Day 12 5/29/15 Flashcards
UTI Routes of Infection
- ascending infection (70%)
- hematogenous infection
UTI Organism Virulence Factors
- bacterial adhesion: pili
- “O” antigens (certain strains are more resistent)
- endotoxin: dec. ureteric perstalsis
UTI Host Defense Mechanisms
- mechanical: bladder emptying, ureteric peristalsis, mucus
- chemical: prostatic secretions, urine osmolality, blood groups Ag’s
- immunological: PMNs, shedding urothelial cells
UTI Predisposing Factors
- females>males
- catheterization
- dec. urine flow/urine stasis
- calculi
- vesicoureteral reflux
- immune compromise
- kidey/UT disease
- pregenancy
UTI Clinical Manifestations
- covert bacteria
- sx reflective of level of infection
- recurrent sx in men usually reflects UT disease
- in early childhood, sx are nonspecific including irritability and convulsions
UTI Complications
- recurrence
- acute pyelonephritis
- renal/perinephric abscess
- papillary necrosis (diabetes)
- staghorn calculi (proteus)
- chronic pyelonephritis/renal scarring
Chronic Pyelonephritis Causes (2)
- UTI that has reached the kidneys
- urinary tract tract obstruction
- vesicoureteral reflux (VUR)
Vesicoureteral Reflux (VUR)
• Primary − Congenital abnormality of VU anatomy − Common in infants − Decreases in freq & severity during childhood − Usually mild
• Secondary − Congenital malformations − Neurogenic bladder (paraplegia, spina bifida) − Obstruction − Older children, adults
Reflux Nephropathy
Chronic Non-Obstructive Pyelonephritis
• Severe, persistent reflux + infection
− Allows organisms to access renal parenchyma
• Renal scars directly over dilate calyces
− More extensive at poles (compound vs. simple
papillae)
− Often unilateral or unequal bilateral
Papillary Renal Cell Carcinoma
- incidence:
- gross pathology:
- microscopic pathology:
- staging and prognosis:
- incidence: 10% to 15% of renal cancers
- gross pathology: unlike clear cell RCCs, papillary carcinomas are frequently multifocal
- microscopic pathology: Papillary growth pattern
- staging and prognosis: Better than clear cell RCC
Clear Cell Renal Cell Carcinoma
- incidence:
- clinical features:
- imaging features:
- gross pathology:
- microscopic pathology:
- staging and prognosis:
-incidence: Most common type, accounting for 70% to 80% of renal cell cancers, males > females
-clinical features:Clinical:
o Hematuria
o Arises in the renal cortex, has a propensity to invade the renal vein and can extend
into the inferior vena cava up to the heart.
o Regional lymph nodes may be enlarged. Hematogenous spread to lungs may occur
-imaging features:
o Ball-like mass of renal cortex
o Engorged, tumor-filled renal vein with extension to inferior vena cava
o Look for metastatic disease
-gross pathology:
o Most often as single tumor, somewhat spherical, yellowish gray mass, variegated appearance, focal hemorrhage, 20% are cystic
- microscopic pathology: three cell types are generally recognized -clear, granular, and spindle
- staging and prognosis: ~5 year survival rate
Renal Medullary Carcinoma
- incidence:
- clinical features:
- imaging features:
- urinary findings:
- gross pathology:
- microscopic pathology:
- staging and prognosis:
- incidence:
- clinical features:
- imaging features:
- urinary findings:
- gross pathology:
- microscopic pathology:
- staging and prognosis:
Chromophobe Renal Carcinoma
- incidence: Represents 5% of renal cell cancers
- microscopic pathology: Cells with prominent cell membranes and pale eosinophilic cytoplasm, usually with a halo around the nucleus. Histologic distinction from oncocytoma can be difficult
- staging and prognosis: Excellent compared with that of the clear cell and papillary cancers
Chromophobe Renal (Bellini Duct) Carcinoma
- incidence
- pathology
- prognosis:
- incidence: 1% or less of renal epithelial neoplasms
- microscopic pathology:Nests of malignant cells enmeshed within a prominent fibrotic stroma, typically in a medullary location
- staging and prognosis: Associated with aggressive behavior and poor prognosis. For the majority of patients surgical treatment will not result in a cure, early detection is key
Familial Renal Cell Carcinoma (RCC)
- incidence: 4% of renal cell cancers
- associated with Von-Hippel-Lindau syndrome
- clinical findings: hemangioblastomas of the cerebellum and retina, develop renal cysts and bilateral, often multiple, renal cell carcinomas