References
- Masaki Y, Nakajima A, Iwao H, Kurose N, Sato T, Nakamura T, et al. Japanese variant of multicentric castleman's disease associated with serositis and thrombocytopenia–a report of two cases: is TAFRO syndrome (Castleman- Kojima disease) a distinct clinicopathological entity? J Clin Exp Hematop. 2013;53(1):79–85.
- Iwaki N, Sato Y, Takata K, Kondo E, Ohno K, Takeuchi M, et al. Atypical hyaline vascular-type castleman's disease with thrombocytopenia, anasarca, fever, and systemic lymphadenopathy. J Clin Exp Hematop. 2013;53(1):87–93.
- Ozawa T, Kosugi S, Kito M, Onishi M, Kida T, Nakata S, et al. Efficacy of rituximab for TAFRO syndrome, a variant type of multicentric Castleman's disease (in Japanese). Rinsho Ketsueki. 2014;55(3): 350–5.
- Kojima M, Nakamura N, Tsukamoto N, Otuski Y, Shimizu K, Itoh H, et al. Clinical implications of idiopathic multicentric castleman disease among Japanese: a report of 28 cases. Int J Surg Pathol. 2008;16(4):391–8.
- Takai K, Nikkuni K, Shibuya H, Hashidate H. Thrombocytopenia with mild bone marrow fibrosis accompanied by fever, pleural effusion, ascites and hepatosplenomegaly (in Japanese). Rinsho Ketsueki. 2010;51(5):320–5.
- Kojima M, Nakamura N, Tsukamoto N, Yokohama A, Itoh H, Kobayashi S, et al. Multicentric Castleman's disease representing effusion at initial clinical presentation: clinicopathological study of seven cases. Lupus. 2011;20(1):44–50.
- Kawabata H, Takai K, Kojima M, Nakamura N, Aoki S, Nakamura S, et al. 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). J Clin Exp Hematop. 2013;53(1):57–61.
- Kubokawa I, Yachie A, Hayakawa A, Hirase S, Yamamoto N, Mori T, et al. The first report of adolescent TAFRO syndrome, a unique clinicopathologic variant of multicentric Castleman's disease. BMC Pediatr. 2014;14(1):139.
- Suda T, Katano H, Delsol G, Kakiuchi C, Nakamura T, Shiota M, et al. HHV-8 infection status of AIDS-unrelated and AIDS-associated multicentric Castleman's disease. Pathol Int. 2001; 51(9):671–9.
- Masaki Y. A novel variant of multicentric Castleman's disease associated with anasarca and thrombocytopenia;TAFRO syndrome (in Japanese). Ketsueki naika. 2014;68(1):97–102.
- Kawabata H, Kadowaki N, Nishikori M, Kitawaki T, Kondo T, Ishikawa T, et al. Clinical features and treatment of multicentric castleman's disease: a retrospective study of 21 Japanese patients at a single institute. J Clin Exp Hematop. 2013;53(1):69–77.
- Fajgenbaum DC, van Rhee F, Nabel CS. HHV-8-negative, idiopathic multicentric Castleman disease: novel insights into biology, pathogenesis, and therapy. Blood. 2014;123(19):2924–33.
- Peterson BA, Frizzera G. Multicentric Castleman's disease. Semin Oncol. 1993;20(6):636–647.
- Takai K, Nikkuni K, Momoi A, Nagai K, Igarashi N, Saeki T. Thrombocytopenia with reticulin fibrosis accompanied by fever, anasarca and hepatosplenomegaly: a clinical report of five cases. J Clin Exp Hematop. 2013;53(1):63–8.
- Togasaki E, Ohwada C, Kawajiri C, Shimizu R, Sugita Y, Yamazaki A, et al. Two cases of muticentric Castleman's disease initially presented with massive effusion and edema (in Japanese). Rinsho ketsueki. 2013;54(9):1447.
- Satoh T, Nakamura T, Nakajima A, Iwao H, Miki M, Sakai T, et al. A case of MCD associated with thrombocytopenia and anasarca, so-called TAFRO syndrome (in Japanese). Rinsho ketsueki. 2013;54(9):1447.
- Kawabata H, Kotani S, Matsumura Y, Kondo T, Katsurada T, Haga H, et al. Successful treatment of a patient with multicentric Castleman's disease who presented with thrombocytopenia, ascites, renal failure and myelofibrosis using tocilizumab, an anti-interleukin-6 receptor antibody. Intern Med. 2013;52(13):1503–7.
- Tedesco S, Postacchini L, Manfredi L, Goteri G, Luchetti MM, Festa A, et al. Successful treatment of a Caucasian case of multifocal Castleman's disease with TAFRO syndrome with a pathophysiology targeted therapy - a case report. Exp Hematol Oncol. 2015;4(1):3.
- Inoue M, Ankou M, Hua J, Iwaki Y, Hagihara M, Ota Y. Complete resolution of TAFRO syndrome (thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly) after immunosuppressive therapies using corticosteroids and cyclosporin A: a case report. J Clin Exp Hematop. 2013;53(1):95–9.
- Koduri PR, Parvez M, Kaza S, Pappu P, Anuradha S. Castleman-Kojima disease in a South Asian adolescent. J Clin Exp Hematop. 2014;54(2):163–6.
- Awano N, Inomata M, Sonoda Y, Kondoh K, Ono R, Moriya A, et al. A case of multicentric castleman's disease of mixed-type, which showed constellation of symptoms, i.e., thrombocytopenia, anasarca, anemia, fever, myelofibrosis, and lymphadenopathy. J Clin Exp Hematop. 2013;53(1):101–5.
- Pauwels P, Dal Cin P, Vlasveld LT, Aleva RM, van Erp WF, Jones D. A chromosomal abnormality in hyaline vascular Castleman's disease: evidence for clonal proliferation of dysplastic stromal cells. Am J Surg Pathol. 2000;24(6):882–8.