Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
1.
Rev Med Interne ; 43(1): 31-38, 2022 Jan.
Artigo em Francês | MEDLINE | ID: mdl-33736891

RESUMO

Looking at the urine for diagnostic purposes, once performed by ancient Egyptians, can still provide some valuable clues in modern medicine. Several diseases have been named after their associated urine color and this underlines the clinical value of visual urine inspection: blue diaper disease, purple urine bag syndrome, black urine disease or porphyria. Abnormal urine color could be challenging for the clinician: it may reveal neoplastic disease (urologic cancer; melanoma), cell lysis (rhabdomyolysis; hemolysis), infection (lymphatic filariasis; malaria), enzyme deficiency (porphyria; alkaptonuria), medication or food intake. In this article, we present the diagnostic approach, the mechanisms involved and the main causes of abnormal urine color.


Assuntos
Nefropatias , Rabdomiólise , Cor , Humanos , Síndrome
2.
Rev Med Interne ; 40(4): 232-237, 2019 Apr.
Artigo em Francês | MEDLINE | ID: mdl-30773236

RESUMO

Many factors can contribute to the risk of venous thrombosis observed in hemolytic diseases. Some mechanisms are related to hemolysis by itself, while others seem more specific to each disease. Despite recent advances in the quantification of this risk and in understanding its physiopathology, the association of hemolysis with venous thrombosis is often unknown. The purpose of this general review is to clarify the main pro-thrombotic mechanisms during hemolysis and to synthesize the clinical data currently available. We will focus on the main types of hemolytic pathologies encountered in current practice, namely paroxysmal nocturnal hemoglobinuria, hemoglobinopathies, auto-immune hemolytic anemia and thrombotic microangiopathies.


Assuntos
Doenças Hematológicas , Hemólise/fisiologia , Anemia Hemolítica/sangue , Anemia Hemolítica/complicações , Anemia Hemolítica/diagnóstico , Doenças Hematológicas/sangue , Doenças Hematológicas/classificação , Doenças Hematológicas/diagnóstico , Doenças Hematológicas/etiologia , Humanos , Fatores de Risco , Trombose/complicações , Trombose/diagnóstico , Trombose Venosa/diagnóstico , Trombose Venosa/etiologia
4.
J Mal Vasc ; 40(6): 384-90, 2015 Dec.
Artigo em Francês | MEDLINE | ID: mdl-26205796

RESUMO

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired disorder of hematopoietic stem cells. Somatic mutation in the phosphatidylinositol glycan class A (PIG-A), X-linked gene, is responsible for a deficiency in glycosphosphatidylinositol-anchored proteins (GPI-AP). The lack of one of the GPI-AP complement regulatory proteins (CD55, CD59) leads to hemolysis. The disease is diagnosed with hemolytic anemia, marrow failure and thrombosis. Thromboembolic complication occurs in 30% of patient after 10 years of follow-up and is the first event in one out of 10 patients. The two most common sites are hepatic and cerebral veins. These locations are correlated with high risk of death. Currently, these data are balanced with the use of a monoclonal antibody (Eculizumab), which has significantly improved the prognosis with a survival similar to general population after 36 months of follow-up. Anticoagulant treatment is recommended after a thromboembolic event but has no place in primary prophylaxis.


Assuntos
Hemoglobinúria Paroxística/sangue , Trombofilia/etiologia , Trombose/etiologia , Anticorpos Monoclonais Humanizados/uso terapêutico , Anticoagulantes/uso terapêutico , Transplante de Medula Óssea , Antígenos CD55/fisiologia , Antígenos CD59/fisiologia , Complexo de Ataque à Membrana do Sistema Complemento/antagonistas & inibidores , Complexo de Ataque à Membrana do Sistema Complemento/imunologia , GMP Cíclico/metabolismo , Gerenciamento Clínico , Endotélio Vascular/patologia , Feminino , Seguimentos , Glicosilfosfatidilinositóis/metabolismo , Hemoglobinúria Paroxística/complicações , Hemoglobinúria Paroxística/genética , Hemoglobinúria Paroxística/terapia , Humanos , Masculino , Proteínas de Membrana/deficiência , Proteínas de Membrana/genética , Óxido Nítrico/metabolismo , Guias de Prática Clínica como Assunto , Trombofilia/tratamento farmacológico , Trombose/tratamento farmacológico , Trombose/prevenção & controle
5.
J Mal Vasc ; 39(4): 274-7, 2014 Jul.
Artigo em Francês | MEDLINE | ID: mdl-24907197

RESUMO

Paroxysmal nocturnal haemoglobinuria (PNH) is a rare hematologic disorder that can exceptionally be complicated by splanchnic thrombosis and intestinal necrosis. The discovery of multiple and dispersed distal ischemia of the small bowel is a real problem because the therapeutic approach depends on the range and the number of the segments to resect and also on the risk of recurrence of new peri-operative ischemic lesions. We report the case of a patient suffering from PNH, operated with the diagnosis of mesenteric infarction. We discovered multiple distal ischemic lesions of the gut extending from the first duodenum to the penultimate loop without perforation. Resection was then ruled out and curative anticoagulation was initiated. Outcome was favorable with restitution ad integrum of the digestive lesions without progression to secondary stenosis. Discovery of distal ischemic lesions without perforation in patients with PNH does not necessarily require resection. Curative anticoagulation can avoid surgery that may be insufficient.


Assuntos
Anticoagulantes/uso terapêutico , Duodeno/irrigação sanguínea , Hemoglobinúria Paroxística/complicações , Heparina/uso terapêutico , Isquemia Mesentérica/etiologia , Anticoagulantes/efeitos adversos , Transfusão de Sangue , Terapia Combinada , Contraindicações , Danazol/uso terapêutico , Duodeno/diagnóstico por imagem , Epistaxe/induzido quimicamente , Feminino , Ácido Fólico/uso terapêutico , Hemorragia Gengival/induzido quimicamente , Hemoglobinúria Paroxística/tratamento farmacológico , Hemoglobinúria Paroxística/terapia , Heparina de Baixo Peso Molecular/efeitos adversos , Heparina de Baixo Peso Molecular/uso terapêutico , Humanos , Isquemia Mesentérica/diagnóstico , Isquemia Mesentérica/tratamento farmacológico , Pessoa de Meia-Idade , Tomografia Computadorizada por Raios X , Procedimentos Desnecessários
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA