Post-transplantation donor-derived Sezary syndrome in a patient with A91V PRF1 variant hemophagocytic lymphohistiocytosis.
作者信息
S Mehta Rohtesh, Torres Cabala Carlos A, DiNardo Courtney D, Daver Naval, Dabaja Bouthaina, Rezvani Katy, Champlin Richard E, Shpall Elizabeth, Duvic Madeleine
机构信息
Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
出版信息
Am J Hematol. 2021 Sep 1;96(9):E350-E353. doi: 10.1002/ajh.26266. Epub 2021 Jun 28.
PMID:34096089
Abstract
摘要
相似文献
1
Post-transplantation donor-derived Sezary syndrome in a patient with A91V PRF1 variant hemophagocytic lymphohistiocytosis.
Am J Hematol. 2021 Sep 1;96(9):E350-E353. doi: 10.1002/ajh.26266. Epub 2021 Jun 28.
2
Hemophagocytic lymphohistiocytosis with a hemizygous PRF1 c.674G>A mutation.伴有 PRF1 c.674G>A 杂合突变的噬血细胞性淋巴组织细胞增生症。
Am J Med Sci. 2023 Nov;366(5):387-394. doi: 10.1016/j.amjms.2023.07.005. Epub 2023 Jul 17.
3
Neuromyelitis optica, atypical hemophagocytic lymphohistiocytosis and heterozygous perforin A91V mutation.视神经脊髓炎、非典型噬血细胞性淋巴组织细胞增生症与穿孔素A91V杂合突变
J Neuroimmunol. 2017 Oct 15;311:10-13. doi: 10.1016/j.jneuroim.2017.08.003. Epub 2017 Aug 15.
4
Prevalence and disease predisposition of p.A91V perforin in an aged population of European ancestry.欧洲血统老年人群中p.A91V穿孔素的患病率及疾病易感性
Blood. 2020 Feb 20;135(8):582-584. doi: 10.1182/blood.2019003487.
5
Perforin gene mutation in familial haemophagocytic lymphohistiocytosis: the first reported case from Hong Kong.家族性噬血细胞性淋巴组织细胞增生症中的穿孔素基因突变：香港首例报告病例。
Hong Kong Med J. 2014 Aug;20(4):339-42. doi: 10.12809/hkmj134041.
6
Case Report: Chronic inflammatory demyelinating polyradiculoneuropathy rather than hemophagocytic lymphohistiocytosis-the initial phenotype of PRF1 gene mutation.病例报告：慢性炎症性脱髓鞘性多发神经病而非噬血细胞性淋巴组织细胞增多症——PRF1 基因突变的初始表型。
Front Immunol. 2023 Dec 11;14:1306338. doi: 10.3389/fimmu.2023.1306338. eCollection 2023.
7
Primary hemophagocytic lymphohistiocytosis in adults: the utility of family surveys in a single-center study from China.成人原发性噬血细胞性淋巴组织细胞增生症：来自中国单中心研究的家族调查的作用。
Orphanet J Rare Dis. 2018 Jan 22;13(1):17. doi: 10.1186/s13023-017-0753-7.
8
Type 2 familial hemophagocytic lymphohistiocytosis in half brothers: A case report.同父异母兄弟中的2型家族性噬血细胞性淋巴组织细胞增生症：一例报告
Medicine (Baltimore). 2018 Jul;97(30):e11577. doi: 10.1097/MD.0000000000011577.
9
[Flow cytometry in the diagnosis of hemophagocytic lymphohistiocytosis in a case with fatal outcome].[流式细胞术在一例预后不良的噬血细胞性淋巴组织细胞增生症诊断中的应用]
Orv Hetil. 2014 Mar 9;155(10):389-95. doi: 10.1556/OH.2014.29790.
10
Perforin gene variant A91V in young patients with severe COVID-19.重症 COVID-19 年轻患者中的穿孔素基因变体 A91V
Haematologica. 2020 Dec 1;105(12):2844-2846. doi: 10.3324/haematol.2020.260307.
Zotero 插件