Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report

Introduction: Antiphospholipid antibody syndrome is a rare systemic autoimmune disease that produces a hypercoagulable state with risk of thrombosis. The ACR/EULAR APS 2023 criteria are used for diagnosis. With respect to treatment, anticoagulants and antiplatelet agents are the most used. Mixed con...

Ամբողջական նկարագրություն

Պահպանված է:
Մատենագիտական մանրամասներ
Հիմնական հեղինակ: Falconi-Toro, Daniel (author)
Այլ հեղինակներ: Bedón-Galarza , Ricardo (author), Bedoya-Dávila , Michelle (author)
Ձևաչափ: article
Լեզու:spa
Հրապարակվել է: 2024
Խորագրեր:
Առցանց հասանելիություն:https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/6426
Ցուցիչներ: Ավելացրեք ցուցիչ
Չկան պիտակներ, Եղեք առաջինը, ով նշում է այս գրառումը!
_version_ 1838811480546344960
author Falconi-Toro, Daniel
author2 Bedón-Galarza , Ricardo
Bedoya-Dávila , Michelle
author2_role author
author
author_facet Falconi-Toro, Daniel
Bedón-Galarza , Ricardo
Bedoya-Dávila , Michelle
author_role author
collection Revista Ciencias Médicas
dc.creator.none.fl_str_mv Falconi-Toro, Daniel
Bedón-Galarza , Ricardo
Bedoya-Dávila , Michelle
dc.date.none.fl_str_mv 2024-05-27
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/6426
10.29166/rfcmq.v49i2.6426
dc.language.none.fl_str_mv spa
dc.publisher.none.fl_str_mv Quito: Universidad Central del Ecuador
dc.relation.none.fl_str_mv https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/6426/8331
dc.rights.none.fl_str_mv Derechos de autor 2024 Daniel Falconi
http://creativecommons.org/licenses/by-nc-nd/4.0
info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv Revista de la Facultad de Ciencias Médicas (Quito); Vol. 49 No. 2 (2024): Revista de la Facultad de Ciencias Médicas (Quito); 42-49
Revista de la Facultad de Ciencias Médicas (Quito); Vol. 49 Núm. 2 (2024): Revista de la Facultad de Ciencias Médicas (Quito); 42-49
2737-6141
2588-0691
reponame:Revista Ciencias Médicas
instname:Universidad Central del Ecuador
instacron:UCE
dc.subject.none.fl_str_mv síndrome antifosfolipídico
enfermedad mixta del tejido conjuntivo
embolia pulmonar
lupus eritematoso sistémico
presentación de caso
Antiphospholipid Syndrome
Mixed Connective Tissue Disease
Pulmonary Embolism
Lupus Erythematosus, Systemic
Case Reports
dc.title.none.fl_str_mv Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
Síndrome antifosfolipídico trombótico en una mujer con enfermedad mixta del tejido conectivo. Reporte de caso-Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Artículo evaluado por pares
description Introduction: Antiphospholipid antibody syndrome is a rare systemic autoimmune disease that produces a hypercoagulable state with risk of thrombosis. The ACR/EULAR APS 2023 criteria are used for diagnosis. With respect to treatment, anticoagulants and antiplatelet agents are the most used. Mixed connective tissue disease is a systemic autoimmune disease that presents the association of clinical manifestations of other autoimmune entities. Objective: To describe the presentation of two rare autoimmune systemic diseases together, with the purpose of contributing a practical approach to diagnosis and management. Case presentation: A 37-year-old patient is described who presented an episode of pulmonary thromboembolism secondary to antiphospholipid antibody syndrome and who for 6 months had symptoms compatible with mixed connective tissue disease. The patient had to undergo surgery and subsequently responded to treatment. Discussion: This case revealed the presence of two autoimmune entities, antiphospholipid antibody syndrome and mixed connective tissue disease presented together and whose debut of complications was a pulmonary thromboembolism, also finding the presence of multiple positive autoantibodies between these antiphospholipid and anti-U1 antibodies snRNP, which represents a diagnostic challenge when differentiating between other connective tissue diseases such as systemic lupus erythematosus, cutaneous systemic sclerosis, mixed connective tissue disease and rheumatoid arthritis. The treatment decision was based on the patient's characteristics and clinical condition at the time of diagnosis. Conclusions: Antiphospholipid antibody syndrome entails the presence of a thrombotic episode; on the other hand, its association with a mixed connective tissue disease is rare and may increase its morbidity and mortality.
eu_rights_str_mv openAccess
format article
id REVCMED_13bed22f7042cf9f34c4403ee334c8f5
identifier_str_mv 10.29166/rfcmq.v49i2.6426
instacron_str UCE
institution UCE
instname_str Universidad Central del Ecuador
language spa
network_acronym_str REVCMED
network_name_str Revista Ciencias Médicas
oai_identifier_str oai:revistadigital.uce.edu.ec:article/6426
publishDate 2024
publisher.none.fl_str_mv Quito: Universidad Central del Ecuador
reponame_str Revista Ciencias Médicas
repository.mail.fl_str_mv *
repository.name.fl_str_mv Revista Ciencias Médicas - Universidad Central del Ecuador
repository_id_str *
rights_invalid_str_mv Derechos de autor 2024 Daniel Falconi
http://creativecommons.org/licenses/by-nc-nd/4.0
