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Anatomy, Abdomen and Pelvis: Kidneys

Editor: Stephen W. Leslie Updated: 9/15/2025 4:33:11 PM

Introduction

The kidneys are paired retroperitoneal organs located between the T12 and L3 vertebrae, positioned lateral to the spine and adjacent to multiple abdominal structures. Each kidney comprises the renal parenchyma—divided into cortex and medulla containing nephrons, the functional units—and the collecting system, which conveys urine to the ureter (see Image. Kidney Anatomy). The kidneys perform essential roles in excreting nitrogenous wastes, regulating electrolytes and acid-base balance, controlling blood pressure, reabsorbing vital substances, and producing hormones such as erythropoietin and calcitriol.

The kidneys hold clinical significance due to their roles in waste excretion, electrolyte and acid-base regulation, blood pressure control, and hormone production, making preservation of renal function essential in disease management. In surgery, the kidney’s end-artery vascular anatomy requires careful protection of accessory renal arteries and the Brodel line, while nephron-sparing techniques enable targeted parenchymal resection to preserve renal function and minimize ischemia. A thorough understanding of renal anatomy and physiology enables clinicians to optimize diagnostic, medical, and surgical interventions while minimizing complications.

Structure and Function

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Structure and Function

Gross Anatomy and Anatomical Relations of the Kidney

The kidneys are a pair of bean-shaped retroperitoneal organs, exhibiting medial concavity and lateral convexity, with an average weight of 160 to 162 g in men and 135 to 136 g in women.[1] The left kidney is generally slightly larger and approximately 10 g heavier than the right kidney. Typical dimensions include a length of 10 to 12 cm, a width of 5 to 7 cm, and a thickness of 3 to 5 cm, comparable in size to a closed fist. Both kidneys are normally positioned between the transverse processes of T12 and L3.

The upper renal poles are usually oriented slightly medial and posterior relative to the lower poles.[2] The right kidney typically occupies a slightly more inferior position than the left, reflecting displacement by the liver.[3] Kidney size correlates positively with total body surface area, height, and weight, and decreases with age due to progressive loss of renal parenchyma.[4][5]

Each kidney is positioned immediately inferior to its respective adrenal (suprarenal) gland. The upper pole of both kidneys lies anterior to the diaphragm, which covers the upper 1/3 of each renal unit, and is frequently crossed by the overlying 12th rib. The lower pole of both kidneys is located anterior to the psoas muscle and the lateral aspect of the quadratus lumborum.

The right kidney relates posteriorly to the ascending colon, medially to the 2nd part of the duodenum, and anteriorly to the liver, separated from the hepatic surface by the hepatorenal recess. The left kidney lies posterior to the descending colon, the tail of the pancreas (which may extend sufficiently to cover the renal hilum), the greater curvature of the stomach (which can overlie the superomedial renal surface), and the spleen, to which it is connected via the splenorenal ligament. The kidneys are aligned slightly obliquely, parallel to the ipsilateral psoas muscle. The colon is positioned anterior to both kidneys.[6][7][8]

The lower poles of the kidneys are more lateral, anterior (superficial), and farther apart than the upper poles.[9] These poles are more susceptible to traumatic injury due to limited protection from the lower rib cage.[10] In a 2010 Korean study, Joon et al measured the longitudinal axis of the kidneys and found a mean coronal angle of 16.8° (range, 15° to 20°) relative to the spine. This angle may be reduced in the presence of accessory renal arteries.

At the medial margin of each kidney lies the renal hilum, where the renal artery enters the kidney, and the renal vein and pelvis exit the renal sinus.[11][12] The renal vein is positioned anterior to the renal artery, with the renal pelvis located posterior to both.[13][14] The renal pelvis represents the superior end of the ureter and typically receives 2 or 3 major calyces, with each major calyx drained by 2 or 3 minor calyces, although considerable variation exists.[15] Minor calyces are indented by the renal papillae, which form the apices of the renal pyramids. A renal pyramid, together with its overlying cortical tissue, constitutes a renal lobe.[16]

Each kidney is enclosed by a 2-layered capsule and surrounded by perinephric fat, the Gerota fascia anteriorly, and the Zuckerkandl fascia posteriorly. The anterior renal fascia is termed "Gerota fascia," while the posterior renal fascia is called "Zuckerkandl fascia."[17] In common usage, the Gerota fascia frequently refers collectively to both fasciae. Perinephric adipose tissue is thickest along the borders of the kidneys and extends into the renal sinus at the renal hilum.

