Immunoreactivity of Wilms tumor 1 (WT1) as an additional evidence supporting hemangiomatous rather than inflammatory origin in the etiopathogenesis of angiolymphoid hyperplasia with eosinophilia.

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Tokat F., Lehman J., Sezer E., Cetin E., Ince Ü., Durmaz E.

Dermatology practical & conceptual, cilt.8, ss.28-32, 2018 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 8
  • Basım Tarihi: 2018
  • Doi Numarası: 10.5826/dpc.0801a06
  • Dergi Adı: Dermatology practical & conceptual
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
  • Sayfa Sayıları: ss.28-32
  • Anahtar Kelimeler: angiolymphoid hyperplasia with eosinophilia, Wilms tumor 1, GLUT1, hemangioma
  • Acıbadem Mehmet Ali Aydınlar Üniversitesi Adresli: Evet

Özet

Background: Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare vascular proliferative disorder mainly located in the periauricular region. The etiopathogenesis of ALHE is unknown, and it is still controversial as to whether the entity represents a benign vascular neoplasm or an inflammatory process.