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1.
Semin Dial ; 2024 May 21.
Article in English | MEDLINE | ID: mdl-38773836
2.
Saudi J Kidney Dis Transpl ; 32(1): 245-248, 2021.
Article in English | MEDLINE | ID: mdl-34145140

ABSTRACT

Fungal peritonitis (FP) is a rare complication of peritoneal dialysis (PD). Candida tropicalis infections are rarely reported in literature. The authors present the first case of FP with peritoneal abscess due to C. tropicalis in a 22-year-old woman admitted to our hospital with septic shock. Abdominal tomography demonstrated an abscess in peritoneal space and intraluminal bubble appearance in femoral venous and arterial circulation. PD fluid specimens and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis revealed fungus growth of C. tropicalis. Fluconazole therapy was administered accompanied by catheter removal and mechanical ventilation with vasopressor support. The patient recovered after 23 days of hospitalization and was discharged. FP represents high mobility and mortality unless infection source control and appropriate antimicrobial therapy are implemented accompanied by PD catheter removal. The use of MALDI-TOF MS for PD-related peritonitis pathogen identification can promote early identification and appropriate antibiotic therapy, especially in C. tropicalis infection.


Subject(s)
Candida tropicalis , Candidiasis/diagnosis , Peritoneal Dialysis , Peritonitis/diagnosis , Female , Humans , Peritonitis/microbiology , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Young Adult
3.
J. bras. nefrol ; 42(4): 484-488, Oct.-Dec. 2020. tab, graf
Article in English, Portuguese | LILACS | ID: biblio-1154625

ABSTRACT

ABSTRACT Introduction: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. Case presentation: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephrotic syndrome for 2 weeks. The patient was diagnosed with ING by percutaneous renal biopsy results, which showed global nodular mesangial matrix expansion, with linear staining accentuation of glomerular and tubular basement membrane for Immunoglobulin G (IgG) and albumin on immunofluorescence. Conclusions: ING is a rare disease with a poor renal prognosis and wide diagnostic approach; we highlight the importance of analyzing every piece of detail together to reach a definitive diagnosis.


RESUMO Introdução: A glomerulosclerose nodular idiopática (GNI) tem um padrão histológico glomerular vasculopático. Apresentação do caso: Os autores apresentam o caso de uma mulher latino-americana, de 44 anos, fumante, com hipertensão e doença arterial periférica; com síndrome nefrótica por 2 semanas. Ela foi diagnosticada com GNI por biópsia renal percutânea, que mostrou expansão generalizada da matriz mesangial nodular, com acentuação de coloração linear na membrana basal glomerular e tubular para imunoglobulina G (IgG) e albumina à imunofluorescência. Conclusões: A GNI é uma doença rara, com mau prognóstico renal, e com necessidade de uma ampla abordagem diagnóstica. Demonstramos aqui a importância de se analisar todos os detalhes em conjunto para realizar um diagnóstico definitivo.


Subject(s)
Humans , Female , Adult , Diabetic Nephropathies/diagnosis , Hypertension , Nephrotic Syndrome , Diagnosis, Differential , Kidney
4.
J Bras Nefrol ; 42(4): 484-488, 2020.
Article in English, Portuguese | MEDLINE | ID: mdl-32776085

ABSTRACT

INTRODUCTION: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. CASE PRESENTATION: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephrotic syndrome for 2 weeks. The patient was diagnosed with ING by percutaneous renal biopsy results, which showed global nodular mesangial matrix expansion, with linear staining accentuation of glomerular and tubular basement membrane for Immunoglobulin G (IgG) and albumin on immunofluorescence. CONCLUSIONS: ING is a rare disease with a poor renal prognosis and wide diagnostic approach; we highlight the importance of analyzing every piece of detail together to reach a definitive diagnosis.


Subject(s)
Diabetic Nephropathies , Hypertension , Nephrotic Syndrome , Adult , Diabetic Nephropathies/diagnosis , Diagnosis, Differential , Female , Humans , Kidney
6.
Arq. neuropsiquiatr ; 76(12): 827-830, Dec. 2018. tab
Article in English | LILACS | ID: biblio-983865

ABSTRACT

ABSTRACT Restless legs syndrome (RLS) is a frequent complication of hemodialysis that has been associated with poor quality of life and increased risk for complications. Nevertheless, few studies regarding this entity exist in resource-limited settings. Objectives: To determine the prevalence of RLS among Mexican patients on hemodialysis; and compare these patients with a control group of the same population. Methods: We recruited 105 hemodialysis patients. Restless legs syndrome was diagnosed according to the updated criteria set out by the International RLS Study Group. We selected patients who did not meet the criteria, as controls. Results: We found an RLS prevalence of 18%. The RLS patients had a significantly higher prevalence of iron deficiency anemia and uremic pruritus. None of the patients reported RLS symptoms prior to hemodialysis initiation. Conclusions: Restless legs syndrome is common among Mexican patients on hemodialysis. Larger studies are required to address the impact of RLS in hemodialysis patients.


