keyword
https://read.qxmd.com/read/38634580/-morphological-predictors-of-water-electrolyte-disorders-in-patients-with-preventive-ileostomy-after-rectal-resection-for-cancer
#21
JOURNAL ARTICLE
A I Maksimkin, Z A Bagatelia, V M Kulushev, E N Gordienko, M S Lebedko, S S Anikina, E P Shin
OBJECTIVE: To analyze morphological changes in wall of functioning and non-functioning small intestine in patients with preventive ileostomy and to determine histological predictors of water-electrolyte disorders. MATERIAL AND METHODS: We prospectively analyzed 57 patients >18 years old who underwent rectal resection with preventive ileostomy between January 2022 and November 2023. Anthropometric data included gender, age, body mass index, ECOG and ASA classes...
2024: Khirurgiia
https://read.qxmd.com/read/38633918/tubulointerstitial-nephritis-and-uveitis-a-case-report
#22
Michael Mira, Yuriy Khanin, Miroslav Sekulic, David Jordanovski
Tubulointerstitial nephritis and uveitis (TINU) is a rare disease of unknown pathogenesis that is characterized by tubulointerstitial nephritis and uveitis. Currently, there are over 250 reported cases of TINU syndrome. TINU syndrome typically presents with mild uveitis and nephritis that is self-limited; however, in this case, the symptoms were severe making it different from previous case reports. We present a case of a 29-year-old female with a history of cytomegalovirus (CMV) with a recent diagnosis of bilateral uveitis who was admitted for worsening systemic symptoms...
March 2024: Curēus
https://read.qxmd.com/read/38633468/tinu-a-multisystemic-inflammatory-disorder-case-report-and-literature-review
#23
Juan Montejo-Hernández, Jorge Rico-Fontalvo, Jose Cabrales, Shuchi Anand, María Cristina Martínez-Ávila, Claudia Duran-Merino, Luis Arias-Restrepo, Camilo Andrés Gómez Duran
Background . The syndrome of tubulointerstitial nephritis and uveitis (TINU) is a rare oculorenal condition, mainly seen in children and women. The underlying cause of this disease is unknown. Case Presentation . We report a 24-year-old male without any past medical history, diagnosed with bilateral uveitis and azotemia. Biopsy revealed tubulointerstitial nephritis, consistent with TINU syndrome. Fluorescein angiogram revealed peripheral retinal vasculitis. Discussion . TINU is a rare disorder that needs to be distinguished from sarcoidosis, Sjogren's disease, and tuberculosis...
2024: Case Reports in Nephrology
https://read.qxmd.com/read/38633257/development-of-a-nomogram-for-membranous-nephropathy-prediction-in-patients-with-primary-sj%C3%A3-gren-s-syndrome-a-6-year-retrospective-study
#24
JOURNAL ARTICLE
Lihui Guo, Shan Zhao, Xudong Liu
OBJECTIVES: Nephritis is a life-threatening complication of primary Sjögren's syndrome (pSS), with membranous nephropathy (MN) being prevalent. Renal biopsy is the gold standard for MN diagnosis, but it is invasive and cannot be repeatedly performed. This study aimed to develop a nomogram for the prediction of MN in patients with pSS. METHODS: This retrospective study included patients with pSS admitted to the Rheumatology and Immunology Department of the First Affiliated Hospital of China Medical University between January 2015 and January 2021...
2024: Frontiers in Immunology
https://read.qxmd.com/read/38632863/stepwise-algorithm-using-computed-tomography-and-magnetic-resonance-imaging-for-differential-diagnosis-of-fat-poor-angiomyolipoma-in-small-renal-masses-a-prospective-validation-study
#25
JOURNAL ARTICLE
Masahiro Toide, Hajime Tanaka, Masaki Kobayashi, Motohiro Fujiwara, Yuki Nakamura, Shohei Fukuda, Koichiro Kimura, Yuma Waseda, Soichiro Yoshida, Ukihide Tateishi, Yasuhisa Fujii
OBJECTIVES: To validate the diagnostic accuracy of a stepwise algorithm to differentiate fat-poor angiomyolipoma (fp-AML) from renal cancer in small renal masses (SRMs). METHODS: We prospectively enrolled 223 patients with solid renal masses <4 cm and no visible fat on unenhanced computed tomography (CT). Patients were assessed using an algorithm that utilized the dynamic CT and MRI findings in a stepwise manner. The diagnostic accuracy of the algorithm was evaluated in patients whose histology was confirmed through surgery or biopsy...
