keyword
https://read.qxmd.com/read/36291403/intrinsic-kidney-pathology-in-children-and-adolescents-following-covid-19-vaccination-a-systematic-review
#21
REVIEW
Henry H L Wu, Mohan Shenoy, Philip A Kalra, Rajkumar Chinnadurai
Global COVID-19 vaccination programs for children and adolescents have been developed with international clinical trial data confirming COVID-19 mRNA vaccine safety and efficacy for the pediatric population. The impact of COVID-19 vaccination in the kidneys is thought to be explained by a complex immune-mediated relationship between the two, although the pathophysiological mechanisms of how COVID-19 vaccination potentially induces kidney pathology are not presently well known. Whilst intrinsic kidney pathologies following COVID-19 vaccination have been reported in adults, such cases are only being recently reported with greater frequency in children and adolescents...
September 26, 2022: Children
https://read.qxmd.com/read/36253737/a-rare-case-of-immunoglobulin-a-dominant-post-infectious-glomerulonephritis-iga-pign-in-a-young-patient
#22
JOURNAL ARTICLE
A Saghar, G Klaus, B Trutnau, M Kömhoff, H J Gröne, S Weber
BACKGROUND: Immunoglobulin A dominant postinfectious glomerulonephritis (IgA PIGN) is a unique medical entity that is rare in the paediatric population. It usually presents with severe renal failure, heavy proteinuria, hypertension, and hypocomplementemia and frequently has an unfavourable prognosis. IgA PIGN generally occurs in association with staphylococcal infections and diabetes mellitus in adult patients. Other pathogens include Escherichia coli and Streptococcus sp. Immunofluorescence studies of kidney biopsy samples show IgA as dominant or codominant antibody...
October 17, 2022: BMC Nephrology
https://read.qxmd.com/read/36090503/twenty-year-follow-up-of-patients-with-epidemic-glomerulonephritis-due-to-streptococcus-zooepidemicus-in-brazil
#23
JOURNAL ARTICLE
Sergio Wyton Pinto, Helbert do Nascimento Lima, Thalles Trindade de Abreu, Alba Otoni, Paulo Cesar Koch Nogueira, Ricardo Sesso
Introduction: Post-streptococcal glomerulonephritis (PSGN) has a good prognosis in children, but few studies have evaluated the long-term renal outcomes in adults with PSGN. Methods: In a follow-up study, 47 predominantly adult patients with PSGN due to group C Streptococcus zooepidemicus were reassessed 20 years after an outbreak in Nova Serrana, Brazil. We evaluated clinical characteristics, renal outcomes, and the trajectory of the estimated glomerular filtration rate (eGFR) by the creatinine-based chronic kidney disease-epidemiology collaboration equation from 5 follow-up assessments...
September 2022: KI Reports
https://read.qxmd.com/read/36065409/a-case-of-paediatric-anti-glomerular-basement-membrane-disease-associated-with-thrombotic-thrombocytopenic-purpura
#24
Joseph McAllister, Pradeep Nagisetty, Kay Tyerman
Anti-GBM disease is a rare vasculitis that causes rapid progressive glomerulonephritis and pulmonary haemorrhage. It is usually an adult diagnosis with isolated paediatric cases reported. Thrombotic thrombocytopenic purpura (TTP) is a rare thrombotic microangiopathy mainly affecting adults that causes multiorgan ischaemia, microangiopathic haemolytic anaemia, and thrombocytopenia. We present the first paediatric case of concurrent anti-GBM disease and TTP. A 14-year-old boy presented with acute kidney failure and severe pulmonary haemorrhage due to anti-GBM disease, confirmed on auto-antibody testing...
2022: Case Reports in Nephrology
https://read.qxmd.com/read/35875713/glomerulopathy-in-patients-with-dermatomyositis-in-early-active-disease-clinical-pathological-and-capillaroscopic-manifestations-and-response-to-treatment
#25
JOURNAL ARTICLE
Saeedeh Shenavandeh, Mahsa TorabiJahromi, Sahand Mohammadzadeh
INTRODUCTION: Idiopathic inflammatory myopathies (IIMs) are a group of systemic connective tissue diseases that present with muscular and extra-muscular manifestations. There are few reports on kidney involvement, especially in dermatomyositis (DM) patients. We evaluated the clinical, laboratory, capillaroscopy, and kidney pathology of patients with DM, who presented with proteinuria during the first year, and followed them for response to treatment. MATERIAL AND METHODS: We evaluated 205 patients with proximal muscle weakness or high muscle enzymes, who referred to the nailfold capillaroscopy clinic from April 2010 to October 2021...
