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Posterior reversible encephalopathy syndrome associated with use of anlotinib to treat squamous cell carcinoma of the cervix: case report and literature review.
Lin, Jietao; Chen, Wenmin; Zhong, Sha; Qian, Kai; Chen, Hanrui; Lin, Lizhu.
Affiliation
  • Lin J; The First Affiliated Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guagnzhou, Guangdong, China.
  • Chen W; Baiyun Hospital of the First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guagnzhou, Guangdong, China.
  • Zhong S; First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
  • Qian K; First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
  • Chen H; The First Affiliated Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guagnzhou, Guangdong, China.
  • Lin L; The First Affiliated Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guagnzhou, Guangdong, China.
Front Pharmacol ; 14: 1255785, 2023.
Article in En | MEDLINE | ID: mdl-38169843
ABSTRACT

Background:

Posterior reversible encephalopathy syndrome (PRES), a neurological disorder with an unknown aetiology, is characterised by visual impairment, headache, vomiting, seizures, and transient alterations in consciousness. Case report We present the case of a 49-year-old woman with advanced cervical carcinoma who received second-line therapy with oral anlotinib (12 mg, days 1-14, every 21 days) and injectable tislelizumab (200 mg, day 1, every 21 days). After 7 days of anlotinib administration, she began experiencing symptoms suggestive of PRES and was diagnosed on day 11. Interruption of anlotinib and supportive treatment led to recovery of her binocular vision. The Naranjo score (+5) graded the causality of this reaction as probable, suggesting the possibility that the event may have been an adverse reaction to anlotinib. Ethics This case report was approved by the Ethics Committee of the First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine (Reference no. K-2023-068, 2023/06/09). Informed consent was obtained from the patient and her family.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Aspects: Ethics Language: En Journal: Front Pharmacol Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Aspects: Ethics Language: En Journal: Front Pharmacol Year: 2023 Document type: Article