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1.
Am J Hematol ; 79(1): 46-9, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15849762

RESUMO

Intravascular lymphoma (IVL) is a rare and usually fatal disease that belongs to the class of high-grade malignant lymphomas and which is characterized by proliferation of neoplastic lymphoid cells exclusively within the lumina of small blood vessels. Its polymorphic and nonspecific clinical manifestations make antemortem diagnosis very difficult. We report herein a case of IVL revealed by fatal, precapillary, pulmonary arterial hypertension and associated with long-lasting fever. Extensive investigation of the usual causes of pulmonary arterial hypertension was negative. The diagnosis of intravascular lymphoma was made on postmortem analysis, revealing diffuse and sometimes complete obliterations of the lumina of small blood vessels by large B-cell lymphoma, including pulmonary capillaries. Thus, we propose that IVL must be added to the spectrum of etiologies of subacute pulmonary arterial hypertension, notably in the context of associated fever, both entities requiring emergency diagnosis. For this purpose, blood collected via pulmonary capillary-wedge aspiration for cytologic examination may be associated with right-sided heart catheterization when this latter procedure is suitable.


Assuntos
Hipertensão Pulmonar/etiologia , Linfoma de Células B/patologia , Linfoma Difuso de Grandes Células B/patologia , Neoplasias Vasculares/patologia , Idoso , Evolução Fatal , Feminino , Humanos , Hipertensão Pulmonar/patologia , Insuficiência de Múltiplos Órgãos
2.
Presse Med ; 33(19 Pt 2): 1367-9, 2004 Nov 06.
Artigo em Inglês | MEDLINE | ID: mdl-15615247

RESUMO

INTRODUCTION: Aseptic endocarditis or/and endomyocardial fibrosis are rarely reported in Behçet's disease. OBSERVATION: We report on a case of a 21-year-old man living in Algeria, revealed by verrucous tricuspid valvulitis extending to the ventricular endomyocardium and complicated with right heart failure, initially misdiagnosed and treated as infective endocarditis occurring on rheumatic cardiac after-effects. DISCUSSION; We discuss the lack of specificity of Jones criteria and emphasize the need to include cardiac involvement in Behçet's disease in the differential diagnosis of rheumatic fever carditis. This message is notably important in some countries where the prevalence of these two entities are among the highest in the world.


Assuntos
Síndrome de Behçet/complicações , Síndrome de Behçet/diagnóstico , Endocardite/etiologia , Fibrose Endomiocárdica/etiologia , Cardiopatia Reumática/diagnóstico , Valva Tricúspide/patologia , Adulto , Fibrose Endomiocárdica/patologia , Humanos , Masculino , Cardiopatia Reumática/patologia , Disfunção Ventricular Direita/etiologia
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