Uni Week 1 Notes Flashcards

(35 cards)

1
Q

Identify the location of the kidneys and their position relative to surrounding structures and organs

A

The kidneys are retroperitoneal organs typically located on either side of the vertebral column extending from approximately the T12 to L3 vertebrae[cite: 8 They are positioned posterior to the peritoneum and anterior to the muscles of the posterior abdominal wall[cite: 8].

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2
Q

Describe the changes in kidney position with respiration and body position

A

The kidneys are mobile organs and can shift their position with respiration descending with inspiration and with changes in body position such as moving from supine to upright[cite: 9].

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3
Q

Describe the renal fascia and the adipose capsule of the kidneys

A

The kidneys are enveloped by a fibrous renal capsule which is then surrounded by an adipose capsule (perirenal fat)[cite: 10 This adipose capsule is enclosed by the renal fascia (Gerota’s fascia) which anchors the kidneys to surrounding structures and helps hold them in place[cite: 10].

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4
Q

Understand the arterial blood supply of the kidneys including the origins pathways and branching patterns of the renal arteries within the kidneys

A

The kidneys receive their arterial blood supply primarily from the renal arteries which originate directly from the abdominal aorta[cite: 11 Within the kidney the renal artery typically divides into segmental arteries which then branch into interlobar arteries arcuate arteries and interlobular arteries supplying blood to the renal cortex and medulla[cite: 11].

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5
Q

Describe the venous drainage of the kidneys and identify the main tributaries that contribute to the formation of the renal veins such as the interlobar veins and arcuate veins

A

Venous drainage of the kidneys occurs via the renal veins which typically drain into the inferior vena cava[cite: 12 Within the kidney the venous drainage largely mirrors the arterial supply with interlobular veins draining into arcuate veins then into interlobar veins and finally converging to form the renal vein[cite: 12].

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6
Q

Identify the origin of renal nerves and the innervation pathway to the kidneys

A

The renal nerves primarily originate from the renal plexus which receives sympathetic innervation from the T10-L1 segments of the spinal cord[cite: 13 These nerves follow the renal arteries to innervate the kidneys[cite: 13].

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7
Q

Define the structures that comprise the renal hilum

A

The renal hilum is the concave medial border of the kidney where structures such as the renal artery renal vein and renal pelvis enter and exit the kidney[cite: 15].

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8
Q

Identify the renal cortex with renal columns renal medulla and renal pyramids and understand the microstructures found within these internal structures of the kidney

A

Internally the kidney consists of an outer renal cortex and an inner renal medulla[cite: 17 The renal cortex extends into the medulla as renal columns separating the renal pyramids of the medulla[cite: 17 The medulla contains conical structures called renal pyramids[cite: 17 Microstructures within these regions include nephrons collecting ducts and associated vasculature[cite: 17].

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9
Q

Describe the structures of the renal pelvis including the minor and major calyces

A

The renal pelvis is a funnel-shaped structure located within the renal hilum formed by the convergence of major calyces[cite: 18 The major calyces in turn are formed by the joining of several minor calyces which collect urine from the renal papillae at the apex of the renal pyramids[cite: 18].

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10
Q

Identify the path of urine drainage by the kidney

A

Urine produced by the nephrons drains into collecting ducts then into the renal papillae followed by the minor calyces major calyces renal pelvis ureter bladder and finally exits the body via the urethra[cite: 19].

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11
Q

Identify the components of the renal corpuscle

A

The renal corpuscle consists of the glomerulus a tuft of capillaries and Bowman’s capsule (or glomerular capsule) which surrounds the glomerulus[cite: 22].

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12
Q

Compare and contrast the structural and functional differences between a cortical nephron and a juxtamedullary nephron

A

Cortical nephrons have short loops of Henle that primarily remain in the renal cortex while juxtamedullary nephrons have long loops of Henle that extend deep into the renal medulla[cite: 23 Juxtamedullary nephrons play a crucial role in the production of concentrated urine[cite: 23].