2022: Reumatologia
https://read.qxmd.com/read/35310798/rapidly-progressive-glomerulonephritis-in-children
#26
REVIEW
Khemchand N Moorani, Madiha Aziz, Farhana Amanullah
Rapidly progressive glomerulonephritis (RPGN), characterized by a rapid development of nephritis with loss of kidney function in days or weeks, is typically associated histologically, with crescents in most glomeruli; and is a challenging problem, particularly in low resource settings. RPGN is a diagnostic and therapeutic emergency requiring prompt evaluation and treatment to prevent poor outcomes. Histopathologically, RPGN consists of four major categories, anti-glomerular basement membrane (GBM) disease, immune complex mediated, pauci-immune disorders and idiopathic /overlap disorders...
January 2022: Pakistan Journal of Medical Sciences Quarterly
https://read.qxmd.com/read/35123445/thrombotic-microangiopathy-with-transiently-positive-direct-coombs-test-in-an-adult-with-poststreptococcal-acute-glomerulonephritis-a-case-report
#27
JOURNAL ARTICLE
Dan Inoue, Takashi Oda, Sachiko Iwama, Takahiko Hoshino, Mitsuya Mukae, Takashi Sakai, Aki Kojima, Takahiro Uchida, Tadasu Kojima, Kentaro Sugisaki, Tomohiro Tomiyasu, Noriko Yoshikawa, Muneharu Yamada
BACKGROUND: To date, a few case reports have described the association between poststreptococcal acute glomerulonephritis (PSAGN) and hemolytic anemia/thrombocytopenia, both with or without a pathology similar to that of thrombotic microangiopathy (TMA). However, the detailed mechanism leading to the complication of TMA in PSAGN patients remains to be clarified. In contrast, infection with neuraminidase-producing Streptococcus pneumoniae is a well-known cause of TMA, and it has been reported that transient positivity of the direct Coombs test is observed in up to 90% of such patients...
February 5, 2022: BMC Nephrology
https://read.qxmd.com/read/35053628/intrinsic-kidney-pathology-following-covid-19-infection-in-children-and-adolescents-a-systematic-review
#28
REVIEW
Henry H L Wu, Mohan Shenoy, Philip A Kalra, Rajkumar Chinnadurai
Introduction: COVID-19 infections resulting in pathological kidney manifestations have frequently been reported in adults since the onset of the global COVID-19 pandemic in December 2019. Gradually, there have been an increased number of COVID-19-associated intrinsic kidney pathologies in children and adolescents reported as well. The pathophysiological mechanisms between COVID-19 and the onset of kidney pathology are not fully known in children; it remains a challenge to distinguish between intrinsic kidney pathologies that were caused directly by COVID-19 viral invasion, and cases which occurred as a result of multisystem inflammatory syndrome due to the infection...
December 22, 2021: Children
https://read.qxmd.com/read/34881426/antibiotics-for-treatment-of-sore-throat-in-children-and-adults
#29
REVIEW
Anneliese Spinks, Paul P Glasziou, Chris B Del Mar
BACKGROUND: Sore throat is a common reason for people to present for medical care and to be prescribed antibiotics. Overuse of antibiotics in primary medicine is a concern, hence it is important to establish their efficacy in treating sore throat and preventing secondary complications.  OBJECTIVES: To assess the effects of antibiotics for reducing symptoms of sore throat for child and adult patients. SEARCH METHODS: We searched CENTRAL 2021, Issue 2, MEDLINE (January 1966 to April week 1, 2021), Embase (January 1990 to April 2021), and two trial registries (searched 6 April 2021)...
December 9, 2021: Cochrane Database of Systematic Reviews
https://read.qxmd.com/read/34823573/inferior-vena-cava-thrombosis-as-a-possible-cause-of-nephrotic-range-proteinuria-two-case-reports
#30
JOURNAL ARTICLE
Yana Apostolova, Patricia Mehier, Salah D Qanadli, Menno Pruijm
BACKGROUND: Nephrotic-range proteinuria is a common reason for nephrological consultation in clinical practice. The differential diagnosis is wide, and generally focuses on different forms of glomerulonephritis, but other causes should not be overlooked, as illustrated in this article. CASE PRESENTATIONS: We report two female patients with nephrotic-range proteinuria. In the first case, a 46 year old Caucasian patient who suffered from extreme obesity (Body mass index (BMI) 77 kg/m2 ), acute kidney injury and nephrotic-range proteinuria were discovered during an emergency consultation for acute abdominal pain...
