Kidneys

• renal κ light chain amyloid deposition
  7 August 2012

  References
  Unique Pattern of Renal κ Light Chain Amyloid Deposition With Histiocytic Transdifferentiation of Tubular Epithelial Cells. Hemminger J, Satoskar A, Brodsky SV, Calomeni E, Nadasdy GM, Kovach P, Hofmeister CC, Nadasdy T. Am J Surg Pathol. 2012 Aug;36(8):1253-7. PMID: #22790864#

• hyperplastic intralobar nephrogenic rest with botryoid protrusion
  24 April 2012

  Nephrogenic rests are nodular collections of undifferentiated renal blastema cells in the postnatal kidney that are recognized as putative precursor lesions of Wilms tumor.
  References
  Single-nucleotide polymorphism in WT1 gene in a hyperplastic intralobar nephrogenic rest with botryoid protrusion. Mizuno K, Hayashi Y, Tozawa K, Iwatsuki S, Kojima Y, Kohri K. Urology. 2010 Jul;76(1):149-52. PMID: (...)

• congenital nephrotic syndrome, finnish type
  20 April 2012

  nephrotic syndrome finnish type; FINNISH CONGENITAL NEPHROSIS; CNF NEPHROTIC SYNDROME, CONGENITAL; NPHS
  The nephrotic syndrome type 1 (NPHS1), also known as "Finnish congenital nephrosis", is caused by homozygous or compound heterozygous mutation in the gene encoding nephrin (NPHS1; MIM.602716) on chromosome 19q13.1.
  The nephrotic syndrome is characterized clinically by proteinuria, hypoalbuminemia, hyperlipidemia, and edema. Kidney biopsies show nonspecific histologic changes such as (...)

• VHL-associated renal cell carcinoma
  22 March 2012

  Genetics
  Germline mutations in the VHL tumor suppressor gene cause von Hippel-Lindau (VHL) disease and somatic VHL mutations occur in the majority of clear cell renal cell carcinoma (cRCC).
  In VHL, cRCC GISTIC analysis identified four statistically significant regions of copy number gain and four statistically significant regions of deletion that occurred in >10% of tumors analyzed.
  Sporadic cRCC without detectable VHL mutations had, on average, more copy number abnormalities than VHL (...)

• DICER1-associated Wilms tumor
  24 February 2012

  References
  Extending the phenotypes associated with DICER1 mutations. Foulkes WD, Bahubeshi A, Hamel N, Pasini B, Asioli S, Baynam G, Choong CS, Charles A, Frieder RP, Dishop MK, Graf N, Ekim M, Bouron-Dal Soglio D, Arseneau J, Young RH, Sabbaghian N, Srivastava A, Tischkowitz MD, Priest JR. Hum Mutat. 2011 Dec;32(12):1381-4. PMID: #21882293#
  DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome. Slade I, (...)

• chronic pyelonephritis
  11 February 2012

  Digital cases
  UI:731 : Acute and chronic pyelonephritis
  UI:746 : Acute and chronic pyelonephritis
  See also
  pyelonephritis

• pyelonephritis
  11 February 2012

  Digital cases
  UI:731 : Acute and chronic pyelonephritis
  UI:746 : Acute and chronic pyelonephritis
  See also
  pyelic anomalies
  nephritis

• acute pyelonephritis
  11 February 2012

  Digital cases
  UI:731 : Acute and chronic pyelonephritis
  UI:746 : Acute and chronic pyelonephritis
  See also
  pyelonephritis

• renal abcess
  11 February 2012

  abcess of the kidney
  Digital case
  UI:989 : Pseudomonas abscesses of the kidney
  See also
  abcess
  Pseudomonas aeruginosa

• renal epithelial and stromal tumor
  27 January 2012

  REST

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