keyword
Keywords lupus, nephropathy, proteinuri...

lupus, nephropathy, proteinuria, dialysis

https://read.qxmd.com/read/38379641/case-report-thrombotic-thrombocytopenic-purpura-in-a-pregnant-woman-with-lupus-membranous-nephropathy-a-diagnostic-challenge
#1
Marina Leiva, Gustavo Navarro, J Daniel Carpio, Leopoldo Ardiles
A 27-year-old female at 20th week of pregnancy was admitted with edema, foamy urine, but normal blood pressure. Her blood count was normal, she had proteinuria of 3 g/day, creatinine 0.4 mg/dl, albumin 2.4 g/dl, and cholesterol 355 mg/dl. Antinuclear antibodies 1/160, but Anti-DNA, anticardiolipin antibodies and lupus anticoagulant were negative, with normal serum C3 and C4. A renal biopsy showed secondary membranous glomerulopathy, most likely lupus class V pure. Steroids, azathioprine, and aspirin were initiated, up to 28 weeks of pregnancy, when she developed severe hypertension, photopsia, headache, anasarca, extensive bruising of the extremities, severe anemia, thrombocytopenia, and creatinine rose to 2...
2024: Front Nephrol
https://read.qxmd.com/read/38344713/clinicopathologic-features-of-antibrush-border-antibody-disease
#2
JOURNAL ARTICLE
Joel D Murphy, Tiffany N Caza, Clarissa A Cassol, Aaron Storey, Josephine M Ambruzs, Christie Boils, Patrick D Walker, Shree Sharma, Nidia Messias, Randolph Hennigar, Nicole K Andeen, Christine VanBeek, Matthew Palmer, Lakshna Sankar, Pooja Sanghi, Kumar Dinesh, Lance Dicker, Anatoly Urisman, Christopher P Larsen
INTRODUCTION: Antibrush border antibody disease (ABBA) is an autoimmune tubulointerstitial kidney disease that primarily affects older individuals and results in progressive kidney failure. It is rare with only 20 reported cases. Here, we describe a case series to further define the clinicopathologic spectrum and natural history, and to inform management. METHODS: We identified 67 patients with ABBA who underwent kidney biopsy, including 65 native and 2 transplants...
February 2024: KI Reports
https://read.qxmd.com/read/38337366/implementation-of-kidney-biopsy-in-one-of-the-poorest-countries-in-the-world-experience-from-zinder-hospital-niger
#3
JOURNAL ARTICLE
Hassane Moussa Diongolé, Zeinabou Maiga Moussa Tondi, Abdoulazize Garba, Kabirou Ganiou, Laouali Chaibou, Djibrilla Bonkano, Illiassou Aboubacar, Abdoul Aziz Seribah, Abdoul Madjid Abdoulaye Idrissa, Akinfenwa Atanda, Lionel Rostaing
Kidney biopsy (KB) has become essential in the nephrologist's approach to kidney diseases, both for diagnosis, treatment, and prognosis. Our objective is to describe the preliminary results of KBs in Niger, one of the poorest countries in the world. This is a descriptive cross-sectional study that took place over 36 months in the nephrology/dialysis department of the Zinder National Hospital. Biopsy results were obtained in less than 5 working days. Patients were responsible for covering the cost of the kidney biopsy...
January 24, 2024: Journal of Clinical Medicine
https://read.qxmd.com/read/37530940/hydroxychloroquine-in-nephrology-current-status-and-future-directions
#4
REVIEW
Indu Ramachandra Rao, Ashwija Kolakemar, Srinivas Vinayak Shenoy, Ravindra Attur Prabhu, Shankar Prasad Nagaraju, Dharshan Rangaswamy, Mohan Varadanayakanahalli Bhojaraja
Hydroxychloroquine is one of the oldest disease-modifying anti-rheumatic drugs in clinical use. The drug interferes with lysosomal activity and antigen presentation, inhibits autophagy, and decreases transcription of pro-inflammatory cytokines. Owing to its immunomodulatory, anti-inflammatory, anti-thrombotic effect, hydroxychloroquine has been an integral part of therapy for systemic lupus erythematosus and lupus nephritis for several decades. The therapeutic versatility of hydroxychloroquine has led to repurposing it for other clinical conditions, with recent studies showing reduction in proteinuria in IgA nephropathy...
November 2023: Journal of Nephrology
https://read.qxmd.com/read/37218706/ckd-therapy-to-improve-outcomes-of-immune-mediated-glomerular-diseases
#5
REVIEW
Hans-Joachim Anders, Gema M Fernandez-Juarez, Augusto Vaglio, Paola Romagnani, Jürgen Floege
The management of immunoglobulin A nephropathy, membranous nephropathy, lupus nephritis, anti-neutrophil cytoplasmic antibody-associated vasculitis, C3 glomerulonephritis, autoimmune podocytopathies and other immune-mediated glomerular disorders is focused on two major treatment goals, preventing overall mortality and the loss of kidney function. Since minimizing irreversible kidney damage best serves both goals, the management of immune-mediated kidney disorders must focus on the two central pathomechanisms of kidney function decline, i...