The region immediately surrounding the kidneys constitutes the retroperitoneum. This region encompasses the portion of the abdominal cavity and pelvis lying between the posterior parietal peritoneum anteriorly and the posterior abdominal wall. Structures contained within the retroperitoneum include the pancreas (excluding the tail embedded in the splenorenal ligament), ascending and descending colon, duodenum (except the 1st segment), adrenal glands, kidneys, ureters, renal vessels, abdominal aorta, inferior vena cava, and posterior bladder wall.[18] Further details are provided in the companion StatPearls reference “Anatomy, Abdomen and Pelvis, Retroperitoneum.”[19]

Internal Structure and Functional Anatomy of the Kidney

Each kidney comprises 2 primary regions: the renal parenchyma and the collecting system (pyelocalyceal system). The renal parenchyma is subdivided into 2 macroscopically and functionally distinct areas, the cortex and the medulla, each containing specific segments of the nephron, the functional unit of the kidney (see Image. Nephron and Vasculature.)

The renal cortex forms the outer portion of the renal parenchyma. This area contains most nephron components, including renal corpuscles, proximal and distal convoluted tubules, collecting tubules, and cortical collecting ducts. The cortex surrounds both the renal medulla and sinus and can be divided into 2 regions. The renal mantle denotes the peripheral layer of cortical tissue that covers the base of each renal pyramid. Renal columns (columns of Bertin), also referred to as "cortical septa," are extensions of cortical tissue that project inward from the mantle toward the renal sinus, flanking each renal pyramid.[20]

The renal medulla lies between the cortex and the renal sinus. This portion is organized into renal pyramids, which contain medullary rays that extend from adjacent cortical tissue into the medulla. Medullary rays consist of the descending and ascending limbs of the loop of Henle, as well as the medullary collecting ducts.[21] Each renal pyramid, together with its associated overlying cortex, constitutes a renal lobe, the anatomical unit of the kidney.[22] Urine from each lobe drains through a single renal papilla, located at the apex of the pyramid (area cribrosa), into a minor calyx. On average, each kidney contains approximately 9 renal lobes.[23]

The renal collecting system receives urine from the renal parenchyma via the collecting ducts and conveys it to the ureter. The system begins with a variable number of minor calyces, each typically enclosing a single renal papilla. Most kidneys (70%) contain 7 to 9 minor calyces, with 2 or 3 converging to form a major calyx.[24]

A minor calyx may drain a single papilla (simple calyx) or multiple papillae (compound calyx). Compound calyces, more frequently observed in the upper renal poles, form when 2 to 3 adjacent minor calyces merge, producing a major calyx. Major calyces subsequently unite to form the renal pelvis, a funnel-shaped structure that marks the transition to the proximal ureter.[25] Variability in intrarenal anatomy influences the selection and success of kidney procedures, including ureteroscopy, extracorporeal shockwave lithotripsy, and percutaneous nephrolithotomy.[26]

Nephrons are the functional units of the kidney, with each adult kidney containing approximately 1 to 1.5 million nephrons, occasionally exceeding 2.5 million.[27][28][29] Each nephron begins with an afferent arteriole that supplies a capillary tuft, the glomerulus.[30] The glomerulus is enclosed by the Bowman capsule, a double-layered epithelial structure. Together, these structures constitute the renal corpuscle. The efferent arteriole exits the glomerulus and gives rise to a secondary capillary network, including peritubular capillaries and vasa recta, which supply the renal tubules (see Image. Filtration Apparatus of the Glomerulus).[31]

