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When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma

Arterial leiomyosarcomas account for up to 21% of vascular leiomyosarcomas, with 56% of arterial leiomyosarcomas occurring in the pulmonary artery. While isolated cases of primary pulmonary artery leiomyosarcoma document survival up to 36 months after treatment, these uncommon, aggressive tumors are...

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Autores principales: Muganlinskaya, Nargiz, Guzman, Amanda, Dahagam, Chanukya, Selinger, Stephen R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677584/
https://www.ncbi.nlm.nih.gov/pubmed/26653696
http://dx.doi.org/10.3402/jchimp.v5.29624
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author Muganlinskaya, Nargiz
Guzman, Amanda
Dahagam, Chanukya
Selinger, Stephen R.
author_facet Muganlinskaya, Nargiz
Guzman, Amanda
Dahagam, Chanukya
Selinger, Stephen R.
author_sort Muganlinskaya, Nargiz
collection PubMed
description Arterial leiomyosarcomas account for up to 21% of vascular leiomyosarcomas, with 56% of arterial leiomyosarcomas occurring in the pulmonary artery. While isolated cases of primary pulmonary artery leiomyosarcoma document survival up to 36 months after treatment, these uncommon, aggressive tumors are highly lethal, with 1-year survival estimated at 20% from the onset of symptoms. We discuss a rare case of a pulmonary artery leiomyosarcoma that was originally diagnosed as a pulmonary embolism (PE). A 72-year-old Caucasian female was initially diagnosed with ‘saddle pulmonary embolism’ based on computerized tomographic angiography of the chest 2 months prior to admission and placed on anticoagulation. Dyspnea escalated, and serial computed tomography scans showed cardiomegaly with pulmonary emboli involving the right and left main pulmonary arteries with extension into the right and left upper and lower lobe branches. An echocardiogram on admission showed severe pulmonary hypertension with a pulmonary artery pressure of 82.9 mm Hg, and a severely enlarged right ventricle. Respiratory distress and multiorgan failure developed and, unfortunately, the patient expired. Autopsy showed a lobulated, yellow mass throughout the main pulmonary arteries measuring 13 cm in diameter. The mass extended into the parenchyma of the right upper lobe. On microscopy, the mass was consistent with a high-grade primary pulmonary artery leiomyosarcoma. Median survival of patients with primary pulmonary artery leiomyosarcoma without surgery is one and a half months, and mortality is usually due to right-sided heart failure. Pulmonary artery leiomyosarcoma is a rare but highly lethal disease commonly mistaken for PE. Thus, we recommend clinicians to suspect this malignancy when anticoagulation fails to relieve initial symptoms. In conclusion, early detection and suspicion of pulmonary artery leiomyosarcoma should be considered in patients refractory to anticoagulation, prompting initiation of early intervention.
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spelling pubmed-46775842016-01-05 When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma Muganlinskaya, Nargiz Guzman, Amanda Dahagam, Chanukya Selinger, Stephen R. J Community Hosp Intern Med Perspect Case Report Arterial leiomyosarcomas account for up to 21% of vascular leiomyosarcomas, with 56% of arterial leiomyosarcomas occurring in the pulmonary artery. While isolated cases of primary pulmonary artery leiomyosarcoma document survival up to 36 months after treatment, these uncommon, aggressive tumors are highly lethal, with 1-year survival estimated at 20% from the onset of symptoms. We discuss a rare case of a pulmonary artery leiomyosarcoma that was originally diagnosed as a pulmonary embolism (PE). A 72-year-old Caucasian female was initially diagnosed with ‘saddle pulmonary embolism’ based on computerized tomographic angiography of the chest 2 months prior to admission and placed on anticoagulation. Dyspnea escalated, and serial computed tomography scans showed cardiomegaly with pulmonary emboli involving the right and left main pulmonary arteries with extension into the right and left upper and lower lobe branches. An echocardiogram on admission showed severe pulmonary hypertension with a pulmonary artery pressure of 82.9 mm Hg, and a severely enlarged right ventricle. Respiratory distress and multiorgan failure developed and, unfortunately, the patient expired. Autopsy showed a lobulated, yellow mass throughout the main pulmonary arteries measuring 13 cm in diameter. The mass extended into the parenchyma of the right upper lobe. On microscopy, the mass was consistent with a high-grade primary pulmonary artery leiomyosarcoma. Median survival of patients with primary pulmonary artery leiomyosarcoma without surgery is one and a half months, and mortality is usually due to right-sided heart failure. Pulmonary artery leiomyosarcoma is a rare but highly lethal disease commonly mistaken for PE. Thus, we recommend clinicians to suspect this malignancy when anticoagulation fails to relieve initial symptoms. In conclusion, early detection and suspicion of pulmonary artery leiomyosarcoma should be considered in patients refractory to anticoagulation, prompting initiation of early intervention. Co-Action Publishing 2015-12-11 /pmc/articles/PMC4677584/ /pubmed/26653696 http://dx.doi.org/10.3402/jchimp.v5.29624 Text en © 2015 Nargiz Muganlinskaya et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Muganlinskaya, Nargiz
Guzman, Amanda
Dahagam, Chanukya
Selinger, Stephen R.
When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
title When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
title_full When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
title_fullStr When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
title_full_unstemmed When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
title_short When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
title_sort when a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677584/
https://www.ncbi.nlm.nih.gov/pubmed/26653696
http://dx.doi.org/10.3402/jchimp.v5.29624
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