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Hemolytic anemia due to pyruvate kinase deficiency coexistent with the alpha thalassemia trait and chronic myeloid leukemia.

作者信息

Shrestha Nirmal, Khurana Harshit, Verghese Renjith, Mishra Yogendra

机构信息

Armed Forces Medical College, Pune, India.

Armed Forces Medical College, Pune, India.

出版信息

Hematol Transfus Cell Ther. 2024 Nov;46 Suppl 5(Suppl 5):S305-S308. doi: 10.1016/j.htct.2024.04.130. Epub 2024 Sep 12.

DOI:10.1016/j.htct.2024.04.130
PMID:39307622
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11670578/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21a0/11670578/ac70dbdbcc99/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21a0/11670578/905f516667d4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21a0/11670578/ac70dbdbcc99/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21a0/11670578/905f516667d4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21a0/11670578/ac70dbdbcc99/gr2.jpg

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Hemolytic anemia due to pyruvate kinase deficiency coexistent with the alpha thalassemia trait and chronic myeloid leukemia.丙酮酸激酶缺乏所致的溶血性贫血与α地中海贫血性状及慢性髓性白血病共存。
Hematol Transfus Cell Ther. 2024 Nov;46 Suppl 5(Suppl 5):S305-S308. doi: 10.1016/j.htct.2024.04.130. Epub 2024 Sep 12.
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[ELECTROPHORETIC STUDY OF THE SOLUBLE PROTEINS OF ERYTHROCYTIC STROMA. II. ERYTHROCYTES OF HEMOPATHIC SUBJECTS].
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本文引用的文献

1
Safety and efficacy of mitapivat, an oral pyruvate kinase activator, in adults with non-transfusion dependent α-thalassaemia or β-thalassaemia: an open-label, multicentre, phase 2 study.口服丙酮酸激酶激活剂米他匹法特在非输血依赖型α地中海贫血或β地中海贫血成人患者中的安全性和有效性：一项开放标签、多中心、2期研究。
Lancet. 2022 Aug 13;400(10351):493-501. doi: 10.1016/S0140-6736(22)01337-X.
2
Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency.米他培坦治疗丙酮酸激酶缺乏症的安全性和疗效。
N Engl J Med. 2019 Sep 5;381(10):933-944. doi: 10.1056/NEJMoa1902678.
3
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.
解决丙酮酸激酶缺乏症的诊断差距：丙酮酸激酶缺乏症诊断的共识建议。
Am J Hematol. 2019 Jan;94(1):149-161. doi: 10.1002/ajh.25325. Epub 2018 Nov 28.
4
Coexistence of alpha-thalassemia and a new pyruvate kinase variant: PK Fukien.α地中海贫血与一种新的丙酮酸激酶变异体：福建丙酮酸激酶的共存。
Acta Haematol. 1983;69(1):3-8. doi: 10.1159/000206830.
5
An unusual hematological syndrome with pyruvate-kinase deficiency and thalassemia minor in the kindreds.
Acta Haematol. 1968;39(6):345-58. doi: 10.1159/000208980.
6
Haemolytic anaemia with hereditary pyruvate kinase instability developing acute leukaemia.
Scand J Haematol. 1975 May;14(4):249-57. doi: 10.1111/j.1600-0609.1975.tb02424.x.
7
Chronic myelomonocytic leukemia associated with hereditary pyruvate kinase deficiency and multiple acquired erythrocyte abnormalities.慢性粒单核细胞白血病伴遗传性丙酮酸激酶缺乏及多种获得性红细胞异常。
Acta Haematol. 1979;61(3):168-74. doi: 10.1159/000207651.