- A Case of Renal Cell Carcinoma in Autosomal Dominant Polycystic Kidney Disease Hemodialyzed
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Hur SH, Song KS, Park JW, Shin SK, Kang DO, Kim JH, Koo JH, Kim SR
- KMID: 2307322
- Korean J Nephrol.
- 1999 Sep;18(5):836-840.
The development of renal cell carcinoma in auto-sornal dominant polycystic kidney disease hemodialyzed was rarely found. A sixty-six year old man has been hemodialyzed for four years. His end-stage renal... -
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- Autosomal Dominant Polycystic Kidney Desease Coexisting with Renal Dysplasia. First Case Described and Followed Since Prenatal Period
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Truyols C
- KMID: 2435352
- Child Kidney Dis.
- 2018 Apr;22(1):28-30.
- doi: 10.3339/jkspn.2018.22.1.28
Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent hereditary renal disease and causes terminal chronic renal failure. ADPKD is characterized by bilateral multiple renal cysts, which are produced... -
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- Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
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Bennett WM
- KMID: 1717937
- Korean J Intern Med.
- 2009 Sep;24(3):165-168.
- doi: 10.3904/kjim.2009.24.3.165
Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition.... -
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- Segmental Cystic Disease of the Kidney: A Case Report
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Han SB, Chung SH, Cho JH
- KMID: 2024544
- J Korean Radiol Soc.
- 2008 Jun;58(6):613-616.
- doi: 10.3348/jkrs.2008.58.6.613
Segmental cystic disease of the kidney is a rare form of cystic disease of the kidney that manifests as variable sized, numerous cysts that are localized in a segment of... -
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- A Case of Transitional Cell Carcinoma Associated with Adult Polycystic Kidney Disease
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Yea SH, Jeong YB, Jeong DH, Kim JH, Park YI, Jo SY
- KMID: 1914392
- Korean J Urol.
- 1997 Aug;38(8):877-881.
Some cases of renal malignancy associated with adult (autosomal dominant) polycystic kidney disease have been reported. Most of these malignancies were diagnosed as renal cell carcinoma. But the case of... -
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- Genetic diagnosis of autosomal dominant polycystic kidney disease: linkage analysis versus direct mutation analysis
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Lee KB
- KMID: 2311824
- Kidney Res Clin Pract.
- 2016 Jun;35(2):67-68.
- doi: 10.1016/j.krcp.2016.04.004
No abstract available. -
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- Obturator hernia in autosomal dominant polycystic kidney disease
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Jung JH, Song JH, Ahn SH
- KMID: 2416087
- Kidney Res Clin Pract.
- 2018 Jun;37(2):178-179.
- doi: 10.23876/j.krcp.2018.37.2.178
No abstract available. -
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- A Case Report: Prenatal Ultrasonographic Diagnosis of Autosomal Dominant Polycystic Kidney Disease
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Lee EH, Shin MC
- KMID: 2261797
- Korean J Obstet Gynecol.
- 2000 Jan;43(1):109-112.
Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disorder characterized by renal cyst formation, hypertension, and end-stage renal disease. For many years, ADPKD was considered an adult disease. In... -
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- Autosomal Dominant Polycystic Kidney Disease Complicated by Aldosterone-producing Adrenal Adenoma
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Park DJ, Yang JI, Choi YM, Kang MJ, Kim HJ, Lee SS, Lee JD, Chang SH, Chung SI, Kwon SI
- KMID: 1990109
- Korean J Nephrol.
- 1998 Nov;17(6):968-972.
We report the case of a 34-year-old woman with autosomal dominant polycystic kidney disease associated with primary aldosteronism due to left adrenal adenoma. Although autosomal dominant polycystic kidney disease could... -
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- A Case of Dilated Cardiomyopathy Associated with Autosomal Dominant Polycystic Kidney Disease
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Choe SC, Jeon ES, Hwang SD
- KMID: 1571916
- J Korean Soc Echocardiogr.
- 2001 Dec;9(2):152-156.
Autosomal dominant polycystic kidney disease is a systemic disorder with cystic manifestations in the kidneys, liver, pancreas, seminal vesicles, and meninges; its noncystic manifestations affect mostly the vascular, cardiac, and... -
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- A Case of ESRD Caused by ADPKD (Autosomal Dominant Polycystic Kidney Disease) in a 17-year-old Patient
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Kim JS, Han BG, Choi SO
- KMID: 2079171
- Korean J Nephrol.
- 2001 Mar;20(2):328-331.
