Atypical hyaline vascular-type castleman's disease with thrombocytopenia, anasarca, fever, and systemic lymphadenopathy.
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Two Cases of Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis/Renal Failure, and Organomegaly (TAFRO) Syndrome with High Serum Procalcitonin Levels, Including the First Case Complicated with Adrenal HemorrhagingThe first report of adolescent TAFRO syndrome, a unique clinicopathologic variant of multicentric Castleman's disease.Successful treatment of a Caucasian case of multifocal Castleman's disease with TAFRO syndrome with a pathophysiology targeted therapy - a case report.TAFRO syndrome: 2 cases and review of the literature.Clinicopathologic analysis of TAFRO syndrome demonstrates a distinct subtype of HHV-8-negative multicentric Castleman disease.TAFRO syndrome successfully treated with tocilizumab: A case report and systematic review.Proposed diagnostic criteria, disease severity classification and treatment strategy for TAFRO syndrome, 2015 version.A case of TAFRO syndrome, a variant of multicentric Castleman's disease, successfully treated with corticosteroid and cyclosporine A.Diffuse Large B-cell Lymphoma during Corticosteroid Therapy for TAFRO Syndrome.TAFRO Syndrome Associated with EBV and Successful Triple Therapy Treatment: Case Report and Review of the Literature.Magnetic resonance imaging of bone marrow for TAFRO syndrome.International, evidence-based consensus diagnostic criteria for HHV-8-negative/idiopathic multicentric Castleman disease.Elevated serum interferon γ-induced protein 10 kDa is associated with TAFRO syndrome.Successful treatment by tocilizumab without steroid in a very severe case of TAFRO syndromeCharacterization of patients with systemic lupus erythematosus who meet the diagnostic criteria for TAFRO syndrome.Successful Treatment of TAFRO Syndrome with Tocilizumab, Prednisone, and Cyclophosphamide.Thalidomide for tocilizumab-resistant ascites with TAFRO syndrome.TAFRO Syndrome with Disseminated Intravascular Coagulation Successfully Treated with Tocilizumab and Recombinant Thrombomodulin.Comprehensive analysis of 225 Castleman's diseases in the oral maxillofacial and neck region: a rare disease revisited.High proportion of TAFRO syndrome in Thai adult Castleman's disease patients: a 10-year experience.Membranoproliferative glomerulonephritis-like findings for TAFRO syndrome, associated with an anterior mediastinal tumor: A case report.
P2860
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P2860
Atypical hyaline vascular-type castleman's disease with thrombocytopenia, anasarca, fever, and systemic lymphadenopathy.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Atypical hyaline vascular-type ...... and systemic lymphadenopathy.
@ast
Atypical hyaline vascular-type ...... and systemic lymphadenopathy.
@en
type
label
Atypical hyaline vascular-type ...... and systemic lymphadenopathy.
@ast
Atypical hyaline vascular-type ...... and systemic lymphadenopathy.
@en
prefLabel
Atypical hyaline vascular-type ...... and systemic lymphadenopathy.
@ast
Atypical hyaline vascular-type ...... and systemic lymphadenopathy.
@en
P2093
P356
P1476
Atypical hyaline vascular-type ...... and systemic lymphadenopathy.
@en
P2093
Katsuyoshi Takata
Kyotaro Ohno
Mai Takeuchi
Noriko Iwaki
Shinji Nakao
Tadashi Yoshino
Yasuharu Sato
Yorihisa Orita
P356
10.3960/JSLRT.53.87
P50
P577
2013-01-01T00:00:00Z