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13
Q

Differentiate between the histology of the glomerular capsule renal tubules and collecting duct

A

The glomerular capsule (Bowman’s capsule) has a parietal layer of simple squamous epithelium and a visceral layer composed of podocytes[cite: 24 The renal tubules (proximal convoluted tubule loop of Henle distal convoluted tubule) exhibit different epithelial cell types and brush borders depending on their function[cite: 24 Collecting ducts are lined with principal cells and intercalated cells[cite: 24].

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14
Q

Define the basic renal processes of glomerular filtration tubular reabsorption tubular secretion

A

Glomerular filtration is the process by which blood plasma is filtered from the glomerulus into Bowman’s capsule[cite: 25 Tubular reabsorption is the selective return of substances from the renal tubule back into the blood[cite: 25 Tubular secretion is the selective transfer of substances from the blood into the renal tubule for excretion[cite: 25].

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15
Q

Describe the sequential events and key developmental stages involved in the formation of the urinary system

A

The urinary system develops from intermediate mesoderm and involves sequential stages of kidney formation: pronephros mesonephros and metanephros[cite: 28 32].

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16
Q

Identify the different sources of cells that contribute to the formation of specific structures within the urinary system such as the nephrons and collecting ducts

A

Nephrons develop from the metanephric blastema (metanephric mesoderm) while the collecting ducts renal calyces renal pelvis and ureter develop from the ureteric bud an outgrowth of the mesonephric duct[cite: 29].

17
Q

Describe the three stages in kidney formation during embryonic development. (Pronephros mesonephros and metanephros)

A

The pronephros is the most rudimentary and transient stage[cite: 32 The mesonephros develops next and functions for a short period during embryonic life[cite: 32 The metanephros is the definitive kidney that develops last and becomes the permanent kidney[cite: 32].

18
Q

Describe the process of nephrogenesis including the differentiation of the metanephric blastema formation of nephron structures and establishment of the renal vasculature

A

Nephrogenesis involves the induction of the metanephric blastema by the ureteric bud leading to the differentiation of the blastema into renal vesicles which then develop into S-shaped bodies forming the renal corpuscle and renal tubules[cite: 33 Concurrently blood vessels invade the developing nephron to establish the renal vasculature[cite: 33].

19
Q

Explain the process of embryonic development of the rest of the urinary system including the formation of ureters bladder and urethra

A

The ureters develop from the ureteric buds[cite: 37 The bladder and urethra develop from the urogenital sinus[cite: 37 39].

20
Q

Explain the purpose of the urorectal septum

A

The urorectal septum is a mesodermal ridge that divides the cloaca into an anterior urogenital sinus and a posterior anorectal canal[cite: 38].

21
Q

Discuss the origin and development of the bladder from the urogenital sinus

A

The bladder primarily develops from the vesical part of the urogenital sinus[cite: 39 The cranial part of the urogenital sinus forms the urinary bladder[cite: 39].

22
Q

Compare and contrast the embryological development of the urethra between males and females

A

In males the urethra is formed from the phallic part of the urogenital sinus and the fusion of the urethral folds[cite: 40 In females the urethra is much shorter and develops from the vesical and pelvic parts of the urogenital sinus with the urethral folds remaining separate[cite: 40].

23
Q

Discuss the aetiology clinical findings morphological features and management of autosomal dominant polycystic kidney disease (PKD)

A

Autosomal dominant PKD is a genetic disorder caused by mutations in the PKD1 or PKD2 genes leading to the development of numerous cysts in the kidneys[cite: 44 Clinical findings include hypertension renal pain hematuria and progressive renal failure[cite: 44 Morphological features involve bilaterally enlarged kidneys with multiple cysts of varying sizes[cite: 44 Management focuses on controlling symptoms blood pressure and slowing the progression of renal disease often requiring dialysis or kidney transplantation in end-stage renal disease[cite: 44].

24
Q

Discuss the aetiology clinical findings morphological features and management of autosomal recessive polycystic kidney disease

A

Autosomal recessive PKD is a genetic disorder caused by mutations in the PKHD1 gene leading to the formation of multiple small cysts in the collecting ducts[cite: 45 It often presents in infancy or childhood with enlarged kidneys hypertension and liver involvement[cite: 45 Management is supportive focusing on treating hypertension renal failure and liver complications[cite: 45].

