Smith Isaac, Aoun Raissa, Lalchan Rebecca
Department of Neurology, NYU Langone, New York, NY, USA.
Case Rep Neurol. 2024 Jul 25;16(1):213-220. doi: 10.1159/000540259. eCollection 2024 Jan-Dec.
The pathophysiology of idiopathic intracranial hypertension (IIH) is not fully characterized, and less is known about its development in transgender patients. Several cases of IIH in transgender patients have been reported, but fewer cases have been published that identify a cerebrospinal fluid (CSF) leak as a complication of IIH in this population. These patients can serve as an important study population, as an association between exogenous testosterone use in karyotypical females and development of IIH may support a hormonally mediated mechanism of development of this disease.
We describe the case of a 33-year-old obese (BMI: 30.58 kg/m) female-to-male transgender patient on exogenous testosterone for 15 years who presented with 1 month of acute or chronic headache with profuse rhinorrhea. Fundoscopic exam revealed disk pallor and edema consistent with a Frisen grade 3 papilledema. Nasal secretion was positive for beta-2 transferrin, consistent with CSF. Computed tomography head demonstrated a 5-mm defect in the medial left middle cranial fossa, bilateral optic nerve prominence and tortuosity, and abnormal arachnoid granulations concerning for IIH. After a successful endoscopic endonasal repair of the left lateral sphenoid recess leak, our patient continued to report headaches, was started on acetazolamide, and noted improvement in symptoms.
The case described herein further supports the growing body of evidence that implicates a hormonal mechanism of action in the development of IIH. Importantly, it also addresses the need for increased study and conversation about rare neurologic diseases in transgender patients.
特发性颅内高压(IIH)的病理生理学尚未完全明确,对于其在跨性别患者中的发展了解更少。已有数例跨性别患者发生IIH的报道,但关于脑脊液(CSF)漏作为该人群IIH并发症的病例报道较少。这些患者可作为重要的研究人群,因为核型女性使用外源性睾酮与IIH发展之间的关联可能支持该病发展的激素介导机制。
我们描述了一名33岁肥胖(BMI:30.58kg/m)的女性向男性转变的跨性别患者,使用外源性睾酮15年,出现1个月的急性或慢性头痛伴大量鼻漏。眼底检查发现视盘苍白和水肿,符合弗里森3级视乳头水肿。鼻分泌物β-2转铁蛋白检测呈阳性,与脑脊液一致。头颅计算机断层扫描显示左侧中颅窝内侧有一个5毫米的缺损,双侧视神经突出和迂曲,以及与IIH相关的异常蛛网膜颗粒。在成功进行内镜下经鼻修复左侧蝶窦隐窝漏后,我们的患者仍持续报告头痛,开始使用乙酰唑胺,并注意到症状有所改善。
本文所述病例进一步支持了越来越多的证据,即激素作用机制与IIH的发展有关。重要的是,它还强调了对跨性别患者罕见神经系统疾病加强研究和交流的必要性。