April 17, 2024: International Journal of Urology: Official Journal of the Japanese Urological Association
https://read.qxmd.com/read/38632537/giant-retinal-pigment-epithelium-tears-with-membranous-nephropathy-a-case-report-and-literature-review
#26
REVIEW
Rui Dou, Yanhua Chu, Quanhong Han, Wei Zhang, Xue Bi
BACKGROUND: Kidney and eye diseases may be closely linked. Tears of the retinal pigment epithelium (RPE) have been reported to be related to kidney diseases, such as IgA nephropathy and light-chain deposition disease. However, pigment epithelium tears associated with membranous nephropathy have not been reported or systematically analysed. CASE PRESENTATION: A 68-year-old man presented with decreased right eye visual acuity. Optical coherence tomography (OCT) revealed cystic macular edema, localized serous detachment of the retina and loss of the outer retinal structure in the right eye and retinal pigment epithelium detachment (PED) combined with serous detachment of the retina in the left eye...
April 17, 2024: BMC Ophthalmology
https://read.qxmd.com/read/38630340/alect2-amyloidosis-with-concurrent-igg4-related-interstitial-nephritis-membranous-nephropathy-and-diabetic-kidney-disease-a-case-report-and-literature-review
#27
JOURNAL ARTICLE
Muhammad Shaheen, Anchit Bharat, Allon N Friedman, Shunhua Guo
Leukocyte chemotactic factor-2 amyloidosis (ALECT2) is a recently described subtype of amyloidosis. IgG4-related disease is a rare fibroinflammatory condition characterized by dense interstitial lymphoplasmacytic infiltrates and fibrosis. Membranous nephropathy and diabetic nephropathy are common causes of nephrotic syndrome. Here we report a 49-year-old Hispanic male patient with diabetes mellitus who presented with jaundice and pruritus. IgG4-related autoimmune pancreatitis was diagnosed through laboratory workup and ampulla biopsy...
April 17, 2024: Journal of Nephrology
https://read.qxmd.com/read/38628656/deep-lymph-node-enlargement-and-renal-failure-caused-by-hypercalcemia%C3%A2-associated-sarcoidosis-a-case-report
#28
Zezhou Liu, Zhigang Tang, Jingping Yuan, Ke Su, Yonghong Jian, Hongyan Liu
Sarcoidosis is a rare disease that severely affects the lungs and superficial lymph nodes. In addition, this disease can also affect the skin, eyes and kidneys to varying degrees. The present report described a 32-year-old male patient who was admitted to Renmin Hospital of Wuhan University (Wuhan, China) due to joint pain in the extremities. He was diagnosed with uncorrectable hypercalcemia. A lymph node biopsy revealed the hypercalcemia to be associated with sarcoidosis, with the patient also demonstrating renal failure and lymph node enlargement...
May 2024: Experimental and Therapeutic Medicine
https://read.qxmd.com/read/38627675/the-role-of-pirnas-in-predicting-and-prognosing-in-cancer-a-focus-on-pirna-823-a-systematic-review-and-meta-analysis
#29
Mohammad Taghizadeh, Tohid Jafari-Koshki, Vahid Jafarlou, Mortaza Raeisi, Leila Alizadeh, Yousef Roosta, Somaieh Matin, Rahele Jabari, Daniel Sur, Abbas Karimi
INTRODUCTION: This article examines the potential of using liquid biopsy with piRNAs to study cancer survival outcomes. While previous studies have explored the relationship between piRNA expression and cancer patient outcomes, a comprehensive investigation is still lacking. To address this gap, we conducted a systematic review and meta-analysis of existing literature. METHODS: We searched major online databases up to February 2024 to identify articles reporting on the role of piRNA in cancer patient survival outcomes...
April 16, 2024: BMC Cancer
https://read.qxmd.com/read/38627670/review-on-epidemiology-disease-burden-and-treatment-patterns-of-iga-nephropathy-in-select-apac-countries
#30
REVIEW
Omer Zaidi, Fen Du, Zhaoli Tang, Sandipan Bhattacharjee, Kristin Pareja
BACKGROUND: Immunoglobulin type A (IgA) nephropathy is the most common primary glomerulonephritis (GN) worldwide with higher rates in East and Pacific Asia compared to North America and Europe. Despite high reported prevalence of IgAN in these countries, the overall disease prevalence across Asia is not available. Treatment patterns of IgAN patients across Asian countries have also not been summarized. The aim of this study was to review and summarize evidence on IgA nephropathy prevalence, treatment patterns, and humanistic and economic burden in mainland China, Taiwan, South Korea, Japan, and Australia...
