Renal Pathology, Copy

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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