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Articles

• alveolar rhabdomyosarcoma
  25 November 2003

  Images
  Alveolar rhabdomyosarcoma.
  https://twitter.com/histiocytosisX/status/699599913013923840
  https://twitter.com/seattlequinns/status/855202143564742656
  ARMS : focal desmin w/ diffuse myogenin in A-RMS (PCR + PAX3-FOXO1)
  https://twitter.com/histiocytosisX/status/730475540524699649
  Compact ARMS : Alveolar rhabdomyosarcoma may lack alveolar spaces. Solid nodules uniform round cells,fibrous septa. DIFFUSE myogenin.
  https://twitter.com/JMGardnerMD/status/856870953011347456 (...)

• mixed gonadal dysgenesis
  22 December 2005

  asymmetric gonadal dysgenesis; 46,XY disorders of sex development

• hepatocellular carcinoma
  28 April 2004

  HCC
  Digital cases
  HPC:150 (HPC:150) : Hepatocellular carcinoma, well-differentiated, grade 2.
  HPC:117 (HPC:117) : Hepatocellular carcinoma in Alagille disease.
  Hepatocellular Carcinoma, FNA and Core Biopsy by Ed Euthman.
  Definition: HCC is the fifth most common cancer in the world. The incidence of HCC has doubled in the United States over the past 25 years and the incidence and mortality rates of HCC seem likely to double again over the next 10–20 years.
  Macroscopy (...)

• Leydig cell tumor
  13 February 2006

  Leydig cell adenoma
  Digital cases
  HPC:119 : Leydig cell tumor.
  JRC:18782 : Testis intestitial cell tumor
  Images
  Leydig cell tumor
  https://twitter.com/MayoClinicPath/status/743120235230699520
  https://twitter.com/seattlequinns/status/857024877034848256
  Synopsis
  Leydig cell proliferation
  round cell proliferation
  fusiform cell proliferation
  Leydig cells
  abundant eosinophilic cytoplasm
  characteristic nuclear-rich zones separated by nuclear-free zones
  crystals of Reinke (...)

• fibrous dysplasia
  3 December 2003

  fibrous dysplasia of bones; osseous fibrous dysplasia
  Definition: Fibrous dysplasia is a skeletal developmental anomaly of the bone-forming mesenchyme that manifests as a defect in osteoblastic differentiation and maturation. Virtually any bone in the body can be affected. It is a nonhereditary disorder of unknown cause.
  Images
  Fibrous dysplasia of bone
  https://twitter.com/KUSAURAP/status/738883221824245760
  https://twitter.com/drsys02/status/857135375495688193 (...)

• C-cell hyperplasia
  3 November 2003

  C-cell hyperplasia; hyperplasia of thyroid C-cells; hyperplasia of C-cells; thyroid C cell hyperplasia

• congenital lobar hyperinflation
  22 June 2005

  congenital lobar emphysema, infantile lobar emphysema

• infantile hemangioma
  11 March 2004

  juvenile hemangioma, cellular hemangioma of infancy, common hemangioma of infancy; GLUT1+ infantile hemangioma
  Digital Cases (Digital slides)
  HPC/106 : GLUT1+ infantile hemangioma
  HPC:186 : GLUT1+ infantile hemangioma
  HPC:385 : GLUT1+ infantile hemangioma
  Clinical synopsis
  The typical infantile hemangioma appears postnataly, grows quickly, and regresses gradually in the first few years of life. Approximately one third of IH are present at birth.
  Infantile hemangiomas progress (...)

• osteochondroma
  18 March 2004

  solitary osteochondroma
  Digital case (Digital slides)
  HPC:396 : Osteochondroma
  Images
  Osteochondroma https://twitter.com/KUSAURAP/status/745057733565526016 https://twitter.com/MArnold_PedPath/status/734893844592893952 https://twitter.com/E_Heidi_Cheek/status/873941616712704000
  Cytogenetics
  loss of distal 8q (#11793371#)
  Predisposition
  multiple osteochondromas (or hereditary multiple exostoses (HME) or osteochnondromatosis) type 1 (MIM.133700): EXT1 germline mutations type 2 (...)

• epulis
  15 December 2004

  (gr. epi-: above; oulon: gingiva)

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