April 16, 2024: BMC Nephrology
https://read.qxmd.com/read/38627208/covid-19-and-renal-allograft-rejection-insight-from-controlled-and-non-controlled-studies
#31
JOURNAL ARTICLE
Ahmed Daoud, Karim Soliman, Maria Aurora Posadas Salas, Genta Uehara, Sakshi Vaishnav, Wisit Cheungpasitporn, Michael J Casey
AIM: Kidney transplant recipients (KTRs), due to their immunosuppressed status, are potentially more susceptible to both the severe effects of COVID-19 and complications in their transplanted organ. The aim of this study is to investigate whether COVID-19 infection increases the risk of rejection in kidney transplant recipients (KTRs). METHODS: This study involved a detailed literature review, conducted using PubMed, with the search being completed by September 7th, 2023...
December 2024: Renal Failure
https://read.qxmd.com/read/38625385/renal-manifestations-in-adult-onset-still-s-disease-a-systematic-review
#32
P V Akhila Arya, Erica Marnet, Madhumita Rondla, Jia Wei Tan, Dileep Unnikrishnan, Gregory Buller
OBJECTIVE: We aimed to review the literature on the clinical presentation, renal pathology, treatment, and outcome of renal manifestations in adult-onset Still's disease (AOSD). METHODS: We used PRISMA guidelines for our systematic review and included all English-language original articles from inception till September 15, 2023, on AOSD and kidney involvement in any form. Data on patient demographics, diagnostic criteria, clinical presentation, renal pathology, treatment employed including dialysis, outcome, cause of death were collected and analyzed...
April 16, 2024: Rheumatology International
https://read.qxmd.com/read/38624051/the-diagnostic-significance-of-c4d-deposits-as-an-immunohistochemical-proof-of-complement-activation-in-kidney-glomerular-pathologies-and-kidney-transplantation
#33
JOURNAL ARTICLE
Stanislav Hresko, Martina Madarova, Miroslava Dobosova, Nikola Palusekova, Petra Niznerova, Stanislav Ziaran, Ivan Varga
C4d, a split product of C4 activation in classical and lectin pathways of the complement system activation, has been regarded as a footprint of tissue damage in antibody-mediated rejection in transplantology. The introduction of C4d staining into daily clinical practice aroused an ever-increasing interest in the role of antibody-mediated mechanisms in kidney allograft rejection. However, this marker of complement activation is also important in other various kidney glomerular pathologies such as immunoglobulin A nephropathy, membranoproliferative glomerulonephritis, lupus nephritis, and others...
2024: Bratislavské Lekárske Listy
https://read.qxmd.com/read/38623282/reclassification-of-genetic-testing-results-a-case-report-demonstrating-the-need-for-structured-re-evaluation-of-genetic-findings
#34
Clara Schott, Samantha Colaiacovo, Cadence Baker, Matthew A Weir, Dervla M Connaughton
RATIONALE: Alport Syndrome (AS) is a progressive genetic condition characterized by chronic kidney disease (CKD), hearing loss, and eye abnormalities. It is caused by mutations in the genes COL4A3, COL4A4 , and COL4A5 . Heterozygous mutations in COL4A4 and COL4A3 cause autosomal dominant Alport Syndrome (ADAS), and a spectrum of phenotypes ranging from asymptomatic hematuria to CKD, with variable extra-renal features. In the past, heterozygous mutations in these genes were thought to be benign, however recent studies show that about 30% of patients can progress to CKD, and 15% can progress to end stage kidney disease (ESKD)...
2024: Canadian Journal of Kidney Health and Disease
https://read.qxmd.com/read/38622386/study-on-fine-grained-visual-classification-of-low-resolution-urinary-erythrocyte
#35
JOURNAL ARTICLE
Qingbo Ji, Tingshuo Yin, Pengfei Zhang, Qingquan Liu, Changbo Hou
The morphological analysis test item of urine red blood cells is referred to as "extracorporeal renal biopsy," which holds significant importance for medical department testing. However, the accuracy of existing urine red blood cell morphology analyzers is suboptimal, and they are not widely utilized in medical examinations. Challenges include low image spatial resolution, blurred distinguishing features between cells, difficulty in fine-grained feature extraction, and insufficient data volume. This article aims to improve the classification accuracy of low-resolution urine red blood cells...
