- Prenatal diagnosis of caudal regression syndrome: A case report
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Park JE, Cho IA, Lee DH, Shin JK, Lee SA, Lee JH, Paik WY
- KMID: 2078023
- Korean J Obstet Gynecol.
- 2011 May;54(5):265-268.
- doi: 10.5468/KJOG.2011.54.5.265
Caudal regression syndrome is rare congenital defect, characterized by the absence of the sacrum, and defects of variable portion of lumbar spine, associated with anomalies from different systems. Although hyperglycemia... -
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- Gastric duplication cyst associated with dorsal pancreatic agenesis and a cystic pulmonary lesion
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Lim SM, Lee H, Jeon EJ, Oh JH, Lee SH, Choi SW, Lee S
- KMID: 2257333
- Korean J Med.
- 2009 Feb;76(2):203-208.
Gastric duplication cysts and dorsal pancreatic agenesis are rare congenital anomalies, and little is known of the association between these two anomalies. A 17-year-old woman was admitted with a cystic... -
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- A Case of Colonic Duplication Cyst Mimicking Gastrointestinal Stromal Tumor
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Jung HC, Jung SW, Jeong ID, Bang SJ, Shin JW, Park NH, Kim YM, Choi DH, Kim DH
- KMID: 2174121
- Intest Res.
- 2009 Jun;7(1):64-67.
Duplications of the gastrointestinal tract are rare congenital malformations that are usually present during the first decade of life. However, a smaller number of cases may remain occult until adulthood.... -
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- A Case Report of Bile Duct Duplication Arising from the Hepatic Hilum
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Gong EJ, Jang EK, Yoon YH, Ahn SH, Hyun YS, Hwang DW, Lee SK
- KMID: 2264297
- Korean J Med.
- 2012 Apr;82(4):465-469.
Anatomic variation in the hepatobiliary tract is relatively common, although bile duct duplication is rare. Detection of biliary tract variation is important because it is closely related to complications such... -
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- Clinical Experience of Currarino Syndrome
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Kim T, Cho MJ, Kim DY, Kim SC, Kim IK
- KMID: 1447931
- J Korean Assoc Pediatr Surg.
- 2011 Jun;17(1):65-71.
Currarino syndrome is a hereditary syndrome characterized by the triad of a sacral bony defect, presacral mass and anorectal malformation. We retrospectively reviewed 13 Currarino syndrome patients who were treated... -
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- Prenatally Detected Congenital Perineal Mass Using 3D Ultrasound which was Diagnosed as Lipoblastoma Combined with Anorectal Malformation: Case Report
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Ahn KH, Boo YJ, Seol HJ, Park HT, Hong SC, Oh MJ, Kim T, Kim HJ, Kim YT, Kim SH, Lee KW
- KMID: 1792965
- J Korean Med Sci.
- 2010 Jul;25(7):1093-1096.
- doi: 10.3346/jkms.2010.25.7.1093
We report a case of prenatally diagnosed congenital perineal mass which was combined with anorectal malformation. The mass was successfully treated with posterior sagittal anorectoplasty postnatally. On ultrasound examination at... -
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- Impact of a Newly Developed Short Double-Balloon Enteroscope on Stent Placement in Patients with Surgically Altered Anatomies
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Tsutsumi K, Kato H, Okada H
- KMID: 2412199
- Gut Liver.
- 2017 Mar;11(2):306-311.
- doi: 10.5009/gnl16441
A newly developed short double-balloon enteroscope with a working channel enlarged to a diameter of 3.2 mm is a novel innovation in stent placement for patients with surgically altered anatomies.... -
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