A 16-year-old male patient was admitted to our hospital in March 2012 with chief complaints
of systemic lymphadenopathy for> 4 years with significant enlargement in the bilateral …

To the Editor, Idiopathic multicentric Castleman disease (iMCD) represents a group of poorly
understood lymphoproliferative disorders with limited treatment options. 1 Despite …

Multicentric Castleman disease (MCD) is an indolent lymphoproliferative disorder of
unknown etiology. Due to the absence of specific histological features in Castleman …

A 20-year-old Turkish male presented with fatigue, abdominal pain, weight loss, and night
sweats. Physical examination revealed hepatosplenomegaly and axillary lymphadenopathy; …

Multicentric Castleman disease is a rare lymphoproliferative disorder of unknown cause. It is
especially rare in children. The authors describe a 4-year-old girl that presented with …

Castleman's disease is an atypical lymphoproliferative disorder, associated with
dysregulated overproduction of interleukin-6 (IL-6) and with systemic manifestations [1] …

Castleman9s disease represents an atypical lymphoproliferative disorder which is non-
clonal but can turn malignant in the form of lymphoma, Kaposi9s sarcoma or plasma cell …

Background Castleman disease (CD) is a rare polyclonal lymphoproliferative disorder of
unclear etiology. Standard therapy for unicentric CD is surgical resection. Radiotherapy can …

Castleman disease is a rare B-cell lymphoproliferative disorder characterized by lymph
node enlargement with or without constitutional signs. Herein, we describe a unique patient …

Human herpes virus-8 (HHV8)-negative, idiopathic multicentric Castleman disease (iMCD)
is a rare lymphoproliferative disorder sustained by pro-inflammatory cytokines, including …