A patient with WT syndrome and Castleman disease.

  title={A patient with WT syndrome and Castleman disease.},
  author={Canan Vergin and Nazan Çeting{\"u}l and K Kavakli and S Oztop and Ferda Ozkinay and Mahmut Çoker and G{\"u}ng{\"o}r Nişli and Saliha Soydan and Erol Balik and Orkun Akar},
  journal={Acta paediatrica Japonica : Overseas edition},
  volume={37 1},
WT syndrome, an autosomal dominant condition, combines hematological abnormalities with mild lib defects. Anemia, pancytopenia, leukemia and lymphoma can occur at varying ages from childhood to middle age. Limb defects include ulnar and radial defects, bifid or hypoplastic thumbs and cutaneous syndactyly. Castleman disease is characterized by tumorous masses of lymphoid tissue showing plasma cell or hyaline vascular type changes in histological specimens. A 13 year old boy, diagnosed as WT… CONTINUE READING
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