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TAFRO Syndrome: A Syndrome or a Subtype of Multicentric Castleman Disease?

Biomedicines, 2024-03, Vol.12 (3), p.652

Takai, Kazue

2024

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2019 Updated diagnostic criteria and disease severity classification for TAFRO syndrome

International journal of hematology, 2020-01, Vol.111 (1), p.155-158

2020

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Optimal treatments for TAFRO syndrome: a retrospective surveillance study in Japan

International journal of hematology, 2021-01, Vol.113 (1), p.73-80

2021

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Castleman-Kojima Disease (TAFRO Syndrome) : A Novel Systemic Inflammatory Disease Characterized by a Constellation of Symptoms, Namely, Thrombocytopenia, Ascites (Anasarca), Microcytic Anemia, Myelofibrosis, Renal Dysfunction, and Organomegaly : A Status Report and Summary of Fukushima (6 June, 2012) and Nagoya Meetings (22 September, 2012)

Journal of Clinical and Experimental Hematopathology, 2013, Vol.53(1), pp.57-61

2013

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Proposed diagnostic criteria, disease severity classification and treatment strategy for TAFRO syndrome, 2015 version

International journal of hematology, 2016-06, Vol.103 (6), p.686-692

2016

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Castleman disease and TAFRO syndrome

Annals of hematology, 2022-03, Vol.101 (3), p.485-490

2022

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Clinicopathologic analysis of TAFRO syndrome demonstrates a distinct subtype of HHV‐8‐negative multicentric Castleman disease

American journal of hematology, 2016-02, Vol.91 (2), p.220-226

2016

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TAFRO Syndrome: A Disease Requiring Immediate Medical Attention

Internal Medicine, 2023/01/01, Vol.62(1), pp.27-32

2023

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Is TAFRO syndrome a subtype of idiopathic multicentric Castleman disease?

American journal of hematology, 2019-09, Vol.94 (9), p.975-983

2019

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Epidemiological analysis of multicentric and unicentric Castleman disease and TAFRO syndrome in Japan

Journal of Clinical and Experimental Hematopathology, 2019, Vol.59(4), pp.175-178

2019

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Patient’s age and d-dimer levels predict the prognosis in patients with TAFRO syndrome

International journal of hematology, 2021-08, Vol.114 (2), p.179-188

2021

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Correction to: Patient’s age and D‑dimer levels predict the prognosis in patients with TAFRO syndrome

International journal of hematology, 2021-08, Vol.114 (2), p.301-302

2021

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Thrombocytopenia with Reticulin Fibrosis Accompanied by Fever, Anasarca and Hepatosplenomegaly : A Clinical Report of Five Cases

Journal of Clinical and Experimental Hematopathology, 2013, Vol.53(1), pp.63-68

2013

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Multimodality Imaging of Subcutaneous Panniculitis-like T-cell Lymphoma

Internal Medicine, 2011, Vol.50(11), pp.1265-1265

2011

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Successful Remission of Evans Syndrome Associated with Graves' Disease by Using Propylthiouracil Monotherapy

Internal Medicine, 2011, Vol.50(6), pp.621-625

2011

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Clinical features of polycythemia vera and essential thrombocythemia in Japan: retrospective analysis of a nationwide survey by the Japanese Elderly Leukemia and Lymphoma Study Group

International journal of hematology, 2006-06, Vol.83 (5), p.443-449

2006

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Treatment with R-bendamustine followed by Y-90 ibritumomab tiuxetan for relapsed/refractory low-grade B-cell lymphoma

Annals of oncology, 2017-10, Vol.28 Suppl 9, p.ix81

2017

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Thrombocytopenia with Reticulin Fibrosis Accompanied by Fever, Anasarca and Hepatosplenomegaly: A Clinical Report of Five Cases

Journal of Clinical and Experimental Hematopathology, 2013-06, Vol.53 (1), p.63-68

