unilateral absence of a pulmonary artery (uapa): case report and literature review

نویسندگان

hosseinali jelvehmoghadam anesthesiology research center, loghman hakim medical center, shahid beheshti university of medical sciences, tehran, iran

maziar mobasher department of critical care, shahid madani medical center, alborz university of medical sciences, karaj, iran.

sevak hatamian alborz university of medical sciences

hooman bahrami motlagh beheshti university of medical sciences

چکیده

one of the more infrequent congenital diseases with a wide spectrum of symptoms and more complications of the right side of pulmonary artery (63% according to ten harkel) is unilateral pulmonary artery agenesis (upaa). the clinical presentation is variable, and many patients can be asymptomatic for many years and even throughout their lives. although the disease more frequently appears in childhood with moderate to severe respiratory symptoms, some patients continue living with the disease up to adulthood. the abnormality is sometimes concurrent with cardiac anomalies. patients with uapa may be asymptomatic or may present with recurrent pulmonary infections. in a report, a 25-year old woman who had inductional termination of pregnancy at 35 week last menstrual period (lmp) in a rural hospital due to preeclampsia reported as the uapa patient.

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عنوان ژورنال:
archives of anesthesiology and critical care

جلد ۲۰۱۶، شماره ۰۵، صفحات ۰-۰

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