April 15, 2024: J Imaging Inform Med
https://read.qxmd.com/read/38621786/extracellular-mitochondrial-components-as-new-biomarkers-for-lupus-nephritis
#36
JOURNAL ARTICLE
Sharath Gowda, Khushboo Rana, Ankit Kumar, Pradip Kumar Prajapati, Namisha Patel, Sapan Pandya, Ratika Srivastava
Major reason for mortality among systemic lupus erythematosus patients is renal failure due to the deposition of immune complexes in the glomeruli. Being a chronic disease with multiple relapses and remissions across the lifespan, it's important to know the degree of nephritis for diagnosis as well as the long-term clinical management of the patients. Currently, renal biopsy is being used as the gold standard to diagnose and define the stages of the disease. However, renal biopsy being invasive only provides a localized picture of nephritis, and has the risk of bleeding...
April 15, 2024: Lupus
https://read.qxmd.com/read/38619321/transplant-nephropathology-wherefrom-wherein-and-whereto
#37
REVIEW
Kim Solez, Garabed Eknoyan
Renal pathology is a relatively recent entry in nephrology. While diseases of the kidney are old, their study began in the 19th century with the report of Richard Bright of the lesions of end-stage kidney disease. Its easy diagnosis from albuminuria soon elevated Bright's nephritis into a leading cause of death. The transformative events in the care of these cases were renal replacement therapy that converted a fatal into a chronic disease, and kidney biopsy that allowed study of the course and pathogenesis of kidney disease...
April 2024: Clinical Transplantation
https://read.qxmd.com/read/38618866/a-fast-and-efficient-liquid-chromatography-tandem-mass-spectrometry-method-for-measuring-l-and-d-amino-acids-in-the-urine-of-patients-with-immunoglobulin-a-nephropathy
#38
JOURNAL ARTICLE
Zhijian Zha, Ruihua Wang, Qian Wang, Fahui Chen, Ziyang Ye, Yafeng Li
Immunoglobulin nephropathy (IgAN) stands as the most prevalent primary glomerular nephropathy globally, typically diagnosed through an invasive renal biopsy. Emerging research suggests the significant involvement of chiral amino acids in kidney disease progression. This study introduces a nonderivative LC-tandem mass spectrometry approach, offering efficient separation outcomes within 15 min for identifying chiral amino acids in human urine samples. Subsequently, using this method, the analysis of l- and d-amino acids in the urine of both patients with IgAN and healthy individuals was conducted...
April 15, 2024: Biomedical Chromatography: BMC
https://read.qxmd.com/read/38617465/use-of-a-belatacept-based-immunosuppression-for-kidney-transplantation-from-donors-after-circulatory-death-a-paired-kidney-analysis
#39
JOURNAL ARTICLE
Rita Eid, Anne Scemla, Magali Giral, Nadia Arzouk, Dominique Bertrand, Marie-Noëlle Peraldi, Laurent Mesnard, Helene Longuet, Mehdi Maanaoui, Geoffroy Desbuissons, Edouard Lefevre, Renaud Snanoudj
BACKGROUND: Efficacy and safety of belatacept have not been specifically reported for kidney transplantations from donors after circulatory death. METHODS: In this retrospective multicenter paired kidney study, we compared the outcome of kidney transplantations with a belatacept-based to a calcineurin inhibitor (CNI)-based immunosuppression. We included all kidney transplant recipients from donors after uncontrolled or controlled circulatory death performed in our center between February 2015 and October 2020 and treated with belatacept (n = 31)...
May 2024: Transplantation Direct
https://read.qxmd.com/read/38615998/single-nucleotide-polymorphism-snp-chromosomal-microarray-as-a-diagnostic-tool-for-mucinous-tubular-and-spindle-cell-carcinoma-a-validation-study
#40
JOURNAL ARTICLE
Kaitlyn J Nielson, Ross Rowsey, Surendra Dasari, William R Sukov, Benjamin R Kipp, Aditya Raghunathan, Rumeal D Whaley, Kingsley Ebare, Melissa L Stanton, Jordan P Reynolds, Vidit Sharma, R Houston Thompson, Stephen A Boorjian, Bradley C Leibovich, Loren Herrera Hernandez, Rafael E Jimenez, John C Cheville, Sounak Gupta
Mucinous tubular and spindle cell carcinoma (MTSCC) shows significant overlap with papillary renal cell carcinoma (PRCC), and harbor recurrent copy-number alterations (CNA). We evaluated 16 RCC with features suggestive of MTSCC using chromosomal microarrays. The cohort was comprised of 8 females and males, each, with an age range of 33-79 years (median, 59), and a tumor size range of 3.4-15.5 cm (median, 5.0). Half the tumors were high-grade (8/16, 50%) with features such as necrosis, marked cytologic atypia, and sarcomatoid differentiation, and 5/16 (31%) were high stage (≥pT3a)...
April 12, 2024: Human Pathology
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