ABSTRACT
Lymphangiomas are rare congenital malformations of the lymphatic system. Authors present a case with giant, septated, axillary thoraco-abdominal lymphangioma. Diagnosis was made at 19 weeks’ gestation by antenatal ultrasonography. The case underwent prenatal expectation treatment.
ABSTRACT
Cervical branchial cleft cysts are uncommon lesion that are developed from remnants of branchial apparatus in embryonal period. These cysts are found in infancy, childhood and adult by recurrent symptoms related to inflammation. It is difficult to find these cysts with antenatal ultrasonography and differential diagnosis from other cervical cysts is difficult too. We experienced a case of fetal cervical branchial cleft cyst that was found with antenatal ultrasonography and diagnosed with surgical biopsy, so we report our case with brief review of literatures.
Subject(s)
Adult , Humans , Biopsy , Branchial Region , Branchioma , Diagnosis, Differential , Fetus , InflammationABSTRACT
Congenital pleural effusions are uncommon. The majority of cases are due to chylothorax, hydrops fetalis, and infection. Effusions of this nature are, for the most part, self-limited. We experienced a rare case of a congenital unilateral pleural effusion due to an extralobar sequestraion with pulmonary lymphangiectasia. Pleural effusion was found by antenatal ultrasonography and confirmed by CT scans and CT angiography of the chest in the neonatal period. The patient underwent an open thoracotomy where extralobar sequestraion located between the diaphragm and the left lower lobe was removed. His postoperative course was uncomplicated and there was complete resolution of the pleural effusion.
Subject(s)
Humans , Angiography , Bronchopulmonary Sequestration , Chylothorax , Diaphragm , Hydrops Fetalis , Pleural Effusion , Thoracotomy , Thorax , Tomography, X-Ray Computed , UltrasonographyABSTRACT
OBJECTIVE: We evaluated the association between perinatal prognosis and the presence of septation in cystic hygroma deteted by antenatal ultrasonography. METHODS: During a 5-year period, 65 cases of cystic hygroma were diagnosed by antenatal ultrasonography. 31 cases were included in this study. Fetal karyotyping, hydrops, and associated anomalies were compared between septated and non-septated groups. Statistical analysis was performed using Fisher exact test. RESULTS: There were 24 cases of septated cystic hygromas, and 7 cases of nonseptated cystic hygromas. Sixty-three percent of the septated cystic hygromas had accompanying hydrops and other anomalies (15/24), versus 28% (2/7) in the nonseptated group (p=0.022). Other anomalies such as cleft lip and palate, omphalocele, and club foot were more frequently seen in the septated group. Nine of 14 cases of septated cystic hygroma that underwent karyotying showed aneuploidy (64%), compared with 0% (0 of 6 cases) aneuploidy rate in the nonseptated cystic hygroma group (p=0.014). CONCLUSION: Abnormal fetal karyotyping, hydrops, and other anomalies are more likely to be associated in fetuses with septated cystic hygroma. So, the presence of septation may be the useful prognostic indicator of cystic hygroma.
Subject(s)
Aneuploidy , Cleft Lip , Edema , Fetus , Foot , Hernia, Umbilical , Karyotyping , Lymphangioma, Cystic , Palate , Prognosis , UltrasonographyABSTRACT
OBJECTIVE: To determine the proportion and the types of CNS anomalies among congenital anomalies detected through prenatal ultrasonography. MATERIALS AND METHODS: Between November 1997 and December 2000, 624 cases of singleton pregnancies were terminated at Department of Obstetrics and Gynecology, CHA Hospital due to lethal congenital anomalies detected through prenatal ultrasound. Forty-three of 624 termination cases had CNS anomalies. Autopsy and chromosomal study was carried out on ten and six cases respectively. Incidence, maternal age and parity, sex ratio and body weight of the terminated fetuses, gestational age at which anomaly was detected, associated anomalies were evaluated. RESULTS: The incidence of CNS anomalies was 0.21%(43 in 20,805), and maternal age was between 30 and 34 in 20cases. The fetus was male in 25 cases, female in 11 cases and indefinite in 7 cases. Anomalies were detected between 17-20 weeks in 12 cases. Body weights of the terminated fetuses were below 500grams in 23 cases. Anencephaly was the most common with 11 cases(25.6%), hydrocephalus ranked second with 8 cases(18.6%). Two cases had associated anomalies of Meckel-Gruber syndrome features. CONCLUSION: CNS anomalies are frequent and have a severe prognosis. Contemporary ultrasound is much accurate in evaluating CNS anomalies. Still, minor anomalies and those cases without associated anomalies are difficult to detect. Even after diagnosis, CNS anomalies are mostly void of prenatal corrective treatment. Fortuitous investigation is needed for prenatal neural axis anomaly detection.
