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Case Reports in Nephrology

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https://read.qxmd.com/read/30775040/acute-interstitial-nephritis-in-a-patient-with-non-small-cell-lung-cancer-under-immunotherapy-with-nivolumab
#1
Panagiotis I Georgianos, Vasilios Vaios, Eleni Leontaridou, Georgia Karayannopoulou, Triantafyllia Koletsa, Athanasios Sioulis, Elias V Balaskas, Pantelis E Zebekakis
Immune-checkpoint-inhibitors (ICPIs) represent a novel class of immunotherapy against several malignancies. These agents are associated with several "immune-mediated" adverse effects, but the reported renal toxicity of ICPIs is less well defined. We present the case of a 60-year-old man with a history of non-small cell lung cancer, who developed acute kidney injury (AKI) approximately 3.5 months after initiation of immunotherapy with nivolumab. Urinalysis revealed sterile pyuria, without microscopic hematuria or proteinuria...
2019: Case Reports in Nephrology
https://read.qxmd.com/read/30733880/high-lyso-gb3-plasma-levels-associated-with-decreased-mir-29-and-mir-200-urinary-excretion-in-young-non-albuminuric-male-patient-with-classic-fabry-disease
#2
Sebastián Jaurretche, Germán R Perez, Graciela Venera
Renal involvement is associated with a greater morbidity and mortality in Fabry disease. Pathological albuminuria, the first Fabry nephropathy clinical manifestation, can occur from early childhood, although histological lesions such as tubulo-interstitial fibrosis and glomerulosclerosis are present or may precede the onset of pathological albuminuria. In renal cells, exposure to Lyso-Gb3 is correlated with increased expression of Transforming Growth Factor- β eta (TGF- β ). miR-21, miR-192, and miR-433 that promote fibrosis are activated by TGF- β , and miR-29 and miR-200 that suppress fibrosis are inhibited by TGF- β ...
2019: Case Reports in Nephrology
https://read.qxmd.com/read/30729052/silicone-induced-granulomatous-reaction-causing-severe-hypercalcemia-case-report-and-literature-review
#3
Gulshan Man Singh Dangol, Hilmer Negrete
A 67-year-old woman presented to the hospital with complaints of abdominal pain. Physical exam was significant for signs of severe dehydration, mild epigastric tenderness and multiple non-tender hard nodules over her arms and thighs. Incidental finding of severe hypercalcemia led to negative workups for hyperparathyroidism, vitamin D intoxication, and malignancy. However, elevated levels of 1,25-hydroxy vitamin D raised the possibility of granulomatous diseases. Imaging and patient report revealed silicone-induced foreign body granulomatous reaction as the cause of hypercalcemia...
2019: Case Reports in Nephrology
https://read.qxmd.com/read/30675407/combining-acute-kidney-injury-with-gastrointestinal-pathology-a-clue-to-acute-oxalate-nephropathy
#4
Benjamin Fox, Nishkarsh Saxena, Leah Schuppener, Laura Maursetter
Acute oxalate nephropathy (AON) is an increasingly recognized cause of acute kidney injury (AKI). Herein, we present two cases of biopsy-proven acute oxalate nephropathy in patients with gastrointestinal malabsorption, coincidentally both stemming from cholangiocarcinoma. The first is a 73-year-old male who presented with syncope and was found to have severe, oliguric AKI in the setting of newly diagnosed, nonresectable cholangiocarcinoma. The second is a 64-year-old man with remote resection of cholangiocarcinoma who presented after routine laboratory monitoring showed significant AKI...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30671269/peritonitis-due-to-moraxella-osloensis-an-emerging-pathogen
#5
Sreedhar Adapa, Purva Gumaste, Venu Madhav Konala, Nikhil Agrawal, Amarinder Singh Garcha, Hemant Dhingra
Peritonitis is a very serious complication encountered in patients undergoing peritoneal dialysis and healthcare providers involved in the management should be very vigilant. Gram-positive organisms are the frequent cause of peritonitis compared to gram-negative organisms. There has been recognition of peritonitis caused by uncommon organisms because of improved microbiological detection techniques. We report a case of peritonitis caused by Moraxella osloensis (M. osloensis), which is an unusual cause of infections in humans...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30662780/clinical-and-complement-long-term-follow-up-of-a-pediatric-patient-with-c3-mutation-related-atypical-hemolytic-uremic-syndrome
