نتایج جستجو برای: renal involvement

تعداد نتایج: 393927  

Journal: :iranian journal of cancer prevention 0
mohammad mohsen mazloomfard resident of urology ladan ajori babak javanmard aida moeini hooman bahrami-motlagh

abstract ureteralstump’s metastasis of renal cell carcinoma is rare. we report a32-year-old femalewith a huge metastatic involvement of the ureteralstump and utero-cervical structures about 2 years after a left radical nephrectomy. she underwent en-bloc resection of the massin conjunctionwith total ureterectomy, bladder cuff excision and hysterectomy.the patient was referred to oncology departm...

Journal: :Kidney & blood pressure research 2007
Romana Rysavá

Primary (AL amyloidosis) is a systemic disease characterized by an amyloid deposition process in many organs, with unsatisfactory survival of patients. The monoclonal light chains form the fibrils that deposit and accumulate in tissues. Renal involvement is very frequent in AL amyloidosis and could lead to development of nephrotic syndrome followed by the renal failure in many cases. Classic th...

Journal: :International journal of urology : official journal of the Japanese Urological Association 2011
Daniel D Sackett Pooja Singh Costas D Lallas

Historically, urologists were the primary surgeons in renal transplantation. Specialization and increased complexity of the field of transplantation, coupled with a de-emphasis of vascular surgical training in urology, has created a situation where many renal transplants are carried out by surgeons with a general surgery background. Because of its genitourinary nature, however, urological input...

Journal: :The Journal of the Association of Physicians of India 1993
P P Varma O P Kalra K Joshi V Sakhuja K S Chugh

Fabry's disease is a sphingolipid storage disorder which is caused by mutations within the gene responsible for the expression of the lysosomal hydrolase, oc-galactosidase A ( 1). The enzyme defect results in the progressive deposition of uncleaved glycosphingolipids within lysosomes of endothelial, perithelial and smooth muscle cells. The major clinical features may be divided into cutaneous l...

2014
Giovanni Palladini Ute Hegenbart Paolo Milani Christoph Kimmich Andrea Foli Anthony D. Ho Marta Vidus Rosin Riccardo Albertini Remigio Moratti Giampaolo Merlini Stefan Schönland

Immunoglobulin light-chain (AL) amyloidosis is caused by a usually small plasma cell clone synthesizing light chains undergoing conformational changes that lead to their aggregationanddeposition in tissues. This process leads toprogressivemultiple organdysfunction anddeath if left untreated.Advanced, irreversibleorgandamageatpresentation is the main limitation to improve theoutcomeofpatientswit...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2001
N Bossini S Savoldi F Franceschini S Mombelloni M Baronio I Cavazzana B F Viola B Valzorio C Mazzucchelli R Cattaneo F Scolari R Maiorca

BACKGROUND Primary Sjögren's syndrome is a connective tissue disorder affecting primarily the lacrimal and salivary glands, resulting in xerophtalmia and xerostomia. Extraglandular manifestations are frequent and may include renal involvement. METHODS We studied the prevalence and nature of kidney involvement in 60 Italian patients with primary Sjögren's syndrome, diagnosed according to the E...

2011
Haldane Porteous Nadia Morgan Julio Lanfranco Monica Garcia-Buitrago Larry Young Oliver Lenz

INTRODUCTION Type 4 renal tubular acidosis is an uncommon clinical manifestation of systemic lupus erythematosus and has been reported to portend a poor prognosis. To the best of our knowledge, this is the first case report which highlights the successful management of a patient with systemic lupus erythematosus complicated by type 4 renal tubular acidosis who did not do poorly. CASE PRESENTA...

Journal: :Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia 2016
Hugo Abensur Marlene Antônia Dos Reis

Every cell in the human body has globotriaosylceramide accumulation (Gb3) in Fabry disease due to the mutation in gene of the enzyme α-galactosidase A. It is a disease linked to sex. The main clinical features are: cutaneous angiokeratomas; acroparestesias and early strokes; decreased sweating and heat intolerance; ocular changes; myocardial hypertrophy, arrhythmias; gastrointestinal disorders ...

Journal: :Proceedings 2012
Gates Colbert Daniel Richey John C Schwartz

Renal and urogenital disease is a prevalent finding of extrapulmonary Mycobacterium tuberculosis. Patients can present with unusual complaints not immediately suspicious for tuberculosis. We describe a 38-year-old man who presented with vomiting and an acute kidney injury. Imaging studies showed nodules throughout the lungs, retroperitoneum, abdominal viscera, and kidneys. Asymmetrical hydronep...

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