Pathology specimens of kidney surgical
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Transcript of Pathology specimens of kidney surgical
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Pathological Specimens of Kidney –
II Surgical
Dr Prashant Bansal
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Urolithiasis
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Urolithiasis
Incidence:
Etiology:
Clinical
Features:
Lab:
Path:
Clinical
Course:
Environmental, metabolic, infectious.
Develop silently until episode of renal
colic. Cause obstruction, pain, infection,
hydronephrosis, and hydroureter.
Gross or mcroscopic hematuria. Chemical
analysis to identify type of stone.
Characteristic radiographic findings.
May recur. Complications are the
problem.
Calcium phosphate or oxalate - Hard,
sharp. Uric acid - Smooth. Staghorn - Cast
of calyceal system.
Common, male predominance.
Treatment: Surgery, lithotomy, or ultrasonic
lithotripsy to remove stone. Treatment of
metabolic process, if indicated. Adequate
hydration.
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Urolithiasis
1-5%, environment, males, pelvis
Renal colic, dull ache in loins
Urinary tract infection recurrent.
Factors affecting:
Urine pH, Infection, Metabolic,
Pyrophosphates and citrate inhibit.
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Urolithiasis
Calcium oxalate (or phosphate) 75%
Magnesium ammonium phosphate (struvite, or "triple phosphate")
12%
Uric acid 6%
Cystine 1%
Other 6%
Infection
Stone
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Hypercalcemia / Hypercalciuria
Primary (increased intestinal absorption of Ca)
Idiopathic (most common)
Milk-alkali syndrome
Vitamin D excess
Sarcoidosis
Secondary (release of Ca from bones)
Renal osteodystrophy
Hyperparathyroidism
Osteolytic metastases (e.g. breast cancer)
Paraneoplastic syndromes (PTrP)
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Staghorn Calculus
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Urolithiasis with hydronephrosis
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Hydronephrosis
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Hydronephrosis:
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Urolithiasis – sites of impaction
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Hydronephrosis
Urolithiasis
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Causes of Obstructive Uropathy
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Renal Tumours
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Renal tumors
Benign
Adenoma
Oncocytoma
Angiomyolipoma
Fibroma (rare!)
Malignant:
Renal cell carcinoma (common – adults)
Wilm’s tumor (childhood)
Transitional cell carcinoma of renal pelvis
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Angiomyolipoma (Benign)
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Renal Papillary Adenoma
Papillary
Common
Histopathology similar to renal
Cell Carcinoma.
< 3cm – benign
> 3cm - malignant
All tumors considered
malignant until proved
otherwise.
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Oncocytoma (DCT epithelia, benign)
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Renal Cell Carcinoma
Incidence:
Etiology:
Clinical
Features:
Lab:
Path:
Clinical
Course:
Cells of proximal convoluted tubule. Risk
factors are smoking, obesity, analgesic
abuse, APCKD.
Hematuria*, flank pain, palpable mass.
Frequently metastasize (lungs, bone, skin,
liver, brain).
Gross or microscopic hematuria.
Specific Dx by radiographic techniques.
5-yr. survival 40%. Poor prognosis with
metastases.
Gross: Large yellow mass with hemorrhage
and necrosis. Invade renal vein.
Micro: Usually clear or granular cells with
little anaplasia. Other histologic variants
(“great mimicker”).
5th and 6th decades, most common
primary renal malignancy.
Treatment: Chemotherapy, surgery, immunotherapy.
Synonyms: Hypernephroma, clear cell carcinoma.
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Renal Cell Carcinoma
Most common renal tumor
Peak age – 60y M:F = 3:1
Incidence increasing world wide
Tobacco; Obesity, genetics (VHLgene, familial cases)
Von Hippel-Lindau syndrome
Hemangioblastoma cerebellum retina
Bilateral renal cysts,
Clear cell type RCC – common.
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RCC - Pathology
Yellow orange tumor –Hypernephroma.
Partially encapsulated
Extends into renal vein
tubular clear cell (77%)
papillary (15%)
granular, chromophobe, sarcomatoid (5%)
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Renal Cell Carcinoma:
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Renal Cell Carcinoma:
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Renal Cell Carcinoma:
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Renal Cell Carcinoma:
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RCC – Clinical Features:
Classical triad (hematuria, flank pain, mass) (<10%)
Hematuria (50%) most common symptom
Metastases-hematogenous and local abdominal
Paraneoplastic syndromes (PTH, Epo, amyloid)
5 year survival = 40%
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Wilm's Tumor
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Wilm’s Tumor
Incidence:
Etiology:
Clinical
Features:
Lab:
Path:
Clinical
Course:
Embryonic renal tissue (metanephric
blastema). Genetic abnormalities.
Palpable abdominal mass. Abdominal
pain, fever, anorexia, nausea/vomiting.
Hematuria.
No specific clinical laboratory findings.
Diagnosis by radiographic techniques.
5-yr. Survival 80%. Metastases to lung,
liver, bone, brain.
Gross: Solitary/multiple cystic mass,
sharply delineated. Soft, bulging, gray-
white with focal hemorrhage and necrosis.
Micro: Triphasic mesenchymal stroma,
tubules, and solid areas (blastema).
Primitive glomeruli, skeletal muscle,
cartilage, bone, etc. (embryonic tissues)
Most common renal tumor of
childhood. Peak age - 2.5 - 3.5 years.
Treatment: Prompt resection with chemotherapy ±
radiotherapy.
Synonyms: Nephroblastoma.
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Wilm's Tumor
Childhood tumor (2-5y) 98%< 10 years
Most common tumor in childhood
Sporadic, unilateral (90%)
Bilateral more common in familial cases (20%)
Familial syndromic (5%), nonsyndromic (5%)
WAGR sy – Aniridia, genital abn, Mental Ret. WT1
Beckwith Wiedemann sy - Hemihypertrophy – WT2
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Wilms Tumor Features:
Lobulated tumors mass –encapsulated
Histology: mixture of immature cells metanephric, stromal, tubular
Chemotherapy + surgery = 5 years = 90%
Children < 2 years better prognosis
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Transitional Cell Carcinoma:
5-10% of adult renal ca.
Etiology: Analgesic abuse, dye, rubber etc..
Multiple common.
Malignant cells in urine
Desquamated tissue may cause obstruction.
Hematuria & pain.
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Transitional cell Carcinoma:
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Transitional cell Carcinoma: