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2.
Gynecol Obstet Fertil ; 42(10): 686-91, 2014 Oct.
Artigo em Francês | MEDLINE | ID: mdl-25245839

RESUMO

OBJECTIVES: Breast magnetic resonance imaging (MRI) has attained a solid position in the diagnosis of breast cancer but its benefit is still to be confirmed in the preoperative staging. The authors assessed the impact of preoperative breast MRI on surgical management of breast cancer in two university hospitals. PATIENTS AND METHODS: This retrospective review was realized in two university hospitals and concerned all patients with breast carcinoma who had a surgical first therapy. We selected 89 patients who underwent preoperative breast MRI in the period between January 2008 and December 2009. RESULTS: The sensitivity of breast MRI for detecting breast tumor was 95%. Fourteen percent of patients had a multifocal disease, 10% a multicentric disease and 2% a synchronous bilateral cancer. The correlation of radiological tumor size with histopathological size was r=0.68 in IRM compared to r=0.45 in conventional imaging (P<0.001). Nineteen additional biopsies were performed and 9.9% of false-positive findings were detected. Retrospectively, planned surgical management was altered in 9% of patients, resulted from use of breast MRI. Six patients had conversion of planned breast conservation to mastectomy and two patients underwent contralateral lumpectomy after discover synchronous bilateral cancer. DISCUSSION AND CONCLUSION: Breast MRI was very sensitive for the detection of breast carcinoma and improved local staging in almost 9% of patients. But, low specificity of this imaging requires a systematically validation of additional lesions by biopsy before surgical planning.


Assuntos
Neoplasias da Mama/patologia , Neoplasias da Mama/cirurgia , Imageamento por Ressonância Magnética , Mastectomia/métodos , Cuidados Pré-Operatórios , Adulto , Idoso , Biópsia , Reações Falso-Positivas , Feminino , Hospitais Universitários , Humanos , Mastectomia Segmentar , Pessoa de Meia-Idade , Estadiamento de Neoplasias/métodos , Estudos Retrospectivos , Sensibilidade e Especificidade
3.
Rev Neurol (Paris) ; 163(11): 1039-47, 2007 Nov.
Artigo em Francês | MEDLINE | ID: mdl-18033042

RESUMO

INTRODUCTION: Acute myelitis accounts for 4 to 5 percent of all cases of neuroborreliosis. In the literature, simultaneous spinal MRI and cerebrospinal fluid (CSF) investigations are presented for only 8 cases. We describe here 3 cases of acute Lyme myelitis. METHOD: In a cohort of 45 patients with neuroborreliosis, diagnosed between January 1998 and January 2005, 3 had acute myelitis. Clinical, biological and radiological data were studied. CASE REPORTS: The three patients had motor, sensorial and sphincter involvement. Extra-spinal involvement, such as fever and headache for one, facial nerve palsy for the second and subarachnoid hemorrhage for the third, was also noted. Pleocytosis varied from 10 to 520 white cells per mm3. Lyme serology was positive in CSF for all. Intrathecal anti-Borrelia antibody index was positive or intermediate for all three patients. Spinal cord MRI revealed a large hyperintense zone involving more than 3 vertebral segments. Myelitis was central, posterior or transverse in the axial plane. The clinical course was favorable after a three-week course of appropriate antibiotics. CONCLUSION: These 3 cases and the others from the literature show the diversity of the clinical and radiological features of acute myelitis: transverse, central or posterior myelitis. Thus, Lyme serology in CSF in indicated for patients presenting acute myelitis, particularly in endemic areas.