Distal to the Bowman capsule, the nephron progresses through the following segments: proximal convoluted tubule, proximal straight tubule (thick descending limb of the loop of Henle), thin descending limb, thin ascending limb, distal straight tubule (thick ascending limb), distal convoluted tubule, and collecting duct. Multiple collecting tubules from distinct nephrons unite to form the collecting duct, which continues as the medullary collecting duct and ultimately as the papillary duct. Papillary ducts open at the apex of the renal pyramids, forming the area cribrosa, through which urine drains into the renal pelvis and the pyelocalyceal system.[32][33]

Kidney Functions

The kidneys perform several essential functions, including the excretion of nitrogenous waste products such as ammonia and urea; the regulation of electrolytes, including sodium, potassium, and calcium; and the maintenance of acid-base balance via hydrogen ion excretion and bicarbonate reabsorption.[34][35] These organs contribute to the regulation of blood pressure and intravascular volume through the renin-angiotensin-aldosterone system.[36] The kidneys also reabsorb vital substances, including glucose, amino acids, phosphate, calcium, and water.[37][38] In addition, these paired structures secrete critical hormones such as erythropoietin, which stimulates red blood cell production, and calcitriol, the active form of vitamin D, which regulates calcium and phosphate metabolism.[39][40]

Embryology

The human kidney develops from the intermediate mesoderm. Nephrogenesis occurs in 3 successive phases: the pronephros, mesonephros, and metanephros.

The pronephros, located in the cervical region of the developing embryo, comprises vestigial excretory units (nephrotomes) that are nonfunctional in humans and appear transiently during the 4th week of development.[41] As the pronephros regresses, the mesonephros arises from the intermediate mesoderm, extending from the upper thoracic to the upper lumbar regions. This transient embryonic kidney consists of excretory units that elongate, form loops, and develop capillary tufts surrounded by the Bowman capsule, forming primitive renal corpuscles. Each excretory tubule drains into a longitudinal collecting duct, the mesonephric (Wolffian) duct, which empties into the early cloaca. Approximately 40 pairs of functional excretory units develop and can drain small amounts of fluid into the early amniotic cavity.[42]

By the 6th week of development, paired mesonephric organs are fully formed, but regression occurs between the 8th and 10th weeks. In the male body, the mesonephric duct is retained and differentiates into components of the reproductive tract, including the epididymis, vas deferens, seminal vesicles, and ejaculatory ducts.[43]

The metanephros, which gives rise to the permanent kidney, appears during the 5th week of development and comprises excretory units derived from the metanephric mesoderm. Metanephric development depends on reciprocal interactions between the metanephric blastema and the ureteric bud. As the distal segment of the mesonephric duct fuses with the cloaca, surrounding mesoderm forms the metanephric blastema. This blastema secretes signaling factors that induce the formation of the ureteric bud as an evagination of the mesonephric duct.[44]

WT1, a transcription factor, regulates signal production. WT1 mutations are associated with nephroblastoma (Wilms tumor) and other syndromes, including Denys-Drash, Frasier, and WAGR (Wilms tumor, aniridia, genitourinary anomalies, and developmental delay).[45][46] This interaction drives ureteric bud dilation, which forms the renal pelvis and ureter, and subsequently splits into major calyces by the end of the 6th week.

Early splitting of the ureteric bud can result in a bifid ureter. Buds then arise from the calyces and are stimulated to divide into collecting tubules at the 7th week, which are incorporated into the developing tubules at the periphery to become minor calyces. Successive generations of collecting tubules continue to develop and converge to form renal pyramids. Tubules induce the surrounding metanephric tissue via fibroblast growth factor 2 (FGF2) and bone morphogenetic protein 7 (BMP7) to form S-shaped tubules and capillaries that differentiate into glomeruli.

