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A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report

Patient: Female, 25-year-old Final Diagnosis: High-risk pulmonary embolism • hyperhomocysteinemia • primary antiphospholipid syndrome Symptoms: Arterial hypotension • sudden-onset dyspnea • tachycardia • tachypnea Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Challenging differential diagno...

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Autores principales: Muñoz-Moreno, Juan-Manuel, Ramos-Yataco, Anthony, Salcedo-Davila, Emanuel, Alcalde-Loyola, Carlos, Halanoca-Quispe, Carina, Requena-Armas, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106094/
https://www.ncbi.nlm.nih.gov/pubmed/37041727
http://dx.doi.org/10.12659/AJCR.939078
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author Muñoz-Moreno, Juan-Manuel
Ramos-Yataco, Anthony
Salcedo-Davila, Emanuel
Alcalde-Loyola, Carlos
Halanoca-Quispe, Carina
Requena-Armas, Carlos
author_facet Muñoz-Moreno, Juan-Manuel
Ramos-Yataco, Anthony
Salcedo-Davila, Emanuel
Alcalde-Loyola, Carlos
Halanoca-Quispe, Carina
Requena-Armas, Carlos
author_sort Muñoz-Moreno, Juan-Manuel
collection PubMed
description Patient: Female, 25-year-old Final Diagnosis: High-risk pulmonary embolism • hyperhomocysteinemia • primary antiphospholipid syndrome Symptoms: Arterial hypotension • sudden-onset dyspnea • tachycardia • tachypnea Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Challenging differential diagnosis BACKGROUND: High-risk pulmonary embolism (PE) occurs when the pulmonary circulation is suddenly occluded by a thrombus and is a life-threatening medical emergency. In young and otherwise healthy individuals, there may be un-diagnosed underlying risk factors for PE that require investigation. This report presents the case of a 25-year-old woman admitted as an emergency with a high-risk large and occlusive PE, later diagnosed with primary antiphospholipid syndrome (APS) and hyperhomocysteinemia. CASE REPORT: A 25-year-old woman presented with sudden-onset dyspnea after elective cholecystectomy. One year earlier, the patient had lower limb deep vein thrombosis without an identified predisposing cause, and she received anticoagulation for 6 months. On physical examination, she had right leg edema. Laboratory tests revealed elevated levels of troponin, pro-B-type natriuretic peptide, and D-dimer. Computed tomography pulmonary angiography (CTPA) demonstrated a large and occlusive PE, and an echocardiogram showed right ventricular dys-function. Successful thrombolysis was performed with alteplase. On repeat CTPA, a significant reduction in filling defects in the pulmonary vasculature was observed. The patient evolved uneventfully and was discharged home on a vitamin K antagonist. Due to unprovoked recurrent thrombotic events, suspicion of underlying thrombophilia was raised, and hypercoagulability studies confirmed primary APS and hyperhomocysteinemia. CONCLUSIONS: This report presents the case of a life-threatening high-risk PE in a previously healthy young woman and highlights the importance of emergency management followed by investigation and treatment of underlying risk factors for venous thromboembolism, including APS and hyperhomocysteinemia.
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spelling pubmed-101060942023-04-17 A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report Muñoz-Moreno, Juan-Manuel Ramos-Yataco, Anthony Salcedo-Davila, Emanuel Alcalde-Loyola, Carlos Halanoca-Quispe, Carina Requena-Armas, Carlos Am J Case Rep Articles Patient: Female, 25-year-old Final Diagnosis: High-risk pulmonary embolism • hyperhomocysteinemia • primary antiphospholipid syndrome Symptoms: Arterial hypotension • sudden-onset dyspnea • tachycardia • tachypnea Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Challenging differential diagnosis BACKGROUND: High-risk pulmonary embolism (PE) occurs when the pulmonary circulation is suddenly occluded by a thrombus and is a life-threatening medical emergency. In young and otherwise healthy individuals, there may be un-diagnosed underlying risk factors for PE that require investigation. This report presents the case of a 25-year-old woman admitted as an emergency with a high-risk large and occlusive PE, later diagnosed with primary antiphospholipid syndrome (APS) and hyperhomocysteinemia. CASE REPORT: A 25-year-old woman presented with sudden-onset dyspnea after elective cholecystectomy. One year earlier, the patient had lower limb deep vein thrombosis without an identified predisposing cause, and she received anticoagulation for 6 months. On physical examination, she had right leg edema. Laboratory tests revealed elevated levels of troponin, pro-B-type natriuretic peptide, and D-dimer. Computed tomography pulmonary angiography (CTPA) demonstrated a large and occlusive PE, and an echocardiogram showed right ventricular dys-function. Successful thrombolysis was performed with alteplase. On repeat CTPA, a significant reduction in filling defects in the pulmonary vasculature was observed. The patient evolved uneventfully and was discharged home on a vitamin K antagonist. Due to unprovoked recurrent thrombotic events, suspicion of underlying thrombophilia was raised, and hypercoagulability studies confirmed primary APS and hyperhomocysteinemia. CONCLUSIONS: This report presents the case of a life-threatening high-risk PE in a previously healthy young woman and highlights the importance of emergency management followed by investigation and treatment of underlying risk factors for venous thromboembolism, including APS and hyperhomocysteinemia. International Scientific Literature, Inc. 2023-04-12 /pmc/articles/PMC10106094/ /pubmed/37041727 http://dx.doi.org/10.12659/AJCR.939078 Text en © Am J Case Rep, 2023 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Muñoz-Moreno, Juan-Manuel
Ramos-Yataco, Anthony
Salcedo-Davila, Emanuel
Alcalde-Loyola, Carlos
Halanoca-Quispe, Carina
Requena-Armas, Carlos
A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report
title A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report
title_full A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report
title_fullStr A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report
title_full_unstemmed A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report
title_short A 25-Year-Old Woman with a High-Risk Large and Occlusive Pulmonary Embolism, Later Diagnosed with Primary Antiphospholipid Syndrome and Hyperhomocysteinemia: A Case Report
title_sort 25-year-old woman with a high-risk large and occlusive pulmonary embolism, later diagnosed with primary antiphospholipid syndrome and hyperhomocysteinemia: a case report
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106094/
https://www.ncbi.nlm.nih.gov/pubmed/37041727
http://dx.doi.org/10.12659/AJCR.939078
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