Subject(s)
Female , Humans , Male , Pregnancy , Anencephaly , Autopsy , Axis, Cervical Vertebra , Body Weight , Central Nervous System , Diagnosis , Fetus , Gestational Age , Gynecology , Hydrocephalus , Incidence , Maternal Age , Obstetrics , Parity , Prognosis , Sex Ratio , Ultrasonography , Ultrasonography, PrenatalABSTRACT
Hemangioendothelioma is the most common tumor of liver in infancy characterized by heart failure due to arteriovenous shunt and thrombocytopenia. Recently with the advance of technology, this tumor can be diagnosed with antenatal ultrasonography. We report a case of hemangioendothelioma that demonstrates huge abdominal mass with increased blood flow in liver detected by ultrasonography.
Subject(s)
Heart Failure , Hemangioendothelioma , Liver , Thrombocytopenia , UltrasonographyABSTRACT
OBJECTIVE: To obtain clinically useful data regarding prenatal diagnosis, proper antepartum counseling and obstetric management in pregnancies with fetal dysplastic kidney disease. METHODS: We retrospectively reviewed 13 cases of MCDK(Multicystic dysplastic kidney) and PCDK(Polycystic dysplastic kidney), diagnosed by antenatal ultrasound and delivered from June 1994 through July 1999 at Ajou University School of Medicine, Department of Obstetrics and Gynecology, with regard to prenatal ultrasonographic findings, perinatal outcomes, maternal complications and associated fetal anomalies. RESULTS: The incidence of MCDK and PCDK was one in 1,066 and one in 2,398 births, respectively. Of the 9 cases of MCDK, one case was terminated due to severely associated anomaly, and 6 cases were delivered by spontaneous labor or pitocin induction at term, of which 1 case was delivered by pitocin induction at 36 weeks gestation due to intrauterine fetal death. Two cases were delivered by cesarean section. There were no neonatal deaths in 7 cases of MCDK and they have been followed up to date, and alive. Of the 4 cases of PCDK, 3 cases were terminated by induced abortion or induced vaginal delivery, and 1 case was delivered by cesarean section, which was combined with hypertrophic cardiomyopathy, and the baby died within 24 hours after birth. Perinatal complications consisted of small for gestational age, urinary tract infection, hydronephrosis, acute respiratory failure, acute renal failure, periventricular hemorrhage and laryngomalacia in the neonatal period. CONCLUSION: It is suggested that antenatal ultrasonography and genetic analysis to evaluate accurate diagnosis and associated anomalies should be performed to manage and councel properly the pregnancies with fetal dysplastic kidney disease.
Subject(s)
Female , Humans , Pregnancy , Abortion, Induced , Acute Kidney Injury , Cardiomyopathy, Hypertrophic , Cesarean Section , Counseling , Diagnosis , Fetal Death , Gestational Age , Gynecology , Hemorrhage , Hydronephrosis , Incidence , Kidney Diseases , Kidney , Laryngomalacia , Obstetrics , Oxytocin , Parturition , Prenatal Diagnosis , Respiratory Insufficiency , Retrospective Studies , Ultrasonography , Urinary Tract InfectionsABSTRACT
Holt-Oram Syndrome is an autosomal dominant disorder characterized by the association of upper-limb abnormalities and congenital heart disease. A woman with no family history of genetic disease underwent antenatal sonography at 27 weeks' menstrual age to screen for fetal anomalies. Ultrasonography revealed abnormalities in the upper limbs. The limb abnormalities included abscence of bilateral thumbs and radius: the left humus was short. Pregnancy termination was performed. The postnatal chromosomal analysis revealed a normal 46XX karyotype and the autopsy finding confirmed the Holt-Oram syndrome. We report a case of Holt-Oram Syndrome in fetus with unaffected parents with brief of the literatures.