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1.
Nephrology (Carlton) ; 25(9): 708-713, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32400945

RESUMO

AIM: Clinical presentation and course of Immunoglobulin A nephropathy vary by ethnicity and geography and significance of extracapillary proliferation or crescents (IgAN-C) in Southeast Asia is not well described. We aimed to describe the clinical course of IgAN-C in Singapore. METHODS: Retrospective cohort study of adult biopsy-proven IgAN diagnosed between February 2011 and October 2016 in 2 hospital-based nephrology units. Outcome was chronic kidney disease (CKD) progression, defined as reduction in eGFR ≥50% or end stage renal failure (ESRF). RESULTS: One hundred and forty-five patients were studied. Among individuals with IgAN-C (n = 44, 30%), 38 patients had cellular or fibrocellular crescents in 1 to 25% of the glomeruli and 6 had crescents in >25%. Median eGFR was 54 (33, 83) mL/min/1.73 m2 . Compared to IgAN without crescents, IgAN-C had greater proteinuria (median 2.9 [1.4, 5.4] g/g vs 1.9 [1.1, 3.6] g/g, P = .03) and more had endocapillary hypercellularity (96% vs 39%, P < .001). IgAN-C were also more likely to receive immunosuppressants (66% vs 43%, P = .01) such as prednisolone (63% vs 38%, P = .006) and cyclophosphamide (12% vs 2%, P = .03). Median follow up was 27 (12, 46) months. IgAN-C were more likely to achieve proteinuria reduction ≥50% at 6 months (66% vs 44%, P = .03). CKD progression within 12 months was not different among those with and without crescents (13% vs 10% respectively, P = .73). However, immunosuppressant treatment of IgAN-C was associated with reduced ESRF (0 vs 20%, P = .03). CONCLUSION: Immunosuppressants may attenuate the risk of ESRF in IgAN-C.


Assuntos
Glomerulonefrite por IGA , Falência Renal Crônica , Glomérulos Renais/patologia , Proteinúria , Biópsia/métodos , Estudos de Coortes , Progressão da Doença , Etnicidade , Feminino , Taxa de Filtração Glomerular , Glomerulonefrite por IGA/complicações , Glomerulonefrite por IGA/epidemiologia , Glomerulonefrite por IGA/patologia , Glomerulonefrite por IGA/terapia , Humanos , Imunossupressores/uso terapêutico , Falência Renal Crônica/epidemiologia , Falência Renal Crônica/etiologia , Masculino , Pessoa de Meia-Idade , Proteinúria/diagnóstico , Proteinúria/etiologia , Singapura/epidemiologia
2.
BMC Nephrol ; 19(1): 185, 2018 07 24.
Artigo em Inglês | MEDLINE | ID: mdl-30041621

RESUMO

BACKGROUND: End stage renal disease (ESRD) is on the rise globally. Varicella infection among adult patients with ESRD has been reported to lead to multiple complications and even death. While varicella vaccination has been recommended in paediatric renal patients; recommendation on varicella vaccination among adult patients with ESRD remained sparse. This review is aimed at evaluating the impact of varicella infection among adult patients with ESRD and make a recommendation for vaccination. METHODS: Three databases (PubMed, Embase and Cumulative Index to Nursing and Allied Health Literature (CINAHL)) were searched in April 2018 with keywords 'varicella, chronic kidney failure, chronic kidney disease, renal replacement therapy, kidney transplantation, end stage renal disease, end stage renal failure, chicken pox, vaccine, vaccination and complications'. RESULTS: 29 articles were selected for review. The studies were mainly case reports, and they included measured outcomes: prevalence of seronegativity, impact (morbidity, length of stay, and mortality) of varicella among patients with ESRD, seroconversion rates and safety of varicella vaccination. The prevalence of seronegativity among varicella-infected ESRD adults was found to be at 42 to 100%. Nineteen deaths were reported. At least 54 patients have had complications from varicella infection. Seroconversion rate post vaccination was found to be around 64-94%. CONCLUSION: Varicella is associated with significant morbidity and mortality rates in adult patients with ESRD. Varicella vaccination should be considered for the vulnerable, seronegative patients.