#6
Anna Bjerre, Grethe Bergseth, Judith Krey Ludviksen, Arne Stokke, Vidar Bosnes, Diana Karpman, Tom Eirik Mollnes
We report a pediatric patient with atypical hemolytic uremic syndrome due to a C3 gain-of-function mutation diagnosed in infancy. She was treated from the start with a constant dose of 300 mg eculizumab every second week from the onset and followed by routine complement analyses for six years. Her complement system was completely inhibited and the dose interval was prolonged from 2 to 3 weeks without alteration of the dose and the complement activity continued to be completely inhibited. Blood samples taken immediately before, immediately after, and between eculizumab doses were analyzed for eculizumab-C5 complexes and percentage of total complement activity, using the Wieslab® test, and compared to a pool of sera from 20 healthy controls...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30652035/malignant-hypertension-causing-a-pulmonary-renal-syndrome
#7
Bryan Yong, David A Power
Background: Pulmonary-renal syndrome is characterised by acute kidney injury, haematuria, and haemoptysis and is a well-recognised presentation of diseases such as ANCA vasculitis that require urgent immunosuppression. Case Presentation: A patient presented with a brief history of haemoptysis, acute renal failure, microscopic haematuria, and severe hypertension. The diagnosis was initially not clear so he was treated with antihypertensives, renal replacement therapy, and immunosuppression...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30631615/anticoagulant-related-nephropathy-induced-by-dabigatran
#8
Nazia Sharfuddin, Mahra Nourbakhsh, Alan Box, Hallgrimur Benediktsson, Daniel A Muruve
We describe a case of biopsy-proven dabigatran related nephropathy in a patient without underlying IgA nephropathy. To date, dabigatran related nephropathy was only reported in patients with concurrent or undiagnosed IgA nephropathy, suggesting that it may predispose patients to dabigatran associated injury. The patient is an 81-year-old woman with multiple medical comorbidities, including nonvalvular atrial fibrillation, who was anticoagulated with dabigatran. She presented to hospital with acute kidney injury in the setting of volume overload...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30581638/a-unique-case-of-metformin-associated-lactic-acidosis
#9
Benjamin Gershkovich, Christopher McCudden, Kevin D Burns
Metformin-associated lactic acidosis [MALA] is a potentially fatal condition characterized by an elevation in serum lactate in patients with metformin exposure. An 82-year-old man with no prior renal history was brought to hospital after being found by his family in a confused state. He had a history of type 2 diabetes mellitus, and his medications included regular metformin. On arrival to our hospital he was conscious but confused and noted recent decreased oral intake. Initial investigations revealed severe acidemia (pH <6...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30581637/severe-metabolic-acidemia-in-a-patient-with-aleukemic-leukemia
#10
Moutaz Ghrewati, Faiza Manji, Varun Modi, Chandra Chandran, Michael Maroules
Malignancy associated lactic acidosis is a rare metabolic complication that may accompany various types of malignancies. To date, most cases that have been reported are associated with hematologic malignancies (lymphoma and leukemia). Many theories have been proposed to explain the pathophysiology of lactic acidosis in malignancies. We are reporting an unusual case of a 62-year-old female who presented with a complaint of generalized weakness. Patient was found to have pancytopenia and metabolic acidosis with an anion gap secondary to lactic acid in addition to non-anion gap acidosis (NAGA)...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30519493/denosumab-induced-severe-hypocalcaemia-in-chronic-kidney-disease
