A Case of Unilateral Pulmonary Artery Agenesis

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Unilateral pulmonary artery agenesis: a case series.

BACKGROUND Unilateral pulmonary artery agenesis (UPAA) is a rare congenital anomaly due to a malformation of the sixth aortic arch of the affected side during embryogenesis. The diagnosis is usually set at adolescence, however it can remain asymptomatic and late diagnosis is possible. DESCRIPTION We present a case series of three female patients, aged 18, 49 and 68 years old, with history of ...

متن کامل

Isolated unilateral pulmonary artery agenesis.

A 33-year-old woman with a history of psoriasis presented with asymmetric oligoarthritis. She had no cardiovascular symptoms. Naproxen and steroids were started with the diagnosis of psoriatic arthritis. Routine chest X-ray showed a small left hemithorax with a right-sided aortic arch and decreased left-sided pulmonary vasculature. A CTscan (Picture A) demonstrated the absence of the left pulmo...

متن کامل

Incidentally detected isolated unilateral pulmonary artery agenesis.

We are reporting here, a case of an incidentally detected, isolated, unilateral pulmonary artery agenesis on contrast enhanced Computed Tomography (CT) of the chest in a 39-year-old male patient.

متن کامل

Pneumothorax in a Patient with Unilateral Pulmonary Artery Agenesis

A 17-year-old Japanese woman presented with right chest pain and exertional dyspnea. The patient had a history of isolated unilateral absence of the right pulmonary artery (UAPA) and pulmonary hypertension from early childhood. Chest radiography revealed right-sided pneumothorax and a small lung volume with mediastinal and tracheal shift to the right as well as right diaphragm elevation (Pictur...

متن کامل

Pulmonary Artery Agenesis: A Case Series

Pulmonary artery agenesis is a rare congenital abnormality in which atresia was encountered in the short segment of the right or left pulmonary arteries. It can be isolated or associated with cardiac abnormalities such as tetralogy of Fallot, septal defects or pulmonary stenosis. The majority of cases are diagnosed in childhood whereas some cases yield no symptoms until adulthood. We evaluated ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Chest

سال: 2016

ISSN: 0012-3692

DOI: 10.1016/j.chest.2016.08.1342