RESUMEN El síndrome de piernas inquietas (SPI) es una complicación de la hemodiálisis que se ha asociado con menor calidad de vida y riesgo aumentado de complicaciones. Sin embargo, existen pocos estudios acerca de esta entidad en escenarios de recursos limitados. Objetivos: Determinar la prevalencia de SPI en pacientes mexicanos en hemodiálisis, y comparar las características con un grupo control de la misma población. Métodos: Reclutamos 105 pacientes en hemodiálisis. El SPI se diagnosticó de acuerdo con los criterios actualizados del grupo de estudio internacional del síndrome de piernas inquietas. Seleccionamos a los pacientes que no cumplieron dichos criterios como controles. Resultados: Encontramos una prevalencia de SPI del 18%. Los pacientes con SPI tenían una prevalencia más alta de anemia ferropénica, y prurito urémico. Ninguno de los pacientes reportó síntomas de SPI previo a iniciar la hemodiálisis. Conclusiones: El SPI es frecuente en pacientes mexicanos en hemodiálisis; se requieren estudios más grandes para evaluar el impacto del síndrome en ésta población.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Restless Legs Syndrome/etiology , Renal Dialysis/adverse effects , Kidney Failure, Chronic/complications , Restless Legs Syndrome/epidemiology , Case-Control Studies , Comorbidity , Prevalence , Renal Dialysis/statistics & numerical data , Anemia, Iron-Deficiency/complications , Anemia, Iron-Deficiency/epidemiology , Diabetes Complications , Diabetes Mellitus/epidemiology , Hypertension/complications , Hypertension/epidemiology , Kidney Failure, Chronic/therapy , Kidney Failure, Chronic/epidemiology , Mexico/epidemiology
7.
Arq Neuropsiquiatr ; 76(12): 827-830, 2018 12.
Article in English | MEDLINE | ID: mdl-30698206

ABSTRACT

OBJECTIVES: Restless legs syndrome (RLS) is a frequent complication of hemodialysis that has been associated with poor quality of life and increased risk for complications. Nevertheless, few studies regarding this entity exist in resource-limited settings. To determine the prevalence of RLS among Mexican patients on hemodialysis; and compare these patients with a control group of the same population. METHODS: We recruited 105 hemodialysis patients. Restless legs syndrome was diagnosed according to the updated criteria set out by the International RLS Study Group. We selected patients who did not meet the criteria, as controls. RESULTS: We found an RLS prevalence of 18%. The RLS patients had a significantly higher prevalence of iron deficiency anemia and uremic pruritus. None of the patients reported RLS symptoms prior to hemodialysis initiation. CONCLUSIONS: Restless legs syndrome is common among Mexican patients on hemodialysis. Larger studies are required to address the impact of RLS in hemodialysis patients.


Subject(s)
Kidney Failure, Chronic/complications , Renal Dialysis/adverse effects , Restless Legs Syndrome/etiology , Adult , Aged , Anemia, Iron-Deficiency/complications , Anemia, Iron-Deficiency/epidemiology , Case-Control Studies , Comorbidity , Diabetes Complications , Diabetes Mellitus/epidemiology , Female , Humans , Hypertension/complications , Hypertension/epidemiology , Kidney Failure, Chronic/epidemiology , Kidney Failure, Chronic/therapy , Male , Mexico/epidemiology , Middle Aged , Prevalence , Renal Dialysis/statistics & numerical data , Restless Legs Syndrome/epidemiology
8.
Ther Apher Dial ; 21(5): 459-464, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28805348

ABSTRACT

Intradialytic hypotension is common complication in stage 5 chronic kidney disease patients on hemodialysis. Incidence ranges from 15 to 30%. These patients have levocarnitine deficiency. A randomized, placebo-controlled quadruple-blinded trial was designed to demonstrate the levocarnitine efficiency on intradialytic hypotension prevention. Patients were randomized into four groups, to receive levocarnitine or placebo. During the intervention period, levocarnitine and placebo was administered 0 and 30 min before each hemodialysis session, respectively. During the trial, 33 patients received 1188 hemodialysis sessions. We identified 239 (21.3%) intradialytic hypotension episodes. The intradialytic hypotension episodes were less frequent in the levocarnitine group (9.3%, 60 IH events) (P < 0.001). Hemodialysis is frequently perplexed by intradialytic hypotension episodes. Levocarnitine supplementation before each hemodialysis session efficiently diminishes the intradialytic hypotension episodes. This is a new application method that must be considered and explored.


Subject(s)
Carnitine/administration & dosage , Hypotension/prevention & control , Kidney Failure, Chronic/therapy , Renal Dialysis/methods , Adult , Carnitine/deficiency , Double-Blind Method , Female , Humans , Hypotension/epidemiology , Hypotension/etiology , Male , Middle Aged , Prospective Studies , Renal Dialysis/adverse effects , Treatment Outcome
9.
Pneumologia ; 65(3): 161-3, 2016.
Article in English | MEDLINE | ID: mdl-29542896

ABSTRACT

Mycobacterium tuberculosis as a cause of both chylothorax and chylous ascites is extremely rare. A 46-year-old non-adherent woman with AIDS and pulmonary tuberculosis presented to our clinic with dyspnea, pleuritic chest and abdominal pain. Chest x-ray demonstrated a left pleural effusion. Contrast-enhanced CT showed free abdominal fluid. Thoracentesis revealed a chylothorax, and paracentesis a chylous ascites. AFB staining and PCR for M. tuberculosis (GeneXpert MTB/ RIF Assay) were both negative. Malignant cells cytology also tested negative. Tuberculosis could account for both chylothorax and chylousascites, as she clinically improved when antituberculous drugs were resumed. Even when PCR tested negative, M. tuberculosis should be included in the differential diagnosis because of its therapeutic and prognostic implications. Keywords: Chylothorax, chylous ascites, Mycobacterium tuberculosis, acquired immunodeficiency syndrom, antituberculous drugs.


Subject(s)
AIDS-Related Opportunistic Infections/complications , Acquired Immunodeficiency Syndrome/complications , Chylothorax/microbiology , Chylous Ascites/microbiology , Immunocompromised Host , Polymerase Chain Reaction , Tuberculosis/complications , Antitubercular Agents/therapeutic use , Chylothorax/diagnosis , Chylothorax/therapy , Chylous Ascites/diagnosis , Chylous Ascites/therapy , Female , Humans , Middle Aged , Paracentesis/methods , Treatment Outcome , Tuberculosis/diagnosis , Tuberculosis/drug therapy
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