November 25, 2021: Journal of Medical Case Reports
https://read.qxmd.com/read/34767075/anti-glomerular-basement-membrane-disease-in-children-a-brief-overview
#31
REVIEW
Thomas Dowsett, Louise Oni
Anti-glomerular basement membrane disease (Anti-GBM), previously known as Goodpasture syndrome, is an extremely rare cause of rapidly progressive glomerulonephritis and chronic kidney disease stage 5 (CKD5) in children. It is associated with acute pulmonary haemorrhage and it has a poor prognosis. It is classified as an autoimmune, small-vessel vasculitis caused by autoantibody formation against the alpha-3 chain in type IV collagen found in the glomerular basement membrane. Evidence of anti-GBM antibodies in serum or histologically are required for diagnosis...
August 2022: Pediatric Nephrology
https://read.qxmd.com/read/34706910/conjunctivitis-episcleritis-and-anterior-uveitis-as-the-first-presenting-features-of-granulomatosis-with-polyangiitis
#32
JOURNAL ARTICLE
Lucas Donato Foster, Michael Nyugen, Edward Margolin
Granulomatosis with polyangiitis (GPA) is a rare disorder characterised by inflammation of small-sized and medium-sized blood vessels that result in damage to various organ systems, but it most commonly affects the respiratory tract and kidneys. It is one of the few entities that can present with ocular inflammation as well as renal impairment at the same time. We describe a case of a 38-year-old man with conjunctivitis, episcleritis, anterior uveitis as a first manifestation of GPA. His presentation with red eye and anterior uveitis prompted further workup, which revealed acute renal failure (creatinine 442 mmol/L), elevated inflammatory markers (erythrocyte sedimentation rate of 85 mmol/hour and C reactive protein of 72 mg/L), and a c-antineutrophil cytoplasmic antibody titre >8...
October 27, 2021: BMJ Case Reports
https://read.qxmd.com/read/34616577/-mycoplasma-pneumoniae-infection-associated-c3-glomerulopathy-presenting-as-severe-crescentic-glomerulonephritis
#33
Lalani De Silva, Dinesha Jayasinghe, Priyani Amarathunga
C3 glomerulopathy (C3GP) is a group of diseases caused by a deregulated complement system, which encompasses both dense deposit disease and C3 glomerulonephritis. Renal manifestations of C3GP are primarily of proliferative glomerulonephritis, and only a few case reports of crescentic glomerulonephritis (CGN) in association with C3GP are available. Here is a case of an adult South-Asian female, who was diagnosed as seropositive acute Mycoplasma pneumoniae infection, with associated systemic manifestations, including immune-type extravascular haemolysis and nephrotic range proteinuria...
2021: Case Reports in Nephrology
https://read.qxmd.com/read/34395134/concomitant-acute-rheumatic-fever-and-acute-post-streptococcal-glomerulonephritis
#34
Somshukla Ghosh, Kelli King-Morris, Joshua Shultz
Acute rheumatic fever (RF) and acute post Streptococcal glomerulonephritis (APSGN) are non-suppurative complications of a Group A Streptococcus (GAS) infection. The concomitant incidence of both complications in a patient is rare because nephritogenic and rheumatogenic strains belong to different serotypes of Group A beta-hemolytic Streptococcus (GABHS). We present a case of a 47-year-old female who had concomitant acute RF and APSGN from a  Streptococcus pyogenes  infection. It is important to have a high clinical suspicion for the sequela of GABHS infection in the setting of cardiac and renal disease following upper respiratory infection (URI) symptoms even in adults and in geographic locations with the nearly undetectable burden of acute RF because of the importance of secondary prophylaxis with an antibiotic...
July 2021: Curēus
https://read.qxmd.com/read/34379888/pediatric-p-anca-vasculitis-following-covid-19
#35
Yaron Fireizen, Cyrus Shahriary, Maria E Imperial, Inderpal Randhawa, Nastasia Nianiaris, Bugsu Ovunc
BACKGROUND: Perinuclear anti-neutrophil cytoplasmic antibodies (P-ANCA) are associated with a multisystem vasculitis affecting small blood vessels in the body. A handful of adult patients who developed vasculitis post-COVID-19 have been reported. Although SARS-CoV-2 has been shown to drive an exaggerated immune response in the pediatric population, such as in Multisystem Inflammatory Syndrome in Children (MIS-C), only one case of vasculitis following COVID-19 has been reported previously in children...