Autosomal dominant polycystic kidney disease (ADPKD) is probably the common human disorder inherited by an autosomal dominant mechanism with worldwide prevalence of 1 out of 500-1,000 individuals. Progressive decline in... -
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- A Case of Emphysematous Pyelonephritis in a Autosomal Dominant Polycystic Kidney Disease Patient Successfully Treated by Medical Treatment
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Ha HK, Choi WW, Kwon SH, Jung IS, Kim YI, Lee JS, Song CS, Oh YK, Lee JG, Cho SB
- KMID: 1889340
- Korean J Nephrol.
- 2002 Sep;21(5):861-864.
Emphysematous pyelonephritis is an uncommon and potentially life-threatening infectious disease. Although there is still controversy about optimal treatment of emphysematous pyelonephritis, published results indicate that the mortality rate in the... -
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- Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report
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Jeong GH, Park BS, Jeong TK, Ma SK, Yeum CH, Kim SW, Kim NH, Choi KC
- KMID: 2157637
- J Korean Med Sci.
- 2003 Apr;18(2):284-286.
- doi: 10.3346/jkms.2003.18.2.284
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases... -
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- Autosomal Dominant Polycystic Kidney Desease Coexisting with Renal Dysplasia. First Case Described and Followed Since Prenatal Period
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Truyols C
- KMID: 2435372
- Child Kidney Dis.
- 2018 Oct;22(2):64-66.
- doi: 10.3339/jkspn.2018.22.2.64
Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent hereditary renal disease and causes terminal chronic renal failure. ADPKD is characterized by bilateral multiple renal cysts, which are produced... -
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- A Case of Spontaneous Rupture of the Autosomal Dominant Polycystic Kidney associated with Ureteral Calculi
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Kim HW, Suh HJ, Lee DH, Lee JH
- KMID: 2289948
- Korean J Urol.
- 1999 Apr;40(4):520-522.
Spontaneous rupture of the kidney is a relatively uncommon disease. It occurs secondary to various kinds of underlying disease such as infection, hydronephrosis, calculous disease, benign or malignant tumor, renal... -
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- Pathogenesis and New Treatment of Autosomal Dominant Polycystic Kidney Disease
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Kim SW
- KMID: 2080176
- Korean J Nephrol.
- 2011 May;30(3):231-238.
The discovery of the genes and their respective proteins that are associated with autosomal dominant polycystic kidney disease (ADPKD) has revolutionized the field of ADPKD biology. Recent studies indicate that... -
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- Papillary Adenoma Identified in Removed Polycystic Kidneys during Kidney Transplantation in Autosomal Dominant Polycystic Kidney Disease Patient
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Chai MH, Park H, Kim Y, Kim JS, Kim SH, Eom M, Yang JW, Han BG, Choi SO
- KMID: 1941321
- J Korean Soc Transplant.
- 2014 Dec;28(4):246-249.
- doi: 10.4285/jkstn.2014.28.4.246
Kidney transplantation is the preferred treatment in end stage renal disease for autosomal dominant polycystic kidney disease (ADPKD) patients. Removal of the native kidney is not usually recommended for ADPKD... -
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- Multifocal Renal Cell Carcinoma of Different Histological Subtypes in Autosomal Dominant Polycystic Kidney Disease
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Na KY, Kim HS, Park YK, Chang SG, Kim YW
- KMID: 1439878
- Korean J Pathol.
- 2012 Aug;46(4):382-386.
- doi: 10.4132/KoreanJPathol.2012.46.4.382
Renal cell carcinoma (RCC) in autosomal dominant polycystic kidney (ADPKD) is rare. To date, 54 cases of RCC in ADPKD have been reported. Among these, only 2 cases have different... -
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- Hypokalemic Hypertension Leading to a Diagnosis of Autosomal Dominant Polycystic Kidney Disease
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Vutthikraivit W, Assanatham M, Sriphrapradang C
- KMID: 2328425
- Electrolyte Blood Press.
- 2016 Jun;14(1):11-15.
- doi: 10.5049/EBP.2016.14.1.11
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disease. Hypertension is common and occurs before decline in renal function. However, the coexistence of hypertension and hypokalemia... -
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- Polycystic Kidney Disease Presenting as Subarachnoid Hemorrhage Due to Ruptured Cerebral Aneurysm: An Autopsy Case
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Choi YD, Lee HY, Kim YS
- KMID: 1593790
- Korean J Pathol.
- 2006 Dec;40(6):469-471.
Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disorder characterized by multiple expanding cysts in both kidneys, and they ultimately destroy the renal parenchyma and cause renal failure. Intracranial... -
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