Lecture 4: Renal Disorders & Tumors PDF
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Ain Shams University
Marwa Shakweer
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Summary
This presentation covers renovascular disorders and renal tumors, including an overview of the anatomy of the kidney, vascular diseases, benign and malignant nephrosclerosis, RCC, and Wilm's tumor. It explains causes, pathologic features, risk factors, and clinical consequences. The presentation also contains illustrations.
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Lecture 4 Renovascular disorders Renal tumors Prof. Marwa Shakweer Head of pathology dep.BUC Professor of pathology , Ain Shams Univeristy Kidney Glomeruli Tubules Blood vessels Inter...
Lecture 4 Renovascular disorders Renal tumors Prof. Marwa Shakweer Head of pathology dep.BUC Professor of pathology , Ain Shams Univeristy Kidney Glomeruli Tubules Blood vessels Interstitial tissue MM.shakweer ILOs Identify types of renovascular disorders, causes, pathogenesis, and clinicopathologic features Classify tumors of the kidney, describe its pathologic features and list its complications MM.shakweer Vascular diseases of the kidney Renal artery stenosis Benign nephrosclerosis (on top of benign hypertnesion) Malignant nephrosclerosis (on top of malignant hypertension) MM.shakweer Renal artery stenosis Atherosclerosis Fibromuscular dysplasia Vasculitis Effect: leads to secondary hypertentsion MM.shakweer Benign nephrosclerosis It is the term used for abnormalities of the kidney induced by benign hypertension Gross: both kidneys are reduced in size The outer surface is finely granular The cut surface shows irregular atrophy of the cortex with loss of differentiation between cortex and medulla Microscopic: a) Large arteries: fibromuscular hyperplasia b) Arteriols: thickening and hyalinization of the walls and narrow lumens leading to diffuse ischemic atrophy of the nephrons MM.shakweer MM.shakweer Malignant nephrosclerosis May arise without preexisting hypertension. May occur on top of malignant hypertension Gross: petechial hemorrhages on cortical surface (flee bitten kidney) Microscopic : fibrinoid necrosis, hyperplastic arteriolosclerosis (onion skin appearance), necrotizing glomerulitis MM.shakweer Hyperplastic arterioloscleroiss, fibrinoid necrosis MM.shakweer Clinical course It is characterised by papilledema, encephalopathy, renal failure Increased intracranial pressure causes headache, nausea, vomiting and visual impairment 90% of deaths are caused by uremia and 10% by cerebral hemorrhage and cardiac failure MM.shakweer Tumors of the kidney Tumors of Tumors of pelvicalyceal kidney tissue system Benign: papilloma, Benign: adenoma, fibroma, lipoma, oncoctyoma fibroma, hemangioma Malignant: a) primary: renal cell carcinoma, Wilm’s tumor Malignant: b) secondary: metastatic from lung breast prostate transitional cell Sarcoma (osteosarcoma) carcinoma Malignant melanoma, choriocarcinoma MM.shakweer Renal cell carcinoma It arises from epithelial cells of renal tubules Age: 60-70 Male to female: 2:1 Risk factors: Smoking Polycystic kidney on top of chronic dialysis Genetic factors: - Clear RCC: von hippel lindau disease (AD) VHL gene is TSG - Papillary RCC: MET protooncogene MM.shakweer Gross Well demarkated and centered in the cortex The cut surface is solid, golden yellow with areas of HNC Extension to the renal pelvis is early and extension to the capsule is late MM.shakweer Microscopic 1- clear cell RCC: clear cells arranged in solid masses, cords, tubules or cysts with papillary structures. The stroma is scanty and very vascular with areas of hemorrhage and necrosis 2- papillary RCC: branching papillae covered by single layer of cells with large nuclei and small amount of cytoplasm 3- chromophobe RCC: large cells with granular esinophilic cytoplasm MM.shakweer MM.shakweer Spread Local: early infiltrate the pelvis , later iinfiltrate the capsule and perinephric fat Blood : lung , bone , brain (due to renal vein invasion) N.B invasion of left renal vein leads to varicocele Lymphatic spread: to lumber group of lymph nodes MM.shakweer Clinical manifestations 1- painless hematuria 2- flank pain and mass in the region of the kidney in late cases 3- manifestations dt metastasis to lung and bones 4- anemia, fever, weight loss 5- Paraneoplastic syndrome: a) Polycythemia due to secretion of erythropoetic stimulating substance b) Hypercalcemia dt production of PT like hormone c) Gynecomastia as result of gonadotrophin and placental lactogen production MM.shakweer Wilm’s tumor Age: children (2-5y) Arise from embryonic cells Gross: rapidly growing tumor destroying kidney tissue and infiltrating renal capsule Infiltration of the renal pelvis and ureter is rare and late MM.shakweer Microscopic (three components) Blastematous areas: small rounded cells with very scanty cytoplasm Mesenchymal elements: spindle cells and may show differentiation to smooth muscles, skeletal muscle, cartilage Epithelial component: anaplastic masses of malignant epithelial cells and may show glandular, tubular or glomerular formations MM.shakweer MM.shakweer MM.shakweer Clinical presentation Large abdominal mass Hematuria Abdominal pain Intestinal obstruction MM.shakweer Spread Local: renal tissue destruction, invasion of renal capsule, adrenal cortex, bowl, liver, vertebrea Blood: lung liver brain Lymphatics : to regional lymph nodes MM.shakweer Thank you