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Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma
Scimitar syndrome is a rare congenital anomaly which is characterised by anomalous pulmonary venous drainage of the either entire right lung or part of it into the inferior vena cava or portal vein or hepatic vein or right atrium occasionally. This can be associated with hypoplasia of the right lung...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046800/ https://www.ncbi.nlm.nih.gov/pubmed/35496752 http://dx.doi.org/10.1016/j.radcr.2022.03.077 |
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author | Dasari, Nikhila Valapala, Venkat Narayana Goutham Anim, Roopa |
author_facet | Dasari, Nikhila Valapala, Venkat Narayana Goutham Anim, Roopa |
author_sort | Dasari, Nikhila |
collection | PubMed |
description | Scimitar syndrome is a rare congenital anomaly which is characterised by anomalous pulmonary venous drainage of the either entire right lung or part of it into the inferior vena cava or portal vein or hepatic vein or right atrium occasionally. This can be associated with hypoplasia of the right lung, dextroposition, underdevelopment of right pulmonary artery and anomalous systemic arterial supply from the descending aorta to the hypoplastic lung. A 36 year old female came with history of swelling in the right breast which turned up to be right breast fibroadenoma. Routine chest radiograph revealed scimitar syndrome which was confirmed on CECT chest. |
format | Online Article Text |
id | pubmed-9046800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90468002022-04-29 Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma Dasari, Nikhila Valapala, Venkat Narayana Goutham Anim, Roopa Radiol Case Rep Case Report Scimitar syndrome is a rare congenital anomaly which is characterised by anomalous pulmonary venous drainage of the either entire right lung or part of it into the inferior vena cava or portal vein or hepatic vein or right atrium occasionally. This can be associated with hypoplasia of the right lung, dextroposition, underdevelopment of right pulmonary artery and anomalous systemic arterial supply from the descending aorta to the hypoplastic lung. A 36 year old female came with history of swelling in the right breast which turned up to be right breast fibroadenoma. Routine chest radiograph revealed scimitar syndrome which was confirmed on CECT chest. Elsevier 2022-04-20 /pmc/articles/PMC9046800/ /pubmed/35496752 http://dx.doi.org/10.1016/j.radcr.2022.03.077 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Dasari, Nikhila Valapala, Venkat Narayana Goutham Anim, Roopa Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma |
title | Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma |
title_full | Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma |
title_fullStr | Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma |
title_full_unstemmed | Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma |
title_short | Scimitar syndrome – An incidental diagnosis in a case of fibroadenoma |
title_sort | scimitar syndrome – an incidental diagnosis in a case of fibroadenoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046800/ https://www.ncbi.nlm.nih.gov/pubmed/35496752 http://dx.doi.org/10.1016/j.radcr.2022.03.077 |
work_keys_str_mv | AT dasarinikhila scimitarsyndromeanincidentaldiagnosisinacaseoffibroadenoma AT valapalavenkatnarayanagoutham scimitarsyndromeanincidentaldiagnosisinacaseoffibroadenoma AT animroopa scimitarsyndromeanincidentaldiagnosisinacaseoffibroadenoma |