Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 37
Filter
1.
Chem Commun (Camb) ; 53(36): 5024-5027, 2017 May 02.
Article in English | MEDLINE | ID: mdl-28429026

ABSTRACT

The N-difluoromethyl triazolo-ß-aza-ε-amino acid present in the core of peptides led to constrained conformations due to CH-F and NH-F interactions. Pseudotetrapeptides were obtained in excellent yields directly by click chemistry between azidodifluoroacetamides and alkynes, both linked to an amino acid. This work demonstrates that the N-difluoromethyltriazole scaffold can induce extended structures to ß-strand mimics.


Subject(s)
Hydrocarbons, Fluorinated/chemistry , Peptidomimetics/chemistry , Triazoles/chemistry , Click Chemistry , Molecular Structure
3.
Nephrologie ; 22(2): 49-51, 2001.
Article in French | MEDLINE | ID: mdl-11385901

ABSTRACT

The short-lived results of angioplasty for venous stenosis of a dialysis access led to stent placement. Its migration is a rare but dangerous complication, because of its final destination, that is right heart or pulmonary artery. We report on such a case and compare it with three cases found in literature.


Subject(s)
Angioplasty/adverse effects , Catheters, Indwelling/adverse effects , Foreign-Body Migration/diagnostic imaging , Kidney Failure, Chronic/therapy , Pulmonary Artery/diagnostic imaging , Renal Dialysis , Stents , Venous Thrombosis/etiology , Adult , Female , Humans , Radiography, Thoracic , Venous Thrombosis/therapy
5.
Nephrologie ; 21(5): 247-52, 2000.
Article in French | MEDLINE | ID: mdl-11068774

ABSTRACT

Twenty patients with severe Schönlein-Henoch nephritis were selected on a histologically basis of diffuse proliferative endo- and/or extracapillary glomerulonephritis during a period of 12 years in Champagne-Ardenne. There were 15 men and 5 women, mean age 44.1 years. An infectious history was found in 40%, an urinary tract cancer in 15%. In all cases there was purpura, in 80% joint pain and in 50% digestive symptoms. Clinical presentation at diagnosis included, in all cases, hematuria (gross in 50%) and proteinuria (of nephrotic range in 80%); there was hypertension in 60% and renal failure in 80%. Histology found, in all cases, mesangial IgA and often C3 deposits, with a diffuse endocapillary proliferation in 10%, extra-capillary proliferation in 30% and both endo-extracapillary in 60%; 45% of the patients had crescents in greater than 50% of glomeruli. The outcome, after steroid and immunosuppressive treatment, was end-stage renal failure in 25%, moderate renal failure in 20%, or normal renal function in 55% with a mean follow-up period of 4.6 years. These severe nephritis were associated with repetitive and often necrotic purpura, frequent joint pain and severe digestive symptoms. The analysis of initial renal presentation confirmed the bad prognosis of nephrotic syndrome, renal failure and especially hypertension, which were well correlated with the severity and diffusion of proliferative lesions. Despite a worse known prognosis, these nephritis responded to an aggressive and early treatment.


Subject(s)
Glomerulonephritis/complications , Glomerulonephritis/etiology , IgA Vasculitis/complications , IgA Vasculitis/physiopathology , Adult , Aged , Female , Glomerulonephritis/physiopathology , Humans , Kidney/pathology , Kidney Glomerulus/pathology , Male , Middle Aged
6.
Nephrologie ; 20(2): 81-6, 1999.
Article in French | MEDLINE | ID: mdl-10227028

ABSTRACT

We report on six cases of leptospirosis observed in fifteen years in our department of nephrology. The contamination is two times from professional origin and four times linked to water leisures, during hot season, from june to september for the majority. Two serotypes are found: L. icterohaemorragiae characterized by marked jaundice, and L. patoc with anicteric form. Acute renal failure, five times oliguro-anuric, necessitates in the six cases hemodialysis (two to six sessions). Meningitis is found in four patients, associated in one case to an encephalitis and a polyradiculoneuritis. In one case, there were interstitial pulmonary lesions, in one another, a myocarditis with conduction disorders, responsible of the only death of this series, and finally, in three cases, a gastrointestinal hemorrhage. Bacteriological diagnosis seems little profitable and microagglutination remains the reference technique, helped by the IgM detecting through ELISA, looking forward to the evaluation of PCR (Polymerase Chain Reaction).


