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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2023
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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. |
format | Online Article Text |
id | pubmed-10106094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
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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