2013

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Does more intensive therapy have effects on mantle cell lymphoma? A clinical experience from the Lymphoma Treatment Study Group in Japan

International journal of hematology, 2011-05, Vol.93 (5), p.684-686

2011

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Thrombocytopenia with mild bone marrow fibrosis accompanied by fever, pleural effusion, ascites and hepatosplenomegaly

Rinshō ketsueki, 2010-05, Vol.51 (5), p.320

2010

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Elevated serum interferon γ-induced protein 10 kDa is associated with TAFRO syndrome

Scientific reports, 2017-02, Vol.7 (1), p.42316-42316, Article 42316

2017

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TAFRO Syndrome: A Disease Requiring Immediate Medical Attention

Internal Medicine, 2022, pp.9622-22

2022

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The clinicopathological comparison among nodal cases of idiopathic multicentric Castleman disease with and without TAFRO syndrome

Human pathology, 2018-07, Vol.77, p.130-138

2018

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The potential role of follicular helper T cells in idiopathic multicentric Castleman disease with and without TAFRO syndrome

Pathology, research and practice, 2019-10, Vol.215 (10), p.152563-152563, Article 152563

2019

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TAFRO Syndrome: A Syndrome or a Subtype of Multicentric Castleman Disease?

2019 Updated diagnostic criteria and disease severity classification for TAFRO syndrome

Optimal treatments for TAFRO syndrome: a retrospective surveillance study in Japan

Proposed diagnostic criteria, disease severity classification and treatment strategy for TAFRO syndrome, 2015 version

Castleman disease and TAFRO syndrome

Clinicopathologic analysis of TAFRO syndrome demonstrates a distinct subtype of HHV‐8‐negative multicentric Castleman disease

TAFRO Syndrome: A Disease Requiring Immediate Medical Attention

Is TAFRO syndrome a subtype of idiopathic multicentric Castleman disease?

Epidemiological analysis of multicentric and unicentric Castleman disease and TAFRO syndrome in Japan

Patient’s age and d-dimer levels predict the prognosis in patients with TAFRO syndrome

Correction to: Patient’s age and D‑dimer levels predict the prognosis in patients with TAFRO syndrome

Thrombocytopenia with Reticulin Fibrosis Accompanied by Fever, Anasarca and Hepatosplenomegaly : A Clinical Report of Five Cases

Multimodality Imaging of Subcutaneous Panniculitis-like T-cell Lymphoma

Successful Remission of Evans Syndrome Associated with Graves' Disease by Using Propylthiouracil Monotherapy

Clinical features of polycythemia vera and essential thrombocythemia in Japan: retrospective analysis of a nationwide survey by the Japanese Elderly Leukemia and Lymphoma Study Group

Treatment with R-bendamustine followed by Y-90 ibritumomab tiuxetan for relapsed/refractory low-grade B-cell lymphoma

Clinical value of assessing the response to imatinib monitored by interphase FISH and RQ-PCR for BCR-ABL in peripheral blood for long-term survival of chronic phase CML patients: results of the Niigata CML-multi-institutional co-operative clinical study

Thrombocytopenia with Reticulin Fibrosis Accompanied by Fever, Anasarca and Hepatosplenomegaly: A Clinical Report of Five Cases

Does more intensive therapy have effects on mantle cell lymphoma? A clinical experience from the Lymphoma Treatment Study Group in Japan

Thrombocytopenia with mild bone marrow fibrosis accompanied by fever, pleural effusion, ascites and hepatosplenomegaly

Elevated serum interferon γ-induced protein 10 kDa is associated with TAFRO syndrome

TAFRO Syndrome: A Disease Requiring Immediate Medical Attention

The clinicopathological comparison among nodal cases of idiopathic multicentric Castleman disease with and without TAFRO syndrome

The potential role of follicular helper T cells in idiopathic multicentric Castleman disease with and without TAFRO syndrome

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