Subject(s)
Acute Kidney Injury/etiology , Leptospirosis/complications , Abattoirs , Adult , Agglutination Tests , Animals , Encephalitis/etiology , Enzyme-Linked Immunosorbent Assay , Fatal Outcome , France , Gastrointestinal Hemorrhage/etiology , Humans , Immunoglobulin M/blood , Leptospira/classification , Leptospira/isolation & purification , Leptospirosis/diagnosis , Leptospirosis/epidemiology , Male , Meningitis, Bacterial/etiology , Mice , Middle Aged , Myocarditis/etiology , Occupational Diseases , Rats , Renal Dialysis , Retrospective Studies , Wound Infection
7.
Presse Med ; 28(13): 683-5, 1999 Apr 03.
Article in French | MEDLINE | ID: mdl-10228475

ABSTRACT

BACKGROUND: Renal sarcoidosis exceptionally presents as a unilateral pyelic pseudotumor as in this case where it was associated with granulomatous nephropathy. CASE REPORT: A 33-year-old man had a two-year history of systemic sarcoidosis with no renal involvement. He developed renal failure related to interstitial granulomatous nephropathy associated with a pyelic localization leading to unilateral hydronephrosis. Urine drainage associated with corticosteroid therapy provided a favorable course. DISCUSSION: Renal involvement in sarcoidosis is usually the consequence of hypercalcemia and hypercalciuria related to ectopic secretion of calcitriol by the sarcoidosic granulomas, with urinary lithiasis and nephrocalcinosis leading to renal failure and also granluomatous interstitial nephropathy. Glomerulopathy or obstructive nephropathy are rarely reported. Intraluminal localizations such as the pyelic lesion in our case are exceptional but must be detected early since they respond to corticosteroid therapy.


Subject(s)
Kidney Diseases/diagnosis , Kidney Pelvis/pathology , Renal Insufficiency/etiology , Sarcoidosis/complications , Adrenal Cortex Hormones/therapeutic use , Adult , Biopsy , Drainage , Humans , Hydronephrosis/etiology , Hydronephrosis/therapy , Kidney Diseases/etiology , Kidney Diseases/pathology , Kidney Diseases/therapy , Male , Renal Insufficiency/diagnosis , Renal Insufficiency/therapy , Sarcoidosis/pathology , Treatment Outcome
8.
Presse Med ; 27(2): 60-3, 1998 Jan 17.
Article in French | MEDLINE | ID: mdl-9768051

ABSTRACT

BACKGROUND: A well-established manifestation of neoplastic disease, nephrotic syndrome is infrequently associated with thymoma. Only 18 cases have been reported in the literature. CASE REPORTS: A 65-year-old man and a 60-year-old woman were seen for nephrotic syndrome. Minimal change renal disease was observed in the first patient whose nephrotic syndrome was steroid resistant. The second patient had membranous glomerulopathy and pure red cell aplasia. In both cases, nephrotic syndrome revealed thymoma. DISCUSSION: The histological lesions in 17 of the 18 biopsied cases reported in the literature were minimal change in 10, focal segmental glomerulonephritis in 4, proliferative glomerulonephritis in 2, and membranous glomerulopathy in only one. The outcome of the nephrotic syndrome was dependent on the success of the thymoma treatment. Some patients responded to steroid and immunosuppressive agents. Pure red cell aplasia is uncommon and prognosis is poor. It can be successfully treated with cyclosporin A as in our second case.


Subject(s)
Glomerulonephritis/diagnosis , Nephrotic Syndrome/diagnosis , Thymoma/diagnosis , Thymus Neoplasms/diagnosis , Adult , Aged , Biopsy , Female , Glomerulonephritis/complications , Glomerulonephritis/drug therapy , Glomerulonephritis/pathology , Humans , Immunosuppressive Agents/therapeutic use , Kidney/pathology , Male , Middle Aged , Nephrotic Syndrome/complications , Nephrotic Syndrome/drug therapy , Nephrotic Syndrome/pathology , Steroids/therapeutic use , Thymoma/complications , Thymoma/drug therapy , Thymus Neoplasms/complications , Thymus Neoplasms/drug therapy , Treatment Outcome
11.
Presse Med ; 24(23): 1075-7, 1995 Jun 24.
Article in French | MEDLINE | ID: mdl-7567808

ABSTRACT

OBJECTIVES: In order to better establish a prevention strategy based on mupirocin, we evaluated nasal carriage of Staphylococcus aureus in haemodialysis patients over a 15 month period. METHODS: Search for Staphylococcus aureus in the nasal cavities was made every 2 months in 92 chronic dialysis patients. These patients were divided into 3 groups according to the nature of the carriage: non-permanent, intermittent or permanent. RESULTS: Among the 80 patients retained for analysis, there were 27.5% with intermittent carriage and 11.25% with permanent carriage. Factors which appeared to protect against carriage were rural residence and home self-dialysis. CONCLUSION: Repeated long-term search for nasal carriage of Staphylococcus aureus has provided reliable data for each patient and gave information on the effects of epidemiological conditions and health care structures.


