Horseshoe kidney

Horseshoe kidney, also known as ren arcuatus (in Latin), renal fusion or super kidney, is a congenital disorder affecting about 1 in 500 people that is more common in men, often asymptomatic, and usually diagnosed incidentally.[1][2] In this disorder, the patient's kidneys fuse together to form a horseshoe-shape during development in the womb. The fused part is the isthmus of the horseshoe kidney. The abnormal anatomy can affect kidney drainage resulting in increased frequency of kidney stones and urinary tract infections as well as increase risk of certain renal cancers.[1]

Horseshoe kidney
Other namesRenal fusion

Fusion abnormalities of the kidney can be categorized into two groups: horseshoe kidney and crossed fused ectopia. The 'horseshoe kidney' is the most common renal fusion anomaly.[3]

Signs and symptomsEdit

Axial CT image of the abdomen showing a horseshoe kidney.

Although often asymptomatic, the most common presenting symptom of patients with a horseshoe kidney is abdominal or flank pain. However, presentation is often non-specific.[1] Approximately a third of patients with horseshoe kidneys remain asymptomatic throughout their entire life with over 50% of patients having no medical issues related to their renal fusion when followed for a 25 year period.[1] As a result, it is estimated that approximately 25% of patients with horseshoe kidneys are diagnosed incidentally with ultrasound or CT imaging.[1]

Associated conditionsEdit

Patients with a horseshoe kidney can develop sequelae related to the abnormal anatomy and present with symptoms related to them.[citation needed]

The general categories a horseshoe kidney may increase the risk for fall under the following categories:

  • Kidney obstruction – commonly causes ureteropelvic junction obstruction (UPJ)[1] which is a blockage at the area where the ureter connects to the renal pelvis. This can lead to urinary stasis which can promote infection and stone formation.[4]
  • Kidney infections – associated with vesicoureteral reflux (present in approximately 50% of all patients with renal fusion) which is an abnormal reflux of urine back into the ureters that increases risk of urinary tract infections.[1]
  • Kidney stones – deviant orientation of kidneys combined with slow urine flow and kidney obstruction may increase the risk of developing kidney stones. Treatment is further complicated if patient possesses aberrant skeletal anatomy.[5] It is estimated approximately 36% of patients with horseshoe kidneys will develop kidney stones.[6]
  • Kidney cancer – increased frequency of certain renal cancers such as transitional cell tumors, Wilms tumors, and carcinoid tumors.[1]
  • Heart abnormalities – ventricular septal defect[7]
  • Neurological abnormalities - encephalocoele, myelomeningocoele, spina bifida[7]
  • Skeletal abnormalities - kyphosis, scoliosis, hemeivertebra, and micrognathia.[7]
  • Genitourinary abnormalities - septate vagina, bicornuate uterus, hypospadias, undescended testis, adult polycystic kidney disease, and more than two kidneys.[7]
  • Genetic abnormalities - Turner syndrome, Down syndrome, Patau syndrome, Edward syndrome, oro-cranial-digital syndrome[7]
Intravenous pyelogram showing horseshoe kidney.


There have been several proposed factors that may contribute to the development of a horseshoe kidney. Different exposures to the developing fetus such as different teratogens (e.g. thalidomide, ethanol, ACE inhibitors, cocaine, gentamicin, corticosteroids, NSAIDs, and vitamin A) have been hypothesized.[8][2][9] Impairment of a developing embryo's nephrogenic cell migration or abnormal migration of the kidneys due to fetal structural abnormalities is another potential factor.[8][2] However, no definitive genetic cause has been identified.[8][9]


Kidneys are normally located in the retroperitoneal space between the T12 and L3 vertebrae after ascending from the pelvis during development to rest underneath the adrenal glands.[1] In patients with this condition, the horseshoe kidney ascent is commonly arrested by the inferior mesenteric artery due to the central fusion of the kidneys.[10] However, this is present in only 40% of cases, and, in 20% of cases, the fused kidney remains in the pelvis.[1] Its ascension may also be restricted by its own renal artery.[11] Additionally, during normal development, the kidneys undergo a 90 degree medial rotation while ascending. However, due to the renal fusion, this rotation is impaired resulting in abnormal placement of the ureters. This in turn can lead to urinary stasis and drainage issues.[1] Furthermore, approximately 70% of kidneys in normal individuals are supplied by a single renal artery with the remaining 30% having embryonic collateral or accessory arteries.[1] With horseshoe kidneys, the majority are supplied by derivatives of the abdominal aorta or common illiac arteries depending on the final position of the kidneys.[1][12]