November 8, 2023: Nephrology, Dialysis, Transplantation
https://read.qxmd.com/read/37098711/-kidney-biopsy-in-subsaharan-africa
#6
JOURNAL ARTICLE
K J N'Dah, W M Tia, D A Lagou, M C Guei, A D Abouna, I Touré, K H Oka, Aar Kobenan, S Diopo, S Delma, I Cherif, E Amékoudi, B S Ouattara, K H Yao, N C Ackoundou, K L Adonis, G V Yao, D A Gnionsahié, Mijm Diomandé
MATERIALS AND METHODS: We carried out a retrospective and descriptive study on biopsies examined between January 2015 and December 2019, in the pathological departments of University Teaching Hospital of Bouaké and Cocody-Abidjan. The KB came from four countries (Côte d'Ivoire, Togo, Guinea-Conakry and Burkina Faso). Optical microscopy and/or direct immunofluorescence techniques were used. All biopsy samples including epidemiological, clinical and pathological data and an optical microscopy and/or direct immunofluorescence study were included...
April 26, 2023: Néphrologie & Thérapeutique
https://read.qxmd.com/read/37016569/-kidney-biopsy-in-subsaharan-africa
#7
JOURNAL ARTICLE
K J N'Dah, W M Tia, D A Lagou, M C Guei, A D Abouna, I Touré, K H Oka, Aar Kobenan, S Diopo, S Delma, I Cherif, E Amékoudi, B S Ouattara, K H Yao, N C Ackoundou, K L Adonis, G V Yao, D A Gnionsahié, Mijm Diomandé
UNLABELLED: Kidney biopsy (KB) is a significant advance in the management of nephropathies. In sub-Saharan Africa, few studies have been carried out. The objective of our study was to evaluate the indication, to determine the epidemiological and histological characteristics of the nephropathies diagnosed in sub-Saharan Africa. MATERIALS AND METHODS: We carried out a retrospective and descriptive study on biopsies examined between January 2015 and December 2019, in the pathological departments of University Teaching Hospital of Bouaké and Cocody-Abidjan...
April 5, 2023: Néphrologie & Thérapeutique
https://read.qxmd.com/read/36420256/implications-of-rituximab-pharmacokinetic-and-pharmacodynamic-alterations-in-various-immune-mediated-glomerulopathies-and-potential-anti-cd20-therapy-alternatives
#8
REVIEW
Jan Miroslav Hartinger, Vojtech Kratky, Zdenka Hruskova, Ondrej Slanar, Vladimir Tesar
The specific B-cell depleting anti-CD20 monoclonal antibody rituximab (RTX) is effective in terms of the treatment of various immune-mediated glomerulopathies. The administration of RTX has been shown to be reliable and highly effective particularly in patients with ANCA-associated vasculitis, which is manifested predominantly with non-nephrotic proteinuria. Stable long-term B-cell depletion is usually readily attained in such patients using standard dosing regimens. However, in patients with nephrotic syndrome and non-selective proteinuria, the RTX pharmacokinetics is altered profoundly and RTX does not maintain high enough levels for a sufficiently long period, which may render RTX treatment ineffective...
2022: Frontiers in Immunology
https://read.qxmd.com/read/36251213/primary-membranous-nephropathy-an-endless-story
#9
REVIEW
Ponticelli Claudio
Primary membranous nephropathy (PMN) is an autoimmune disease caused by the attack of autoantibodies against podocyte antigens leading to the in situ production of immune complexes. However, the etiology is unknown and the pathogenesis is still far from being completely elucidated. MN is prevalently idiopathic or primary, but in about 20-30% of cases it is secondary to chronic infections, systemic diseases, exposure to drugs, or malignancy. The differentiation between primary and secondary MN may be difficult, particularly when MN precedes signs and symptoms of the original disease, as in some cases of cancer or systemic lupus erythematosus...
March 2023: Journal of Nephrology
https://read.qxmd.com/read/35994230/kidney-biopsy-during-pregnancy-a-difficult-decision-a-case-series-reporting-on-20-patients-from-mexico
#10
JOURNAL ARTICLE
Bernardo Moguel González, Marcos Garcia Nava, Oralia Alejandra Orozco Guillén, Virgilia Soto Abraham, Enzo Vasquez Jimenez, Bernardo Rodriguez Iturbe, Magdalena Madero Rovalo
BACKGROUND: Kidney biopsy is a routine procedure in the diagnosis of kidney disease, but during pregnancy it carries potential adverse effects for both mother and child, aside from the challenges of obtaining adequate tissue samples. Nevertheless, a precise diagnosis is necessary when specific and potentially toxic treatments are to be used during pregnancy. The present report presents our experience with regard to the usefulness and safety of kidney biopsies during pregnancy. METHODS: Retrospective analysis of clinical indications, complications, histopathological diagnoses, and treatment of patients who had kidney biopsies done at a single academic center during gestation weeks 11-30 between January 2015 and January 2019...
