Nakayama Shoko, Yokote Taiji, Kobayashi Kichinosuke, Hirata Yuji, Akioka Toshikazu, Miyoshi Takuji, Takubo Takayuki, Tsuji Motomu, Hanafusa Toshiaki
Department of Internal Medicine (I), Osaka Medical College, Takatsuki, Osaka 569-0801, Japan.
Endocrine. 2009 Jun;35(3):290-2. doi: 10.1007/s12020-009-9171-5. Epub 2009 Apr 15.
A patient having acute myeloid leukemia (AML) with multilineage dysplasia, developed hyponatremia and showed all symptoms of the syndrome of inappropriate antidiuretic hormone secretion (SIADH) through a mechanism similar to tumor lysis. Retrospective immunohistochemical analysis of blast cells was positive for antidiuretic hormone (ADH) protein. According to us, this is the first case report of SIADH in an AML patient with multilineage dysplasia, showing blast cells immunostained for ADH, which clearly demonstrated that the tumor cells produced ADH.
一名患有多系发育异常的急性髓系白血病(AML)患者发生了低钠血症,并通过类似于肿瘤溶解的机制表现出抗利尿激素分泌不当综合征(SIADH)的所有症状。对原始细胞进行回顾性免疫组化分析显示抗利尿激素(ADH)蛋白呈阳性。据我们所知,这是首例关于多系发育异常的AML患者发生SIADH的病例报告,该患者原始细胞ADH免疫染色阳性,清楚地表明肿瘤细胞产生了ADH。