Prenatal diagnosis of an obstructive mediastinal bronchogenic cyst

1995 ◽  
Vol 5 (2) ◽  
pp. 194-196
Author(s):  
Chandrakant R. Patel ◽  
Kevin L. Muise ◽  
Marc M. Levine

SummaryWe report a patient with a mediastinal cyst compressing the left atrium that was diagnosed prenatally by fetal echocardiography. Postnatally, attempted aspiration guided by computerized tomography was unsuccessful. Because of respiratory distress, the cyst was removed surgically. Pathological examination revealed a bronchogenic cyst.

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Livia Teresa Moreira Rios ◽  
Edward Araujo Júnior ◽  
Luciano Marcondes Machado Nardozza ◽  
Antonio Fernandes Moron ◽  
Marília da Glória Martins

Bronchogenic cysts arise from abnormal buds from the primitive esophagus and tracheobronchial tree, which do not extend to the site where alveolar differentiation occurs. Bronchogenic cysts are typically unilocular mucus field lesions arising from posterior membranous wall of the air way. The prenatal diagnosis usually is realized by two-dimensional ultrasound showing the large unilocular cystic image in the chest fetus. The prenatal percutaneous aspiration can reduce the risk of heart compression and permit better respiratory conditions to newborn. We present a case of a primiparous pregnant 23 year-old-woman prenatal ultrasound showed a large unilocular cyst in the left hemithorax with compression of the normal left lung tissue and contralateral mediastinal shift. This cyst was percutaneously aspirated without subsequent reaccumulation of fluid. The newborn did not have respiratory distress and the computed tomography scan confirmed the finding of a fluid-filled cyst in the left chest. The chest X-ray showed the displacement of the heart and the mediastinum from the left to the right. The prenatal diagnosis of bronchogenic cyst is very important to assess the degree of the compression of the normal lung and the mediastinum shift. Furthermore, the prenatal diagnosis permits planning delivery in the tertiary hospital with multidisciplinary team because of the risk of respiratory distress.


2002 ◽  
Vol 2 (4) ◽  
pp. 251-260
Author(s):  
J. M. Martínez ◽  
O. Gómez ◽  
M. del Río ◽  
B. Puerto ◽  
A. Borrell ◽  
...  

2021 ◽  
pp. 1-3
Author(s):  
Claire Bertail-Galoin

Abstract A fistula between the pulmonary artery and the left atrium is a rare entity and its diagnosis is uncommon in the neonatal period. There are more reported surgical treatments in the literature than with a transcatheter closure. We report the case of a prenatal diagnosis of a large fistula between the right pulmonary artery and the left atrium with successful transcatheter closure with an Amplatzer duct occluder II 6/4 mm.


2017 ◽  
Vol 5 (2) ◽  
pp. 193-196 ◽  
Author(s):  
Ramush Bejiqi ◽  
Ragip Retkoceri ◽  
Hana Bejiqi

BACKGROUND: Cardiac rhabdomyoma (CRs) are the most common primary tumour of the heart in infants and children. Usually are multiple and, basing on the location can cause a haemodynamic disturbance, dysrhythmias or heart failure during the fetal and early postnatal period. CRs have a natural history of spontaneous regression and are closely associated with tuberous sclerosis complex (TSC). It has an association with tuberous sclerosis (TS), and in those, the tumour may regress and disappear completely, or remain consistent in size. AIM: We aimed to evaluate the prenatal diagnosis, clinical presentation and outcome of CRs and their association with TSC in a single centre. The median follow-up period was three years (range: 6 months - 5 years). MATERIAL AND METHODS: We reviewed medical records of all fetuses diagnosed prenatally with cardiac rhabdomyoma covering the period January 2010 to December 2016 which had undergone detailed ultrasound evaluation at a single centre with limited technical resources. RESULTS: Twelve fetuses were included in the study; mostly had multiple tumours and a total of 53 tumours were identified in all patients - the maximum was one fetus with16 tumours. All patients were diagnosed prenatally by fetal echocardiography. In two patient's haemodynamic disturbances during the fetal period was noted and pregnancies have been terminated. After long consultation termination of pregnancy was chosen by the parents in totally 8 cases. In four continuing pregnancies during the first year of live tumours regressed. TSC was diagnosed in all patients during the follow-up. CONCLUSIONS: Cardiac rhabdomyoma are benign from the cardiovascular standpoint in most affected fetuses. An early prenatal diagnosis may help for an adequate planning of perinatal monitoring and treatment with the involvement of a multidisciplinary team. Large tumour size, the number of tumours and localisation may cause hydrops, and they are significantly associated with poor neonatal outcome.


1987 ◽  
Vol 7 (6) ◽  
pp. 407-411 ◽  
Author(s):  
Lawrence D. Platt ◽  
Greggory R. Devore ◽  
Janet Horenstein ◽  
Zdena Pavlova ◽  
Bruce Kovacs ◽  
...  

2014 ◽  
Vol 15 (7) ◽  
pp. 831-831 ◽  
Author(s):  
Hisao Yoshikawa ◽  
Makoto Suzuki ◽  
Raisuke Iijima ◽  
Masato Nakamura ◽  
Kaoru Sugi

2014 ◽  
Vol 115 (02) ◽  
pp. 98-100
Author(s):  
T. Maly ◽  
V. Mihal ◽  
K. Michalkova ◽  
T. Tichy ◽  
C. Neoral ◽  
...  

1987 ◽  
Vol 6 (1) ◽  
pp. 57-68 ◽  
Author(s):  
T. Barton ◽  
R. Harris ◽  
J. Weinman ◽  
L. Allan ◽  
D. Crawford

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