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Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report
Splanchnetopia accompanied with atrial septal defect is a rare congenital malformation clinically. Recent studies show that the patients are susceptible to lung disease. We present a case of a 62-year-old man who presented to our hospital with cough, palpitation and short of breath after activity. O...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358318/ https://www.ncbi.nlm.nih.gov/pubmed/28352381 http://dx.doi.org/10.4021/cr20e |
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author | Bao, Ning Zhang, Yu |
author_facet | Bao, Ning Zhang, Yu |
author_sort | Bao, Ning |
collection | PubMed |
description | Splanchnetopia accompanied with atrial septal defect is a rare congenital malformation clinically. Recent studies show that the patients are susceptible to lung disease. We present a case of a 62-year-old man who presented to our hospital with cough, palpitation and short of breath after activity. On physical examination, we found cyanosis of lips and face, swollen jugular vein, bubble sounds at the lung bottom, irregular heart rhythm, the large liver under the left rib and the lower limbs edema. Laboratory studies revealed white blood cell 18.6 × 10(9)/L and neutrophils 73.9%. Electrocardiogram showed disappearance of P wave and substituted F wave with irregular R-R interval. Ultrasound cardiogram indicated that there was a 24 mm-long gap in the middle of the atrial septal. Dextrocardia, pulmonary artery extrudes and infection of lung were found by chest x-ray. The abdomen ultrasound indicated organ flip. Clinical diagnosis was congenital heart disease, splanchnectopia, atrial septal defect, Eisenmenger’s syndrome, atrial flutter, cardiac function class III and pneumonia. The patient left hospital after 2-week treatment. Its clinical significance is when the thoracic and celiac organs are ill, the position of the symptoms and physical signs are contrary to the normal place. Therefore, we should make a careful and systematic examination of the patients in order to avoid misdiagnosis and delay in treatment. |
format | Online Article Text |
id | pubmed-5358318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53583182017-03-28 Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report Bao, Ning Zhang, Yu Cardiol Res Case Report Splanchnetopia accompanied with atrial septal defect is a rare congenital malformation clinically. Recent studies show that the patients are susceptible to lung disease. We present a case of a 62-year-old man who presented to our hospital with cough, palpitation and short of breath after activity. On physical examination, we found cyanosis of lips and face, swollen jugular vein, bubble sounds at the lung bottom, irregular heart rhythm, the large liver under the left rib and the lower limbs edema. Laboratory studies revealed white blood cell 18.6 × 10(9)/L and neutrophils 73.9%. Electrocardiogram showed disappearance of P wave and substituted F wave with irregular R-R interval. Ultrasound cardiogram indicated that there was a 24 mm-long gap in the middle of the atrial septal. Dextrocardia, pulmonary artery extrudes and infection of lung were found by chest x-ray. The abdomen ultrasound indicated organ flip. Clinical diagnosis was congenital heart disease, splanchnectopia, atrial septal defect, Eisenmenger’s syndrome, atrial flutter, cardiac function class III and pneumonia. The patient left hospital after 2-week treatment. Its clinical significance is when the thoracic and celiac organs are ill, the position of the symptoms and physical signs are contrary to the normal place. Therefore, we should make a careful and systematic examination of the patients in order to avoid misdiagnosis and delay in treatment. Elmer Press 2011-06 2011-05-20 /pmc/articles/PMC5358318/ /pubmed/28352381 http://dx.doi.org/10.4021/cr20e Text en Copyright 2011, Bao et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bao, Ning Zhang, Yu Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report |
title | Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report |
title_full | Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report |
title_fullStr | Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report |
title_full_unstemmed | Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report |
title_short | Splanchnectopia Accompanied With Atrial Septal Defect: A Case Report |
title_sort | splanchnectopia accompanied with atrial septal defect: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358318/ https://www.ncbi.nlm.nih.gov/pubmed/28352381 http://dx.doi.org/10.4021/cr20e |
work_keys_str_mv | AT baoning splanchnectopiaaccompaniedwithatrialseptaldefectacasereport AT zhangyu splanchnectopiaaccompaniedwithatrialseptaldefectacasereport |