| Turkish Journal of Cancer |
| 2009, Volume 39, Number 3, Page(s) 110-114 |
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| A case of multicentric HHV-8 positive Castleman's disease presenting with marked lymphocytosis |
| SİMTEN DAĞDAŞ1, MURAT ALBAYRAK2, ÖZLEM ŞAHİN BALÇIK2, GÜLSÜM ÖZET1, FUNDA CERAN1, SELİM EREKUL3 |
1Ankara Numune Education and Research Hospital, Department of Hematology, Ankara-Turkey 2Ankara Oncology Education and Research Hospital, Department of Hematology, Ankara-Turkey 3Ankara University School of Medicine, Department of Pathology, Ankara-Turkey |
Castleman's disease is a rare lymphoproliferative disease
which is morphologically and clinically heterogeneous. Histopathologically
it is classified into hyaline vascular, plasma
cell and mixed variants and clinically into unicentric and
multicentric types. Although it presents with diverse clinical
and laboratory findings, as far as we know, there is no case
in the literature that presents with such a marked lymphocytosis
which can simulate chronic lymphocytic leukemia.
In this report, a case of Castleman's disease, that is HHV-
8 positive multicentric hyaline vascular type and displaying
marked lymphocytosis is presented. [Turk J Cancer
2009;39(3):110-114]
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