung Kang
HAHong-Min Ahn
Hong-Min Ahn
SHSun-Hwi Hwang
Sun-Hwi Hwang
SLSi Hak Lee
Si Hak Lee
Jang S, et al. Ann Surg Treat Res. 2020 Oct;99(4):205-212. https://doi.org/10.4174/astr.2020.99.4.205

1 January 2024 in Annals of Surgical Treatment and Research
Verified
Journal Article
Open access
PDF file
YJYe-Chan Jeong
Ye-Chan Jeong
AKAyoung Kang
Ayoung Kang
DKDaypimg Ko
Daypimg Ko
JYJoong Kee Youn
Joong Kee Youn
HKHyun-Young Kim
Hyun-Young Kim
Jeong YC, et al. Ann Surg Treat Res. 2024 Jun;106(6):322-329. https://doi.org/10.4174/astr.2024.106.6.322

1 December 2020 in Korean Journal of Clinical Oncology
Verified
Journal Article
Open access
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AKAyoung Kang
Ayoung Kang
SCSung Hwan Cho
Sung Hwan Cho
BPByung-Soo Park
Byung-Soo Park
GSGyung Mo Son
Gyung Mo Son
HKHyun Sung Kim
Hyun Sung Kim
TKTae Un Kim
Tae Un Kim
An extragastrointestinal stromal tumor (EGIST) is a gastrointestinal stromal tumor that arises outside of the gastrointestinal tract. Most EGISTs are located in the omentum, mesentery, and retroperitoneum. The occurrence of an EGIST at the perianal region is very rare. Herein, we report our experience with EGISTs in the perianal area and review the literature. A 70-year-old man presented to our hospital with a 2-year history of anal discomfort. A pelvic magnetic resonance imaging scan showed a homogenous, well-defined, soft tissue density mass. The patient underwent mass excision, and the pathological examination confirmed that the mass was an EGIST. The size of the tumor was 4.3×3.2 cm, and the mitotic count was 1 per 50 high-power fields. The tumor cells were immunohistochemically positive for KIT and CD34 but were negative for S-100 and alpha-smooth muscle actin. There were no other abnormal findings in the gastrointestinal tract; upon pathological review, this case was confirmed as perianal EGIST. Therefore, EGIST should be considered as a differential diagnosis of perianal masses.

8 August 2025 in Medicine
Verified
Journal Article
Open access
DIDongwon Im
Dongwon Im
AKAyoung Kang
Ayoung Kang
SKSoo-Hong Kim
Soo-Hong Kim
SLSang Su Lee
Sang Su Lee
HJHyuk Jae Jung
Hyuk Jae Jung
Rationale: Deep vein thrombosis (DVT) is rare in pediatric patients. Congenital inferior vena cava (IVC) anomalies are asymptomatic; however, these can cause DVT in younger patients rarely. Patient concerns: In this case, a 14-year-old male patient was referred to our hospital for lower abdominal pain. Diagnoses: At the first hospital he visited, computed tomography revealed a thrombus in the veins of the abdomen and lower extremities; however, an accurate diagnosis could not be made because the thrombus was thought to be inconsistent with abdominal pain. Close examinations revealed swelling of the lower extremities and pain while walking. Contrast-enhanced computed tomography revealed the absence of IVC (AIVC), resulting in DVT at the external iliac, gonadal, inferior mesenteric, and collateral veins of the right pelvic cavity. Interventions: The patient received anticoagulation therapy. Outcomes: At a follow-up 6 months later, his symptoms improved, and a thrombus was not found. AIVC could cause DVT. Lessons: DVT is rare in pediatric patients and is difficult to diagnose when the initial symptoms are vague. Conservative treatments are the most commonly used treatment; long-term follow-up is needed.

1 January 2026 in Translational Pediatrics
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Journal Article
Open access
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HKHansol Kim
Hansol Kim
AKAyoung Kang
Ayoung Kang
SKSoo-Hong Kim
Soo-Hong Kim
JKJae Young Kim
Jae Young Kim
TPTaejin Park
Taejin Park
YLYeoun Joo Lee
Yeoun Joo Lee
Original Article Is surgery always necessary for multiple magnet ingestion in children?—evidence for an endoscopy-first approach Hansol Kim, Ayoung Kang, Soo-Hong Kim, Jae Young Kim, Taejin Park, Taek Jin Lim, Yeoun Joo Lee

30 May 2025 in Journal of Medicine and Life Science
Verified
Journal Article
Open access
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AKAyoung Kang
Ayoung Kang
SKSoo-Hong Kim
Soo-Hong Kim
HKHae-Young Kim
Hae-Young Kim
Choledochal cyst (CC) is a rare biliary tract disease characterized by cystic dilation of the biliary duct that requires surgical resection because of its malignant potential and associated complications. Minimally invasive surgeries (MIS), such as laparoscopy and robotics, have been increasingly used for the treatment of CC. This study investigated the current treatment trends and outcomes of pediatric CC in Korea, with a focus on MIS. We reviewed papers and conference abstracts on pediatric CC in Korea, published between 2000 and 2024. The incidence of CC in Korea is similar to that in Japan, with a rate of 1 in 13,000 individuals and a male-to-female ratio of 1:3 to 1:4. Type I CC was the most common (73.8%), followed by type IVA (16.0%). The first pediatric laparoscopy for CC in Korea was performed in 2006, and the first robotic surgery was in 2011. According to national surveys conducted by the Korean Association of Pediatric Surgeons in 2002 and 2017, all surgeries performed in the 2000s were open procedures. By the late 2010s, 54.3% of surgeries had been performed using MIS (laparoscopy, 31.1%; robotic surgery, 23.2%). Although few institutions have reported MIS outcomes for CC in Korea, laparoscopic surgery has been shown to be safe and cosmetically favorable. The surgical outcomes of robotic surgery are similar, but with challenges such as longer operation times, difficulties in small patients, and higher costs. Although laparoscopic surgery is currently the standard treatment in Korea, robotic surgery may become another standard procedure if the technological limitations can be overcome.