一名患有未确诊的 Sturge-Weber 综合征的难民的非典型癫痫发作和复发:来自有限环境的病例报告。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL International Medical Case Reports Journal Pub Date : 2024-06-22 eCollection Date: 2024-01-01 DOI:10.2147/IMCRJ.S472356
Awab H Saad, Saeed Mohammed Omar, Abeir Abbas Elgilli, Ibtehal Abdalwahid Abdalmjeed Omer, Morouj Hussein Jalaleldeen
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引用次数: 0

摘要

背景:斯特吉-韦伯综合征(Sturge-Weber Syndrome,SWS)是一种复杂罕见的遗传性神经-皮肤疾病,其特点是存在葡萄酒色斑、眼部和颅内血管瘤病,导致癫痫发作、眼部和口腔异常:我们报告了一名 39 岁、无糖尿病、无高血压的女性难民,她最初因贫血导致心力衰竭而接受输血治疗。入院后,她出现多次局灶性至双侧癫痫发作、严重烦躁、失语和右侧偏瘫,因此住进了重症监护室。复查病史和体格检查发现,她的左侧眼部有淡淡的葡萄酒色斑,最初未引起注意,20 年前曾有过无诱因癫痫发作的远期病史。影像学检查发现顶叶钙化,确诊为 SWS。因此,为了全面了解患者的诊断并确定治疗策略,患者接受了多学科治疗,包括神经内科、眼科、耳鼻喉科和理疗科的会诊。通过连续 3 天静脉注射苯妥英,并通过鼻胃管将卡马西平口服剂量提高到每天 1 克,成功控制了癫痫发作。遗憾的是,由于缺乏人员或资源,无法对 SWS 患者进行其他重要评估,如高级神经影像学、精神科、整形外科和神经外科评估,以及牙科复查:本病例突显了未确诊的 SWS 患者罕见的成人癫痫发作以及在未服用抗癫痫药物近二十年后再次发作的情况。该病例还强调了全面病史和临床检查的重要性,因为如果这名患者在入院时没有出现癫痫发作,她可能会被漏诊为 SWS。我们的研究还显示了在资源有限的情况下管理如此复杂的病情所面临的挑战。
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An Atypical Seizure Onset and Re-Emergence in a Refugee with an Undiagnosed Sturge-Weber Syndrome: A Case Report from a Limited Setting.

Background: Sturge-Weber syndrome (SWS) is a complex rare genetic neuro-cutaneous disorder characterized by the presence of a port-wine stain, ophthalmic and intracranial angiomatosis leading to seizures, ocular, and oral abnormalities.

Case presentation: We report a 39-year-old, non-diabetic, non-hypertensive female refugee who presented initially with heart failure due to anemia for which she received blood transfusions. Later on admission, she developed multiple focal to bilateral seizures, severe irritability, aphasia, and right-sided hemiplegia, leading to admission to the ICU. A repeat medical history and examination revealed a faint left-sided ophthalmic port-wine stain that was initially unnoticed and a remote history of unprovoked seizures 20 years ago. Imaging revealed parietal calcifications and confirmed the diagnosis of SWS. Thus, a multidisciplinary approach was taken to fully understand the patient's diagnosis and determine a treatment strategy, involving consultations with the neurology, ophthalmology, otolaryngology, and physiotherapy departments. Successful seizure control was achieved by administering IV phenytoin for 3 days and the up-titrating of oral carbamazepine to 1g daily through a nasogastric tube. Unfortunately, due to the unavailability of personnel or resources, other important assessments for patients with SWS, such as advanced neuroimaging, psychiatric, plastic and neuro-surgery evaluations, as well as dentistry reviews, could not be conducted.

Conclusion: This case highlights the rare occurrence of adult-onset seizures in an undiagnosed SWS and their re-emergence after almost two decades without anti-seizure medications. It also highlights the importance of a comprehensive history and clinical examination, as this patient's diagnosis of SWS could have been missed if she had not experienced seizures on admission. Our study also demonstrates the challenges associated with managing such a complex condition in settings with limited resources.

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来源期刊
International Medical Case Reports Journal
International Medical Case Reports Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
1.40
自引率
0.00%
发文量
135
审稿时长
16 weeks
期刊介绍: International Medical Case Reports Journal is an international, peer-reviewed, open access, online journal publishing original case reports from all medical specialties. Submissions should not normally exceed 3,000 words or 4 published pages including figures, diagrams and references. As of 1st April 2019, the International Medical Case Reports Journal will no longer consider meta-analyses for publication.
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