نتایج جستجو برای: multicystic dysplastic kidney

تعداد نتایج: 225892  

Journal: :Journal of medical genetics 1996
R Torra L Alós J Ramos X Estivill

We report two brothers with a cystic malformation of the kidneys, liver, and pancreas. In both cases the malformation was fatal and the children died shortly after birth. The pathological findings, consisting of multicystic dysplastic kidneys, dilated and dysgenetic bile ducts, dilated pancreatic ducts, and polysplenia, correspond to those reported by Ivemark as renal-hepatic-pancreatic dysplas...

Journal: :Indian Journal of Pathology and Microbiology 2011

Journal: :The journal of the Japanese Practical Surgeon Society 1977

2013
Faten HAMMEDI Rim HADHRI Manel NJIMA Imed KRICHENE Houda MAHMOUDI Adnène MOUSSA

Cystic partially differentiated nephroblastoma is a rare tumor of the kidney usually affecting infants. It should be distinguished from Wilms’ tumor with multicystic areas and multilocular cystic nephroma. Multilocular cystic nephroma is a benign tumor whereas Wilms’ tumor with multicystic areas is at the malignant end of the range of classification of such tumours. Cystic partially differentia...

Journal: :Journal of the American Society of Nephrology : JASN 2006
Peter C Harris Kyongtae T Bae Sandro Rossetti Vicente E Torres Jared J Grantham Arlene B Chapman Lisa M Guay-Woodford Bernard F King Louis H Wetzel Deborah A Baumgarten Philip J Kenney Mark Consugar Saulo Klahr William M Bennett Catherine M Meyers Qin Jean Zhang Paul A Thompson Fang Zhu J Philip Miller

Data from serial renal magnetic resonance imaging of the Consortium of Radiologic Imaging Study of PKD (CRISP) autosomal dominant polycystic kidney disease (PKD) population showed that cystic expansion occurs at a consistent rate per individual, although it is heterogeneous in the population, and that larger kidneys are associated with more rapid disease progression. The significance of gene ty...

Journal: :Diagnostic and Interventional Imaging 2015

Journal: :International journal of clinical and experimental pathology 2014
Hakan Ozturk Serap Karaaslan

BACKGROUND The multilocular cystic nephroma (MLCN) is a unilateral cystic neoplasm of the kidney exhibiting benign biological behavior. The etiology and histopathogenesis of the disease is controversial (dysplastic/hamartomous/neoplastic). MLCNs show bimodal age distribution, with peak incidence occurring at 2-4 years of age and between the fourth and sixth decades. The male to female ratio in ...

Journal: :Journal of medical genetics 1998
P M Czarnecki D L Van Dyke S Vats G L Feldman

geal atresia" and renal agenesis and renal dysplasia with von Maeyer-RokitanskiKuster complex.'4 As yet, there is no consistent detectable chromosomal or metabolic cause of the 3C syndrome, including the 22ql 1.2 deletion discussed here. In the 16 families known to have children with the 3C syndrome, four males and 14 females, two had two affected daughters, three are related, and five belong t...

Journal: :Il Giornale di chirurgia 2011
E Falidas A Ntasi S Mathioulakis K Vlachos G Anyfantakis S Boutzouvis C Villias

Multicystic nephroma is a relatively rare tumor of the kidney presenting unclear histological origin. Abdominal mass is a common onset sign in children while abdominal flank pain or abdominal discomfort, hematuria and recurrent urinary tract infections usually affect adults. Preoperative diagnosis is impossible especially in the adult variant of the tumor where clear cells carcinoma with cystic...

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