The distal glomerulus connects with the connecting tubules, while the Bowman capsule surrounds the proximal glomerulus, forming the renal corpuscle. The tubule extends into the proximal convoluted tubule, loop of Henle, and distal convoluted tubule. Collectively, these tubules and renal corpuscles constitute the nephron, the functional renal excretory unit. The majority of nephrons (60%) form during the latter half of gestation.[47] Nephrons become functional and urine-producing by the 12th week and continue to develop until approximately 1 million per kidney are present at birth (range, 250,000 to over 2 million).[48][49][50]

The causes of this wide variation in nephron number are not fully understood, but likely contributors include genetic factors, in utero environmental differences, maternal health and nutrition, developmental anomalies, and toxic exposures during gestation.[51][52] Individuals born with a low nephron count exhibit increased susceptibility to renal disease and kidney failure later in life.[53][54]

Blood Supply and Lymphatics

Approximately 20% of total cardiac output, or 1 to 1.1 L/min, is delivered to the kidneys.[55][56][57] With a normal glomerular filtration rate of 120 mL/min, 180 L of fluid per day is filtered from the blood into the renal nephrons. Average urine output is approximately 1.5 L daily, indicating that 178.5 L of fluid initially filtered by the glomeruli must be reabsorbed.[58] This process requires a highly specialized tubular reabsorption system supported by extensive peritubular microvascular networks for efficient fluid return to the systemic circulation.[59][60][61][62]

Renal perfusion is supplied via the renal arteries, which branch from the aorta just below the superior mesenteric artery and enter the hilum at the level of L2. While typically singular, renal arteries may be duplicated or accompanied by accessory arteries, all of which are end arteries that must be preserved during surgery or transplantation. The longer right renal artery passes posterior to the inferior vena cava. Each renal artery divides into anterior and posterior branches, described relative to the renal pelvis. The anterior branch receives 75% of renal blood flow, while the posterior branch supplies the posterior segment as the posterior segmental artery.

The 1st branch of the renal artery is typically the inferior suprarenal (adrenal) artery, although considerable variability exists.[63][64][65] The anterior branch further divides into 4 main segmental arteries:

  • Superior segmental artery, also known as the apical segmental artery
  • Anterosuperior segmental artery, also referred to as the superior segmental artery
  • Anteroinferior segmental artery, also referred to as the middle segmental artery
  • Inferior segmental artery

Each segmental artery subsequently divides into interlobar, arcuate, and interlobular arteries.[66][67][68] The interlobar arteries extend parallel between major calyces. These vessels then branch into arcuate arteries, which traverse the base of the renal pyramids within the cortex. Interlobular arteries arise from the arcuate arteries and extend into the renal cortex, eventually forming afferent arterioles, peritubular capillaries, and efferent arterioles that contribute to the vasa recta and peritubular capillary networks.[69] Some interlobular branches supply the renal capsule, renal pelvis, and proximal ureter (see Image. Kidney Blood Supply).

Renal veins mirror the path of the arteries anteriorly. The left renal vein is several centimeters longer than the right vein, crossing the midline to reach the IVC located to the right of the abdominal aorta at the L2 or L3 level.[70][71] This anatomical difference often favors the selection of the left kidney for transplantation over the right kidney.

The term "nutcracker syndrome" refers to entrapment of the left renal vein caused by compression between the superior mesenteric artery and the aorta. The left renal vein passes posterior to the superior mesenteric artery and anterior to the aorta en route to the IVC, placing it at risk of compression.[72] Clinical manifestations are generally nonspecific and may include abdominal pain, hypotension, intermittent flank pain, and microscopic hematuria. Management typically involves endovascular stenting, though left renal vein transposition may be required in selected cases.[73][74] Further details are available in the companion StatPearls reference, "Nutcracker Syndrome and Left Renal Vein Entrapment."[75]

The left testicular (gonadal) vein usually drains into the higher-pressure left renal vein, whereas the right testicular (gonadal) vein empties directly into the lower-pressure IVC.[76] These anatomical differences account for the higher prevalence of left-sided varicoceles and explain why an isolated right-sided varicocele may indicate IVC obstruction, potentially due to tumor thrombus extending from the right renal vein.[77]

Renal lymphatic drainage, and potentially that of the proximal ureters, occurs via lymphatic channels. These channels enter the aortic lymphatic chain on the left and the right lateral IVC lymphatics on the right.[78][79]

Nerves

Innervation of the kidneys, suprarenal glands, and a portion of the proximal ureters is provided by the renal nerve plexus, which contains both sympathetic and parasympathetic fibers.[80] The plexus receives input from the abdominopelvic splanchnic nerves.

