Recurrent Hodgkin's Disease Presenting as a Clinically Isolated Cavernous Sinus Syndrome.

IF 0.9 Q4 CLINICAL NEUROLOGY
Case Reports in Neurological Medicine Pub Date : 2021-08-07 eCollection Date: 2021-01-01 DOI:10.1155/2021/3946231
Aayesha Jalaluddin Soni, Edward Bernard Lee-Pan
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引用次数: 0

Abstract

Background: Hodgkin's disease involving the central nervous system is uncommon and is usually seen in patients with uncontrolled systemic disease or those who have had multiple episodes of recurrent disease. Common symptoms of intracranial Hodgkin's disease are motor and/or sensory deficits, headache, papilloedema, coma, and seizures. The rarity of Hodgkin's disease presenting with intracranial involvement is marked, but patients presenting with cavernous sinus syndrome is even rarer. Despite its rarity, the presence of a cavernous sinus syndrome in a patient with a known history of Hodgkin's disease warrants full utilization of modern diagnostic techniques in terms of investigation. Case Presentation. A 34-year-old woman, known with previous Hodgkin's lymphoma and now in remission for the past 7 years, presented with signs and symptoms suggestive of a left cavernous sinus syndrome. She was otherwise systemically well with no other complaints. Extensive investigations revealed no obvious cause for the cavernous sinus syndrome. A CT chest revealed subclinical axillary lymphadenopathy, which on excisional biopsy confirmed recurrent Hodgkin's disease. The patient's sole clinical presentation of her recurrent disease was the cavernous sinus syndrome, with no other clinically obvious systemic signs or symptoms to suggest a relapse. This was treated with steroids, and clinical improvement was noted; she was referred to oncology for extensive chemotherapy.

Conclusions: Whilst there is a paucity of literature around this topic, it must be remembered by the clinician that cavernous sinus syndrome may be the sole clinical presentation of recurrent Hodgkin's disease. Even though it is reported that lymphomatous involvement in the brain usually occurs late in the disease process, this case is evidence that cavernous sinus syndrome may precede other systemic signs and symptoms. Recognising this possibility will ensure a rigorous search for Hodgkin's disease, an early and effective diagnosis, and a better prognosis in affected patients.

Abstract Image

复发何杰金氏病表现为临床孤立的海绵窦综合征。
背景:累及中枢神经系统的霍奇金病并不常见,通常见于全身性疾病不受控制或多次复发的患者。颅内何杰金氏病的常见症状是运动和/或感觉缺陷、头痛、乳头水肿、昏迷和癫痫发作。以颅内累及为表现的何杰金氏病是罕见的,但以海绵窦综合征为表现的患者更是罕见。尽管其罕见,存在海绵窦综合征的患者有何杰金氏病的已知历史值得充分利用现代诊断技术方面的调查。案例演示。34岁女性,已知既往何杰金氏淋巴瘤,目前在过去的7年缓解,提出的体征和症状提示左侧海绵窦综合征。除此之外,她全身都很好,没有别的毛病。广泛的调查显示海绵窦综合征没有明显的病因。胸部CT显示亚临床腋窝淋巴结病,切除活检证实复发何杰金氏病。患者复发的唯一临床表现是海绵窦综合征,没有其他临床明显的全身体征或症状提示复发。这是用类固醇治疗,并注意到临床改善;她被转到肿瘤科接受广泛的化疗。结论:虽然关于这一主题的文献很少,但临床医生必须记住,海绵窦综合征可能是复发性霍奇金病的唯一临床表现。尽管有报道称淋巴瘤累及大脑通常发生在疾病过程的晚期,但本病例证明海绵窦综合征可能先于其他全身体征和症状。认识到这种可能性将确保对何杰金氏病进行严格的研究,早期有效的诊断,以及对受影响患者更好的预后。
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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