Assuntos
Doença de Lyme/complicações , Mielite/etiologia , Doença Aguda , Idoso , Antibacterianos/uso terapêutico , Anticorpos Antibacterianos/análise , Anticorpos Antibacterianos/líquido cefalorraquidiano , Western Blotting , Borrelia burgdorferi/imunologia , Estudos de Coortes , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Leucocitose/etiologia , Doença de Lyme/tratamento farmacológico , Doença de Lyme/patologia , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Mielite/tratamento farmacológico , Mielite/patologia , Mielite Transversa/tratamento farmacológico , Mielite Transversa/etiologia , Mielite Transversa/patologia , Medula Espinal/patologia
4.
Proc Biol Sci ; 270(1525): 1703-12, 2003 Aug 22.
Artigo em Inglês | MEDLINE | ID: mdl-12964998

RESUMO

In North America, the pea aphid Acyrthosiphon pisum encompasses ecologically and genetically distinct host races that offer an ideal biological system for studies on sympatric speciation. In addition to its obligate symbiont Buchnera, pea aphids harbour several facultative and phylogenetically distant symbionts. We explored the relationships between host races of A. pisum and their symbiotic microbiota to gain insights into the historical process of ecological specialization and symbiotic acquisition in this aphid. We used allozyme and microsatellite markers to analyse the extent of genetic differentiation between populations of A. pisum on pea, alfalfa and clover in France. In parallel, we examined: (i) the distribution of four facultative symbionts; and (ii) the genetic variation in the Buchnera genome across host-associated populations of A. pisum. Our study clearly demonstrates that populations of A. pisum on pea, clover and alfalfa in France are genetically divergent, which indicates that they constitute distinct host races. We also found a very strong association between host races of A. pisum and their symbiotic microbiota. We stress the need for phylogeographic studies to shed light on the process of host-race formation and acquisition of facultative symbionts in A. pisum. We also question the effects of these symbionts on aphid host fitness, including their role in adaptation to a host plant.


Assuntos
Afídeos/genética , Buchnera/genética , Frequência do Gene/genética , Repetições de Microssatélites/genética , Filogenia , Simbiose/genética , Adaptação Biológica , Animais , Primers do DNA , Ecossistema , Fabaceae , França , Seleção Genética , Análise de Sequência de DNA
5.
Ann Med Interne (Paris) ; 152(3): 147-51, 2001 Apr.
Artigo em Francês | MEDLINE | ID: mdl-11431571

RESUMO

OBJECTIVE: The aim of this study was to report our experience with autoimmune neuropathies associated with hematological disorders and to describe their etiological and clinical polymorphism. PATIENTS AND METHODS: A retrospective study was conducted in five patients with autoimmune peripheral neuropathies with anti-MAG (myelin-associated glycoprotein) antibodies. RESULTS: Autoimmune neuropathies were associated with Waldenström's macroglobulinemia (n=2), Hodgkin disease (n=1), chronic lymphocytic leukemia (n=1) and idiopathic polyclonal B lymphoproliferation (n=1). Most of the patients had a sensorial polyneuropathy, predominant in the legs, exhibiting slow progress. Our patients showed a disappointing response to chemotherapy with stabilization or short response.


Assuntos
Anticorpos Anti-Idiotípicos/sangue , Anticorpos Anti-Idiotípicos/imunologia , Doenças Autoimunes/etiologia , Doenças Autoimunes/imunologia , Doenças Hematológicas/complicações , Doença de Hodgkin/complicações , Leucemia Linfocítica Crônica de Células B/complicações , Transtornos Linfoproliferativos/complicações , Glicoproteína Associada a Mielina/imunologia , Polineuropatias/etiologia , Polineuropatias/imunologia , Macroglobulinemia de Waldenstrom/complicações , Adulto , Idoso , Idoso de 80 Anos ou mais , Doenças Autoimunes/sangue , Progressão da Doença , Feminino , Doença de Hodgkin/tratamento farmacológico , Humanos , Leucemia Linfocítica Crônica de Células B/tratamento farmacológico , Transtornos Linfoproliferativos/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Polineuropatias/sangue , Estudos Retrospectivos , Resultado do Tratamento , Macroglobulinemia de Waldenstrom/tratamento farmacológico
6.
Nat Genet ; 28(2): 119-20, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11381253

RESUMO

Chorea-acanthocytosis (CHAC, MIM 200150) is an autosomal recessive neurodegenerative disorder characterized by the gradual onset of hyperkinetic movements and abnormal erythrocyte morphology (acanthocytosis). Neurological findings closely resemble those observed in Huntington disease. We identified a gene in the CHAC critical region and found 16 different mutations in individuals with chorea-acanthocytosis. CHAC encodes an evolutionarily conserved protein that is probably involved in protein sorting.


