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RENAL PATHOLOGY
DEPARTEMEN PATOLOGI ANATOMIFK UMI
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KELAINAN-KELAINAN YANG DAPAT
DIJUMPAI PADA GINJAL:
KELAINAN KONGENITAL
CYSTIC DISEASE PADA GINJAL
GLOMERULAR DISEASE TUBULES AND INTERSTITIUM DISEASE
BLOOD VESSEL DISEASE
URINARY TRACT OBSTRUCTION
RENAL CALCULI STONE
TUMOR PADA GINJAL
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ANOMALI KONGENITAL PADA GINJAL :
1. Agenesis Kidney
2. Hypoplasia : kegagalan ginjal untuk
berkembang mencapai ukuran yang normal
3. Ectopic Kidney: adanya ectopic foci akibatgangguan perkembangan bagian
metaneprhros pada masa embryo
4. Horseshoe kidney : bersatunya polus
superior dan inferior sehingga berbentukseperti ladam kuda
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CYSTIC DISEASE OF THE KIDNEY
Cystic renal Dysplasia
Polycystic Kidney Disease :- Autosomal dominan (adult)
- Autosomal resesif (childhood)
Medullary cystic
Acquired cystic (dialysis associated) Localized (simple) renal cyst
Renal cyst in hereditary malformationsyndromes
Glomerulocystic disease Extraparenchymal renal cyst
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POLYCYSTIC KIDNEY DISEASE
(AUTOSOMAL DOMINANT - ADULT)
Kelainan herediter dengan karakteristikadanya kista-kista yang biasanya padakedua ginjal merusak parenkimginjal menyebabkan gagal ginjal
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POLYCYSTICKIDNEY
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GLOMERULAR DISEASE
Sering merupakan problem utama pada nefrologiTerbanyak : Glomerulonefritis kronis
penyebab utama gagal ginjal kronik
Biasanya diawali dengan penyakit sistemik, spt :
SLE, hipertensi, polyarteritis nodosa, DM
Manifestasi Klinis :
- Acute nefrotik syndrom
- Papillary progressive glomerlonefritis- Cronic renal failure
- Asymptomatik ( proteinuria atau hematuria)
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Contd
Perubahan morfologi :
hipersellularity
- biasanya disertai dengan proliferasi selluler
dari sel mesangial atau endothelial
- infiltrasi leukosit- Crescent formation
penebalan basement membrane
hialinisasi dan sklerosis
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Hyaline arteriolosclerosisThe lesions are characterized by glassy thickening of arterial and arteriolar walls. Inthis section an involved arteriole (arrow) is adjacent to a sclerotic glomerulus(asterisk). Hyaline arteriolosclerosisis seen in elderly patients, with or withouthypertension or diabetes, and in patients with long-standing diabetes but the lesions
are most common and most severe in hypertensive patients.
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PENY. PADA TUBULUS DAN INTERSTITIUM
Terdiri dari 2 kelompok :1. Iskemik atau tubular injury
Acute tubular necrosis
Acute renal failure
2. Tubulointerstitial nefritis
Penyebab
utama gagalginjal akut
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Note : necrosis and sloughing of epithelial cells of the proximal convolutedtubules.
The glomeruli and distal convoluted tubules are preserved
Acute tubular necrosis
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Tubulointerstitial nefritis
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TUMOR PADA
GINJAL
BENIGN
MALIGNANT
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TUMOR GINJAL BENIGN
1. Renal Papillary Adenoma
2. Renal Fibroma(Hamartoma)3. Angiomyolipoma
4. Oncocytoma
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Renal Cell Carcinoma
( Adenocarcinoma Ginjal )- Clear Cell Ca (70% - 80%)
- Papillary Ca (10% - 15%)
- Chromophobe Renal Ca
- Collecting Duct Ca
(Bellini Duct)
Urothelial Ca pada pelvisrenalis
Tumor
GinjalMalignant
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RENAL CELL CARCINOMA
Merupakan suatu keganasan yang berasal dariepitel tubulus renal
90% dari seluruh kasus keganasan yang terjadi
pada ginjal
Etiologi belum jelas, diduga ada hubungan
dengan asap rokok, paparan zat arsenic pada
industri
Gejala : trias simptom hematuri, nyeri danteraba massa pada daerah pinggang
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Multilocular cystic renal cell carcinoma
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Chromophobe renal cell carcinoma (RCC).Typical homogeneously tan coloured tumour of thelower pole of the kidney.
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Chromophobe renal cell carcinoma
Chromophobe renal cell carcinoma comprises about 5% of epithelial renalneoplasms. Microscopically, it is composed of variably-sized cells with abundantpale reticular or flocculent cytoplasm.
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Renal cell carcinoma was formerly known as hypernephroma and is also calledadenocarcinoma of the kidney.The most common type, clear cell carcinoma, is illustrated here. The number of cells
with clear cytoplasm vs eosinophilic granular cytoplasm varies from tumor to tumorand in different sections in an individual tumor
Renal cellcarcinoma
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Clear Cell Renal Cell Carcinoma
Grading Renal Cell Carcinoma: Fuhrman Grade 1
Fuhrman nuclear gradingsystem correlated well
with survival in patientswith renal cell carcinoma.Grade 1 tumors haveround, uniform nucleiwith inconspicuous orabsent nucleoli.
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Renal Cell Carcinoma : Fuhrman Grade 2
Nuclear contours are moreirregular than Grade 1;nuclei are about 15 micronsin diameter. Nucleoli maybe visible at highmagnification.
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Renal Cell Carcinoma : Fuhrman Grade 3
Nuclear contours are
even more irregular.Nuclear diameters canapproach 20 microns.Nucleoli are readilyseen.
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Cystic Renal Cell Carcinoma
Some cases of renal cellcarcinoma are composed largelyof multilocular cysts separated bythin septa containing tumor cells.The cystic nature of this tumor isillustrated in this low-power scan.
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Papillary Renal Cell Carcinoma
Papillary renal cell carcinoma comprises 15% to 18% of renal cell carcinoma.Note the prominent papillary structures many of which enclose clusters offoamy macrophages.
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WILLMS TUMOR
Tumor primer ginjal malignant yang dijumpai pada
anakTerjadi akibat kelainan gen
Makroskopis : massa yang besar , bulat dan solid,
warna coklat keabuan, bisa disertai
hemorrhage, cyst dan nekrosis
Mikroskopis :
dijumpai gambaran komponen triphasic :
blastema, stromal dan epitelKlinis : massa pd abdomen, nyeri, hematuria,
hipertensi
Prognosis baik : nefrektomi dan kemoterapi
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Wilms Tumor
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The triphasic nature of Wilms Tumor is obvious here. The epithelialelements surround nodules of blastema and are attempting for formrosettes. The nodules of blastem are separated by myxoid stroma.
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Wilms' Tumor : Epithelium
The epithelial component in this Wilms tumor consists of primitivecuboidal cells forming tubular structures and rosettes.
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Wilms' Tumor : BlastemaBlastema in WT consists of sheets of densely packed small blue cells withhyperchromatic nuclei, little cytoplasm and conspicuous mitotic activity