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伊立替康联合顺铂治疗复发性卵巢透明细胞癌后出现抗利尿激素分泌不当综合征。

Syndrome of inappropriate antidiuretic hormone secretion following irinotecan-cisplatin administration as a treatment for recurrent ovarian clear cell carcinoma.

作者信息

Kwon Do Youn, Han Gwan Hee, Ulak Roshani, Ki Kyung Do, Lee Jong Min, Lee Seon Kyung

机构信息

Department of Obstetrics and Gynecology, Kyung Hee University Hospital at Gangdong, Seoul, Korea.

Department of Medicine, Graduate School, Kyung Hee University Seoul, Korea.

出版信息

Obstet Gynecol Sci. 2017 Jan;60(1):115-117. doi: 10.5468/ogs.2017.60.1.115. Epub 2017 Jan 19.

Abstract

Syndrome of inappropriate antidiuretic hormone secretion (SIADH) has various causes including central nervous system disorders, pulmonary and endocrine diseases, paraneoplastic syndromes, and use of certain drugs. SIADH induced by chemotherapy with irinotecan-cisplatin is not a common complication. Here, we review a case of SIADH after treatment with irinotecan-cisplatin. A 45-year-old woman received adjuvant chemotherapy (paclitaxel-carboplatin) for ovarian clear cell carcinoma, but the cancer recurred within 9 months of chemotherapy. Subsequently, a second line of combination chemotherapy containing irinotecan-cisplatin was initiated. However, 5 days after chemotherapy administration, her general condition began to deteriorate; her hematological tests revealed hyponatremia. Therefore, it is imperative to consider the possibility of SIADH in patients being treated with irinotecan-cisplatin-based chemotherapy. Proper monitoring of serum sodium levels and assessment of clinical symptoms should be performed in such patients for early diagnosis and prompt management.

摘要

抗利尿激素分泌不当综合征(SIADH)有多种病因,包括中枢神经系统疾病、肺部和内分泌疾病、副肿瘤综合征以及某些药物的使用。由伊立替康-顺铂化疗诱导的SIADH并非常见并发症。在此,我们回顾一例伊立替康-顺铂治疗后发生SIADH的病例。一名45岁女性因卵巢透明细胞癌接受辅助化疗(紫杉醇-卡铂),但化疗后9个月内癌症复发。随后,开始进行含伊立替康-顺铂的二线联合化疗。然而,化疗给药5天后,她的一般状况开始恶化;血液检查显示低钠血症。因此,对于接受基于伊立替康-顺铂化疗的患者,必须考虑发生SIADH的可能性。应对此类患者进行血清钠水平的适当监测和临床症状评估,以便早期诊断和及时处理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f1/5313354/68d5a98d75f7/ogs-60-115-g001.jpg

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