spelling Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case reportSíndrome antifosfolipídico trombótico en una mujer con enfermedad mixta del tejido conectivo. Reporte de caso-Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case reportFalconi-Toro, DanielBedón-Galarza , RicardoBedoya-Dávila , Michellesíndrome antifosfolipídicoenfermedad mixta del tejido conjuntivoembolia pulmonarlupus eritematoso sistémicopresentación de casoAntiphospholipid SyndromeMixed Connective Tissue DiseasePulmonary EmbolismLupus Erythematosus, SystemicCase ReportsIntroduction: Antiphospholipid antibody syndrome is a rare systemic autoimmune disease that produces a hypercoagulable state with risk of thrombosis. The ACR/EULAR APS 2023 criteria are used for diagnosis. With respect to treatment, anticoagulants and antiplatelet agents are the most used. Mixed connective tissue disease is a systemic autoimmune disease that presents the association of clinical manifestations of other autoimmune entities. Objective: To describe the presentation of two rare autoimmune systemic diseases together, with the purpose of contributing a practical approach to diagnosis and management. Case presentation: A 37-year-old patient is described who presented an episode of pulmonary thromboembolism secondary to antiphospholipid antibody syndrome and who for 6 months had symptoms compatible with mixed connective tissue disease. The patient had to undergo surgery and subsequently responded to treatment. Discussion: This case revealed the presence of two autoimmune entities, antiphospholipid antibody syndrome and mixed connective tissue disease presented together and whose debut of complications was a pulmonary thromboembolism, also finding the presence of multiple positive autoantibodies between these antiphospholipid and anti-U1 antibodies snRNP, which represents a diagnostic challenge when differentiating between other connective tissue diseases such as systemic lupus erythematosus, cutaneous systemic sclerosis, mixed connective tissue disease and rheumatoid arthritis. The treatment decision was based on the patient's characteristics and clinical condition at the time of diagnosis. Conclusions: Antiphospholipid antibody syndrome entails the presence of a thrombotic episode; on the other hand, its association with a mixed connective tissue disease is rare and may increase its morbidity and mortality.Introducción: El síndrome de anticuerpos antifosfolípidos es una enfermedad autoinmune sistémica poco frecuente, que produce un estado de hipercoagulabilidad con riesgo de trombosis. Para su diagnóstico se utilizan los criterios ACR/EULAR APS del 2023. Con respecto al tratamiento son los anticoagulantes y antiagregantes plaquetarios los más utilizados. La enfermedad mixta del tejido conectivo es una enfermedad autoinmunitaria sistémica que presenta la asociación de manifestaciones clínicas de otras entidades autoinmunes.  Objetivo: Describir la presentación de dos enfermedades sistémicas autoinmunes poco frecuentes en conjunto, con el propósito de contribuir con un enfoque práctico para el diagnóstico y manejo. Presentación del caso: Se describe una paciente de 37 años que presentó un episodio de tromboembolia pulmonar secundario a síndrome de anticuerpos antifosfolípidos y en los 6 meses previos tuvo síntomas compatibles con enfermedad mixta del tejido conectivo. Discusión: Este caso revelo la presencia de dos entidades autoinmunes, síndrome de anticuerpos antifosfolípidos y enfermedad mixta del tejido conectivo presentadas en conjunto y cuyo debut de complicaciones fue una tromboembolia pulmonar, encontrándose además presencia de múltiples autoanticuerpos positivos entre estas anticuerpos antifosfolipídicos y anti-U1 snRNP, lo que representa un reto diagnóstico al diferenciar entre otras enfermedades del tejido conectivo como lupus eritematoso sistémico, esclerosis sistémica cutánea, enfermedad mixta del tejido conectivo y artritis reumatoide. La decisión del tratamiento se basó en las características del paciente y su condición clínica al momento del diagnóstico. Conclusiones: El síndrome de anticuerpos antifosfolipídicos conlleva la presencia de un episodio trombótico, por otro lado, su asociación con una enfermedad mixta del tejido conectivo es poco frecuente y puede aumentar su morbimortalidad. Quito: Universidad Central del Ecuador2024-05-27info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArtículo evaluado por paresapplication/pdfhttps://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/642610.29166/rfcmq.v49i2.6426Revista de la Facultad de Ciencias Médicas (Quito); Vol. 49 No. 2 (2024): Revista de la Facultad de Ciencias Médicas (Quito); 42-49Revista de la Facultad de Ciencias Médicas (Quito); Vol. 49 Núm. 2 (2024): Revista de la Facultad de Ciencias Médicas (Quito); 42-492737-61412588-0691reponame:Revista Ciencias Médicasinstname:Universidad Central del Ecuadorinstacron:UCEspahttps://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/6426/8331Derechos de autor 2024 Daniel Falconihttp://creativecommons.org/licenses/by-nc-nd/4.0info:eu-repo/semantics/openAccess2024-07-04T14:08:25Zoai:revistadigital.uce.edu.ec:article/6426Portal de revistashttps://revistadigital.uce.edu.ec/Universidad públicahttps://uce.edu.ec/**Ecuador*2737-61412588-0691opendoar:*2024-07-04T14:08:25Revista Ciencias Médicas - Universidad Central del Ecuadorfalse
spellingShingle Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
Falconi-Toro, Daniel
síndrome antifosfolipídico
enfermedad mixta del tejido conjuntivo
embolia pulmonar
lupus eritematoso sistémico
presentación de caso
Antiphospholipid Syndrome
Mixed Connective Tissue Disease
Pulmonary Embolism
Lupus Erythematosus, Systemic
Case Reports
status_str publishedVersion
title Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
title_full Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
title_fullStr Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
title_full_unstemmed Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
title_short Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
title_sort Thrombotic antiphospholipid syndrome in a woman with mixed connective tissue disease. Case report
topic síndrome antifosfolipídico
enfermedad mixta del tejido conjuntivo
embolia pulmonar
lupus eritematoso sistémico
presentación de caso
Antiphospholipid Syndrome
Mixed Connective Tissue Disease
Pulmonary Embolism
Lupus Erythematosus, Systemic
Case Reports
url https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/6426