9q34缺失细胞遗传学异常的急性髓系白血病中继性尿崩症。

Q2 Medicine
Oman Medical Journal Pub Date : 2024-07-31 eCollection Date: 2024-07-01 DOI:10.5001/omj.2024.22
Majd Farajallah, Fatima Alkaabi, Arif Alam, Raya Almazrouei
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引用次数: 0

摘要

急性髓性白血病(AML)很少与中枢性尿崩症(CDI)相关,其潜在的病理生理机制尚不清楚。aml相关CDI病例中最常见的细胞遗传学异常是7号单体,其次是3号染色体异常。我们报告了一例新诊断为AML的9q34缺失(ABL1基因区域)的女性,她出现了多尿和烦渴的症状,调查证实了CDI。这是首次报道的9q34缺失(ABL1基因区域)在AML合并CDI中的细胞遗传学异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Central Diabetes Insipidus in Acute Myeloid Leukemia with Cytogenetic Abnormality of 9q34 Deletion.

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 (ABL1 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 (ABL1 gene region) in AML with CDI.

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来源期刊
Oman Medical Journal
Oman Medical Journal Medicine-Medicine (all)
CiteScore
3.10
自引率
0.00%
发文量
119
审稿时长
12 weeks
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