Farajallah Majd, Alkaabi Fatima, Alam Arif, Almazrouei Raya
Department of Internal Medicine, Tawam Hospital, Al Ain, UAE.
Division of Endocrinology, Tawam Hospital, Al Ain, UAE.
Oman Med J. 2024 Jul 31;39(4):e661. doi: 10.5001/omj.2024.22. eCollection 2024 Jul.
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.
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。