Partial anomalous pulmonary venous connection differential diagnosis: Difference between revisions
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{{Partial anomalous pulmonary venous connection}} | {{Partial anomalous pulmonary venous connection}} | ||
{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto: | {{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh13579@gmail.com], [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu]; '''Assistant Editor(s)-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | ||
==Overview== | ==Overview== |
Latest revision as of 16:54, 2 November 2012
Partial anomalous pulmonary venous connection Microchapters |
Differentiating Partial anomalous pulmonary venous connection from other Diseases |
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Diagnosis |
Treatment |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2], Keri Shafer, M.D. [3]; Assistant Editor(s)-In-Chief: Kristin Feeney, B.S. [4]
Overview
During diagnostic evaluation, it is important to recognize that signs and symptoms of partial anomalous pulmonary venous connection can be similar to other congenital heart diseases.
Differentiation of PAPVC from Total Anomalous Pulmonary Venous Connection (TAPVC)
PAPVC is present in approximately 10% of patients with an ASD. Depending upon the hemodynamics and magnitude and direction of shunting, an ASD may either improve or exacerbate the shunting associated with a PAPVC. These two defects have a common embryologic origin. However, in contrast to PAPVC, in TAPVC all pulmonary venous return is to the right atrium.