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Multicystic dysplastic kidney

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Multicystic dysplastic kidney
Other namesMulticystic renal dysplasia[1]
Diagram of multicystic dysplastic kidney
SpecialtyMedical genetics Edit this on Wikidata
CausesDue to atresia at 10 weeks gestation[2]
Diagnostic methodUltrasound [3]
TreatmentNephrectomy, if needed [4]

Multicystic dysplastic kidney (MCDK) is a condition that results from the malformation of the kidney during fetal development. The kidney consists of irregular cysts of varying sizes. Multicystic dysplastic kidney is a common type of renal cystic disease, and it is a cause of an abdominal mass in infants.[5]

Signs and symptoms

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When a diagnosis of multicystic kidney is made in utero by ultrasound, the disease is found to be bilateral in many cases. Those with bilateral disease often have other severe deformities or polysystemic malformation syndromes.[6] In bilateral cases, the newborn has the classic characteristic of Potter's syndrome.[7][8]

The bilateral condition is incompatible with survival, as the contralateral system frequently is abnormal as well. Contralateral ureteropelvic junction obstruction is found in 3% to 12% of infants with multicystic kidney and contralateral vesicoureteral reflux is seen even more often, in 18% to 43% of infants. Because the high incidence of reflux, voiding cystourethrography usually has been considered advisable in all newborns with a multicystic kidney.[medical citation needed]

Cause

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The cause of multicystic dysplastic kidney can be attributed to genetics. Renal dysplasia can be a consequence of a genetic syndrome, which in turn may affect the digestive tract, nervous system, or other areas of the urinary tract. If the mother had been taking certain prescription drugs such as those for hypertension, this may be a precipitating factor as well.[9]

Pathophysiology

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The mechanism of multicystic dysplastic kidney is a result of an abnormal induction of metanephric mesenchyme. This could be a result of a formation difficulty of the mesonephric duct. Some mutations in genes associated with renal dysplasia (in syndromes) have been determined. The mutations in question occur at EYA1 or SIX1 genes (branchio-oto-renal syndrome). The PAX2 gene is also thought to play a role in MCDK.[4]

The contralateral kidney often undergoes hypertrophy. This is believed to be a compensatory mechanism to the non-functional MCDK. About 90% of patients with an MCDK will have contralateral hypertrophy into adulthood. The impact of contralateral hypertrophy on long-term renal outcomes is unknown.[10]

Diagnosis

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Ultrasound Scan -Vesicoureteral reflux

MCDK is usually diagnosed by ultrasound examination before birth. Mean age at the time of antenatal diagnosis is about 28 weeks[3] A microscopic analysis of urine in individuals with probable multicystic dysplastic kidney should be done.[4] One meta-analysis demonstrated that unilateral MCDK occurs more frequently in males and the greater percentage of MCDK occur on the left side of the body.[11]

Treatment

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MCDK is not treatable. However, the patient is observed periodically for the first few years during which ultrasounds are generally taken to ensure the healthy kidney is functioning properly and that the unhealthy kidney is not causing adverse effects. In severe cases MCDK can lead to neonatal fatality (in bilateral cases), however in unilateral cases the prognosis might be better (it would be dependent on associated anomalies).[12][13]

Epidemiology

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In regard to the epidemiology of multicystic dysplasia kidney, the incidence of MCDK is estimated to be 1 in every 4,000 live births, making it rare in terms of the general population.[9]

References

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  1. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Multicystic dysplastic kidney". www.orpha.net. Retrieved 31 July 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. ^ Doubilet, Peter M.; Benson, Carol B. (2003). Atlas of Ultrasound in Obstetrics and Gynecology: A Multimedia Reference. Lippincott Williams & Wilkins. p. 152. ISBN 9780781736336. Retrieved 2 January 2018.
  3. ^ a b Chang, Ling-Wei; Chang, Fong-Ming; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Cheng, Yueh-Chin; Chen, Hsi-Yao (2002). "Prenatal diagnosis of fetal multicystic dysplastic kidney with two-dimensional and three-dimensional ultrasound". Ultrasound in Medicine & Biology. 28 (7): 853–858. doi:10.1016/s0301-5629(02)00535-5. PMID 12208325.
  4. ^ a b c Multicystic Renal Dysplasia at eMedicine
  5. ^ Multicystic Dysplastic Kidney Imaging at eMedicine
  6. ^ Seseke, F. (2003). "Clinical Aspects of Paediatric Urology". Imaging in Paediatric Urology. pp. 1–67. doi:10.1007/978-3-642-55785-9_1. ISBN 978-3-642-62803-0.
  7. ^ Potter Syndrome~treatment at eMedicine
  8. ^ Lager, Donna J.; Abrahams, Neil (2012-11-07). Practical Renal Pathology, A Diagnostic Approach: A Volume in the Pattern Recognition Series. Elsevier Health Sciences. p. 27. ISBN 978-1455737864.
  9. ^ a b "Kidney Dysplasia". www.niddk.nih.gov. Retrieved 2015-11-24.
  10. ^ Gaither, Thomas W.; Patel, Ankur; Patel, Chandni; Chuang, Kai-wen; Cohen, Ronald A.; Baskin, Laurence S. (2018). "Natural History of Contralateral Hypertrophy in Patients with Multicystic Dysplastic Kidneys". Journal of Urology. 199 (1): 280–286. doi:10.1016/j.juro.2017.06.075. PMID 28645868. S2CID 206633374.
  11. ^ Schreuder, M. F.; Westland, R.; Van Wijk, J. A. E. (2009). "Unilateral multicystic dysplastic kidney: A meta-analysis of observational studies on the incidence, associated urinary tract malformations and the contralateral kidney". Nephrology Dialysis Transplantation. 24 (6): 1810–1818. doi:10.1093/ndt/gfn777. PMID 19171687.
  12. ^ Stevenson, Roger E.; Hall, Judith G.; Everman, David B.; Solomon, Benjamin D. (2015-10-16). Human Malformations and Related Anomalies. Oxford University Press. p. 800. ISBN 9780199386048.
  13. ^ Schwartz, M. William (2012-01-01). The 5 Minute Pediatric Consult. Lippincott Williams & Wilkins. p. 439. ISBN 9781451116564.

Further reading

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