Sympathetic efferents supply the nephrons and renal vasculature exclusively, with dense distribution around the afferent arterioles, thick ascending limbs, and distal convoluted tubules.[81][82][83][84] Preganglionic fibers arise from T8 to L1 and synapse in the inferior mesenteric ganglion.[85][86][87][88][89] Postganglionic fibers follow the renal artery and vein to the kidney, positioning them adjacent to major renal vasculature and rendering them accessible to transcatheter renal denervation procedures.[90][91][92][93] These procedures ablate both afferent and efferent fibers to control blood pressure in cases of otherwise intractable hypertension.[94]

Activation of these sympathetic fibers increases sodium retention, stimulates renin release, and induces renal vasoconstriction, contributing to the development of hypertension.[95][96][97] This mechanism underlies the therapeutic efficacy of transcatheter renal denervation in managing otherwise uncontrolled hypertension.[98][99][100][101]

The sensory renal afferent nerves, comprising both mechanoreceptors (stretch) and chemoreceptors, extend from the renal cortex and proximal ureter, with the highest density in the walls of the renal pelvis.[102][103][104] No sensory fibers are present in the renal medulla, although some are observed in the cortex and proximal ureters.[105][106] These fibers follow the renal artery primarily to the ipsilateral dorsal root ganglia of T12 to L3, then ascend the spinal cord to the brainstem and hypothalamus, where they modulate sympathetic outflow and contribute to blood pressure regulation.[107][108]

Transcatheter renal denervation is approved by the U.S. Food and Drug Administration for the treatment of both afferent and efferent renal nerve fibers using renal arterial ultrasound or radiofrequency ablation. This procedure improves blood pressure control in patients with otherwise difficult, resistant, or intractable hypertension.[109][110][111][112] The procedure preserves renal function, enables the reduction of antihypertensive medications, and demonstrates sustained efficacy in multiple trials.[113][114][115] Additional benefits have been observed in individuals with heart failure and certain arrhythmias. The procedure is contraindicated in patients with significant renal artery stenosis, kidney transplants, untreated secondary hypertension, severe renal failure (glomerular filtration rate < 40 mL/min), or solitary kidneys.[116][117][118][119]

Visceral afferent fibers convey pain signals via sympathetic pathways to the spinal ganglia and spinal cord segments of T11 to L2. Pain is often referred to the corresponding dermatome. Therefore, flank discomfort may originate from the kidney.[120] Renal pain typically results from stretching caused by obstruction and dilation, inflammation, infection, or ischemia.[121] Nonobstructing renal calculi generally do not produce flank pain, renal discomfort, or renal colic.

Physiologic Variants

Physiological anatomical variations of the kidney are relatively common and may have significant implications for diagnosis, surgical planning, and interventional procedures. Some of these variants are discussed below.

Horseshoe kidneys are one of the most recognized renal anomalies, characterized by fusion of the lower poles, typically anterior to the aorta (see Image. Horseshoe Kidney on Computed Tomography). Fusion of the lower poles restricts renal ascent due to obstruction by the superior mesenteric artery, resulting in an atypical lower midline position anterior to the abdominal aorta and anterior-facing renal pelves. Horseshoe kidneys frequently possess multiple accessory renal arteries. These anomalies occur in approximately 1 in 400 individuals and are associated with increased rates of ureteropelvic junction (UPJ) obstruction, nephrolithiasis, and urinary tract infection.

Severe malformations, predominantly affecting the urogenital system, are present in roughly 23% of cases.[122] The anomalous position and orientation of horseshoe kidneys complicate surgical procedures. Additional information is provided in the companion StatPearls reference “Horseshoe Kidney.”[123]

A fused pelvic (pancake) kidney is a rare congenital condition where both kidneys unite into a single pelvic mass. Unlike the more common horseshoe kidney, a pancake kidney is located in the pelvis rather than the abdomen and exhibits complete fusion of the renal units. Fused pelvic kidneys are more prevalent in male individuals and are usually identified in men aged 30 to 60.

