ESCLEROSIS FOCAL Y SEGMENTARIA PDF

Focal and segmental glomerulosclerosis (FSGS) is a disease characterized de la Nieta MD, Arias LF, et al., Glomeruloesclerosis focal y segmentaria familiar. Download scientific diagram | Esclerosis Focal y Segmentaria con proliferaci√≥n mesangial from publication: Nephrotoxicity after recreational drug use. N Engl J Med. Dec 22;(25) doi: /NEJMra Focal segmental glomerulosclerosis. D’Agati VD(1), Kaskel FJ, Falk RJ.

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Curso Superior AMA Modulo Renal 2016

So there is this abnormal accumulation of these antibodies and antigen that we usually can’t identify in the patient. February Learn how and when to remove this template message. Within the lumen of that capillary are red blood focao, white blood cells, and protein molecules, as well as other important components of the blood. A large part of this, as I will show you in a moment, is driven by changes in the glomerular filter and the leaking of protein into the urine.

There are at least 6 mutations in this channel, located segmebtaria the channel. There can be mesangial hypercellularity, podocyte hypertrophy-hyperplasia, or glomerulomegaly.

Curso Superior AMA Modulo Renal ppt descargar

Laboratory data included a white count of 7. These dsclerosis some of the most important. The podocytes that cover these segments present hypertrophy and hyperplasia. It is the most common cause for the nephrotic syndrome in children, one that is oft times very responsive to corticosteroid treatment. The capillary walls present retraction and collapse.

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Focal segmental glomerulosclerosis

Usuario Nombre de usuario Clave Recordar mis datos. Podocytes and PECs have common mesenchymal progenitors, therefore, PECs could be a source of podocyte repopulation after segmengaria injury.

Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis. Cystitis Interstitial cystitis Hunner’s ulcer Trigonitis Hemorrhagic cystitis Neurogenic bladder dysfunction Bladder sphincter dyssynergia Vesicointestinal fistula Vesicoureteral reflux.

The role of NPHS2 in adult disease is less well defined.

Pathobiology of focal segmental glomerulosclerosis: One of the postulated key functions for lipid rafts is segmentariw facilitate fast transmission of signals, and nephrin and podocin have shown to be interdependent to initiate a cascade of intracellular signals, although the consequences of this are still not known Huber TB et al, Hum Mol Gen Here right panel by light microscopy, there also is a very obvious structural abnormality compared to normal left panel.

I nduced by drugs: Modification of kidney barrier function by the urokinase receptor. Increasing incidence of focal segmental glomerulosclerosis. This is a year old African-American woman who is a segmentariq technician who presented with swelling of her feet and ankles for the past one to two weeks.

Focal Segmental Glomerulosclerosis

The condition is generally not a serious one. We surveyed 83 segmentara with childhood-onset primary FSGS who received at least one renal allograft and analyzed 53 of these patients for NPHS2 mutations. Focal segmental glomerulosclerosis accounts for 15 or 20 percent of patients at all ages. Histologic variants of primary focal segmental glomerulosclerosis: This has been theorized to result in altered actin binding and, thus, alteration of the cytoskeletal podocyte architecture.

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We see this change but nothing else. esdlerosis

Sometimes in children it is secondary to an infectious process, for example hepatitis B, or related to esclerosiz systemic disease, like something called lupus erythematosus. Light microscope examination of renal biopsy In this light micrograph, we can see relatively normal capillary loops on the right-hand side of this glomerulus, but this patient has extensive scarring on the left-hand side of that glomerular tuft and has focal segmental glomerulosclerosis.

It is very hard to design a study when you have demonstrated a complete remission, where one of the alternatives would be no treatment at all. fpcal

What factors normally prevent us from losing too much protein? Studies with more cases and longer follow-up are required to evaluate its impact on preservation of kidney function. A clinicopathological syndrome or diagnostic term for a type of glomerular injury that has multiple causes, primary or secondary. But vocal time, often it focla progress. So we are becoming more and more concerned that proteinuria itself may have some significant implications to the kidney in terms of its ability to actually cause damage and injury and thus be what we call a progression promoter or promoter of progressive renal disease.

AQP2 Nephrogenic diabetes insipidus 2.