• Advances in pediatric surgery
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• 제11권1호
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• pp.1-8
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• 2005

With the development of fetal ultrasonography, detection of fetal ovarian cysts has been increased. Although ovarian cyst formation during the perinatal period is a self limiting process, there is still considerable controversy regarding the best treatment of the fetal ovarian cyst. The purpose of this study is to evaluate the natural history of fetal ovarian cysts and to analyze the result of treatment. From 1995 to 2004, 31 consecutive fetuses with ovarian cysts were followed by ultrasonography during the perinatal period. The fetal ovarian cyst was diagnosed by prenatal ultrasonography between 25weeks and 38 weeks and the mean size of the cysts was 5cm (ranged from 2 to 8cm). At birth, 3 cysts disappeared. In 2 cases, the diagnoses were changed to multicystic kidney disease and intestinal duplication. During following up of 26 cysts, 15 cysts have resolved completely. Seven cysts required oophorectomy because of cyst torsion (n=3), differentiation of tumorous condition (n=2), increased size of cyst (n=1), and large size (8cm) of cyst at birth (n=l). Fetal ovarian cyst should primarily be observed, and only in the limited cases, surgical treatment would be required for the risk of complications such as torsion and differentiation from benign to malignant pathology.

• Journal of Yeungnam Medical Science
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• 제38권3호
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• pp.240-244
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• 2021

Imperforate anus is an anomaly caused by a defect in the development of the hindgut during early pregnancy. It is a relatively common congenital malformation and is more common in males. Although there are cases of a solitary imperforate anus, the condition is more commonly found as a part of a wider spectrum of other congenital anomalies. Although urgent reconstructive anorectal surgery is not necessary, immediate evaluation is important and urgent decompressive surgery may be required. Moreover, as there are often other anomalies that can affect management, prenatal diagnosis can help in optimizing perinatal care and prepare parents through prenatal counseling. In the past, imperforate anus was diagnosed by prenatal ultrasonography based on indirect signs such as bowel dilatation or intraluminal calcified meconium. Currently, it is diagnosed by directly checking the perineum with prenatal ultrasonography. Despite advances in ultrasound technology, accurate prenatal diagnosis is impossible in most cases and imperforate anus is detected after birth. Here, we present two cases of imperforate anus in female fetuses that were not diagnosed prenatally.

• Childhood Kidney Diseases
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• 제10권1호
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• pp.33-39
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• 2006

목적 :신생아 수신증은 임신의 약 4.5-7% 정도로 흔하게 나타날 뿐 아니라 산전 초음파의 발달과 함께 조기진단이 가능한 질환이다. 그러나 그 자연 경과에 대한 이해 부족으로, 수술적 중재술의 적절한 시기에 대한 합의가 이루어지지 않은 상태이다. 저자들은 신생아 수신증의 자연경과에 대한 이해와 수술의 위험요소를 분석함으로써, 적절한 치료지침을 제시하고자 하였다. 방법 : 2001년 4월부터 2005년 4월까지 본원에서 태어난 신생아 중, 주산기에 시행한 신 초음파 검사에서 신생아 수신증으로 진단된 환아를 대상으로 하였다. 총 2회 이상의 초음파 검사를 통한 경과 관찰을 하였던 환아들 중, 6개월 이상 추적관찰된 총 69명의 환자를 대상으로 하였다. 환자군은 주산기 신장 초음파에서 신우전후경 길이를 기준으로 분류하였다 각각 환자의 신장 초음파 검사에서 신우전후경 길이 및 SFU 지수를 측정하였고, $^{99m}Tc-MAG3$ 검사 결과를 바탕으로 분석하였다. 수술은 정해진 기준에 따라 시행하였다. 결과 : 신우전후경의 길이가 10 mm 이상인 환자군에서, 10 mm 미만인 환자군에 비해 수술적 중재술을 필요한 경우가 많았다. 또한 SFU 지수가 3 이상인 경우에서, 수술의 빈도가 높아, SFU 지수 3 미만인 환자군과 유의한 차이를 두었다. MAG3 검사 중, 상대 신기능은 수술과의 연관성을 찾기 어려웠으나, 신장 폐색의 정도와 수술 여부와 상호 관계가 있는 것으로 나타났다. 결론 : 신생아 수신증에서 주산기 신장 초음파 검사 상, 신우전후경의 길이가 10 mm가 넘거나, SFU 지수가 3 이상이거나, MAG3 검사 결과 상 폐색이 의심되는 경우에는 수술적 중재술을 통한 적극적인 치료를 고려하는 것이 추천된다. 그리고 신우전후경의 길이가 10 mm 미만이거나 SFU 지수가 2 이하인 경우, 신생아 수신증의 자연 경과를 관찰할 수 있으나 정기적인 경과 관찰이 필요하다.

