Huang Jieming, Li Yiming, Li Yueping, Yu Qianwen, Chen Xiaochun, Ye Qinyong, Chen Ying
Department of Neurology, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Department of Neurology, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, Fuzhou, Fujian, China; Institute of Neuroscience, Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China; Clinical Research Center for Precision Diagnosis and Treatment of Neurological Diseases of Fujian Province, China.
Thromb Res. 2025 Feb;246:109252. doi: 10.1016/j.thromres.2025.109252. Epub 2025 Jan 4.
Protein S deficiency is a rare inherited disease. We report the case of a young man who unexpectedly developed isolated cortical vein thrombosis (ICoVT) associated with a novel PROS1 mutation.
Clinical symptoms were recorded, and physical examinations conducted. Comprehensive laboratory tests included routine coagulation function tests, protein C activity, and antithrombin III levels. Advanced imaging techniques, such as magnetic resonance imaging (MRI), magnetic resonance venography (MRV), and computed tomography angiography (CTA) were employed. We also performed genetic analysis on the patient and his parents.
The patient presented with headaches and paroxysmal convulsions without identifiable triggers. Physical examinations and routine coagulation tests were generally normal, except for a markedly reduced protein S activity at 21.2 %. MRI scans revealed right parietal cerebral hemorrhage and thickening of the cortical vein, characterized by high T1-weighted Imaging and low T2-weighted Imaging and Fluid-Attenuated Inversion Recovery signals. CTA and Doppler ultrasound of the lower limbs showed no abnormalities. Family history revealed that his father had suffered from multiple venous thromboses. Genetic testing identified a missense mutation (c.1912G>T p.Gly638Cys) in both the patient and his father, along with a duplication of approximately 403.6 kb on chromosome 3q26.32-33 in the patient.
This case highlights a novel PROS1 missense mutation and its significant role in development of cortical venous thrombosis. It provides a new insight into the genetic basis of autosomal dominant thrombophilia associated with protein S deficiency (THPH5).
蛋白S缺乏症是一种罕见的遗传性疾病。我们报告了一名年轻男性意外发生孤立性皮质静脉血栓形成(ICoVT)并伴有一种新的PROS1突变的病例。
记录临床症状并进行体格检查。全面的实验室检查包括常规凝血功能检查、蛋白C活性和抗凝血酶III水平。采用了先进的成像技术,如磁共振成像(MRI)、磁共振静脉造影(MRV)和计算机断层血管造影(CTA)。我们还对患者及其父母进行了基因分析。
患者出现头痛和阵发性抽搐,无明确诱因。体格检查和常规凝血检查一般正常,但蛋白S活性显著降低,为21.2%。MRI扫描显示右侧顶叶脑出血和皮质静脉增粗,表现为T1加权成像高信号、T2加权成像和液体衰减反转恢复序列低信号。下肢CTA和多普勒超声检查未见异常。家族史显示他的父亲曾患多发性静脉血栓形成。基因检测在患者及其父亲中均发现一个错义突变(c.1912G>T p.Gly638Cys),同时患者3号染色体q26.32 - 33区域存在约403.6 kb的重复。
本病例突出了一种新的PROS1错义突变及其在皮质静脉血栓形成发展中的重要作用。它为与蛋白S缺乏相关的常染色体显性遗传性易栓症(THPH5)的遗传基础提供了新的见解。