October 2021: Pediatric Pulmonology
https://read.qxmd.com/read/34341369/mortality-and-predictors-of-acute-kidney-injury-in-adults-a-hospital-based-prospective-observational-study
#36
JOURNAL ARTICLE
Abinet Abebe, Kabaye Kumela, Maekel Belay, Bezie Kebede, Yohannes Wobie
Acute kidney injury (AKI) is a major global public health problem. It is expensive to manage and associated with a high rate of prolonged hospitalization and in-hospital mortality. Little is known about the burden of acute kidney injury in moderate to low-income countries. We aim to assess predictors of in-hospital mortality among AKI patients admitted to the medical ward. We prospectively identified patients meeting kidney disease improving global outcomes (KIDGO) AKI definitions from April to August 2019...
August 2, 2021: Scientific Reports
https://read.qxmd.com/read/34178223/-a-study-on-malignant-arterial-hypertension-about-168-cases-at-the-unit-of-nephrology-internal-medecine-of-the-university-hospital-center-treichville-abidjan
#37
Jean Astrid Aka, Cyr Monlet Guei, Serge Didier Konan, Patrick Sery Diopoh, Syndou Sanogo, Hubert Kouamé Yao
Introduction: malignant arterial hypertension (MAH) is a nosologic disorder which has not been described in Nephrology. The purpose of this study was to describe the profile of patients with MAH in the Division of Nephrology and to identify prognostic factors. Methods: we conducted a retrospective, descriptive and analytical study from January 2013 to December 2018 in the Unit of Nephrology of the University Hospital Center in Treichville. The diagnosis of MAH was retained in patients with diastolic blood pressure (DBP) ≥ 130 mmHg, Keith Wegener grade III/IV hypertensive retinopathy, one or multiple visceral, cardiac and/or brain and/or renal diseases...
2021: Pan African Medical Journal
https://read.qxmd.com/read/34130975/anca-associated-glomerulonephritis-in-tuberculosis-a-paradoxical-reaction
#38
JOURNAL ARTICLE
Shane OBrien, Brenda Griffin, Anne Marie McLaughlin, Joseph Keane
We present a case of antineutrophil cytoplasmic antibodies (ANCA)-associated rapidly progressive glomerulonephritis in the context of treatment of pulmonary tuberculosis (TB). A 42-year-old woman was treated for drug-susceptible pulmonary TB and represented with paradoxical worsening of symptoms and radiological features. She was HIV negative. A severe acute kidney injury with features of glomerulonephritis was evident on admission. Perinuclear ANCA and antimyeloperoxidase antibodies were present in serum and renal biopsy was consistent with ANCA-associated vasculitis...
June 15, 2021: BMJ Case Reports
https://read.qxmd.com/read/34097292/more-than-tubular-dysfunction-cystinosis-and-kidney-outcomes
#39
JOURNAL ARTICLE
Bahriye Atmis, Aysun K Bayazit, Derya Cevizli, Deniz Kor, Hatice Busra Fidan, Atil Bisgin, Sebile Kilavuz, Ilker Unal, Kivilcim Eren Erdogan, Engin Melek, Gulfiliz Gonlusen, Ali Anarat, Neslihan Onenli Mungan
BACKGROUND: Cystinosis is a lysosomal storage disease that affects many tissues. Its prognosis depends predominantly on kidney involvement. Cystinosis has three clinical forms: nephropathic infantile, nephropathic juvenile and non-nephropathic adult. Proximal tubular dysfunction is prominent in the infantile form, whereas a combination of glomerular and tubular alterations are observed in the juvenile form. METHODS: Thirty-six children with nephropathic cystinosis were included in the study...
April 2022: Journal of Nephrology
https://read.qxmd.com/read/33893138/crescentic-postinfectious-glomerulonephritis-in-an-adult-patient-with-juvenile-nasopharyngeal-angiofibroma
#40
JOURNAL ARTICLE
Sheryll Anne Manalili, Paolo Nikolai So, Maria Ana Louise Naidas, Anthony Russell Villanueva
Crescentic glomerulonephritis is usually associated with an acute nephritic syndrome with rapidly declining renal function. Postinfectious cases usually have a higher possibility of recovery. Juvenile nasopharyngeal angiofibroma (JNA) is a rare, locally aggressive tumour affecting mostly young men. A 28-year-old man presented with recurrent JNA initially excised 2 years prior. The patient was initially managed as a case of airway obstruction and pneumonia. He developed tea-coloured urine, oedema and acute kidney failure requiring dialysis while awaiting surgery...
April 23, 2021: BMJ Case Reports
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