Occurred in the renal medullary cystic disease has two: medullary sponge kidney and renal units childhood renal tuberculosis - medullary cystic disease.
Medullary sponge kidney caused by congenital dysplasia, in the more than 40 ~ 50-year-old disease, prognosis is good. Patients with renal medullary collecting duct cystic expansion was generally look somewhat like sponges, 70% of renal involvement, each kidney to a number of nipple involvement. Often a result of the stones and infection was not discovered. Expansion of the pool of long-term urinary retention, and often a result of the merger of hypercalciuria stones. Abdominal plain film see normal or mild renal size of the increase, kidney area that clustering of multiple stones (in the nipple area Chengfangshezhuang order). IVP show: medullary collecting duct cystic Zhang, was Shanzhuang, this is the basis for the diagnosis of this disease. Will not be required on the treatment of asymptomatic. Subject to regular review, hypercalciuria g oral dihydrochloride Cypriots to reduce urinary calcium, the merger stone to more drinking water. Infection should be infection control.
Juvenile renal units renal tuberculosis - medullary cystic disease: genetic disease is also known as hereditary tubular interstitial nephritis. Kidney moderately narrow, fine granular surface was irregular. Clinical manifestations of multiple urine, Fan Jie, lethargy, pale and development obstacles in the development of a 20-year-old former uremia. Treatment for symptomatic treatment.
Medullary sponge kidney caused by congenital dysplasia, in the more than 40 ~ 50-year-old disease, prognosis is good. Patients with renal medullary collecting duct cystic expansion was generally look somewhat like sponges, 70% of renal involvement, each kidney to a number of nipple involvement. Often a result of the stones and infection was not discovered. Expansion of the pool of long-term urinary retention, and often a result of the merger of hypercalciuria stones. Abdominal plain film see normal or mild renal size of the increase, kidney area that clustering of multiple stones (in the nipple area Chengfangshezhuang order). IVP show: medullary collecting duct cystic Zhang, was Shanzhuang, this is the basis for the diagnosis of this disease. Will not be required on the treatment of asymptomatic. Subject to regular review, hypercalciuria g oral dihydrochloride Cypriots to reduce urinary calcium, the merger stone to more drinking water. Infection should be infection control.
Juvenile renal units renal tuberculosis - medullary cystic disease: genetic disease is also known as hereditary tubular interstitial nephritis. Kidney moderately narrow, fine granular surface was irregular. Clinical manifestations of multiple urine, Fan Jie, lethargy, pale and development obstacles in the development of a 20-year-old former uremia. Treatment for symptomatic treatment.
