Paroxysmal nocturnal hemoglobinuria complicated with essential thrombocythemia harboring concomitant PIGA, CALR, and ASXL1 mutations

被引：1

作者：

Okamoto, Haruya ^{[1
,2
]}

Uoshima, Nobuhiko ^{[2
]}

Kamitsuji, Yuri ^{[2
]}

Kawata, Eri ^{[2
,3
]}

Komori, Yukiko ^{[2
]}

Sasaki, Nana ^{[2
]}

Tsutsumi, Yasuhiko ^{[2
]}

Tsukamoto, Taku ^{[1
]}

Mizutani, Shinsuke ^{[1
]}

Nannya, Yasuhito ^{[4
,5
]}

Kuroda, Junya ^{[1
]}

机构：

[1] Kyoto Prefectural Univ Med, Dept Med, Div Hematol & Oncol, Kamigyo Ku, 465 Kajii Cho, Kyoto 6028566, Japan

[2] Japan Red Cross Hosp Kyoto Daini, Dept Hematol, Kyoto, Japan

[3] Matsushita Mem Hosp, Dept Hematol, Osaka, Japan

[4] Kyoto Univ, Dept Pathol & Tumour Biol, Kyoto, Japan

[5] Kyoto Univ, Inst Adv Study Human Biol WPI ASHBi, Kyoto, Japan

来源：

ANNALS OF HEMATOLOGY | 2021年 / 100卷 / 08期

关键词：

D O I：

10.1007/s00277-021-04425-y

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：2113 / 2115

页数：3

共 42 条

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[22] An atypical chronic neutrophilic leukemia patient harboring ASXL1 and NRAS mutations associated with monoclonal plasma cell dyscrasia presenting as hemopericardium
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Tao, Lan
Jiang, Xin
Chen, Haoyue
Liu, Chunhua
Sun, Miao
ANNALS OF HEMATOLOGY, 2021, 100 (01) : 273 - 275
[23] An atypical chronic neutrophilic leukemia patient harboring ASXL1 and NRAS mutations associated with monoclonal plasma cell dyscrasia presenting as hemopericardium
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Lan Tao
Xin Jiang
Haoyue Chen
Chunhua Liu
Miao Sun
Annals of Hematology, 2021, 100 : 273 - 275
[24] GATA-1, BUT NOT FOG-1, FLI-1 OR CALR, IS UP-REGULATED IN ESSENTIAL THROMBOCYTHEMIA INDEPENDENTLY FROM JAK2 AND CALR MUTATIONS
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HAEMATOLOGICA, 2015, 100 : 531 - 532
[25] GATA1, BUT NOT FOG1, FLI1 OR CALR, IS UP-REGULATED IN ESSENTIAL THROMBOCYTHEMIA INDEPENDENTLY FROM JAK2 AND CALR MUTATIONS
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HAEMATOLOGICA, 2015, 100 : 170 - 170
[26] Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms
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A Pardanani
J Patel
M Wadleigh
T Lasho
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[27] Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms
Abdel-Wahab, O.
Pardanani, A.
Patel, J.
Wadleigh, M.
Lasho, T.
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Beran, M.
Gilliland, D. G.
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LEUKEMIA, 2011, 25 (07) : 1200 - 1202
[28] Comparative thrombotic risk associated with CALR1, CALR2, and JAK2 V617F mutations in essential thrombocythemia
Neupane, Niraj
Low, Soon K.
Kharel, Himal
Bhattarai, Sanket
Thapa, Sangharsha
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AMERICAN JOURNAL OF HEMATOLOGY, 2024, 99 (01) : E26 - E28
[29] Concomitant Analysis of EZH2 and ASXL1 Mutations In Myelofibrosis, Chronic Myelomonocytic Leukemia and Blast-Phase Myeloproliferative Neoplasms
Abdel-Wahab, Omar
Pardanani, Animesh
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Heguy, Adriana
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BLOOD, 2010, 116 (21) : 1266 - 1266
[30] Myelodysplastic Syndromes with EZH2 Mutations Frequently Show Multilineage Dysplasia, Chromosome 7 Alterations and Concomitant Mutations in ASXL1, RUNX1 and TET2
Sakhdari, Ali
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Bueso-Ramos, Carlos
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Medeiros, L. Jeffrey
Kanagal-Shamanna, Rashmi
MODERN PATHOLOGY, 2018, 31 : 549 - 550

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