Jingjing Yang, Zhanhua Liang, Huajun Jiang
Department of Neurology, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Department of Orthopaedics, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Indian J Dermatol. 2022 Jul-Aug;67(4):480. doi: 10.4103/ijd.ijd_1169_20.
Familial hypercholesterolemia (FH) is one of the inherited metabolic diseases, demonstrating the low-density lipoprotein receptor (LDLR) abnormality and serum cholesterol level marked elevation. FH has become an extremely high incident cause of occlusive coronary heart disease. However, even though hemorheological disorder caused by hyperlipidemia is a risk factor of ischemic cerebrovascular disease, cerebral infarction caused by FH has not been given much attention. We present a 41-year-old man with a family history of hypercholesterolemia was admitted to our hospital with dizziness, vertigo, slurred speech, and weakness in his left limbs. Head CT scan showed multiple acute cerebral infarction in the right frontal and parietal lobes. He had arcus corneae and less obvious signs of cutaneous xanthomas in the hands and knees. Molecular analysis of the LDLR gene identified heterozygous and missense mutation in exon 12 of the LDLR gene. The final diagnosis was cerebral infarction caused by FH. It is worth noting that cerebral infarction may also occur in patients with FH. Even if the most patients do not have any sign or history of cerebral ischemia, they need more attention to precise examination of the brain.
家族性高胆固醇血症(FH)是一种遗传性代谢疾病,表现为低密度脂蛋白受体(LDLR)异常和血清胆固醇水平显著升高。FH已成为闭塞性冠心病的极高发病因。然而,尽管高脂血症引起的血液流变学紊乱是缺血性脑血管病的一个危险因素,但FH所致的脑梗死却未得到足够重视。我们报告一名41岁男性,有高胆固醇血症家族史,因头晕、眩晕、言语不清和左下肢无力入院。头部CT扫描显示右侧额叶和顶叶多发急性脑梗死。他有角膜弓,手部和膝部皮肤黄色瘤体征不明显。LDLR基因的分子分析确定在LDLR基因第12外显子存在杂合错义突变。最终诊断为FH所致脑梗死。值得注意的是,FH患者也可能发生脑梗死。即使大多数患者没有任何脑缺血体征或病史,也需要更重视脑部的精确检查。