Tumoral diseases

Articles

• cutaneous Paget disease
  20 June 2007

  See also : extramammary Paget disease
  Images
  "crushed basal cells" appearance is a clue to cutaneous Paget disease https://twitter.com/nathan_t_harvey/status/817321113487167488 https://twitter.com/JMGardnerMD/status/857595741778440198
  Digital cases
  JRC:5395 : Mammary Paget disease.
  JRC:10822 : Extramammary Paget disease.
  JRC:10823 : Extramammary Paget disease.
  Videos
  Vulvar Paget disease (by Washington Deceit) http://www.youtube.com/v/hRikkqh2SXY
  See also
  cutaneous (...)

• vulvar Paget disease
  20 June 2007

  Video
  Vulvar Paget disease (by Washington Deceit)
  See also
  cutaneous Paget disease

• SMARCB1-associated familial schwannomatosis
  29 April 2007

  INI1-associated familial schwannomatosis

• cancer spreading
  9 March 2007

  Videos
  melanoma as a model of cancer spreading

• pleuropulmonary blastoma and cystic nephroma association
  21 March 2007

  PPBCN association

• neurofibromatosis type 2
  28 October 2003

  NF2

• McCune-Albright syndrome
  27 June 2007

  The McCune-Albright syndrome is characterized by polyostotic fibrous dysplasia, pigment patches of the skin and endocrinologic abnormalities, including precocious puberty, thyrotoxicosis, pituitary gigantism, and Cushing syndrome (MIM.219080). It is usually caused by mosaicism for a mutation in the GNAS1 gene.
  Synopsis
  polyostotic fibrous dysplasia
  pigment patches of the skin
  endocrinologic abnormalities
  precocious puberty
  thyrotoxicosis
  pituitary gigantism
  primary bimorphic (...)

• splenic tumoral invasion
  16 March 2007

  See also
  splenic tumors
  Metastasis

• hereditary leiomyomatosis and renal cell cancer syndrome
  24 September 2003

  HLRCC syndrome; FH-associated RCC; FH-deficient RCC; Reed syndrome
  Definition: Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an autosomal dominant disorder characterized by smooth-muscle tumors of the skin and uterus and/or renal cell carcinoma. The mutation of this condition has been identified in the fumarate hydratase (FH, 1q42.3-q43) gene.
  Mutations in the fumarate hydratase (FH) gene underlie HLRCC, a rare syndrome involving cutaneous and uterine leiomyomata and (...)

• CNPPB syndrome
  21 June 2005

  association cystic nephroma and pleuropulmonary blastoma

0 | 10