One case of surgical treatment of coagulation factor XI deficiency complicated with esophageal cancer: a case report

Author:

Tian Yang,Zheng Zhaowei,Song Nannan,Wang Jun

Abstract

Abstract Background Coagulation factor XI deficiency is an autosomal recessive hereditary disease with a low incidence. It usually occurs after surgery or trauma; Esophageal cancer is a common malignant tumor of the digestive tract in China. But so far, surgery-based comprehensive treatment of esophageal cancer still dominates. Case presentation We report a case of an Asian patient with XI factor deficiency and lower esophageal squamous cell carcinoma who was admitted to our hospital recently. After active preoperative preparation, the operation was successfully performed, and there was no obvious abnormal bleeding during and after the operation. Conclusions Coagulation factor XI deficiency is a relatively rare disease, and patients with the disease will face a greater risk of bleeding during the perioperative period. The encouraging perioperative outcome enables us to have a deeper understanding of surgical treatment strategies for patients with Coagulation factor XI deficiency.

Publisher

Springer Science and Business Media LLC

Reference11 articles.

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3. Chen Y, Chen T, Jiang C, Zhu H, Pan L, Chang H, et al. Genetic analysis of patients with hereditary coagulation factor XI deficiency and literature review. Int J Blood Transf Hematol. 2021;44(02):153–9.

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