Accessory renal arteries comprise a common anatomical variation of renal vascular supply.[124][125] These vessels may arise from the main renal artery, abdominal aorta, or aberrant arterial sources.[126][127] As end arteries, accessory vessels do not form anastomoses within the kidney and are therefore not supplemental.[128] These blood vessels may contribute to the development of UPJ obstruction.[129]

Accessory renal arteries are present in approximately 20% to 30% of the population and must be identified prior to procedures such as nephrectomy, partial nephrectomy, aortic aneurysm repair, renal transplantation, and percutaneous or other uroradiological interventions.[130] The most frequently observed accessory renal artery is an extrahilar branch supplying the superior renal pole.[131] Accessory arteries, particularly those supplying the lower pole, may influence renal angulation.

Other vascular anomalies include a retroaortic left renal vein, where venous drainage from the left kidney to the inferior vena cava passes posterior to the aorta.[132][133][134] The reported incidence ranges from 1.7% to 2.5%.[135][136]

Ectopic kidneys, where the organ remains in an abnormal location due to failed ascent during fetal development, are also observed. The most common form is the pelvic kidney, where the kidney remains in the pelvis rather than ascending to the lumbar region. This anomaly occurs in approximately 1 in 12,000 individuals and is frequently discovered incidentally.[137][138] The adrenal glands are typically in their normal position due to their distinct embryological origins.[139] Additional anomalies include crossed-fused ectopia, UPJ obstruction, and renal duplication.[140][141][142][143][144][145][146]

Surgical Considerations

All intrarenal arteries are generally considered end arteries, with minimal or no significant native collateral circulation under normal physiological conditions.[147] Accessory renal arteries must be preserved during renal surgery, as they supply discrete anatomical regions. Injury can result in localized ischemia and parenchymal loss. In contrast, renal veins freely anastomose and communicate with each other.

The Brodel line is a relatively avascular zone between the anterior and posterior renal end arteries. This landmark extends longitudinally from superior to inferior, located just posterior to the lateral convex border of each kidney. This line represents the optimal site for nephrostomy placement or renal incision to minimize blood loss.[148]

The retroperitoneum is an enclosed space distinct from the peritoneal cavity. Leaving the retroperitoneum intact in cases of renal trauma maintains the tamponade effect and may prevent unnecessary nephrectomy.[149]

Nephron-sparing surgery includes conservative techniques aimed at preserving healthy renal parenchyma as an alternative to total nephrectomy.[150][151] Methods include partial nephrectomy and percutaneous ablation procedures.[152][153] Nephron-sparing surgery is the first-line treatment for small renal masses, with expanding indications.[154] The approach may involve resecting renal tissue supplied by a specific segmental artery, identified intraoperatively by arterial clipping. Both polar and midzone kidney regions can be suitable for nephron-sparing resection of lesions such as small tumors.[155]

Clinical Significance

Intimate knowledge of renal anatomy and its physiological variants is essential for kidney surgery to prevent inadvertent injury, preserve maximal renal function, and optimize outcomes. Renal disease encompasses any structural or functional abnormality of the kidneys. Although etiologies are diverse, progressive loss of renal function is a common endpoint.

Histologically, renal pathologies are classified into 4 major compartments.[156][157] Glomerular diseases include inflammatory glomerulonephritis, often presenting with nephritic syndrome, presenting with hematuria, hypertension, and reduced glomerular filtration rate, as well as proteinuria below 3.5 g/day.[158] Examples of conditions presenting with inflammatory glomerulonephritis include immunoglobulin A nephropathy, postinfectious glomerulonephritis, and lupus nephritis.[159][160][161] Noninflammatory glomerulopathies present with nephrotic syndrome, characterized by proteinuria exceeding 3.5 g/day, hypoalbuminemia, and edema.[162] Examples include minimal change disease, focal segmental glomerulosclerosis, and membranous nephropathy.[163][164][165]

