Archives de pédiatrie – Vol. 11 – N° 1 – p. – La maladie de Cacchi et Ricci chez un enfant de 13 ans – EM|consulte. Kidney Int. Feb;69(4) Medullary sponge kidney (Lenarduzzi-Cacchi -Ricci disease): a Padua Medical School discovery in the s. Gambaro G(1). Cette page est une page de collecte et de diffusion d’informations concernant la maladie de cacchi-ricci (Medullary Sponge Kidney). Venez partager vos.

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This page was last edited on 2 Octoberat Narcotic medication even with large quantities is sometimes not adequate. Views Cachi Edit View history. Non-obstructing stones in MSK can be associated with significant and chronic pain even if dw not passing. The documents contained in this web site are presented for information purposes only. In addition to the typical clinical phenotype of recurrent stone disease, other clinical profiles have now been recognized, that is, an indolent, almost asymptomatic MSK, and a rare form characterized by intractable pain.

Congenital disorders of urinary system Kidney diseases. What is an eponym? While some patients report increased chronic kidney pain, the source of the pain, when a UTI or blockage is not present, is unclear at this time.

If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned caccchi The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties. Infobox medical condition new. Uncomplicated form usually asymptomatic. Retrieved 21 May Urachus Urachal cyst Urachal fistula Urachal sinus. Urachal cyst Urachal fistula Urachal sinus.

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A cafchi cystic disease of the pyramids with dilation of the terminal collecting ducts in the kidneys and multiple small cysts in the maladiee, giving the kidneys a spongy appearance. A rare, autosomal recessive form is associated with Caroli disease.

An eponym is a word derived from the name of a person, whether real or fictional. This pain can often be debilitating and treatment is challenging.

Orphanet: Maladie de Cacchi Ricci

Epispadias Hypospadias Posterior urethral valves. This survey of medical eponyms and the persons behind them is meant as a general interest site only.

Curr Opin Nephrol Hypertens. The pain in this situation can be constant.

List people by country List people alphabetically List eponyms alphabetically List all women alphabetically. Check this box if you wish to receive a copy of your message. Ectopic ureter Megaureter Duplicated ureter. Medical geneticsNephrology.

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Medullary sponge kidney

A medical eponym is thus any word related to medicine, whose name riccl derived from a person. Specialised Social Services Eurordis directory. Hematuria ; Kidney sponge ; Kidney diseases ; Lithiasis ; Child.

Access to the text HTML. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this caccchi. Outline Masquer le plan. An Orphanet summary for this disease is currently under development. Congenital malformations and deformations of urinary system Q60—Q64 The irregular ectatic collecting ducts are often seen in MSK, which are sometimes described as having a “paintbrush-like” appearance, are best seen on intravenous urography.


In addition to the typical clinical phenotype of recurrent stone disease, other clinical profiles have now been recognized, that is, an indolent, almost asymptomatic MSK, and a rare form characterized by intractable, excruciating pain. Only comments written in English can be processed. No information found riicci must under any circumstances be used for medical purposes, diagnostically, therapeutically or rocci. Often, aggressive treatment is unnecessary for people with MSK disease that does not cause any symptoms asymptomatic.

Retrieved 22 August Frequently congenital and familial. Personal information regarding our website’s visitors, including their identity, is confidential. Journal page Archives Contents list. Onset of detection from kaladie weeks of age to 71 years, both sexes equally affected. For all other comments, please send your remarks via contact us. La maladie de Cacchi et Ricci chez un enfant de 13 ans.

MSK was previously believed not to be hereditary but there is more evidence coming forth that may indicate otherwise. In patients with low levels of citrate in the urine hypocitraturia and incomplete distal renal tubular acidosistreatment with potassium citrate helps prevent the formation of new kidney stones.

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