Assuntos
Coreia/genética , Mutação , Proteínas/genética , Proteínas de Saccharomyces cerevisiae , Processamento Alternativo , Animais , Caenorhabditis elegans/genética , Linhagem Celular , Cromossomos Humanos Par 6 , Eritrócitos/fisiologia , Éxons , Proteínas Fúngicas/genética , Regulação da Expressão Gênica , Haplótipos , Humanos , Linhagem , Transporte Proteico , Proteínas/metabolismo , Homologia de Sequência de Aminoácidos , Transcrição Gênica , Proteínas de Transporte Vesicular
7.
Parkinsonism Relat Disord ; 6(2): 107-110, 2000 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-10699392

RESUMO

Two patients with a hyperkinetic syndrome contralateral to acute hemiplegia are presented. One patient showed a right-sided hemiplegia associated with abnormal movements of the left upper limb. In the other patient hemiplegia was localised on the left side while abnormal movements involved the right lower limb. Brain imaging showed acute infarctions (respectively left middle cerebral artery area and right lacunar infarctions) associated with a pre-existing contralateral infarction involving anterior non-primary motor areas. Hyperkinetic syndromes in stroke are mainly related to acute lesion of the contralateral subcortical areas. In our patients, the acute lesions were located ipsilateral to the hyperkinetic body part while the pre-existing lesions were located contralateral to the hyperkinetic side. We speculated that these pre-existing lesions might play a role in the pathophysiology of this clinical syndrome.

9.
J Neuroradiol ; 24(1): 65-7, 1997 Jun.
Artigo em Francês | MEDLINE | ID: mdl-9303946

RESUMO

Epidermoid cysts are rare intradural extramedullary tumors. There are two types of lesions: congenital spinal cysts frequently associated with other bone or skin malformations (spina bifida aperta, dermal sinus ...) and iatrogenic spinal cysts resulting from lumbar puncture. In both situations, clinical and the radiologic findings are similar. We describe an epidermoid cyst in a 52-year-old female affected with a lumbar pain and recent urinary disorders. Symptoms were slow to appear and dependent on the location of the cyst. Epidermoid cyst contained keratin, cholesterol crystals and desquamed epithelial cells. On CT, epidermoid cyst was a hypodense lesion on MR. On T1 weighted images the tumor was hypointense. The signal appeared heterogeneous. There was no enhancement after Gadolinium DTPA injection. Differential diagnosis included: ependymoma, hemangioblastoma, neurinoma, meningioma and metastasis, but all these lesions are enhanced by contrast injection.


Assuntos
Cisto Epidérmico/diagnóstico , Doenças da Coluna Vertebral/diagnóstico , Meios de Contraste , Diagnóstico Diferencial , Dura-Máter/patologia , Ependimoma/diagnóstico , Feminino , Gadolínio , Gadolínio DTPA , Hemangioblastoma/diagnóstico , Humanos , Dor Lombar/diagnóstico , Imageamento por Ressonância Magnética , Meningioma/diagnóstico , Pessoa de Meia-Idade , Neurilemoma/diagnóstico , Compostos Organometálicos , Ácido Pentético/análogos & derivados , Neoplasias da Medula Espinal/diagnóstico , Neoplasias da Coluna Vertebral/diagnóstico , Tomografia Computadorizada por Raios X , Retenção Urinária/diagnóstico
11.
Bull Soc Ophtalmol Fr ; 89(11): 1225-7, 1989 Nov.
Artigo em Francês | MEDLINE | ID: mdl-2630122

RESUMO

The ophthalmologist is often faced with recurrent or apparently primitive uveitis. The specialist in internal medicine almost never meets first with this type of disease. Taking advantage of a seldom seen sarcoidosis case (almost exclusively ocular), the authors point out the interest of a systematic collaboration when confronted with an endocular disease so called "inflammatory", or vascular and in appearance isolated.


Assuntos
Sarcoidose/diagnóstico , Uveíte/etiologia , Doença Crônica , Feminino , Humanos , Medicina Interna , Pessoa de Meia-Idade , Oftalmologia
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