Congenital Cystic Adenomatoid Malformation Diagnosed During First-Trimester Ultrasound Scan
| Autor: | Georges A. Markou, Christophe Poncelet, Georgios Dafereras |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Adult
medicine.medical_specialty Diaphragmatic breathing Prenatal diagnosis Ultrasonography Prenatal Congenital Abnormalities Diagnosis Differential 03 medical and health sciences 0302 clinical medicine Fetus Pregnancy Cystic Adenomatoid Malformation of Lung Congenital Prenatal Diagnosis medicine Humans 030212 general & internal medicine Stage (cooking) Abortion Therapeutic Lung business.industry Gestational age General Medicine Articles medicine.disease Pregnancy Trimester First medicine.anatomical_structure 030228 respiratory system Gestation Female Radiology business |
| Zdroj: | The American Journal of Case Reports |
| ISSN: | 1941-5923 |
| Popis: | Patient: Female, 26 Final Diagnosis: Congenital cystic adenomatoid malformation (CCAM) Symptoms: Inconveniently • polyhydramnios Medication: — Clinical Procedure: Termination of pregnancy Specialty: Obstetrics and Gynecology Objective: Congenital defects/diseases Background: Congenital cystic adenomatoid malformation (CCAM) is mostly reported from the second trimester of pregnancy. We report a case of a microcystic type of CCAM that was suggested by routine ultrasound examination at a gestational age of 12 weeks. Case Report: First-trimester ultrasound screening revealed the presence of a hyperechoic image that occupied the whole of the right lung, without no other any associated complications. The cardiac and aorta deviations with diaphragmatic eversion associated with a poly-hydramnios had subsequently appeared. The diagnosis of CCAM was confirmed histologically after termination of the pregnancy at 25 weeks of gestation. Conclusions: CCAM may occur at a very early stage of fetal lung development. |
| Databáze: | OpenAIRE |
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