Horseshoe kidneys are commonly diagnosed incidentally on abdominal imaging. The diagnosis can be made with many different imaging modalities such as ultrasound, intravenous pyelogram, CT, and MRI.[1]

Common features that can be found on imaging include:

  • Midline symmetrical fusion (present in 90% of cases) or lateral asymmetric fusion (present in 10% of cases) of the lower poles[13]
  • Position of fused kidneys are lower than normal with incomplete medial rotation[13]
  • Renal pelvis and ureters are positioned more anteriorly and ventrally cross the isthmus[13][4]
  • Isthmus that may be positioned below the inferior mesenteric artery[13]
  • Variant arterial supply that can originate from the abdominal aorta or common illiac arteries[1][12][13]
  • Lower poles of kidney that extend ventromedially and may be poorly defined[14]


Symphysiotomy, which involves separating the fused isthmus in order to release the kidneys, used to be a recommended treatment for this condition but has fallen out of favor due to complications and minimal benefit.[1][15] Furthermore, kidneys can remain in their original abnormal location after the surgery.[1][16] Instead, management focuses on treating the sequelae should the patient become symptomatic.[citation needed]

While treatment typically does not differ from that of patients with normal kidney anatomy,[17] kidney stones can warrant a different approach. Extracorporeal shockwave lithotripsy, a possible treatment for kidney stones, can be less effective in patients with horseshoe kidneys due to the abnormal anatomy causing difficulties with localizing the energy to the stones. Also, due to the kidney obstruction that can commonly occur with this renal fusion, clearance of the resulting stone fragments can also be impaired.[1] For this reason, prior to any treatment with shockwave lithotripsy, a UPJ obstruction must first be ruled out as it significantly impair successful treatment.[4] For stones that are less than 1.5 cm, ureteroscopy and shockwave lithotripsy can be first utilized.[4] For stones larger than 1.5 cm or when previous treatment has failed, the stones can instead be removed through a minimally invasive procedure known as percutaneous nephrolithotomy.[4]

Compared to patients with normal kidneys, patients with horseshoe kidneys who undergo treatment with percutaneous nephrolithotomy experience no difference in complications or stone clearance.[4]

Patients will also typically require imaging before any abdominal surgery as the vascular supply to the abnormal kidney can be highly variable between patients.[1] Additionally, the horseshoe kidneys can have a close association with colon which can increase risk of bowel injury.[1]


There is an incidence of 1 in every 500 individuals within a normal population.[1][2]

Males are more likely to develop a horseshoe kidney with a preponderance of 2:1.[1][2]

Certain genetic diseases can predispose patients to developing a horseshoe kidney:

Notable casesEdit


  1. ^ a b c d e f g h i j k l m n o p q r s t u v w x y Kirkpatrick JJ, Leslie SW (2018). Horseshoe Kidney. StatPearls. StatPearls Publishing. PMID 28613757. Retrieved 2019-01-16.
  2. ^ a b c d e f g h Taghavi K, Kirkpatrick J, Mirjalili SA (October 2016). "The horseshoe kidney: Surgical anatomy and embryology". Journal of Pediatric Urology. 12 (5): 275–280. doi:10.1016/j.jpurol.2016.04.033. PMID 27324557.
  3. ^ Glodny B, Petersen J, Hofmann KJ, Schenk C, Herwig R, Trieb T, et al. (January 2009). "Kidney fusion anomalies revisited: clinical and radiological analysis of 209 cases of crossed fused ectopia and horseshoe kidney". BJU International. 103 (2): 224–35. doi:10.1111/j.1464-410X.2008.07912.x. PMID 18710445.
  4. ^ a b c d e f Wein, Alan J.; Kavoussi, Louis R.; Partin, Alan W.; Peters, Craig Andrew (2015-10-23). Campbell-Walsh Urology (Eleventh ed.). Philadelphia, PA. ISBN 9780323263740. OCLC 931870910.
  5. ^ Jung M, Rai A, Wang L, Puttmann K, Kukreja K, Koh CJ (October 2018). "Nephrolithiasis in a 17-Year-Old Male With Seckel Syndrome and Horseshoe Kidneys: Case Report and Review of the Literature". Urology. 120: 241–243. doi:10.1016/j.urology.2018.05.023. PMID 29894776.
  6. ^ Pawar AS, Thongprayoon C, Cheungpasitporn W, Sakhuja A, Mao MA, Erickson SB (January 2018). "Incidence and characteristics of kidney stones in patients with horseshoe kidney: A systematic review and meta-analysis". Urology Annals. 10 (1): 87–93. doi:10.4103/UA.UA_76_17. PMC 5791465. PMID 29416282.
  7. ^ a b c d e Shah HU, Ojili V (2017). "Multimodality imaging spectrum of complications of horseshoe kidney". The Indian Journal of Radiology & Imaging. 27 (2): 133–140. doi:10.4103/ijri.IJRI_298_16. PMC 5510309. PMID 28744072.
  8. ^ a b c Kirkpatrick JJ, Joshua J.; Leslie SW, Stephen W. (2021). Horseshoe Kidney. StatPearls [Internet]: Treasure Island (FL): StatPearls Publishing. PMID 28613757.
  9. ^ a b Woolf AS, Winyard PJ, Hermanns MH, Welham SJ (2003). "Maldevelopment of the human kidney and lower urinary tract: an overview.". In Vize PD, Woolf AS, Bard JB (eds.). In The kidney. Academic Press. pp. 377–393. doi:10.1016/b978-012722441-1/50023-3. ISBN 9780127224411.
  10. ^ Oktem H, Gozil R, Calguner E, Bahcelioglu M, Mutlu S, Kurkcuoglu A, et al. (2008). "Morphometric study of a horseshoe kidney". Medical Principles and Practice. 17 (1): 80–3. doi:10.1159/000109596. PMID 18059107.
  11. ^ Suwannakhan A, Meemon K (2019-05-28). "Horseshoe kidney with extrarenal calyces and malformed renal vessels". European Journal of Anatomy. 20 (4): 355–359.
  12. ^ a b Natsis K, Piagkou M, Skotsimara A, Protogerou V, Tsitouridis I, Skandalakis P (August 2014). "Horseshoe kidney: a review of anatomy and pathology". Surgical and Radiologic Anatomy. 36 (6): 517–26. doi:10.1007/s00276-013-1229-7. PMID 24178305. S2CID 7889789.
  13. ^ a b c d e Gutiérrez M (2013). "Renal anomalies of position, shape and fusion: radiographic analysis" (PDF). Revista de la Federación Ecuatoriana de Radiología. 6: 24–30.
  14. ^ Nahm AM, Ritz E (November 1999). "Horseshoe kidney". Nephrology, Dialysis, Transplantation. 14 (11): 2740–1. doi:10.1093/ndt/14.11.2740. PMID 10534525.
  15. ^ Oderda M, Calleris G, Allasia M, Dalmasso E, Falcone M, Catti M, et al. (February 2017). "Robot-assisted laparoscopic pyeloplasty in a pediatric patient with horseshoe kidney: surgical technique and review of the literature". Urologia. 84 (1): 55–60. doi:10.5301/uro.5000188. PMID 27516351. S2CID 25468419.
  16. ^ Pitts WR, Muecke EC (June 1975). "Horseshoe kidneys: a 40-year experience". The Journal of Urology. 113 (6): 743–6. doi:10.1016/S0022-5347(17)59571-3. PMID 1152146.
  17. ^ Al Otay A, Sarhan O, El-Tholoth HS, Alhelaly A, Al Akrash H, Al Ghanbar M, et al. (July 2018). "Different managements of horseshoe kidney stones, any difference in the outcome?". Urology Annals. 10 (3): 287–290. doi:10.4103/UA.UA_116_17. PMC 6060601. PMID 30089987.
  18. ^ "Renal Pathology". Retrieved 2008-11-26.
  19. ^ Cereda A, Carey JC (October 2012). "The trisomy 18 syndrome". Orphanet Journal of Rare Diseases. 7 (1): 81. doi:10.1186/1750-1172-7-81. PMC 3520824. PMID 23088440.
  20. ^ Kleta R, Brämswig JH (July 2000). "Horseshoe kidney and Turner syndrome". Nephrology, Dialysis, Transplantation. 15 (7): 1094. doi:10.1093/ndt/15.7.1094-b. PMID 10862660.
  21. ^ Ranke MB, Saenger P (July 2001). "Turner's syndrome". Lancet. 358 (9278): 309–14. doi:10.1016/S0140-6736(01)05487-3. PMID 11498234. S2CID 42096888.
  22. ^ Niamien-Attai C, Bacchetta J, Ranchin B, Sanlaville D, Cochat P (October 2017). "[Renal abnormalities in Down syndrome: A review]". Archives de Pédiatrie. 24 (10): 1013–1018. doi:10.1016/j.arcped.2017.07.014. PMID 28893484.
  23. ^ Parkinson. "Mel Gibson Interview - part one". BBC.
  24. ^ Paget ET. "Autopsy Report: Sam Kinison" (PDF). Autopsy Files.

External linksEdit

External resources