پديد آورندگان :
Asgarani F نويسنده , Keyhani M نويسنده , Sharifian R A نويسنده , Toogeh G R نويسنده , Aghanouri R نويسنده , Jalaeekhoo H نويسنده
چكيده لاتين :
Castlemanיs disease (angiofollicular lymphoid hyperplasia) includes a heterogeneous group of lymphoproliferative disorders. The cause of this disease remains uncertain. There are two types of localized Castlemanיs disease: the more common hyaline vascular and the plasma cell types. Mixed variant is an uncommon localized lesion in general population. The lesions can occur in any part of the body that contains lymphoid tissue, although seventy percent are found in the anterior mediastinum. We report a thirty years old boy with Castlemanיs disease who presented with fever, anorexia, weight loss, sweating, anemia and abdominal mass. The histologic examination of the biopsy specimens revealed a mixed hyaline vascular and plasma cell type of Castlemanיs disease.