#11
Ryan Jalleh, Gopal Basu, Richard Le Leu, Shilpanjali Jesudason
Background: Hypocalcaemia is increasingly recognized as a complication of denosumab use in Chronic Kidney Disease (CKD) patients with osteoporosis. Despite Therapeutic Goods Administration (TGA) notifications in 2013, we have subsequently encountered several cases of denosumab-induced hypocalcaemia, raising concern about lack of widespread awareness among prescribing practitioners. Aims: We reviewed the morbidity and healthcare intervention needs of CKD patients with hypocalcaemia attributed to denosumab...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30473895/unusual-case-of-an-infant-with-urinary-tract-infection-presenting-as-cholestatic-jaundice
#12
Rahaf Niazi, Bashaer Baharoon, Afnan Neyas, Meshari Alaifan, Osama Safdar
Neonatal jaundice is considered one of the most common reasons for admission to the pediatric medical ward. We report a case of a 1-month-old infant who presented with jaundice but no fever or any other signs of systemic illnesses. Laboratory test results revealed high direct hyperbilirubinemia, and urine culture showed a urinary tract infection with Enterobacter cloacae as the causative agent. He was admitted to the pediatric medical ward where he was treated with a course of antibiotics for 14 days, and cholestasis resolved completely following a course of antibiotics...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30425869/scleroderma-renal-crisis-debute-with-thrombotic-microangiopathy-a-successful-case-treated-with-eculizumab
#13
Maite Hurtado Uriarte, Carolina Larrarte, Laura Bravo Rey
We had the challenged to treat a 40-year-old female with Systemic Scleroderma who was showing unspecific symptoms. During her time at the hospital she rapidly develops renal dysfunction, associated with hypertension. She required renal replacement therapy initiation and we observed a decline in hemoglobin and platelets numbers. We confirm a microangiopathic hemolytic anemia and rule out other immune diseases or thrombotic thrombocytopenic purpura. Systemic Sclerosis is a chronic immune disorder of unknown origin that it is not completely understood...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30410805/renal-tubular-acidosis-and-hypokalemic-paralysis-as-a-first-presentation-of-primary-sj%C3%A3-gren-s-syndrome
#14
Arun Sedhain, Kiran Acharya, Alok Sharma, Amir Khan, Shital Adhikari
Sjögren's syndrome is an autoimmune disease with multisystem involvement and varying clinical presentation. We report the clinical course and outcome of a case who presented with repeated episodes of hypokalemia mimicking hypokalemic periodic paralysis and metabolic acidosis, which was later diagnosed as distal renal tubular acidosis secondary to primary Sjögren's syndrome. A 50-year-old lady, who was previously diagnosed as hypokalemic periodic paralysis, presented with generalized weakness and fatigue. She was found to have severe hypokalemia with normal anion-gap metabolic acidosis consistent with distal renal tubular acidosis...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30402307/cloudy-dialysate-as-the-initial-presentation-for-lymphoma
#15
Sriram Sriperumbuduri, Deborah Zimmerman
Turbid dialysate in a patient on peritoneal dialysis is usually due to peritonitis and almost all these patients are started on empirical antibiotics pending cultures. However, in few of them with culture negative fluid, this could represent other etiologies like chyle, which requires more intensive investigations, and analysis of fluid itself reveals some rare diagnosis. We present one such report of chylous ascites with prompt investigation leading to a diagnosis of malignancy in a peritoneal dialysis patient...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30364076/a-case-of-hepatic-glomerulosclerosis-with-monoclonal-iga1-%C3%AE%C2%BA-deposits
#16
Yusuke Okabayashi, Nobuo Tsuboi, Naoko Nakaosa, Kotaro Haruhara, Go Kanzaki, Kentaro Koike, Akihiro Shimizu, Akira Fukui, Hideo Okonogi, Yoichi Miyazaki, Tetsuya Kawamura, Makoto Ogura, Akira Shimizu, Takashi Yokoo
