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2.
Gynecol Obstet Fertil ; 42(10): 686-91, 2014 Oct.
Article in French | MEDLINE | ID: mdl-25245839

ABSTRACT

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.


Subject(s)
Breast Neoplasms/pathology , Breast Neoplasms/surgery , Magnetic Resonance Imaging , Mastectomy/methods , Preoperative Care , Adult , Aged , Biopsy , False Positive Reactions , Female , Hospitals, University , Humans , Mastectomy, Segmental , Middle Aged , Neoplasm Staging/methods , Retrospective Studies , Sensitivity and Specificity
3.
Rev Neurol (Paris) ; 163(11): 1039-47, 2007 Nov.
Article in French | MEDLINE | ID: mdl-18033042

ABSTRACT

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.


Subject(s)
Lyme Disease/complications , Myelitis/etiology , Acute Disease , Aged , Anti-Bacterial Agents/therapeutic use , Antibodies, Bacterial/analysis , Antibodies, Bacterial/cerebrospinal fluid , Blotting, Western , Borrelia burgdorferi/immunology , Cohort Studies , Enzyme-Linked Immunosorbent Assay , Female , Humans , Leukocytosis/etiology , Lyme Disease/drug therapy , Lyme Disease/pathology , Magnetic Resonance Imaging , Male , Middle Aged , Myelitis/drug therapy , Myelitis/pathology , Myelitis, Transverse/drug therapy , Myelitis, Transverse/etiology , Myelitis, Transverse/pathology , Spinal Cord/pathology
4.
Proc Biol Sci ; 270(1525): 1703-12, 2003 Aug 22.
Article in English | MEDLINE | ID: mdl-12964998

ABSTRACT

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.


Subject(s)
Aphids/genetics , Buchnera/genetics , Gene Frequency/genetics , Microsatellite Repeats/genetics , Phylogeny , Symbiosis/genetics , Adaptation, Biological , Animals , DNA Primers , Ecosystem , Fabaceae , France , Selection, Genetic , Sequence Analysis, DNA
5.
Ann Med Interne (Paris) ; 152(3): 147-51, 2001 Apr.
Article in French | MEDLINE | ID: mdl-11431571

ABSTRACT

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.


Subject(s)
Antibodies, Anti-Idiotypic/blood , Antibodies, Anti-Idiotypic/immunology , Autoimmune Diseases/etiology , Autoimmune Diseases/immunology , Hematologic Diseases/complications , Hodgkin Disease/complications , Leukemia, Lymphocytic, Chronic, B-Cell/complications , Lymphoproliferative Disorders/complications , Myelin-Associated Glycoprotein/immunology , Polyneuropathies/etiology , Polyneuropathies/immunology , Waldenstrom Macroglobulinemia/complications , Adult , Aged , Aged, 80 and over , Autoimmune Diseases/blood , Disease Progression , Female , Hodgkin Disease/drug therapy , Humans , Leukemia, Lymphocytic, Chronic, B-Cell/drug therapy , Lymphoproliferative Disorders/drug therapy , Male , Middle Aged , Polyneuropathies/blood , Retrospective Studies , Treatment Outcome , Waldenstrom Macroglobulinemia/drug therapy
6.
Nat Genet ; 28(2): 119-20, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11381253

ABSTRACT

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.


Subject(s)
Chorea/genetics , Mutation , Proteins/genetics , Saccharomyces cerevisiae Proteins , Alternative Splicing , Animals , Caenorhabditis elegans/genetics , Cell Line , Chromosomes, Human, Pair 6 , Erythrocytes/physiology , Exons , Fungal Proteins/genetics , Gene Expression Regulation , Haplotypes , Humans , Pedigree , Protein Transport , Proteins/metabolism , Sequence Homology, Amino Acid , Transcription, Genetic , Vesicular Transport Proteins
7.
Parkinsonism Relat Disord ; 6(2): 107-110, 2000 Apr 01.
Article in English | MEDLINE | ID: mdl-10699392

ABSTRACT

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.
Article in French | MEDLINE | ID: mdl-9303946

ABSTRACT

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.


Subject(s)
Epidermal Cyst/diagnosis , Spinal Diseases/diagnosis , Contrast Media , Diagnosis, Differential , Dura Mater/pathology , Ependymoma/diagnosis , Female , Gadolinium , Gadolinium DTPA , Hemangioblastoma/diagnosis , Humans , Low Back Pain/diagnosis , Magnetic Resonance Imaging , Meningioma/diagnosis , Middle Aged , Neurilemmoma/diagnosis , Organometallic Compounds , Pentetic Acid/analogs & derivatives , Spinal Cord Neoplasms/diagnosis , Spinal Neoplasms/diagnosis , Tomography, X-Ray Computed , Urinary Retention/diagnosis
11.
Bull Soc Ophtalmol Fr ; 89(11): 1225-7, 1989 Nov.
Article in French | MEDLINE | ID: mdl-2630122

ABSTRACT

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.


Subject(s)
Sarcoidosis/diagnosis , Uveitis/etiology , Chronic Disease , Female , Humans , Internal Medicine , Middle Aged , Ophthalmology
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