Subject(s)
Nasal Cavity/microbiology , Nasal Mucosa/microbiology , Renal Dialysis/adverse effects , Staphylococcal Infections/epidemiology , Staphylococcus aureus/isolation & purification , Aged , Female , HLA Antigens/analysis , Humans , Male , Middle Aged , Prevalence , Staphylococcal Infections/etiology , Staphylococcal Infections/immunology , Staphylococcal Infections/microbiology
12.
Nephrologie ; 15(2): 129-31, 1994.
Article in French | MEDLINE | ID: mdl-8047197

ABSTRACT

From January 1986 to December 1990, we studied angiographically the subclavian-brachiocephalic vein of 100 patients dialysed on subclavian catheter for 50 (first group) and on internal jugular catheter for the 50 others (second group). These 2 groups are not statistically different for age: 61.6 +/- 11.3 years in the first and 61 +/- 11.1 in the second, for sex: respectively 48% and 56% of women, for time-length of catheter insertion: respectively 31 +/- 21.8 days and 31.7 +/- 16, and for number of dialysis sessions: respectively 13.5 +/- 9.1 and 13.6 +/- 7.1. The type of catheters, the frequency of removal for poor flow (16% in both groups) or for infections (6% in both groups) and the local nursing are similar in the 2 groups. Only the side of cannulation differs: the right side is used in 58% of cases in the first group and 78% in the second one. The angiographic study reveals a stenosis of the vein in 42% of the subclavian group and in 10% of the internal jugular group. The left side presents more risks of stenosis than the right, what can be explained by anatomical features. The strictures, whose severity is variable, are mainly located at and slightly above the junction of jugular and subclavian veins. This significative difference in favour of the internal jugular route asserts its superiority on subclavian route in respect of venous access of dialysed patients.


Subject(s)
Catheterization, Central Venous/adverse effects , Catheters, Indwelling/adverse effects , Jugular Veins/injuries , Renal Dialysis , Subclavian Vein/injuries , Aged , Brachiocephalic Trunk/injuries , Constriction, Pathologic/diagnostic imaging , Constriction, Pathologic/etiology , Female , Humans , Jugular Veins/diagnostic imaging , Male , Middle Aged , Phlebography , Prospective Studies , Risk , Subclavian Vein/diagnostic imaging
13.
Presse Med ; 22(14): 675-9, 1993 Apr 17.
Article in French | MEDLINE | ID: mdl-8511114

ABSTRACT

An IgG kappa light-chain myeloma, remarkable for the presence of inclusions in plasmocytes and proximal renal tubular cells, was discovered during investigations for renal failure associated with partial Fanconi's syndrome. An immunohistochemical study showed that the crystalline inclusions were positive for IgG and kappa light-chain in plasmocytes and exclusively for kappa light-chain in the renal tubular cells. An ultrastructural study showed that the inclusions were localized in lysosomes and had a 55 A periodicity. This case is similar to the forty odd myelomas or light-chain diseases reported in the literature and revealed by Fanconi's syndrome. Their prognosis is good, with a slow progression towards late renal failure. In our patient the preference of lesions for proximal tubular cells, the site of protein catabolism, was particular since in myelomas they are usually located in the distal tubular cells.


Subject(s)
Fanconi Syndrome/complications , Immunoglobulin kappa-Chains , Plasmacytoma/complications , Aged , Fanconi Syndrome/pathology , Female , Fluorescent Antibody Technique , Humans , Kidney/pathology , Kidney/ultrastructure , Microscopy, Electron , Plasma Cells/pathology , Plasma Cells/ultrastructure , Plasmacytoma/pathology , Plasmacytoma/ultrastructure
14.
Nephrologie ; 13(3): 127-33, 1992.
Article in French | MEDLINE | ID: mdl-1641055

