Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
1.
Br J Dermatol ; 175(5): 1049-1051, 2016 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-26992073

RESUMO

We present two cases of patients with systemic autoimmune diseases (one with dermatomyositis and one with CREST syndrome) who presented with a worsening of calcinosis cutis after treatment of osteoporosis with teriparatide. To our knowledge, this association is not described in the literature and might be considered in the spectrum of adverse reactions to teriparatide.


Assuntos
Conservadores da Densidade Óssea/efeitos adversos , Calcinose/induzido quimicamente , Osteoporose/tratamento farmacológico , Dermatopatias/induzido quimicamente , Teriparatida/efeitos adversos , Idoso , Síndrome CREST/complicações , Dermatomiosite/complicações , Feminino , Humanos , Pessoa de Meia-Idade , Osteoporose/complicações
2.
Lupus ; 25(6): 658-62, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26743321

RESUMO

AIM: The aim of this study was to describe a case series of patients with primary or secondary antiphospholipid syndrome (APS) treated with direct oral anticoagulants (DOACs). PATIENTS AND METHODS: Clinical charts of eight patients with thrombotic primary or secondary APS treated with direct oral anticoagulants (DOACs) between January 2012 and May 2015 were reviewed. RESULTS: The mean age was 45 ± 14.36 (range 27-69 years). Four patients had secondary APS (50%). All patients were initially treated with warfarin by a mean time of 70.87 ± 57.32 months (range 17-153 months). Changes in anticoagulation were defined by recurring thrombosis in five patients (62.5%) and life-threatening bleeding in the other three cases. Seven patients (87.5%) received rivaroxaban treatment and one patient (12.5%) apixaban. The mean follow-up period with DOACs was 19 ± 10.06 months (range 2-36 months). There was no recurrence of thrombosis by the time of data collection. CONCLUSIONS: Despite not being the standard treatment in APS, we propose DOACs as a rational alternative for the management of patients with this diagnosis. Further interventional clinical studies are necessary for possible standardization of this therapy in APS patients.


Assuntos
Anticoagulantes/uso terapêutico , Síndrome Antifosfolipídica/tratamento farmacológico , Hemorragia/induzido quimicamente , Trombose/prevenção & controle , Administração Oral , Adulto , Idoso , Anticoagulantes/administração & dosagem , Anticoagulantes/efeitos adversos , Síndrome Antifosfolipídica/complicações , Feminino , Seguimentos , Hemorragia/epidemiologia , Humanos , Pessoa de Meia-Idade , Pirazóis/efeitos adversos , Pirazóis/uso terapêutico , Piridonas/efeitos adversos , Piridonas/uso terapêutico , Recidiva , Estudos Retrospectivos , Rivaroxabana/efeitos adversos , Rivaroxabana/uso terapêutico , Trombose/etiologia , Resultado do Tratamento , Varfarina/efeitos adversos , Varfarina/uso terapêutico
3.
Rheumatol Int ; 34(5): 723-5, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-23292188

RESUMO

We report an adult female patient with Takayasu arteritis (TA) receiving conventional medical treatment and anti-TNF therapy, which developed progressive thoracic and abdominal aortic aneurysms. She developed imminent rupture of the thoracic aneurysm and an endovascular stent-graft (EVSG) was emergency implanted and a year after this procedure the abdominal aneurysm increased in size requiring reoperation and placement of another EVSG. Both procedures had a very good outcome. This case shows the effectivity and security of multiple EVSG implantations in multiple aortic aneurisms in patients with TA.


Assuntos
Aneurisma da Aorta Abdominal/cirurgia , Aneurisma da Aorta Torácica/cirurgia , Implante de Prótese Vascular/instrumentação , Prótese Vascular , Procedimentos Endovasculares/instrumentação , Stents , Arterite de Takayasu/complicações , Arterite de Takayasu/tratamento farmacológico , Adulto , Aneurisma da Aorta Abdominal/diagnóstico , Aneurisma da Aorta Abdominal/etiologia , Aneurisma da Aorta Torácica/diagnóstico , Aneurisma da Aorta Torácica/etiologia , Aortografia/métodos , Produtos Biológicos/uso terapêutico , Feminino , Humanos , Reoperação , Arterite de Takayasu/diagnóstico , Arterite de Takayasu/imunologia , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Fator de Necrose Tumoral alfa/antagonistas & inibidores
4.
Lupus ; 21(10): 1128-30, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22460293

RESUMO

The psychiatric manifestations of three patients with systemic lupus erythematosus (SLE) and neuropathic dysautonomic processes are described. All patients had a severe form of SLE with neurological, renal, articular, pulmonary or haematological manifestations. All three have two types of psychiatric manifestations: (1) a chronic and progressive depression and (2) a complex dissociative disorder during the acute episodes of postural hypotension. A provocative test with SPECT with 99mTc-HmPAO to be done during the episode of orthostatic hypotension may contribute to clinical assessment of complex changes in cerebral regional perfusion.