August 22, 2022: Journal of Nephrology
https://read.qxmd.com/read/33411573/consequences-of-insurance-denials-among-u-s-patients-prescribed-repository-corticotropin-injection-acthar-gel-for-nephrotic-syndrome
#11
JOURNAL ARTICLE
J Bradford Rice, Mary P Panaccio, Alan White, Mark Simes, Emma Billmyer, Nathaniel Downes, John Niewoehner, George J Wan
INTRODUCTION: Repository corticotropin injection (RCI; Acthar Gel) is indicated to induce a diuresis or a remission of proteinuria in nephrotic syndrome (NS) without uremia of the idiopathic type or that due to lupus erythematosus. This study compares patient characteristics and measurable healthcare resource utilization (HCRU) between NS patients who received a prescription for RCI and then were either approved or denied treatment by their insurers. METHODS: A retrospective analysis of adults with NS from January 2015 to December 2018 was conducted using a de-identified open-source claims database...
March 2021: Current Medical Research and Opinion
https://read.qxmd.com/read/30777545/thymoglobulin-resistant-t-cell-mediated-acute-rejection-in-a-pregnant-renal-transplant-recipient-case-report-and-review-of-the-literature
#12
REVIEW
Mohamed Balaha, Torki Al-Otaibi, Osama A Gheith, Medhat A Halim, Mohamed Shaker, Zohair Fayyad, Prasad Nair, Zakaria Zakaria, Hasaneen Abo-Atya, Yahya Makkeyia
To avoid graft rejection during pregnancy, frequent monitoring of serum drug levels is recommended. Pregnancy induces hyperfiltration in transplanted kidneys, as in native kidneys; therefore, detection of rejection can be difficult when monitoring by serum creatinine. If rejection is suspected, ultrasonographguided graft biopsy can be done; once proven, it can be treated with pulse steroids, but data are scarce regarding other agents. Here, we present a 28-year-old pregnant female patient with resistant acute rejection but with successful pregnancy outcome...
January 2019: Experimental and Clinical Transplantation
https://read.qxmd.com/read/26445002/clinicopathological-features-of-membranoproliferative-glomerulonephritis-under-a-new-classification
#13
JOURNAL ARTICLE
Preeti Nargund, Neeraja Kambham, Kshama Mehta, Richard A Lafayette
BACKGROUND: A recent classification of membranoproliferative glomerulonephritis (MPGN) utilizes the presence of immunoglobulin and complements to simplify diagnosis and point towards disease etiology. Here, we evaluate a historic cohort of patients with idiopathic MPGN using the new classification system and correlate it with clinical outcome. METHODS: We identified 281 patients diagnosed with MPGN at Stanford from 2000 to 2012. Patients with hepatitis, systemic lupus erythematosis, lymphomas, and plasma cell dyscrasias were excluded...
December 2015: Clinical Nephrology
https://read.qxmd.com/read/25825329/pregnancy-in-chronic-kidney-disease-questions-and-answers-in-a-changing-panorama
#14
JOURNAL ARTICLE
Giorgina Barbara Piccoli, Gianfranca Cabiddu, Rossella Attini, Federica Vigotti, Federica Fassio, Alessandro Rolfo, Domenica Giuffrida, Antonello Pani, Piero Gaglioti, Tullia Todros
Chronic kidney disease (CKD) is increasingly encountered in pregnancy because of greater diagnostic awareness, which is a reflection of the newer, broader definitions (i.e., any changes in blood or urine composition or at imaging, or a glomerular filtration rate (GFR) of <60 mL/min lasting at least 3 months) and of increased incidence (higher maternal age and better outcomes of several kidney diseases). CKD is extremely heterogeneous and may be described by the degree of GFR reduction (CKD stages), the presence of proteinuria and hypertension and the type of kidney disease; the risk of adverse pregnancy-related events increases as GFR decreases and it is affected by proteinuria and hypertension...
July 2015: Best Practice & Research. Clinical Obstetrics & Gynaecology
https://read.qxmd.com/read/21422635/c1q-nephropathy-presenting-as-acute-renal-failure
#15
JOURNAL ARTICLE
Pavan Malleshappa, Ravi Ranganath, Anup P Chaudhari, Ashwinikumar Ayiangar, Suratkal Lohitaksha
We describe a 42-year-old male patient who presented with high grade fever associated with acute renal failure requiring hemodialysis. Renal biopsy revealed that he had focal proliferative glomerulonephritis on light microscopy, dominant mesangial deposition of C1q by immunofluorescent staining, and electron dense deposits on electron microscopy, with no evidence of systemic lupus erythematosus, compatible with the diagnosis of C1q nephropathy. Intensive treatment with a combination of methyl prednisolone pulse therapy and oral prednisolone was successful in achieving complete remission and disappearance of proteinuria in our patient...