ABSTRACT

From January 1986 to December 1990, we studied angiographically the subclavian-brachiocephalic vein of 100 patients dialysed on subclavian catheter for 50 (first group) and on internal jugular catheter for the 50 others (second group). These 2 groups are not statistically different for age: 61.6 +/- 11.3 years in the first and 61 +/- 11.1 in the second, for sex: respectively 48% and 56% of women, for time-length of catheter insertion: respectively 31 +/- 21.8 days and 31.7 +/- 16, and for number of dialysis sessions: respectively 13.5 +/- 9.1 and 13.6 +/- 7.1. The type of catheters, the frequency of removal for poor flow (16% in both groups) or for infections (6% in both groups) and the local nursing are similar in the 2 groups. Only the side of cannulation differs: the right side is used in 58% of cases in the first group and 78% in the second one. The angiographic study reveals a stenosis of the vein in 42% of the subclavian group and in 10% of the internal jugular group: a dramatic difference in favour of the internal jugular route, whose superiority on subclavian route is asserted in respect of venous access of dialysed patients.


Subject(s)
Catheterization/adverse effects , Jugular Veins/diagnostic imaging , Renal Dialysis/adverse effects , Subclavian Vein/diagnostic imaging , Vascular Diseases/etiology , Aged , Constriction, Pathologic/diagnostic imaging , Constriction, Pathologic/etiology , Female , Humans , Male , Middle Aged , Phlebography , Vascular Diseases/diagnostic imaging
16.
Nephrol Dial Transplant ; 6(10): 722-4, 1991.
Article in English | MEDLINE | ID: mdl-1754109

ABSTRACT

From January 1986 to December 1990 we studied angiographically the subclavian-brachiocephalic vein of 100 patients dialysed by subclavian catheter for 50 (first group) and by internal jugular catheter for the 50 others (second group). These two groups were not statistically different as regards age (61.6 +/- 11.3 years in the first and 61 +/- 11.1 in the second), sex (48% and 56% were women), duration of catheter insertion (31 +/- 21.8 and 31.7 +/- 16 days), and the number of dialysis sessions (13.5 +/- 9.1 and 13.6 +/- 7.1). The type of catheters, the frequency of removal for poor flow (16% in both groups) or infections (6% in both groups), and the local nursing were similar in the two groups. The only difference was the side of cannulation: the right side in 58% of cases in group 1 and 78% in group 2. The angiographic study revealed a stenosis of the vein in 42% of the subclavian group and in 10% of the internal jugular group: a dramatic difference in favour of the internal jugular route, whose superiority over the subclavian route is asserted in respect of venous access of dialysed patients.


Subject(s)
Catheterization, Central Venous/adverse effects , Jugular Veins/diagnostic imaging , Renal Dialysis/adverse effects , Subclavian Vein/diagnostic imaging , Vascular Diseases/etiology , Aged , Female , Humans , Male , Middle Aged , Radiography
19.
Nephrologie ; 11(4): 217-21, 1990.
Article in French | MEDLINE | ID: mdl-2074921

ABSTRACT

It can be difficult to distinguish between primary hyperoxaluria at end-stage renal failure and secondary oxalosis, all the more as primary hyperoxaluria can be latent for a long time and occur at a late stage. A 57 year-old woman, without family nor personal history of urolithiasis, receives regular hemodialysis for a renal failure discovered at end-stage. Eighteen months later, calcium oxalate deposits appear in the skin, bone marrow and both kidneys, suggesting secondary oxalosis. An other 57 year-old woman presents a chronic renal failure due to bilateral urolithiasis, whose surgery has caused a dramatic decrease of renal function requiring regular hemodialysis. Because of apparition of severe bone alterations, a parathyroidectomy is realized, and because of calcium oxalate deposition in the skin and bone marrow, primary hyperoxaluria is suspected. In both observations, the enzyme activity determination in a liver biopsy gives the diagnosis of primary hyperoxaluria.


Subject(s)
Alanine Transaminase/deficiency , Hyperoxaluria, Primary/diagnosis , Kidney Failure, Chronic/complications , Liver/enzymology , Transaminases , Biopsy , Bone Marrow/chemistry , Bone Marrow/pathology , Bone and Bones/pathology , Calcium Oxalate/analysis , Female , Humans , Hyperoxaluria, Primary/complications , Hyperoxaluria, Primary/pathology , Kidney/chemistry , Kidney Failure, Chronic/therapy , Middle Aged , Renal Dialysis , Skin/chemistry , Skin/pathology
SELECTION OF CITATIONS
SEARCH DETAIL
...