Pathology Of The Kidney, Ureters And Bladder Flashcards
(49 cards)
Kidney Differential Diagnoses
- Trauma
- Swelling/Mass/Tumour - non-neoplastic, benign, malignant (primary/secondary)
- Chronic - chronic inflammatory
- Acute - infection, acute inflammation, immunological
- Stone - genetic, metabolic
Causes of Haematuria
Serious causes of haematuria include kidney or bladder cancer; inflammation of the kidney, urethra, bladder, or prostate; polycystic kidney disease; and trauma on urinary tract, among other causes.
Less serious include vigorous exercise and sexual activity.
Causes of Acute Renal Failure
- Pre-renal: When the blood flow to the kidney is impaired. The following can cause an impaired blood flow: Severe blood loss, Heart disease, Liver failure, Some medications like aspirin and ibuprofen, Overuse of NSAIDs
- Renal causes: damage to the kidney, A blood clot formation in kidney, Kidney infections, Drugs like chemotherapy and antibiotics, HUS (hemolytic uremic syndrome), Glomerulonephritis – inflammation of the glomeruli which are the kidney filters, Blood vessel inflammation or vasculitis
- Post-renal: urinary obstruction, Diseases that cause blockage of urine include colon cancer, prostate cancer, cervical cancer, and blood clots
- The risk factors include: Age, Diabetes, High blood pressure, Block in the blood vessels in the arm or legs, Kidney disease, Liver diseases
Causes of Proteinuria
Dehydration, Inflammation, Low blood pressure, Fever, Intense activity, High stress, Kidney stones, Taking aspirin every day, Very low temperatures. high blood pressure, diabetes, Immune disorders such as lupus, Kidney inflammation (glomerulonephritis), multiple myeloma, Preeclampsia, A buildup of protein in your organs (amyloidosis), Cardiovascular disease, Intravascular hemolysis (a condition in which red blood cells are destroyed), Kidney cancer, Heart failure
Kidney functions
fluid and electrolyte balance, resorption of solutes, excretion (of waste e.g. conjugated xenobiotics (substances which are foreign to the body) or urea or excess water), endocrine (renin & bp, erythropoietin & RBCs)
Potter Syndrome
Bilateral renal agenesis - often fatal shortly after birth. Caused by a lack of amniotic fluid.
Renal Hypoplasia
The kidneys don’t fully develop. Can be unilateral or bilateral. Caused by genetic mutations or drugs taking during pregnancy,
Vesicoureteric Reflux
backward flow of urine from the bladder into the kidneys. This causes strong, persistent urge to urinate, pain while passing urine, abdominal pain and fever.
Renal Artery Stenosis
narrowing of the arteries that carry blood to the kidneys. This causes high blood pressure, elevated protein levels in urine, decreased kidney function and swelling.
Familial Mediteranean Fever
A genetic condition that leads to high fever and inflammation of abdomen, lungs and joints.
Can cause kidney failure.
Alport’s Syndrome
Alport syndrome is a genetic condition characterized by kidney disease, hearing loss, and eye abnormalities.
People with Alport syndrome experience progressive loss of kidney function. Almost all affected individuals have blood in their urine (hematuria), which indicates abnormal functioning of the kidneys. Many people with Alport syndrome also develop high levels of protein in their urine (proteinuria). The kidneys become less able to function as this condition progresses, resulting in end-stage renal disease (ESRD).
Autosomal Dominant Polycystic Kidney Disease
A genetic disorder in which numerous fluid-filled cysts develop in the kidney. This causes high blood pressure, back pain, headaches, blood in urine, kidney stones and urinary tract infections. Signs and symptoms often develop during adulthood despite cysts being there since birth/childhood.
Autosomal Recessive Polycystic Disease
A genetic disorder in which numerous fluid-filled cysts develop in the kidney. This causes high blood pressure, back pain, headaches, blood in urine, kidney stones and urinary tract infections. Much rarer than autosomal dominant and is often lethal in early life.
Medullary Sponge Kidney
Medullary sponge kidney is a condition where cysts develop in the urine-collecting ducts and tubules of one or both kidneys. The exact cause of medullary sponge kidney is unknown and there is no cure.
The first sign that a person has medullary sponge kidney is usually a UTI or a kidney stone. UTIs and kidney stones share many of the same signs and symptoms: burning or painful urination, pain in the back, lower abdomen, or groin, cloudy, dark, or bloody urine, foul-smelling urine, fever and chills, vomiting.
Medullary Cystic Disease Complex
Medullary cystic disease complex belongs to group of paediatric cystic renal diseases charaterised by progressive tubular atrophy with glomerulosclerosis (chronic tubulointerstitial nephritis) and multiple small medullary cysts.
Simple Cyst Kidney
Characterised by small, oval or round thin-walled sacs with watery fluid in the kidney. This causes back pain, abdominal pain and fever.
Glomerulonephritis
Inflammation of the kidneys that may involve the glomeruli, tubules or interstitial tissue (functional units of kidney) surrounding them. This causes swelling of the face, hands, feet and legs, blood pressure, blood in urine, and reduced kidney function.
Glomerulopathy
Glomerulopathy is generic disease of the renal glomerulus, impairment of which can lead to hematuria or proteinuria due to injury or dysfunction of the endothelium, glomerular filtration barrier or podocyte.
Glomerular Disease
- Immunological - MHC/HLA association
- Primary - glomerulonephritis or glomerulopathy
- Secondary - vascular, autoimmune e.g. Systemic Lupus Erythematosus, Amyloidosis, Diabetes, Acquired
Goodpasture Syndrome
Goodpasture syndrome is a rare disorder in which your body mistakenly makes antibodies that attack the lungs and kidneys. Lack of energy or tiring easily (fatigue), Nausea, Trouble breathing, Pale skin, Coughing up blood, Burning feeling when urinating, Small amounts of blood in the urine (hematuria), Protein in the urine (proteinuria).
Mesangiocapillary (Membranoproliferative) Glomerulonephritis 1&2
Membranoproliferative glomerulonephritis (MPGN) is an uncommon cause of chronic nephritis that occurs primarily in children and young adults. This entity refers to a pattern of glomerular injury based on the following three characteristic histopathologic findings:
- Proliferation of mesangial and endothelial cells and expansion of the mesangial matrix.
- Thickening of the peripheral capillary walls by subendothelial immune deposits and/or intramembranous dense deposits.
- Mesangial interposition into the capillary wall, giving rise to a double-contour or tram-track appearance on light microscopy.
Type I – Subendothelial deposits Type 2 – Dense deposits in the glomerular basement membrane
Minimal Lesion Glomerulonephritis
Presents with acute onset of nephrotic syndrome, often following a viral upper respiratory tract infection. Most common in children. Treat with steroids. Marked to proteinuria. Sometimes with Hodgkin’s lymphoma or remission with measles.
Focal Segmental Glomerulosclerosis
Focal segmental glomerulosclerosis (FSGS) is a disease in which scar tissue develops on the parts of the kidneys that filter waste out of the blood (glomeruli). FSGS can be caused by a variety of conditions. Marked proteinuria.
Symptoms may include: Foamy urine (from excess protein in the urine), Poor appetite Swelling (called generalized edema, from fluids held in the body), Weight gain.
Causes include: HIV infection, Obesity, Sickle cell disease, Birth defects of the kidneys, Heroin or other drug use, Genetic causes (in rare cases).
Nephrotic Syndrome
Results from excreting too much protein in urine due to a kidney disorder. This causes swelling in ankles, feet and around eyes, foamy urine, obesity, and fatigue.
Hypoalbuminaemia, Oedema and Albuminuria, hyperlipidaemia.
