Horseshoe kidney

13,427views

test

00:00 / 00:00

Horseshoe kidney

5400

5400

Development of the renal system
Ureter, bladder and urethra histology
Kidney histology
Renal system anatomy and physiology
Body fluid compartments
Hydration
Movement of water between body compartments
Horseshoe kidney
Renal agenesis
Potter sequence
Posterior urethral valves
Multicystic dysplastic kidney
Polycystic kidney disease
Vesicoureteral reflux
Alport syndrome
Urinary incontinence
Urinary incontinence: Pathology review
Neurogenic bladder
Bladder exstrophy
Antidiuretic hormone
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Diabetes insipidus and SIADH: Pathology review
Diabetes insipidus
Nephrotic syndromes: Pathology review
Nephritic and nephrotic syndromes: Clinical
Nephritic syndromes: Pathology review
Minimal change disease
Hydronephrosis
Glomerular filtration
Measuring renal plasma flow and renal blood flow
Renal clearance
TF/Px ratio and TF/Pinulin
Regulation of renal blood flow
Sodium homeostasis
Kidney countercurrent multiplication
Urea recycling
Tubular reabsorption and secretion
Tubular reabsorption and secretion of weak acids and bases
Tubular secretion of PAH
Tubular reabsorption of glucose
Distal convoluted tubule
Loop of Henle
Proximal convoluted tubule
Renin-angiotensin-aldosterone system
Free water clearance
Amyloidosis
IgA nephropathy (NORD)
Poststreptococcal glomerulonephritis
Rapidly progressive glomerulonephritis
Lupus nephritis
Potassium homeostasis
Hypophosphatemia
Hyperphosphatemia
Hypermagnesemia
Hypomagnesemia
Hypocalcemia
Hypercalcemia
Hyperkalemia
Hypokalemia
Hyponatremia
Hypernatremia
Phosphate, calcium and magnesium homeostasis
The role of the kidney in acid-base balance
Acid-base disturbances: Pathology review
Physiologic pH and buffers
Renal tubular acidosis
Renal tubular acidosis: Pathology review
Metabolic acidosis
Metabolic and respiratory acidosis: Clinical
Respiratory acidosis
Metabolic alkalosis
Plasma anion gap
Respiratory alkalosis
Metabolic and respiratory alkalosis: Clinical
Acid-base map and compensatory mechanisms
Ornithine transcarbamylase deficiency
Kidney stones: Pathology review
Nitrogen and urea cycle
Goodpasture syndrome
Erythropoietin
Vitamin D
Kidney stones
ACE inhibitors, ARBs and direct renin inhibitors
Kidney stones: Clinical
Hypokalemia: Clinical
Renal tubular defects: Pathology review
Urinary tract infections: Clinical
Urinary tract infections: Pathology review
Lower urinary tract infection
Proteus mirabilis
Staphylococcus saprophyticus
Enterobacter
Klebsiella pneumoniae
Serratia marcescens
Pseudomonas aeruginosa
Renal artery stenosis
Thiazide and thiazide-like diuretics
Carbonic anhydrase inhibitors
Osmotic diuretics
Loop diuretics
Potassium sparing diuretics
Acute kidney injury: Clinical
Renal azotemia
Postrenal azotemia
Prerenal azotemia
Chronic kidney disease
Acute tubular necrosis
Renal papillary necrosis
Medullary cystic kidney disease
Chronic kidney disease: Clinical
Congenital renal disorders: Pathology review
Medullary sponge kidney
Chronic pyelonephritis
Acute pyelonephritis
Neisseria gonorrhoeae
Chlamydia trachomatis
Urethritis
Prostatitis
Schistosomes
Hemolytic-uremic syndrome
Thrombotic thrombocytopenic purpura
Renal cortical necrosis
Renal cell carcinoma
Angiomyolipoma
WAGR syndrome
Nephroblastoma (Wilms tumor)
Non-urothelial bladder cancers
Transitional cell carcinoma
Electrolyte disturbances: Pathology review
Renal failure: Pathology review
Renal and urinary tract masses: Pathology review
Transplant rejection
Graft-versus-host disease
Non-corticosteroid immunosuppressants and immunotherapies
Hypertension
BK virus (Hemorrhagic cystitis)

Assessments

Flashcards

0 / 9 complete

USMLE® Step 1 questions

0 / 1 complete

High Yield Notes

11 pages

Flashcards

Horseshoe kidney

0 of 9 complete

Questions

USMLE® Step 1 style questions USMLE

0 of 1 complete

A 40-year-old woman comes to the clinic for a follow-up appointment after hospitalization for pyelonephritis. The patient has had multiple episodes of urinary tract infections over the past few years. She is otherwise healthy. She does not use tobacco, alcohol or illicit substances. Family history is unremarkable. The patient’s physical exam is normal. A CT of the abdomen obtained during hospitalization is shown below:  


Retrieved from: Wikimedia Commons

Which of the following best explains these findings?  

External References

First Aid

2024

2023

2022

2021

Aorta

horseshoe kidney and p. 597

Down syndrome (trisomy 19)

horseshoe kidney and p. 597

Edwards syndrome (trisomy NaN)

horseshoe kidney and p. 597

Horseshoe kidney p. 597

Turner syndrome p. 725

Hydronephrosis p. 617

horseshoe kidney p. 597

Inferior mesenteric artery p. 370

horseshoe kidney p. 597

Kidney stones p. 620

horseshoe kidney and p. 597

Patau syndrome (trisomy NaN)

horseshoe kidney in p. 597

Renal arteries p. 370, 599

horseshoe kidney p. 597

Renal cell carcinomas p. 617

horseshoe kidney and p. 597

Turner syndrome p. 655

horseshoe kidney p. 597

Ureter p. 597, 639, 643, 644

horseshoe kidney p. 597

Transcript

Watch video only

Content Reviewers

Horseshoe kidney, or sometimes renal fusion, is a congenital disorder where the two kidneys fuse together into one during fetal development, resulting in one large horseshoe-shaped kidney.

Normally during fetal development, the future kidneys develop in the pelvis as a structure called the metanephrose before finally migrating upward into the abdomen and becoming everyone’s favorite organ duo.

For people with horseshoe kidney, their kidneys fused together at some point during development, and there are two main working theories on how this might happen.

The first is mechanical fusion, which happens during the metanephros stage, which is around about the 5th week of gestation.

At this point, the two kidneys are still in the pelvis, and are therefore pretty close together, so close that it’s thought that some flexion or growth of the developing spine and pelvic organs essentially pushes them together, causing the lower or inferior poles of the kidneys to touch and fuse together, forming what’s called a fibrous isthmus, fibrous because it’s composed of connective tissue.

The other theory involves a teratogenic event. Teratogenic meaning something that disrupts fetal development in some way.

In this case it’s thought that the posterior nephrogenic cells, which are the cells that help to form part of the kidney, migrate and rendezvous in the wrong spot, and therefore again form an isthmus connecting the two kidneys, but this time since the isthmus is composed of kidney cells as opposed to connective tissue, it’s called a parenchymal isthmus.

Whichever one happens, now you’ve got this single, horseshoe-shaped kidney in the pelvis.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "HORSESHOE KIDNEY" Annals of Surgery (1925)
  6. "Multimodality imaging spectrum of complications of horseshoe kidney" Indian Journal of Radiology and Imaging (2017)
  7. "Horseshoe kidney: a review of anatomy and pathology" Surgical and Radiologic Anatomy (2013)