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Acute Myeloid Leukemia, Version 3.2023, NCCN Clinical Practice Guidelines in Oncology.急性髓系白血病,第 3 版 2023 年,NCCN 肿瘤学临床实践指南。
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Acute myeloid leukemia with central diabetes insipidus.急性髓系白血病伴中枢性尿崩症
Blood Cells Mol Dis. 2019 May;76:45-52. doi: 10.1016/j.bcmd.2019.01.005. Epub 2019 Jan 24.
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Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel.成人急性髓系白血病的诊断与管理:2017年国际专家小组的欧洲白血病网络(ELN)建议
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Acute myeloid leukemia with monosomy 7, ectopic virus integration site-1 overexpression and central diabetes insipidus: A case report.伴有7号染色体单体、异位病毒整合位点-1过表达及中枢性尿崩症的急性髓系白血病:一例报告
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Myelodysplastic syndrome in transformation to acute myeloid leukemia presenting with diabetes insipidus: due to pituitary infiltration association with abnormalities of chromosomes 3 and 7.
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伴有9q34缺失细胞遗传学异常的急性髓系白血病合并中枢性尿崩症

Central Diabetes Insipidus in Acute Myeloid Leukemia with Cytogenetic Abnormality of 9q34 Deletion.

作者信息

Farajallah Majd, Alkaabi Fatima, Alam Arif, Almazrouei Raya

机构信息

Department of Internal Medicine, Tawam Hospital, Al Ain, UAE.

Division of Endocrinology, Tawam Hospital, Al Ain, UAE.

出版信息

Oman Med J. 2024 Jul 31;39(4):e661. doi: 10.5001/omj.2024.22. eCollection 2024 Jul.

DOI:10.5001/omj.2024.22
PMID:39748863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11694343/
Abstract

Acute myeloid leukemia (AML) is rarely associated with central diabetes insipidus (CDI) with unclear underlying pathophysiological mechanisms. The most commonly reported cytogenetic abnormality in cases of AML-associated CDI is monosomy 7, followed by chromosome 3 abnormalities. We report a case of a woman with newly diagnosed AML with 9q34 deletion ( gene region), who developed symptoms of polyuria and polydipsia with an investigation confirming CDI. This is the first reported case of cytogenetic abnormality of 9q34 deletion ( gene region) in AML with CDI.

摘要

急性髓系白血病(AML)很少与中枢性尿崩症(CDI)相关,其潜在病理生理机制尚不清楚。AML相关CDI病例中最常报道的细胞遗传学异常是7号染色体单体,其次是3号染色体异常。我们报告一例新诊断为AML且存在9q34缺失(基因区域)的女性患者,该患者出现多尿和烦渴症状,检查证实为CDI。这是首例报道的AML伴CDI且存在9q34缺失(基因区域)细胞遗传学异常的病例。