Tumoral diseases

Articles

• pleuropulmonary blastoma and cystic nephroma association
  21 March 2007

  PPBCN association

• 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

• condyloma
  20 June 2007

  condyloma accuminata WP
  Definition: Condylomas are HPV-associated squamous cell papilloma localized on genital ( genital condyloma ) or anal ( anal condyloma ) mucosa.
  Images
  condyloma https://twitter.com/NRiddleMD/status/730566150480744448
  Wikimedia 1: Condyloma acuminatum
  Wikimedia 2 : Condyloma acuminatum
  Genital warts (or condylomata acuminata, venereal warts, anal warts and anogenital warts) are symptoms of a highly contagious sexually transmitted disease caused by some (...)

• 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 (...)

• 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 (...)

• cancer spreading
  9 March 2007

  Videos
  melanoma as a model of cancer spreading

• SMARCB1-associated familial schwannomatosis
  29 April 2007

  INI1-associated familial schwannomatosis

• neurofibromatosis type 2
  28 October 2003

  NF2

• vulvar Paget disease
  20 June 2007

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

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