• Clinical and Experimental Pediatrics
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• 제57권2호
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• pp.75-78
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• 2014

Purpose: This study aimed to investigate the clinical features of macrocephaly at birth in Korea using ultrasonography. Methods: We retrospectively investigated the medical records of full-term birth neonates in Cheil General Hospital & Women's Healthcare Center from January 2000 to June 2012. The following parameters were recorded and analyzed: gestational age, sex, birth weight, height, occipitofrontal circumference (OFC), physical examination, perinatal problems, and ultrasonography results. Macrocephaly was diagnosed when the OFC was greater than two standard deviations, based on the 2007 Korean National Growth Charts. Results: There were 75 neonates with macrocephaly at birth (52 boys and 23 girls), with a mean OFC of $38.1{\pm}0.49cm$. A comparison of the birth weight and height with the OFC value showed that height was correlated with OFC (r=0.35) but birth weight was not correlated with OFC (r=0.06). There were no remarkable findings in 56 cases (75%). Germinal matrix hemorrhage was identified in 10 cases (13%). An enlarged cerebrospinal fluid space was found in 5 cases (6.7%). There were 3 cases of mega-cisterna magna (4%), 1 case of ventriculomegaly, and 1 case of an enlarged interhemispheric space (6 mm) among these patients. In addition, a choroid plexus cyst was seen in 1 case. Mineralizing vasculopathy in both basal ganglia with no evidence of congenital infection was found in 2 cases and an asymptomatic subarachnoid hemorrhage was found in 1 case. Conclusion: Our results indicate that macrocephaly at birth has benign ultrasonography findings and shows a pattern of male dominance.

• Clinical and Experimental Pediatrics
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• 제51권1호
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• pp.89-92
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• 2008

신생아의 피막하 간 혈종은 다양한 원인에 의해서 유발되는데 대부분은 출혈의 양이 적어 임상적으로 발견되기 보다는 부검시 발견되는 경우가 많다. 그러나 출혈의 양이 많아 혈종을 싸고 있는 피막이 파열되고 잇따른 출혈이 발생할 경우에는 창백, 혈관 허탈, 빈혈, 복부팽만, 저산소증, 산혈증 등의 증상을 보이므로 조기에 의심하여 정확한 진단을 내리고 적절한 수술적 치료를 실시하지 않으면 사망률이 높다. 저자들은 태변 흡입후 신생아 가사 소견을 보여 심폐소생술을 실시한 신생아에서 출생후 7일에 발현된 대량 피막하 간 혈종 파열 1례를 경험하였기에 보고하는 바이다.

• Archives of Plastic Surgery
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• 제43권2호
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• pp.153-159
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• 2016

Background The prenatal ultrasound detection of cleft lip with or without cleft palate (CL/P) and its continuous management in the prenatal, perinatal, and postnatal periods using a multidisciplinary team approach can be beneficial for parents and their infants. In this report, we share our experiences with the prenatal detection of CL/P and the multidisciplinary management of this malformation in our institution's Congenital Disease Center. Methods The multidisciplinary team of the Congenital Disease Center for mothers of children with CL/P is composed of obstetricians, plastic and reconstructive surgeons, pediatricians, and psychiatrists. A total of 11 fetuses were diagnosed with CL/P from March 2009 to December 2013, and their mothers were referred to the Congenital Disease Center of our hospital. When CL/P is suspected in the prenatal ultrasound screening examination, the pregnant woman is referred to our center for further evaluation. Results The abortion rate was 28% (3/11). The concordance rate of the sonographic and final diagnoses was 100%. Ten women (91%) reported that they were satisfied with the multidisciplinary management in our center. Conclusions Although a child with a birth defect is unlikely to be received well, the women whose fetuses were diagnosed with CL/P on prenatal ultrasound screening and who underwent multidisciplinary team management were more likely to decide to continue their pregnancy.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제2권1호
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• pp.109-115
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• 1999

Hepatitis C virus (HCV) has been identified as an important cause of posttransfusion hepatitis, but vertical transmission of chronic infected HCV RNA positive mothers has been documented in some cases. The reports of the risk of perinatal infection have been widely varied in the literature. The authors experienced one case of vertical transmission of HCV in an infant of a mother who had hepatitis C during pregnancy. At admission, HCV RNA (+), Ig G anti HCV (+) and Ig M anti HCV (+) were found in the mother. Also at admission, HCV RNA (+), Ig G anti HCV (+), Ig M anti HCV (+), elevation of liver aminotransferase level and hepatosplenomegaly on ultrasonography were found in the baby on day 31. HCV RNA (-), Ig M anti HCV (-) and normal of liver aminotransferase level were noted on day 250 in the serum of the infant. We used reverse transcriptase polymerase chain reaction (RT-PCR) technique to find a very small amount of HCV RNA in the serum. All the findings suggest vertical transmission of HCV RNA from mother to infant during 3rd trimester of pregnancy.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제2권2호
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• pp.262-266
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• 1999

