Castleman Disease: A Multicenter Case Series from Turkey
Objective: Castleman disease (CD) is a rare disease also known as angiofollicular lymph node hyperplasia. The two main histological subtypes are the hyaline vascular and plasma cell variants.
Eren Gündüz +31 more
doaj +1 more source
Kaposi's sarcoma-associated herpesvirus oncoprotein K13 protects against B cell receptor induced growth arrest and apoptosis through NF-κB activation [PDF]
Kaposi's sarcoma-associated herpesvirus (KSHV) has been linked to the development of Kaposi's sarcoma, primary effusion lymphoma and multicentric Castleman's disease (MCD). We have characterized the role of KSHV-encoded viral FLICE inhibitory protein K13
Ahmad +53 more
core +1 more source
Expert Perspective: Diagnosis and Treatment of Castleman Disease
Castleman disease (CD) is a major diagnostic challenge for rheumatologists. Unicentric CD (UCD) involves one enlarged lymph node region, whereas multicentric CD (MCD) involves multiple enlarged lymph node regions. Both UCD and MCD may exhibit a wide range of symptoms that overlap with other immune‐mediated conditions.
Luke Y. C. Chen +2 more
wiley +1 more source
Castle man disease: a case report and review of the literature
The Castleman disease (CD) is a rare disease of unknown etiology, characterized histologically by angiofollicular lymphoid hyperplasia. It comes in two forms, unicentric and multicentric.
Mounir Kettani +6 more
doaj +1 more source
Retroperitoneal Castleman’s disease: advocating a multidisciplinary approach for a rare clinical entity [PDF]
BACKGROUND: Castleman’s disease is a rare and poorly understood disease entity that may resemble more common conditions and represents a clinical challenge to the treating surgeon.
Adriana Sanchez +8 more
core +1 more source
HHV-8-negative multicentric Castleman disease presenting as a crescentic immune complexes membranoproliferative glomerulonephritis. [PDF]
Multicentric Castleman disease is a rare polyclonal lymphoproliferative disorder mainly associated with two renal manifestations: thrombotic microangiopathy and amyloidosis.
Duss, F.R. +3 more
core +1 more source
Increased mTOR activation in idiopathic multicentric Castleman disease.
Idiopathic multicentric Castleman disease (iMCD) is a rare and poorly-understood hematologic disorder characterized by lymphadenopathy, systemic inflammation, cytopenias, and life-threatening multi-organ dysfunction.
Daniel J. Arenas +16 more
semanticscholar +1 more source
Multicentric Castleman Disease
The article is devoted to the discussion of the specific features of Castleman disease, a clinical case of its multicentric variant, and analyzes the patient`s case report, the clinical data and results of the laboratory and instrumental methods of research.
E. N. Shcherbakova +2 more
openaire +2 more sources
Siltuximab for Multicentric Castleman Disease—Letter [PDF]
We read with great interest the article by Deisseroth and colleagues ([1][1]) focusing on the recent global approval of the monoclonal IL6 antibody siltuximab for the treatment of patients with HHV-8-, HIV-negative multicentric Castleman disease (MCD).
Raphael, Teipel +7 more
openaire +2 more sources
It is attempted to employ proteolysis‐targeting chimeras‐based targeted protein degradation to the viral protein “Latency‐associated Nuclear Antigen” from Kaposi's sarcoma‐associated herpesvirus. While ternary complex formation is detected via native mass spectrometry, protein degradation is not observed, presumably due to insufficient permeability ...
Aylin Berwanger +10 more
wiley +1 more source

