WordNet

an impairment of health or a condition of abnormal functioning
either of two bean-shaped excretory organs that filter wastes (especially urea) from the blood and excrete them and water in urine; "urine passes out of the kidney through ureters to the bladder"
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
of or relating to or resembling a cyst
of or relating to a normal cyst (as the gallbladder or urinary bladder)
a closed sac that develops abnormally in some body structure

PrepTutorEJDIC

(体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
女性の話術芸人 =diseur
腎臓;(食品としての)羊(豚など)の腎臓 / 《文》気質,性質,たち(nature)
病気にかかった / 病的な,不健全な(morbid)
胞嚢(ほうのう)性の
胞嚢(ほうのう)

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/11/04 15:07:46」(JST)

wiki en

Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions.^[1] With the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation of disease may be from birth, or much later into adult life. Cystic disease may involve one or both kidneys and may or may not occur in the presence of other anomalies.^[2] A higher incidence of cystic kidney disease is found in the male population and prevalence increases with age. Renal cysts have been reported in more than 50% of patients over the age of 50.^[3] Typically, cysts grow up to 2.88 mm annually and cause related pain and/or hemorrhage.^[4]

Of the cystic kidney diseases, the most common is Polycystic kidney disease; having two prevalent sub-types: autosomal recessive and autosomal dominant polycystic kidney disease.^[5] Autosomal Recessive Polycystic Kidney Disease (ARPKD) is primarily diagnosed in infants and young children. Autosomal dominant polycystic kidney disease (ADPKD) is most often diagnosed in adulthood.^[6]

Another example of cystic kidney disease is Medullary sponge kidney.

^ Bisceglia, M; et al (2007). "Renal cystic diseases: a review". Advanced Anatomic Pathology (13): 26–56.
^ Bisceglia, M; et al (2007). "Renal cystic diseases: a review". Advanced Anatomic Pathology (13): 26–56.
^ Campbell, SC; Novick AC, Bukowski RM (2007). Campbell-Walsh Urology. ed. Neoplasms of the upper urinary tract (9 ed.). Philadelphia: Saunders. pp. 1575–1582.
^ Campbell, SC; Novick AC, Bukowski RM (2007). Campbell-Walsh Urology. ed. Neoplasms of the upper urinary tract (9 ed.). Philadelphia: Saunders. pp. 1575–1582.
^ Bisceglia, M; et al (2007). "Renal cystic diseases: a review". Advanced Anatomic Pathology (13): 26–56.
^ Bisceglia, M; et al (2007). "Renal cystic diseases: a review". Advanced Anatomic Pathology (13): 26–56.

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English Journal

Novel UMOD mutations in familial juvenile hyperuricemic nephropathy lead to abnormal uromodulin intracellular trafficking.

Liu M, Chen Y, Liang Y, Liu Y, Wang S, Hou P, Zhang H, Zhao M.SourceRenal Division, Department of Medicine, Peking University First Hospital, Institute of Nephrology, Peking University, Key Laboratory of Renal Disease, Ministry of Health of China, Key Laboratory of Chronic Kidney Disease Prevention and Treatment, Ministry of Education, Beijing 100034, China.
Gene.Gene.2013 Dec 1;531(2):363-9. doi: 10.1016/j.gene.2013.08.041. Epub 2013 Aug 27.
BACKGROUND: Familial juvenile hyperuricemic nephropathy (FJHN) is an autosomal dominant disorder characterized by hyperuricemia and progressive chronic kidney disease. Uromodulin gene (UMOD) mutations, leading to abnormalities of uromodulin intracellular trafficking contribute to the progress of the
PMID 23988501

Tumor Necrosis on Magnetic Resonance Imaging Correlates With Aggressive Histology and Disease Progression in Clear Cell Renal Cell Carcinoma.

Beddy P, Genega EM, Ngo L, Hindman N, Wei J, Bullock A, Bhatt RS, Atkins MB, Pedrosa I.SourceDepartment of Radiology, St. James Hospital and Trinity College, Dublin, Ireland.
Clinical genitourinary cancer.Clin Genitourin Cancer.2013 Oct 19. pii: S1558-7673(13)00196-1. doi: 10.1016/j.clgc.2013.07.006. [Epub ahead of print]
OBJECTIVE: The study objective was to correlate the magnetic resonance imaging (MRI) features of clear cell renal cell carcinoma (ccRCC) with the histopathologic features and disease progression.METHODS: Institutional review board approval for this retrospective study was obtained; patient consent w
PMID 24145001

Japanese Journal

症例報告長期透析患者の後天性嚢胞性腎疾患に合併した両側腎細胞癌の2例

森山浩之,吉野干城,江崎隆 [他]
広島医学 66(5), 318-324, 2013-05
NAID 40019699183

症例報告原発不明の多発肝腫瘍を認め,剖検で肉腫様腎細胞癌を診断した長期透析患者の1例

長谷川純平,若井幸子,尾本和也
日本透析医学会雑誌 46(2), 201-206, 2013-02
NAID 40019603320

Liver metastasis of sarcomatoid renal cell carcinoma in a hemodialysis patient

長谷川純平,若井幸子,尾本和也
日本透析医学会雑誌 46(2), 201-206, 2013
… Pathologically, we diagnosed sarcomatoid renal cell carcinoma (RCC) arising from the right kidney mass. … To diagnose this disease in the early stage, regular examinations are essential, but, in sarcomatoid renal cell carcinoma, renal tumors remain difficult to diagnosis correctly, even with CT images. …
NAID 130003372764

Related Pictures

★リンクテーブル★

リンク元	「cystic kidney」「嚢胞性腎疾患」「cystic renal disease」
拡張検索	「adult polycystic kidney disease」「autosomal dominant polycystic kidney disease」「autosomal recessive polycystic kidney disease」「polycystic kidney disease」
関連記事	「disease」「kidney disease」「cystic kidney」「cystic」「kidney」