Obstruction of the extrahepatic bile ducts is the most common cause of conjugated hyperbilirubinemia in early infancy. More than 90% of such obstructive lesions are accounted for by extrahepatic biliary atresia. A rare lesion is obstruction of the common duct by impacted, thickened secretions and bile. Bile plug syndrome is defined as extrahepatic obstruction of the bile ducts by bile sludge in term infants without anatomic abnormalities, congenital chemical defects of bile, or hepatocellular lesions. Obstruction of extrahepatic ducts by plugs of biliary material apperas to be due to the inspissation and precipitation of bile and mucus within the lumen of the ducts. Cholestasis and precipitation of bile develop in association with abnormal composition of bile in cystic fibrosis, hepatocellular damage, prolonged erythroblastic jaundice, altered biliary dynamics with total parenteral nutrition, gut dysfunction, diuretic therapy, exchange transfusions and perinatal hemolysis. In those cases, the term inspissated bile syndrome is used. The clinical and laboratory findings in bile plug syndrome are identical to those observed in biliary atresia and choledochal cyst. The diagnosis can be suspected based on the findings of clinical and laboratory examinations together with hepatobiliary imaging, ultrasonography, radionuclide scan and liver biopsy. We experienced a case of spontaneous resolution of bile plug syndrome in a 4-year-old girl. We report this case with brief review related literatures.

• Pediatric Infection and Vaccine
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• 제4권1호
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• pp.79-89
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• 1997

목 적 : 신생아 세균성 뇌막염은 임상 증상이 비특이적이며 여러가지 신경학적 후유증을 남길 수 있는 질환으로 본 저자들은 원인균 특히 그람 양성균과 음성균에 의한 뇌막염을 비 교 분석하여 치료 및 예후의 개선을 도모하고자 본 연구를 시행하였다. 방 법 : 1991년 1월부터 1996년 6월까지 중앙 길병원 신생아 중환자실과 소아과 병동에서 뇌척수액 검사상 균이 배양되었거나 latex agglutination test상 균이 밝혀진 24례를 대상으로 후향적으로 분석하였다. 결 과 : 1) 환아의 분포는 남아 17명, 여아 7명이었고, 그람 양성균에 의한 뇌막염 환아의 평균 출생 체중과 재태 기간은 $2.91{\pm}0.79kg$, $38.4{\pm}2.74$주, 그람 음성균군에서는 $3.30{\pm}0.90kg$, $37.7{\pm}3.33$ 주로 두 군간에 유의한 차이는 보이지 않았다. 2) 선행 요인으로는 미숙아, 태변 착색, 조기 양막 파수, 산모 당뇨병, 임신성 고혈압 등이 있었으며, 임상 증상 및 증후로는 발열, 경련, 수유량 감소, 대천문 팽대 등이 있었고, 증상 발현 시기는 조기 발현형이 11례(그람 양성균 4례, 그람 음성균 7례), 지연 발현형이 13례 (그람 양성균 7례, 그람 음성균 6례)였다. 3) 원인균은 그람 양성균이 11례로 coagulase-negative staphylococci와 group B streptococci가 각 3례, Staphyolococcus aureus와 Streptococcus viridans가 각 2례, enterococci가 1례가 있었으며, 그람 음성균은 13례로 Escherichia coli가 7례, Klebsiella pneumoniae가 3례 Pseudomonas aeruginosa, Acinetobactor, Emterobacter가 각 1례씩 있었다. 4) 뇌척수액 검사상 백혈구 수치는 그람 음성균군에서 통계적으로 유의하게 높았으나 단백 수치와 당 수치는 두 군간에 통계적으로 유의한 차이를 보이지 않았다. 5) 뇌초음파 검사상 그람 양성균군에서는 7례(63.6%)에서, 그람 음성균군에서는 10례 (76.9%)에서 비정상 소견을 보였으나 두 군간에 뇌초음파 검사상 비정상 소견의 빈도에 있어서는 통계적으로 유의한 차이를 보이지 않았다. 6) 항생제 감수성 검사에서 그람 양성균군에서는 penicillin계통, 1세대 cephalosporin, vancomycin에, 그람 음성균군에서는 amikacin과 3세대 cephalosporin에 대해 비교적 높은 감수성을 보였다. 7) 사망율(병원내 사망이나 hopeless discharge)은 20.8%(5례)였으며, 예후는 그람 양성균 군과 그람 음성균군에서 통계적으로 유의한 차이를 보이지 않았다. 결 론 : 신생아 세균성 뇌막염은 그람 양성균과 그람 음성균 간의 빈도와 예후의 차이는 보이지 않았고 예후가 불량하므로 세균성 뇌막염이 의심되는 환아에서는 적극적인 치료가 필요하리라 사료된다.