Tubular diseases are commonly associated with acute kidney injury and electrolyte imbalances.[166][167] Examples include acute tubular necrosis, hereditary tubulopathies, and renal tubular acidosis.[168][169][170] Interstitial diseases encompass disorders such as acute or chronic interstitial nephritis, granulomatous conditions (tuberculosis, sarcoidosis), and amyloidosis, all of which primarily involve the renal interstitial tissue.[171][172][173] Vascular diseases affect the renal vasculature and include vasculitis, systemic lupus erythematosus, systemic sclerosis, and atherosclerotic cardiovascular disease.[174][175][176][177]

Other Issues

Nephrology is the medical specialty dedicated to the study, diagnosis, and nonsurgical management of renal disorders. Such conditions comprise chronic kidney disease, renal failure, diabetic nephropathy, lupus nephritis, hypertensive nephrosclerosis, acute kidney injury, glomerulonephritis, dialysis, medical management of kidney transplantation, and electrolyte disturbances.[178]

Urology, as defined by the American Urological Association, is the medical and surgical discipline that provides care for adults and children with conditions of the genitourinary tract and adrenal glands. The specialty addresses diseases, dysfunctions, infections, and neoplasms of the genitourinary system and male reproductive organs (eg, benign prostatic hyperplasia, prostatitis, bladder and prostate cancer, erectile dysfunction, incontinence, hematuria), as well as renal and adrenal conditions requiring surgical intervention, including kidney stones, tumors, transplant surgery, and congenital renal anomalies.

Media


(Click Image to Enlarge)
<p>Kidney Anatomy

Kidney Anatomy. This illustration shows the internal structure of the kidney, highlighting key features such as the capsule, cortex, medulla, and renal pyramids. Other important labeled components include the minor and major calyces, the renal papilla, artery, vein, and pelvis, fat in the sinus, and the ureter. A clear view of the blood vessels and urine-collecting structures within the kidney is provided.

Contributed by Scott Dulebohn, MD


(Click Image to Enlarge)
<p>Horseshoe Kidney on Computed Tomography

Horseshoe Kidney on Computed Tomography. This axial computed tomography image shows a horseshoe kidney, a congenital anomaly where the lower poles of both kidneys are fused, forming a U-shaped structure. The red outline highlights the fused renal tissue crossing the midline anterior to the vertebral column.

Contributed by S Bhimji, MD


(Click Image to Enlarge)
<p>Nephron and Vasculature

Nephron and Vasculature. The illustration shows the renal corpuscle with the Bowman capsule and glomerulus, the proximal convoluted tubule, nephron loop (descending and ascending limbs), distal convoluted tubule, and the collecting duct. The associated vasculature includes the afferent arteriole, efferent arteriole, peritubular capillaries, and vasa recta.

Cenveo, license: CC BY 3.0


(Click Image to Enlarge)
<p>Filtration Apparatus of the Glomerulus

Filtration Apparatus of the Glomerulus. The illustration labels the glomerular capillary tuft (fenestrated endothelium), afferent and efferent arterioles, and the juxtaglomerular cell, along with the Bowman capsule’s parietal and visceral layers formed by podocytes and their pedicels. Filtrate accumulates in the capsular space and exits into the proximal convoluted tubule.

 

Cenveo, license: CC BY 3.0


(Click Image to Enlarge)
<p>Kidney Blood Supply

Kidney Blood Supply. The renal artery enters at the hilum and divides into segmental, lobar, interlobar, arcuate, and interlobular arteries. Interlobular arteries radiate into the cortex, while interlobar arteries course between renal pyramids. Venous return follows interlobular, arcuate, and interlobar veins, draining into the renal vein at the hilum. The renal capsule forms the outer covering. The cortex contains glomeruli and extends inward as renal columns between pyramids. Medullary pyramids terminate in papillae projecting into minor calyces, which merge into major calyces. Major calyces unite to form the renal pelvis, a funnel-shaped cavity continuous with the ureter, which conducts urine to the bladder.

 

Cenveo, license: CC BY 4.0

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