Tumoral diseases

Articles

• cutaneous Paget disease
  20 June 2007

  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 diseases
  cutaneous (...)

• 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 (...)

• vulvar Paget disease
  20 June 2007

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

• neurofibromatosis type 2
  28 October 2003

  NF2

• splenic tumoral invasion
  16 March 2007

  See also
  splenic tumors
  Metastasis

• CNPPB syndrome
  21 June 2005

  association cystic nephroma and pleuropulmonary blastoma

• pleuropulmonary blastoma and cystic nephroma association
  21 March 2007

  PPBCN association

• SMARCB1-associated familial schwannomatosis
  29 April 2007

  INI1-associated familial schwannomatosis

• cancer spreading
  9 March 2007

  Videos
  melanoma as a model of cancer spreading

• Faisalabad histiocytosis
  18 March 2006

  Definition: Faisalabad histiocytosis is a form of histiocytosis associated with sensorineural deafness and joint contractures.
  Faisalabad histiocytosis (MIM.602782) was first described as a novel autosomal recessive form of histiocytosis in a highly consanguineous family originating from Pakistan.
  Affected individuals were born with joint deformities, sensorineural hearing loss and subsequently developed a generalized lymphadenopathy and swellings in their eyelids that were shown to (...)

0 | 10