25
Define multicystic dysplastic kidney (MCDK) and discuss possible aetiologies
Multicystic dysplastic kidney (MCDK) is a congenital condition where the kidney is replaced by multiple non-communicating cysts and there is little to no normal renal tissue[cite: 46 Possible etiologies include abnormal development of the ureteric bud and metanephric blastema during embryogenesis[cite: 46].
26
Compare and contrast MCDK with PKD
MCDK is typically unilateral involves a non-functional kidney and usually results from a developmental anomaly often sporadic[cite: 46 PKD on the other hand is usually bilateral progressive genetic (autosomal dominant or recessive) and involves the formation of numerous cysts that impair kidney function over time[cite: 46].
27
Discuss the causes morphology changes clinical presentations and possible complications associated with:
28
Ectopic kidney
An ectopic kidney is a kidney that is not located in its usual position often due to abnormal ascent during development[cite: 50 It can be found in the pelvis or other abnormal locations[cite: 50 Clinical presentations can include asymptomatic discovery pain or urinary tract infections due to abnormal drainage[cite: 50 Complications include hydronephrosis and increased susceptibility to injury[cite: 50].
29
Horseshoe kidney
A horseshoe kidney is a congenital anomaly where the two kidneys are fused usually at their lower poles forming a U-shape[cite: 52 This fusion typically occurs as the kidneys ascend during development[cite: 52 Clinical presentations are often asymptomatic but can include increased risk of urinary tract infections kidney stones and hydronephrosis due to abnormal drainage[cite: 52].
30
Cross fused renal ectopia
In cross-fused renal ectopia one kidney crosses the midline and fuses with the other kidney[cite: 54 This leads to both kidneys being on the same side of the body[cite: 54 Clinical presentations vary but can include asymptomatic discovery pain or complications like hydronephrosis[cite: 54].
31
Duplex kidney
A duplex kidney is a kidney with two collecting systems and two ureters[cite: 55 It can be complete with two separate ureters draining into the bladder or incomplete with two ureters joining before reaching the bladder[cite: 55 Clinical presentations include increased risk of urinary tract infections vesicoureteral reflux or obstruction[cite: 55].
32
Describe the aetiology types and clinical presentations of renal agenesis
Renal agenesis is the complete absence of one or both kidneys[cite: 56 Unilateral renal agenesis is more common and often asymptomatic with the remaining kidney undergoing compensatory hypertrophy[cite: 56 Bilateral renal agenesis is lethal leading to Potter sequence due to oligohydramnios[cite: 56 The etiology involves a failure of the ureteric bud to develop or induce the metanephric blastema[cite: 56].
33
Define the primary functions of the kidneys including filtration reabsorption secretion and excretion
The kidneys filter waste products and excess water from the blood to form urine (filtration)[cite: 61 They reabsorb essential substances back into the blood (reabsorption)[cite: 61 They also secrete certain waste products and excess ions into the filtrate (secretion)[cite: 61 Finally they eliminate urine from the body (excretion)[cite: 61].
34
Identify the endocrine functions of the kidneys such as the production and secretion of renin erythropoietin and calcitriol
The kidneys produce and secrete renin which is involved in blood pressure regulation[cite: 62 They also produce erythropoietin which stimulates red blood cell production[cite: 62 Additionally the kidneys convert calcidiol to calcitriol (the active form of vitamin D) which is crucial for calcium homeostasis[cite: 62].
35
Describe the functions of the kidneys that are related to the maintenance of fluid and electrolyte balance blood pressure regulation and acid-base homeostasis
The kidneys regulate fluid balance by controlling water reabsorption and excretion[cite: 63 They maintain electrolyte balance by selectively reabsorbing or excreting various ions like sodium potassium calcium and phosphate[cite: 63 Through the renin-angiotensin-aldosterone system and by regulating fluid volume they play a critical role in long-term blood pressure regulation[cite: 63 The kidneys also contribute to acid-base homeostasis by excreting hydrogen ions and reabsorbing bicarbonate ions[cite: 63].