Longino Elizabeth S, Lindquist Nathan R, Cass Nathan D, Brignola Emily, Thompson Reid C, Haynes David S
Department of Otolaryngology-Head and Neck Surgery, Vanderbilt University Medical Center, Nashville, TN.
Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, TN.
Otol Neurotol Open. 2022 Oct 26;2(4):e020. doi: 10.1097/ONO.0000000000000020. eCollection 2022 Dec.
Few case reports have described primary central nervous system lymphoma (PCNSL) presenting as a cerebellopontine angle (CPA) lesion in HIV-positive patients. We describe a rare presentation of rapidly progressing PCNSL of the CPA/internal auditory canal (IAC) as labyrinthitis with initial negative MRI in an HIV-positive patient.
A 58-year-old male with well-controlled HIV presented with sudden left sensorineural hearing loss, tinnitus, and imbalance. Vestibular testing suggested an uncompensated left peripheral vestibular weakness. MRI demonstrated facial and cochleovestibular nerve enhancement within the CPA and IAC. The presumptive diagnosis of labyrinthitis was made. Two months later, he presented to his infectious disease provider with left facial weakness and disequilibrium and was treated for presumed Bell's palsy. One month later, he presented with left corneal reflex dysfunction, decreased visual acuity, diplopia, and worsening ataxia. Repeat MRI demonstrated a new 3.6 cm lesion of the left CPA/IAC with vasogenic edema. Despite location, the mass lacked the brainstem compression characteristic of other extra-axial CPA masses such as vestibular schwannoma. Flow cytometry and cytology from cerebrospinal fluid was consistent with primary central nervous system large B-cell lymphoma.
We present a unique case of rapidly progressing PCNSL of the CPA/IAC in an HIV-positive patient, presenting initially as labyrinthitis with negative MRI followed by development of multiple cranial neuropathies and 3-month repeat MRI demonstrating a large CPA mass. In HIV-positive patients with a similar initial presentation, PCNSL should considered early in the diagnostic evaluation with close clinical monitoring and a low threshold for repeat imaging.
少数病例报告描述了原发性中枢神经系统淋巴瘤(PCNSL)在HIV阳性患者中表现为桥小脑角(CPA)病变。我们描述了1例罕见的HIV阳性患者,其CPA/内耳道(IAC)的PCNSL迅速进展,最初表现为迷路炎,MRI检查结果为阴性。
一名58岁男性,HIV病情控制良好,出现突发左侧感音神经性听力损失、耳鸣和平衡失调。前庭测试提示左侧外周前庭功能未代偿性减弱。MRI显示CPA和IAC内面神经及耳蜗前庭神经强化。初步诊断为迷路炎。两个月后,他因左侧面部无力和平衡失调就诊于传染病专科医生,被诊断为疑似贝尔麻痹并接受治疗。一个月后,他出现左侧角膜反射功能障碍、视力下降、复视和共济失调加重。复查MRI显示左侧CPA/IAC有一个新的3.6 cm病变,并伴有血管源性水肿。尽管病变位于该部位,但该肿块缺乏其他CPA轴外肿块(如前庭神经鞘瘤)的脑干压迫特征。脑脊液的流式细胞术和细胞学检查结果与原发性中枢神经系统大B细胞淋巴瘤相符。
我们报告了1例HIV阳性患者中CPA/IAC的PCNSL迅速进展的独特病例,最初表现为迷路炎,MRI检查结果为阴性,随后出现多发性颅神经病变,3个月后复查MRI显示CPA有一个大肿块。对于有类似初始表现的HIV阳性患者,在诊断评估早期应考虑PCNSL,密切进行临床监测,并降低重复成像的阈值。