网织红细胞增多作为一个警示信号：1例8号染色体三体骨髓增生异常综合征患者获得性椭圆形红细胞增多症的罕见病例 - Suppr

Reticulocytosis As a Whistleblower: A Rare Case of Acquired Elliptocytosis in a Myelodysplastic Syndrome Patient With Trisomy 8.

作者信息

Hage-Sleiman Mehdi, Zhu Jaja, Guérineau Hippolyte, Ronez Emily, Jondeau Katayoun, Kosmider Olivier, Picard Véronique, Denguir Maha, Maillon Agathe, Clauser Sylvain, Bardet Valérie

机构信息

Service d'Hématologie-Immunologie-Transfusion, Hôpitaux Universitaires Paris Ile De France Ouest, Université Versailles Saint Quentin-Paris-Saclay, Paris, France.

UF d'Hématologie clinique, Hôpitaux Universitaires Paris Ile De France Ouest, Université Versailles Saint Quentin-Paris-Saclay, Paris, France.

出版信息

Hemasphere. 2021 Jan 12;5(2):e517. doi: 10.1097/HS9.0000000000000517. eCollection 2021 Feb.

DOI:10.1097/HS9.0000000000000517

PMID:33458593

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7806241/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d7/7806241/e2a1cb6e47b0/hs9-5-e517-g001.jpg

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Reticulocytosis As a Whistleblower: A Rare Case of Acquired Elliptocytosis in a Myelodysplastic Syndrome Patient With Trisomy 8.网织红细胞增多作为一个警示信号：1例8号染色体三体骨髓增生异常综合征患者获得性椭圆形红细胞增多症的罕见病例

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Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies.孤立性 8 号三体性骨髓增生异常综合征（MDS）：一种常伴有骨髓增生性特征的 MDS 类型？法国骨髓增生异常综合征小组的报告。

Br J Haematol. 2018 Sep;182(6):843-850. doi: 10.1111/bjh.15490. Epub 2018 Jul 13.

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Revised international prognostic scoring system for myelodysplastic syndromes.修订版国际预后积分系统用于骨髓增生异常综合征。

Blood. 2012 Sep 20;120(12):2454-65. doi: 10.1182/blood-2012-03-420489. Epub 2012 Jun 27.

Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study.伴 del(20q) 或 i(20q) 的骨髓增生异常综合征的形态学、细胞遗传学和生存情况：一项多中心研究。

Ann Hematol. 2012 Feb;91(2):203-13. doi: 10.1007/s00277-011-1286-0. Epub 2011 Jul 9.

Depletion of L3MBTL1 promotes the erythroid differentiation of human hematopoietic progenitor cells: possible role in 20q- polycythemia vera.耗尽 L3MBTL1 可促进人造血祖细胞的红细胞分化：在 20q-真性红细胞增多症中的可能作用。

Blood. 2010 Oct 14;116(15):2812-21. doi: 10.1182/blood-2010-02-270611. Epub 2010 Jun 28.

Association between myeloid malignancies and acquired deficit in protein 4.1R: a retrospective analysis of six patients.髓系恶性肿瘤与蛋白4.1R获得性缺陷之间的关联：6例患者的回顾性分析

Am J Hematol. 2008 Apr;83(4):275-8. doi: 10.1002/ajh.21088.

New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients.骨髓增生异常综合征中核型的预后影响及与亚型的相关性新见解：来自2124例患者核心数据集的证据

Blood. 2007 Dec 15;110(13):4385-95. doi: 10.1182/blood-2007-03-082404. Epub 2007 Aug 28.

Spectrin-based skeleton in red blood cells and malaria.红细胞和疟疾中基于血影蛋白的骨架

Curr Opin Hematol. 2007 May;14(3):198-202. doi: 10.1097/MOH.0b013e3280d21afd.

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Reticulocytosis As a Whistleblower: A Rare Case of Acquired Elliptocytosis in a Myelodysplastic Syndrome Patient With Trisomy 8.

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