Assuntos
Doenças do Sistema Nervoso Autônomo/etiologia , Doenças do Sistema Nervoso Autônomo/psicologia , Lúpus Eritematoso Sistêmico/complicações , Lúpus Eritematoso Sistêmico/psicologia , Adolescente , Doenças Autoimunes do Sistema Nervoso/diagnóstico por imagem , Doenças Autoimunes do Sistema Nervoso/etiologia , Doenças Autoimunes do Sistema Nervoso/psicologia , Doenças do Sistema Nervoso Autônomo/diagnóstico por imagem , Encéfalo/irrigação sanguínea , Encéfalo/diagnóstico por imagem , Circulação Cerebrovascular , Depressão/diagnóstico por imagem , Depressão/etiologia , Depressão/psicologia , Transtornos Dissociativos/diagnóstico por imagem , Transtornos Dissociativos/etiologia , Transtornos Dissociativos/psicologia , Feminino , Humanos , Hipotensão Ortostática/diagnóstico por imagem , Hipotensão Ortostática/etiologia , Hipotensão Ortostática/psicologia , Lúpus Eritematoso Sistêmico/diagnóstico por imagem , Compostos Radiofarmacêuticos , Tecnécio Tc 99m Exametazima , Tomografia Computadorizada de Emissão de Fóton Único , Adulto Jovem
5.
Med Hypotheses ; 82(6): 784-91, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24746382

RESUMO

Rheumatoid arthritis (RA) is a complex autoimmune disease of recent evolutionary origin. Genetic drift determines diverse polymorphisms implicated in the susceptibility to RA including the major histocompatibility complex (MHC) class II genes in the so-called shared epitope. These genes originated after the divergence between Homo and Pan from their common ancestry Ardipithecus ramidus about 5 million years ago. Natural selection determined the particular changes in the legs (bipedal position), hands, neck, brain and eusociality in humans which influence the clinical presentation of RA. In this article, we hypothesized that the origin and course of RA may be explainable in the light of evolution.


Assuntos
Artrite Reumatoide/genética , Artrite Reumatoide/patologia , Cromossomos Humanos Par 6/genética , Evolução Molecular , Genes MHC da Classe II/genética , Modelos Biológicos , Articulação Atlantoaxial/patologia , Deriva Genética , Mãos/patologia , Quadril/patologia , Humanos , Seleção Genética
6.
Clin Rheumatol ; 33(3): 415-8, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24402739

RESUMO

New cases of Pneumocystis jirovecii pneumonia (PJP) have recently been reported in patients with systemic lupus erythematosus (SLE) after rituximab therapy. Several factors may contribute to susceptibility to P. jirovecii infection in this type of patients, including the immunological characteristics of the disease, the mechanisms of rituximab action, environmental factors, and the biological characteristics of the fungus. We report two patients with SLE who developed PJP after rituximab therapy.


Assuntos
Anticorpos Monoclonais Murinos/efeitos adversos , Lúpus Eritematoso Sistêmico/tratamento farmacológico , Pneumocystis carinii/isolamento & purificação , Pneumonia por Pneumocystis/etiologia , Antibacterianos/uso terapêutico , Anticorpos Monoclonais Murinos/uso terapêutico , Evolução Fatal , Feminino , Humanos , Lúpus Eritematoso Sistêmico/complicações , Pneumonia por Pneumocystis/tratamento farmacológico , Rituximab , Resultado do Tratamento , Adulto Jovem
7.
Med Hypotheses ; 81(1): 111-3, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23643707

RESUMO

Several clinical cases have shown the association of primary hyperparathyroidism and immune conditions related to B-cell hyperactivity. In some of these cases the treatment of hyperparathyroidism led to the resolution of the autoimmune phenomena. Thus, this paper hypothesizes that high levels of parathyroid hormone (PTH) may modify B lymphocytes function and induce the development of autoimmunity mediated by B-cell hyperactivity.


Assuntos
Linfócitos B/imunologia , Hiperparatireoidismo Primário/imunologia , Humanos , Modelos Teóricos , Hormônio Paratireóideo/fisiologia
8.
Case Rep Rheumatol ; 2012: 517424, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23304614

RESUMO

We report a female patient with rheumatoid arthritis which was refractory to methotrexate, leflunomide, and anti-TNF therapy. She was treated with anti-IL-6 tocilizumab (TCZ), with an early appearance of sterile pustules on erythematous swollen skin of trunk, back, and abdominal area. The lesions were consistent with the diagnosis of acute drug-related generalized exanthematous pustulosis (AGEP). This adverse event was controlled with medical treatment without requiring removal of TCZ.

9.
Case Rep Med ; 2012: 128103, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23251162

RESUMO

Paracoccidioidomycosis is an endemic South American systemic mycosis caused by the dimorphic fungus Paracoccidioides brasiliensis (P. brasiliensis). The main clinical form of disease is pulmonary, but all organs may be involved. We report a case of overinfection by P. brasiliensis in chronic gouty arthritis affecting the proximal phalanx of the right hallux. The patient required proximal amputation and long-term antifungal therapy.

SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa