日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Clinicopathological and transcriptomic profiles of 101 patients with diffuse large B-cell lymphoma/high-grade B-cell lymphoma with double-hit MYC and BCL2 or BCL6 and triple hit

对101例伴有MYC和BCL2或BCL6双重打击以及三重打击的弥漫性大B细胞淋巴瘤/高级别B细胞淋巴瘤患者的临床病理学和转录组学特征进行分析

Miyaoka, Masashi; Carreras, Joaquim; Kikuti, Yara Yukie; Ikoma, Haruka; Nagase, Shunsuke; Ito, Atsushi; Orita, Makoto; Kawada, Hiroshi; Sakai, Rika; Sato, Yasuharu; Nishimura, Midori Filiz; Tsukasaki, Kunihiro; Momose, Shuji; Kameoka, Yoshihiro; Yoshida, Masahiro; Satou, Akira; Kato, Seiichi; Oishi, Naoki; Saito, Akio; Sadahira, Ken; Masugi, Yohei; Nakamura, Naoya

International Consensus Histopathological Criteria for Subtyping Idiopathic Multicentric Castleman Disease Based on Machine Learning Analysis

基于机器学习分析的特发性多中心Castleman病亚型国际共识组织病理学标准

Nishimura, Midori Filiz; Haratake, Tomoka; Nishimura, Yoshito; Nishikori, Asami; Sumiyoshi, Remi; Ujiie, Hideki; Kawahara, Yuri; Koga, Tomohiro; Ueki, Masao; Laczko, Dorottya; Oksenhendler, Eric; Fajgenbaum, David C; van Rhee, Frits; Kawakami, Atsushi; Sato, Yasuharu

The Involvement of PI3K-Akt Signaling in the Clinical and Pathological Findings of Idiopathic Multicentric Castleman Disease-Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis, and Organomegaly and Not Otherwise Specified Subtypes

PI3K-Akt信号通路在特发性多中心Castleman病(血小板减少症、全身水肿、发热、网状纤维化、器官肿大及其他未明确亚型)的临床和病理表现中的作用

Haratake, Tomoka; Nishimura, Midori Filiz; Nishikori, Asami; Gonzalez, Michael V; Ennishi, Daisuke; Lai, You Cheng; Ochi, Sayaka; Tsunoda, Manaka; Fajgenbaum, David C; van Rhee, Frits; Momose, Shuji; Sato, Yasuharu

Kikuchi-Fujimoto disease: investigating comprehensive clinicopathological features and risk factors for recurrence

菊池-藤本病:探讨其全面的临床病理特征和复发风险因素

Nishimura, Midori Filiz; Sakao, Chikako; Kurokawa, Yuka; Nishimura, Yoshito; Nishikori, Asami; Yamamoto, Hidetaka; Sato, Yasuharu

Spontaneous Complete Regression of Aleukaemic Cutaneous Myeloid Sarcoma without Progression to Leukaemia Over a Long-term Follow-up Period

长期随访期间,无白血病性皮肤髓系肉瘤自发性完全消退且未进展为白血病

Higaki-Mori, Hiromi; Yamada, Nanako; Ozaki, Kanae; Nishimura, Midori Filiz; Yoshida, Yuichi

Diagnostic challenges of the idiopathic plasmacytic lymphadenopathy (IPL) subtype of idiopathic multicentric Castleman disease (iMCD): Factors to differentiate from IgG4-related disease

特发性多中心性卡斯尔曼病(iMCD)特发性浆细胞性淋巴结病(IPL)亚型的诊断挑战:与IgG4相关疾病鉴别的因素

Nishikori, Asami; Nishimura, Midori Filiz; Fajgenbaum, David C; Nishimura, Yoshito; Maehama, Kanna; Haratake, Tomoka; Tabata, Tetsuya; Kawano, Mitsuhiro; Nakamura, Naoya; Momose, Shuji; Sumiyoshi, Remi; Koga, Tomohiro; Yamamoto, Hidetaka; van Rhee, Frits; Kawakami, Atsushi; Sato, Yasuharu

Computed tomography findings of idiopathic multicentric Castleman disease subtypes

特发性多中心性卡斯尔曼病亚型的计算机断层扫描表现

Iguchi, Toshihiro; Nishikori, Asami; Sato, Yasuharu; Nishimura, Midori Filiz; Iwaki, Noriko; Kojima, Katsuhide; Asahara, Takashi; Otsuka, Fumio; Maeda, Yoshinobu; Hiraki, Takao

Discrepancy of Hans' criteria for clonally related nodal and pericardiac fluid diffuse large B-cell lymphoma with MYD88 L265P mutation

Hans标准对伴有MYD88 L265P突变的克隆相关淋巴结和心包积液弥漫性大B细胞淋巴瘤的诊断存在差异

Terao, Toshiki; Sato, Yumiko; Kuroda, Yoshiaki; Haratake, Tomoka; Nishimura, Midori Filiz; Sato, Yasuharu; Kuyama, Shoichi

A lymph node lesion of hyper IL-6 syndrome mimicking plasmacytoma, IgG4-related disease, and Castleman disease

高IL-6综合征引起的淋巴结病变,可模拟浆细胞瘤、IgG4相关疾病和卡斯尔曼病。

Matsui, Kenta; Imai, Hiroshi; Kobayashi, Toshiaki; Mizutani, Minoru; Nishimura, Midori Filiz; Sato, Yasuharu; Karube, Kennosuke; Okada, Manato; Usui, Miki; Kawakami, Keiki; Murata, Tetsuya

Analysis of Notch1 protein expression in methotrexate-associated lymphoproliferative disorders

对甲氨蝶呤相关淋巴增生性疾病中 Notch1 蛋白表达的分析

Okatani, Takeshi; Nishimura, Midori Filiz; Egusa, Yuria; Yoshida, Sayako; Nishimura, Yoshito; Nishikori, Asami; Yoshino, Tadashi; Yamamoto, Hidetaka; Sato, Yasuharu