Assuntos
Varicela/diagnóstico , Varicela/epidemiologia , Falência Renal Crônica/diagnóstico , Falência Renal Crônica/epidemiologia , Bases de Dados Factuais/tendências , Humanos , Falência Renal Crônica/virologia
4.
Cureus ; 14(9): e29429, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-36159357

RESUMO

Spontaneous perinephric hematoma is an uncommon but serious condition that is typically caused by tumor hemorrhage or vascular disease such as polyarteritis nodosa. We describe a 78-year-old Chinese gentleman with underlying chronic kidney disease, renal cysts, non-obstructive renal stones, hypertension, ischemic heart disease, and atrial fibrillation who was on rivaroxaban and clopidogrel. He developed spontaneous perinephric hematoma complicated by acute kidney injury, anemia, and myocardial infarction who underwent angioembolization and packed cell transfusion. He did not have further bleeding episodes, and his kidney function improved before discharge.

5.
BMJ Case Rep ; 12(5)2019 May 22.
Artigo em Inglês | MEDLINE | ID: mdl-31122958

RESUMO

Inflammatory conditions manifest with a broad spectrum of signs and symptoms. Panniculitis is such a condition affecting the subcutaneous fat and presents as tender erythematous nodules. It is also associated with a systemic response and has been described in the literature as early as in 1892 by Pfeifer and in the 1920s by Weber and Christian. We present an unusual case of a Caucasian man with recurrent febrile illness, systemic inflammatory response and renal dysfunction requiring acute high dependency care. The authors successfully treated him with an antiproliferative agent, mycophenolate mofetil, which resulted in preventing him from having further episodes.


Assuntos
Paniculite Nodular não Supurativa/diagnóstico , Idoso , Diagnóstico Diferencial , Febre/etiologia , Humanos , Imunossupressores/administração & dosagem , Imunossupressores/uso terapêutico , Masculino , Ácido Micofenólico/administração & dosagem , Ácido Micofenólico/uso terapêutico , Paniculite Nodular não Supurativa/complicações , Paniculite Nodular não Supurativa/tratamento farmacológico , Síndrome
8.
Clin Kidney J ; 9(2): 222-6, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26985372

RESUMO

BACKGROUND: Crescent formation generally reflects severe glomerular injury. There is sparse literature on post-infectious glomerulonephritis (PIGN) with crescents in adults. This retrospective study looked at nine such cases to see if there is a correlation between the severity of presentation, steroid treatment, histological severity and outcome. METHODS: Biopsy reports of all the adults who underwent kidney biopsy from February 2010 to June 2014 in a tertiary care hospital were screened and all the cases with the diagnosis of PIGN with crescents were selected. Clinical presentation, laboratory data, histology, treatment and outcome were analysed. RESULTS: Six patients had evidence of recent/current infection, but all except two were non-streptococcal. The mean creatinine was 360.67 µmol/L (range 70.72-770.85) and the mean estimated glomerular filtration rate (MDRD eGFR) was 30.28 mL/min/1.73 m(2) (range 6.4-111.1) on presentation. All five patients who were treated with steroids had an excellent response. Among the four patients who did not receive steroids, two were left with significant renal impairment (mean MDRD eGFR 23.5 mL/min/1.73 m(2)) at a mean follow-up of 15.5 months (range 10-21). The mean percentage of glomeruli with crescents was 36.13% (range 11.76-100) and except in one, there was no tubular atrophy or interstitial fibrosis and none had glomerulosclerosis. None of the patients progressed to end-stage renal disease. CONCLUSION: Non-streptococcal infections are more common precipitants. There was no correlation between histological and clinical severity. Patients treated with steroids had better renal outcomes.

10.
Ann Indian Acad Neurol ; 16(4): 687-9, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24339610

RESUMO

Three cases with manifestations of right heart failure, shock, metabolic acidosis, and renal failure in varying combination were admitted with paraparesis. Nerve conduction study suggested predominantly motor and mainly axonal type of neuropathy. Rapid reversal of shock, acidosis, and multi-organ dysfunction with timely infusion of thiamine was followed by the complete neurological recovery.

11.
BMJ Case Rep ; 20092009.
Artigo em Inglês | MEDLINE | ID: mdl-21887158

RESUMO

Pregnancy in women with lupus nephritis is associated with increased risk of fetal and maternal complications. The risk of poor outcome is higher if there are signs of disease activity at conception. The presence of hypertension and anti-phospholipid antibodies worsens the prognosis. There are very few therapeutic options in view of the threat of various congenital anomalies and associated comorbidities. Mycofenolate mofetil (MMF) is contraindicated during pregnancy due to risk of congenital anomalies and fetal loss. This is a case of a woman with membranous lupus nephritis, who went into partial remission with rituximab and became pregnant while on maintenance therapy with MMF. Due to lack of alternative options, she continued to be given MMF. She had a successful outcome in spite of the presence of the poor prognostic factors. The baby had asymptomatic non-communicating duplication of the oesophagus, which has never been reported before in association with MMF during pregnancy.

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