March 2011: Saudi Journal of Kidney Diseases and Transplantation
https://read.qxmd.com/read/15912651/-study-of-the-biopsied-nephrotic-syndrome-for-20-years-in-the-cadiz-bay-area-histological-correspondence-renal-prognosis-and-clinical-prognostic-factors
#16
JOURNAL ARTICLE
P L Quirós, M Ceballos, C Remón, A Lozano, R del Castillo, E Aznar, M A Pérez Pérez-Ruilópez, M Rivero, E Fernández Ruiz
AIMS: To analyse the histological correspondence, the renal survival and the clinical prognostic factors in the nephrotic syndrome for more than 20 years in our environment as well as the influence of the nephrotic proteinuria in the renal survival in the different histological particular types of glomerulonephritis. PATIENTS AND METHODS: Among the 542 primary and secondary glomerulonephritis diagnosed by kidney biopsy for two decades in the Cadiz Bay Area, we selected 242 patients whose clinical presentation and the biopsy indication was the nephrotic syndrome...
2005: Nefrología: Publicación Oficial de la Sociedad Española Nefrologia
https://read.qxmd.com/read/11061101/-clinical-course-and-prognostic-factors-in-lupus-nephropathy
#17
JOURNAL ARTICLE
G Gamba, L Quintanilla, M D del Bosque, A Chew-Wong, R Correa-Rotter
BACKGROUND: The present study was designed to know the clinical course of lupus nephritis and the risk factors associated with the development of end stage renal disease. METHODS: This a retrospective study performed in a cohort of 154 patients with biopsy proven lupus nephritis that were seen in our hospital between 1984 and 1990. The clinical records of all patients were reviewed in order to collect the following information at the time of the biopsy: age, sex, number and type of lupus criteria according with the American College of Reumathology, mean arterial pressure, serum creatinine, BUN, and albumin, as well as urinary protein excretion...
July 2000: Revista de Investigación Clínica; Organo del Hospital de Enfermedades de la Nutrición
https://read.qxmd.com/read/10975310/c1q-nephropathy-presenting-as-rapidly-progressive-crescentic-glomerulonephritis
#18
JOURNAL ARTICLE
T Srivastava, V Chadha, E M Taboada, U S Alon
C1q nephropathy is an immune complex glomerulonephritis defined by the presence of mesangial immunoglobulins and complement deposits, most notably C1q, and the absence of clinical and laboratory evidence of systemic lupus erythematosus. Histology in C1q nephropathy is characterized by a slight to severe increase in mesangial cellularity and matrix, with or without segmental sclerosis. C1q nephropathy usually presents with nephrotic-range proteinuria in older children and young adults, and has a poor response to steroids...
September 2000: Pediatric Nephrology
https://read.qxmd.com/read/10430971/familial-clustering-of-end-stage-renal-disease-in-blacks-with-hiv-associated-nephropathy
#19
JOURNAL ARTICLE
B I Freedman, J M Soucie, S M Stone, S Pegram
Human immunodeficiency virus-associated nephropathy (HIVAN) develops more often in HIV-infected blacks than whites. Blacks also show marked familial clustering of other causes of end-stage renal disease (ESRD), particularly diabetes mellitus-, hypertension-, and systemic lupus erythematosus-associated ESRD. We compared the family history of ESRD in 201 blacks with ESRD caused by HIVAN (cases) to that of 50 HIV-infected blacks without renal disease (controls) to determine whether HIV-associated ESRD shows familial aggregation...
August 1999: American Journal of Kidney Diseases
https://read.qxmd.com/read/10414228/-severe-nephrotic-syndrome-with-reversible-acute-kidney-failure-in-lupus-associated-membranous-nephropathy
#20
JOURNAL ARTICLE
C Pauli-Magnus, T Mettang, U Kuhlmann
HISTORY AND CLINICAL FINDINGS: A 20 year old, previously healthy woman presented with a four week history of progressive oedema of the legs and the eyelids and a weight gain of 10 kg. INVESTIGATIONS: Biochemical tests revealed a nephrotic syndrome with a protein-loss in urine of 13.6 g/24 hours and a serum-albumin of 1.2 g/dl. Serological tests showed positive response for antinuclear antibodies, anti-double-stranded-DNA antibodies and cardiolipin antibodies. Renal histology revealed a lupus-associated diffuse membranous nephropathy (WHO-type Vd)...
June 25, 1999: Deutsche Medizinische Wochenschrift
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