Antithrombin III deficiency and idiopathic intracranial hypertension: a case report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2025-01-04 DOI:10.1186/s13256-024-04997-z
Mansoureh Togha, Yousef Mokary, Elham Jafari
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Abstract

Background: Idiopathic intracranial hypertension (IIH) is a condition where the pressure of the cerebrospinal fluid in the brain increases without a known cause. It typically affects adults but can also occur in adolescents and children, although it is less common. Numerous elements, including coagulopathy, have been documented in previous cases as potential etiological factors of IIH. Nonetheless, our objective was to present the insufficiency of a coagulation factor as an additional contributing factor to IIH, a notion that has not been previously reported.

Case presentation: In this case, a 34-year-old West Asian female patient presented with a subacute generalized headache, bilateral blurred vision, and papilledema. The patient's brain magnetic resonance imaging showed flattening of the posterior globe and empty sella, but no other abnormalities were detected. The results of magnetic resonance venography and cerebrospinal fluid analysis were also normal, except for an opening cerebrospinal fluid pressure of 600 mm H2O during the lumbar puncture. Rheumatologic and endocrine disorders were ruled out on the basis of clinical assessment and laboratory tests. The patient was started on acetazolamide (1 g/day, increased to 2 g/day) and furosemide (20 mg/twice a day) and was encouraged to lose weight. These treatments led to some improvement for about 1 year, but her symptoms then worsened without an obvious cause. Given the prolonged duration of the disease and the lack of expected response to treatment, the patient was reevaluated for endocrinopathy and collagen vascular disease, which were negative. An additional workup revealed an antithrombin III (AT III) deficiency, for which the patient was prescribed acetylsalicylic acid (80 mg/day) in addition to the previous medications. As a result, the patient's papilledema, macular thickness, and nerve fiber layer edema decreased, as observed by fundoscopy and optical coherence tomography. Clinical examination and imaging also showed improvement in the patient's symptoms.

Conclusion: This case highlights the importance of considering coagulopathy in cases of IIH and suggests that antiplatelet therapy with acetylsalicylic acid may be beneficial for such patients.

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抗凝血酶III缺乏与特发性颅内高压1例报告。
背景:特发性颅内高压(IIH)是一种脑内脑脊液压力升高而原因不明的情况。它通常影响成年人,但也可能发生在青少年和儿童,尽管不太常见。许多因素,包括凝血功能障碍,在以前的病例中被证明是IIH的潜在病因。尽管如此,我们的目的是提出凝血因子不足作为IIH的一个额外因素,这一概念以前没有报道过。病例介绍:本病例中,34岁的西亚女性患者表现为亚急性全身头痛、双侧视力模糊和乳头水肿。患者的脑磁共振成像显示后球变平,蝶鞍空,但未发现其他异常。磁共振静脉造影和脑脊液分析结果也正常,除了腰椎穿刺时脑脊液压力为600 mm H2O。根据临床评估和实验室检查,排除了风湿病和内分泌疾病。患者开始使用乙酰唑胺(1 g/天,增加到2 g/天)和呋塞米(20 mg/ 2次/天),并鼓励减肥。这些治疗导致了大约1年的一些改善,但随后她的症状在没有明显原因的情况下恶化。考虑到病程延长和治疗效果不佳,对患者进行了内分泌病变和胶原血管病变的重新评估,结果均为阴性。额外的检查显示抗凝血酶III (AT III)缺乏症,为此患者除先前的药物外,还开了乙酰水杨酸(80毫克/天)。结果,眼底镜和光学相干断层扫描观察到患者的乳头水肿、黄斑厚度和神经纤维层水肿减少。临床检查和影像学检查也显示患者的症状有所改善。结论:本病例强调了在IIH病例中考虑凝血功能障碍的重要性,并提示乙酰水杨酸抗血小板治疗可能对这类患者有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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