Cargando…
Partial anomalous pulmonary venous connection associated with hemoptysis: A case report
RATIONALE: Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital anomaly characterized by the failure of fusion of embryologic pulmonary venous system with left atrium. PATIENT CONCERNS: A 45-year-old male patient with PAPVC who was hospitalized because of mild hemoptysis. Image...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571256/ https://www.ncbi.nlm.nih.gov/pubmed/31169699 http://dx.doi.org/10.1097/MD.0000000000015893 |
_version_ | 1783427374086356992 |
---|---|
author | Li, ChengCheng Teng, Peng Yang, Yanyan Ni, Yiming Ma, Liang |
author_facet | Li, ChengCheng Teng, Peng Yang, Yanyan Ni, Yiming Ma, Liang |
author_sort | Li, ChengCheng |
collection | PubMed |
description | RATIONALE: Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital anomaly characterized by the failure of fusion of embryologic pulmonary venous system with left atrium. PATIENT CONCERNS: A 45-year-old male patient with PAPVC who was hospitalized because of mild hemoptysis. Images showed the anomalous vein originated from the left upper pulmonary vein and flowed into the left brachiocephalic vein. No other underlying causes for hemoptysis were detected. DIAGNOSIS: After multi-disciplinary discussion, the patient was diagnosed as PAPVC of left upper pulmonary vein draining into the left brachiocephalic vein with intact atrial septum. INTERVENTIONS: Although surgical correction of PAPVC was feasible, left upper lobectomy was performed as the definitive treatment for both hemoptysis and PAPVC. OUTCOMES: The patient had an uneventful postoperative hospital course and was followed up for nearly 2 years without recurrence of hemoptysis. LESSONS: PAPVC is associated with atrial septal defect in 80% to 90% of cases while isolated PAPVC with intact atrial septum is an extremely rare entity. We present a rare isolated PAPVC patient with hemoptysis. To our best knowledge, PAPVC associated with hemoptysis has never been reported before. |
format | Online Article Text |
id | pubmed-6571256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-65712562019-07-22 Partial anomalous pulmonary venous connection associated with hemoptysis: A case report Li, ChengCheng Teng, Peng Yang, Yanyan Ni, Yiming Ma, Liang Medicine (Baltimore) Research Article RATIONALE: Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital anomaly characterized by the failure of fusion of embryologic pulmonary venous system with left atrium. PATIENT CONCERNS: A 45-year-old male patient with PAPVC who was hospitalized because of mild hemoptysis. Images showed the anomalous vein originated from the left upper pulmonary vein and flowed into the left brachiocephalic vein. No other underlying causes for hemoptysis were detected. DIAGNOSIS: After multi-disciplinary discussion, the patient was diagnosed as PAPVC of left upper pulmonary vein draining into the left brachiocephalic vein with intact atrial septum. INTERVENTIONS: Although surgical correction of PAPVC was feasible, left upper lobectomy was performed as the definitive treatment for both hemoptysis and PAPVC. OUTCOMES: The patient had an uneventful postoperative hospital course and was followed up for nearly 2 years without recurrence of hemoptysis. LESSONS: PAPVC is associated with atrial septal defect in 80% to 90% of cases while isolated PAPVC with intact atrial septum is an extremely rare entity. We present a rare isolated PAPVC patient with hemoptysis. To our best knowledge, PAPVC associated with hemoptysis has never been reported before. Wolters Kluwer Health 2019-06-07 /pmc/articles/PMC6571256/ /pubmed/31169699 http://dx.doi.org/10.1097/MD.0000000000015893 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Research Article Li, ChengCheng Teng, Peng Yang, Yanyan Ni, Yiming Ma, Liang Partial anomalous pulmonary venous connection associated with hemoptysis: A case report |
title | Partial anomalous pulmonary venous connection associated with hemoptysis: A case report |
title_full | Partial anomalous pulmonary venous connection associated with hemoptysis: A case report |
title_fullStr | Partial anomalous pulmonary venous connection associated with hemoptysis: A case report |
title_full_unstemmed | Partial anomalous pulmonary venous connection associated with hemoptysis: A case report |
title_short | Partial anomalous pulmonary venous connection associated with hemoptysis: A case report |
title_sort | partial anomalous pulmonary venous connection associated with hemoptysis: a case report |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571256/ https://www.ncbi.nlm.nih.gov/pubmed/31169699 http://dx.doi.org/10.1097/MD.0000000000015893 |
work_keys_str_mv | AT lichengcheng partialanomalouspulmonaryvenousconnectionassociatedwithhemoptysisacasereport AT tengpeng partialanomalouspulmonaryvenousconnectionassociatedwithhemoptysisacasereport AT yangyanyan partialanomalouspulmonaryvenousconnectionassociatedwithhemoptysisacasereport AT niyiming partialanomalouspulmonaryvenousconnectionassociatedwithhemoptysisacasereport AT maliang partialanomalouspulmonaryvenousconnectionassociatedwithhemoptysisacasereport |