Validated international definition of the thrombocytopenia, anasarca, fever, reticulin fibrosis, renal insufficiency, and organomegaly clinical subtype (TAFRO) of idiopathic multicentric Castleman disease

被引:89
作者
Nishimura, Yoshito [1 ,2 ]
Fajgenbaum, David C. [3 ]
Pierson, Sheila K. [3 ]
Iwaki, Noriko [4 ]
Nishikori, Asami [5 ]
Kawano, Mitsuhiro [6 ]
Nakamura, Naoya [7 ]
Izutsu, Koji [8 ]
Takeuchi, Kengo [9 ,10 ,11 ]
Nishimura, Midori Filiz [12 ]
Maeda, Yoshinobu [13 ]
Otsuka, Fumio [1 ]
Yoshizaki, Kazuyuki [14 ]
Oksenhendler, Eric [15 ,16 ]
van Rhee, Frits [17 ]
Sato, Yasuharu [5 ]
机构
[1] Okayama Univ, Dept Gen Med, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[2] Univ Hawaii, Dept Med, John A Burns Sch Med, Honolulu, HI USA
[3] Univ Penn, Ctr Cytokine Storm Treatment & Lab, Div Translat Med & Human Genet, Perelman Sch Med, Philadelphia, PA USA
[4] Kanazawa Univ, Hematol Resp Med, Grad Sch Med Sci, Kanazawa, Ishikawa, Japan
[5] Okayama Univ, Div Pathophysiol, Grad Sch Hlth Sci, Okayama, Japan
[6] Kanazawa Univ, Dept Rheumatol, Grad Sch Med Sci, Kanazawa, Ishikawa, Japan
[7] Tokai Univ, Dept Pathol, Sch Med, Isehara, Kanagawa, Japan
[8] Natl Canc Ctr, Dept Hematol, Tokyo, Japan
[9] Canc Inst Hosp Japanese Fdn Canc Res, Dept Pathol, Tokyo, Japan
[10] Japanese Fdn Canc Res, Canc Inst, Div Pathol, Tokyo, Japan
[11] Japanese Fdn Canc Res, Canc Inst, Pathol Project Mol Targets, Tokyo, Japan
[12] Okayama Univ, Dept Pathol, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[13] Okayama Univ, Dept Hematol Oncol & Resp Med, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[14] Osaka Univ, Inst Sci & Ind Res, Dept Organ Fine Chem, Osaka, Japan
[15] Hop St Louis, Dept Clin Immunol, Paris, France
[16] Univ Paris, Paris, France
[17] Univ Arkansas Med Sci, Myeloma Ctr, Little Rock, AR 72205 USA
关键词
DIAGNOSTIC-CRITERIA; KOJIMA DISEASE; SEVERITY CLASSIFICATION; CELL LYMPHOMA; VARIANT; JAPANESE;
D O I
10.1002/ajh.26292
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thrombocytopenia, anasarca, fever, reticulin fibrosis, renal insufficiency, and organomegaly (TAFRO) syndrome is a heterogeneous entity manifesting with a constellation of symptoms described above that can occur in the context of idiopathic multicentric Castleman disease (iMCD) as well as infectious diseases, malignancies, and rheumatologic disorders. So, iMCD-TAFRO is an aggressive subtype of iMCD with TAFRO syndrome and often hyper-vascularized lymph nodes. Since we proposed diagnostic criteria of iMCD-TAFRO in 2016, we have accumulated new insights on the disorder and additional cases have been reported worldwide. In this systematic review and cohort analysis, we established and validated a definition for iMCD-TAFRO. First, we searched PubMed and Japan Medical Abstracts Society databases using the keyword "TAFRO" to extract cases. Patients with possible systemic autoimmune diseases and hematologic malignancies were excluded. Our search identified 54 cases from 50 articles. We classified cases into three categories: (1) iMCD-TAFRO (TAFRO syndrome with lymph node histopathology consistent with iMCD), (2) possible iMCD-TAFRO (TAFRO syndrome with no lymph node biopsy performed and no other co-morbidities), and (3) TAFRO without iMCD or other co-morbidities (TAFRO syndrome with lymph node histopathology not consistent with iMCD or other comorbidities). Based on the findings, we propose an international definition requiring four clinical criteria (thrombocytopenia, anasarca, fever/hyperinflammatory status, organomegaly), renal dysfunction or characteristic bone marrow findings, and lymph node features consistent with iMCD. The definition was validated with an external cohort (the ACCELERATE Natural History Registry). The present international definition will facilitate a more precise and comprehensive approach to the diagnosis of iMCD-TAFRO.
引用
收藏
页码:1241 / 1252
页数:12
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