Glomerular immunoglobulin A (IgA) deposition is a common finding in hepatic glomerulosclerosis; thus, this disease is also called hepatic IgA nephropathy. However, only a small number of patients with hepatic IgA nephropathy have active glomerular lesions, so functional decline is slow in most cases. In this report, we describe a 60-year-old man who developed nephrotic syndrome and progressive renal impairment during follow-up for alcoholic liver cirrhosis. A renal biopsy showed a membranoproliferative glomerulonephritis-like pattern; diffuse double-contours of the glomerular basement membrane and focal active glomerular lesions with moderate-to-severe endocapillary proliferation and fibrocellular crescents...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30254775/severe-symptomatic-hyponatremia-secondary-to-escitalopram-induced-siadh-a-case-report-with-literature-review
#17
Rishi Raj, Aasems Jacob, Ajay Venkatanarayan, Mohankumar Doraiswamy, Manjula Ashok
Hyponatremia is a well-known medication related side effect of selective serotonin reuptake inhibitors; despite its association with escitalopram, the newest SSRI is very rare. We did a review of literature and came across only 14 reported case of this rare association of SIADH with escitalopram. We hereby report a case of a 93-year-old female who presented with generalized tonic-clonic seizure and was diagnosed with severe hyponatremia due to escitalopram-induced syndrome of inappropriate antidiuretic hormone secretion (SIADH)...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30210883/-bartonella-endocarditis-mimicking-crescentic-glomerulonephritis-with-pr3-anca-positivity
#18
Joseph Vercellone, Lisa Cohen, Saima Mansuri, Ping L Zhang, Paul S Kellerman
Bartonella henselae is a fastidious organism that causes cat scratch disease, commonly associated with fever and lymphadenopathy but, in rare instances, also results in culture-negative infectious endocarditis. We describe a patient who presented with flank pain, splenic infarct, and acute kidney injury with an active urinary sediment, initially suspicious for vasculitis, which was subsequently diagnosed as B. henselae endocarditis. Bartonella endocarditis may present with a crescentic glomerulonephritis (GN) and elevated PR3-ANCA antibody titers, mimicking ANCA-associated GN, with 54 cases reported in the literature...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30155326/mucin-1-gene-mutation-and-the-kidney-the-link-between-autosomal-dominant-tubulointerstitial-kidney-disease-and-focal-and-segmental-glomerulosclerosis
#19
H Trimarchi, M Paulero, T Rengel, I González-Hoyos, M Forrester, F Lombi, V Pomeranz, R Iriarte, A Iotti
Glomerular diseases are one of the most frequent causes of chronic kidney disease, focal and segmental glomerulosclerosis being one of the commonest glomerulopathies. However, the etiology of this glomerular entity, which merely depicts a morphologic pattern of disease, is often not established and, in most of the patients, remains unknown. Nephrologists tend to assume focal and segmental glomerulosclerosis as a definitive diagnosis. However, despite the increasing knowledge developed in the field, genetic causes of glomerular diseases are currently identified in fewer than 10% of chronic kidney disease subjects...
2018: Case Reports in Nephrology
https://read.qxmd.com/read/30155325/-achromobacter-xylosoxidans-relapsing-peritonitis-and-streptococcus-suis-peritonitis-in-peritoneal-dialysis-patients-a-report-of-two-cases
#20
Rafał Donderski, Magdalena Grajewska, Agnieszka Mikucka, Beata Sulikowska, Eugenia Gospodarek-Komkowska, Jacek Manitius
Peritonitis is considered to be the most common complication of peritoneal dialysis (PD). It is usually caused by Gram positive Staphylococcus epidermidis. Achromobacter xylosoxidans (A. xylosoxidans) and Streptococcus suis (S. suis) are rare pathogens, but there is emerging evidence that they may be also responsible for PD related peritonitis. We described 2 cases of rare peritonitis treated in our center. In our opinion this is the first described case of PD related peritonitis caused by Streptococcus suis...
2018: Case Reports in Nephrology
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