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Livedo racemosa as a marker of increased risk of recurrent thrombosis in patients with negative anti-phospholipid antibodies
Martínez Valle, Ferran; Ordi Ros, Josep; Selva O´Callaghan, Albert; Balada, Eva; Solans Laque, Roser; Vilardell Tarres, Miquel.
Afiliação
  • Martínez Valle, Ferran; Hospital Vall d´Hebron. Vall d´Hebron Research Institute. Research Unit in Systemic Autoinmmune diseases. Barcelona. Spain
  • Ordi Ros, Josep; Hospital Vall d´Hebron. Vall d´Hebron Research Institute. Research Unit in Systemic Autoinmmune diseases. Barcelona. Spain
  • Selva O´Callaghan, Albert; Hospital Vall d´Hebron. Vall d´Hebron Research Institute. Research Unit in Systemic Autoinmmune diseases. Barcelona. Spain
  • Balada, Eva; Hospital Vall d´Hebron. Vall d´Hebron Research Institute. Research Unit in Systemic Autoinmmune diseases. Barcelona. Spain
  • Solans Laque, Roser; Hospital Vall d´Hebron. Vall d´Hebron Research Institute. Research Unit in Systemic Autoinmmune diseases. Barcelona. Spain
  • Vilardell Tarres, Miquel; Hospital Vall d´Hebron. Vall d´Hebron Research Institute. Research Unit in Systemic Autoinmmune diseases. Barcelona. Spain
Med. clín (Ed. impr.) ; 132(20): 767-771, mayo 2009. tab
Artigo em Espanhol | IBECS | ID: ibc-73181
Biblioteca responsável: ES1.1
Localização: BNCS
ABSTRACT
Background and

objective:

Livedo reticularis racemosa and cerebrovascular lesions characterize Sneddon's syndrome. We report 23 patients with livedo racemosa and describe the association with thrombotic events. Our objective was to determine whether livedo racemosa may be an independent clinical marker for the development of thrombotic events in patients who test negative for anti-phospholipid antibodies.

Methods:

Twenty-three patients with widespread livedo racemosa were studied. None of the patients were positive for anti-phospholipid antibodies. The clinical protocol included a register of thrombotic events, fetal death or miscarriages, hypertension, and valvular heart disease. Cerebral MRI and echocardiography were systematically performed in all patients.

Results:

Nineteen patients (82.60%) had thrombotic events. Fifteen (65.21%) had arterial thrombosis and eleven (47.82%) presented venous occlusions. Seven patients (30.43%) had both arterial and venous thrombosis. Fetal losses were recorded in seven cases (30.43%), with a total number of 33; five patients had 3 or more fetal losses. Eleven out of 23 patients (47.82%) had valvular heart disease. Arterial hypertension was detected in 16 (69.56%) patients. Four patients did not have thrombotic events but had other clinical manifestations. After anti-coagulation therapy was withdrawn, a new thrombotic event was observed in 9 out of the 14 treated patients (64.28%).

Conclusions:

Livedo racemosa seems to be a good clinical marker for the detection of hypercoagulable states even in the absence of anti-phospholipid antibodies or other known biologic markers of thrombosis. Long-term anti-coagulation is probably warranted in patients with livedo racemosa and a previous thrombotic event (AU)
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Coleções: Bases de dados nacionais / Espanha Contexto em Saúde: ODS3 - Meta 3.4 Reduzir as mortes prematuras devido doenças não transmissíveis Problema de saúde: Doença Cardiovascular / Doenças da Pele / Tromboembolismo Venoso Base de dados: IBECS Assunto principal: Trombose / Dermatopatias Vasculares Tipo de estudo: Estudo de etiologia / Guia de prática clínica / Estudo prognóstico / Fatores de risco Limite: Feminino / Humanos / Masculino Idioma: Espanhol Revista: Med. clín (Ed. impr.) Ano de publicação: 2009 Tipo de documento: Artigo Instituição/País de afiliação: Hospital Vall d´Hebron/Spain
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Coleções: Bases de dados nacionais / Espanha Contexto em Saúde: ODS3 - Meta 3.4 Reduzir as mortes prematuras devido doenças não transmissíveis Problema de saúde: Doença Cardiovascular / Doenças da Pele / Tromboembolismo Venoso Base de dados: IBECS Assunto principal: Trombose / Dermatopatias Vasculares Tipo de estudo: Estudo de etiologia / Guia de prática clínica / Estudo prognóstico / Fatores de risco Limite: Feminino / Humanos / Masculino Idioma: Espanhol Revista: Med. clín (Ed. impr.) Ano de publicação: 2009 Tipo de documento: Artigo Instituição/País de afiliação: Hospital Vall d´Hebron/Spain
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