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Case Report

[English]
A Case Report of Accessory Cervical Thymus
Ki Yun Lee, Yong Soon Chun, Jeong Su Nam, Nan Joo Lee, Hye Kyoung Yoon
J Korean Assoc Pediatr Surg 2008;14(1):83-87.   Published online June 30, 2008
DOI: https://doi.org/10.13029/jkaps.2008.14.1.83

Accessory cervical thymic tissue has been rarely reported. However, it should be included in the differential diagnosis of neck masses in children, along with branchial anomalies, lymph nodes and other tumors. This lesion occurs along the descending line of the thymus between the angle of mandible and superior mediastinum. A 2-month-old infant presented with an asymptomatic left sided neck mass. MRI revealed a well defined homogeneous mass in the deep lobe of left parotid gland. At operation, an easily identified soft tissue mass was found in the left submandibular area, measuring 3 × 1.5 cm. It was completely excised. Microscopic examination revealed normal thymic tissue.

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Original Articles

[English]
Infantile Hypertrophic Pyloric Stenosis: Clinical Differences of Infantile Hypertrophic Pyloric Stenosis between Premature and Full-term Infants
Suk Koo Lee, Seong Hwan Kim, Woo Yong Lee, Hyun Hahk Kim
J Korean Assoc Pediatr Surg 1998;4(1):34-38.   Published online June 30, 1998
DOI: https://doi.org/10.13029/jkaps.1998.4.1.34

Infantile hypertrophic pyloric stenosis(IHPS) is common in full-term babies, and relatively rare in prematures. The diagnosis of IHPS in premature infants may be obscured because of the lack of classic symptoms and signs and the absence of the standard criteria for ultrasonic diagnosis. The purpose of this study is to discover the clinical differences between premature and full-term infants with pyloric stenosis, and determine the appropriate diagnostic methods for early diagnosis in premature infants. The clinical records of 52 IHPS patients who had been operated upon from October, 1994 to April, 1997 were reviewed. The incidence of IHPS in premature infants was 25 %. The onset of symptom was 4.7 weeks of age in premature, and 2.9 weeks in full-term babies. Diagnosis was established by typical symptoms. signs. and diagnostic imaging studies. In two premature infants, diagnosis was confirmed by upper gastrointestinal(GI) series, because ultrasonography did not meet the diagnostic criteria. Two premature infants initially diagnosed as gastroesophageal reflux by esophagography. were found to have IHPS by upper GI series. For the diagnosis of IHPS, a new set of criteria for premature babies has to be developed.

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[English]
Intestinal Perforations in Very Low Birth Weight Infants
Kim, Dae Yeon , Kim, Seong Chul , Kim, Ai Rhan , Kim, Ki Soo , Pi, Soo Young , Kim, In Koo
J Korean Assoc Pediatr Surg 2001;7(2):112-117.
DOI: https://doi.org/10.13029/jkaps.2001.7.2.112
With the advances in neonatal intensive care, pediatric surgeons experience very low birth weight infants, weighing <1,500 g, more frequently. We report our 14 cases of very low birth weight infants with intestinal perforations without congenital causes, at the Asan Medical Center during the 11-year period from 1989 to 2000. The average birth weight was 919 g (563-1,490), and average gestational age was 206 days (161-286). There were nine males and five females. Operation was performed at an average age of 14.0 days (3-38). Ten neonates with symptomatic PDA were given indomethacin in an attempt to close the ductus. Bowel perforation involved the jejunum in two and ileum in twelve. At laparotomy, there were seven focal intestinal perforations, five typical NEC, one intussusception, and an unknown cause. Four neonates underwent resection and anastomosis of the bowel, and nine underwent exteriorization. One underwent resection and anastomosis after peritoneal drainage. Four patients had postoperative complications; two leakage of anastomosis, one stoma necrosis, and one internal herniation. Seven of fourteen patients survived (50.0%). Seven patients died of septic complication. There was a significant difference in the birth weight and gestational age in survivors compared with those who died (p<0.05). There was an increased risk of bowel perforation in indomethacin treatment for PDA. Careful clinical observation and keen judgment are essential for this particular group of infants.
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