Velez Oquendo Gabriel, Alcantar Sergio, Gupta Sonu
Internal Medicine, Northeast Georgia Medical Center Gainesville, Gainesville, USA.
Internal Medicine, Augusta University Medical College of Georgia, Augusta, USA.
Cureus. 2024 Mar 16;16(3):e56277. doi: 10.7759/cureus.56277. eCollection 2024 Mar.
Carcinomatous meningitis (CM) is characterized by the multifocal dissemination of malignant cells into the cerebrospinal fluid (CSF), pia mater, and subarachnoid space. Involvement can occur in the advanced stage of malignancy, causing multifocal involvement and a wide array of symptoms. Diagnosis requires suspicions and a multimodal approach that includes imaging, lumbar puncture, and diagnostic laboratory evaluation. This case represents a female with a history of non-Hodgkin's lymphoma (NHL) and venous thromboembolism on chronic anticoagulation who presented due to acute encephalopathy, hallucinations, and right cranial nerve III palsy for 10 days before arrival. Computed tomography (CT) and angiography of the brain did not show any intracranial abnormalities. Subsequent magnetic resonance imaging (MRI) was without signs of infarction, hemorrhage, or abnormal enhancement, with the MRI of the orbits showing asymmetric linear enhancement anterior to the superior pons and midbrain on the right. Initial differential included a paraneoplastic syndrome, but there was no obvious evidence of pathological enhancement on MRI. Due to progressive bulbar symptoms, a lumbar puncture was performed with cerebrospinal fluid diagnostic workup with cytology showing monoclonal B-cell proliferation consistent with lymphoma. This case illustrates a rare but specific finding of CM as cranial nerve III palsy symptoms in this patient who did not have imaging findings that would reflect her symptoms on the initial MRI of the brain. Furthermore, diagnosing CM is complex and involves a combination of multiple diagnostic and treatment modalities. It is important to recognize the condition early to improve the patient's quality of life, prolong survival, and stabilize neurological deterioration.
癌性脑膜炎(CM)的特征是恶性细胞多灶性播散至脑脊液(CSF)、软脑膜和蛛网膜下腔。这种累及可发生在恶性肿瘤的晚期,导致多灶性累及和一系列症状。诊断需要怀疑并采用包括影像学、腰椎穿刺和诊断性实验室评估在内的多模式方法。该病例为一名有非霍奇金淋巴瘤(NHL)病史且因静脉血栓栓塞接受长期抗凝治疗的女性,因急性脑病、幻觉和右侧动眼神经麻痹入院前10天就诊。脑部计算机断层扫描(CT)和血管造影未显示任何颅内异常。随后的磁共振成像(MRI)未显示梗死、出血或异常强化迹象,眼眶MRI显示右侧脑桥上部和中脑前方有不对称线性强化。最初的鉴别诊断包括副肿瘤综合征,但MRI上没有明显的病理强化证据。由于进行性延髓症状,进行了腰椎穿刺并对脑脊液进行诊断性检查,细胞学检查显示单克隆B细胞增殖,与淋巴瘤一致。该病例说明了CM的一种罕见但特定的表现,即该患者出现动眼神经麻痹症状,但最初的脑部MRI没有显示出能反映其症状的影像学表现。此外,诊断CM很复杂,需要多种诊断和治疗方式相结合。早期识别这种情况对于提高患者的生活质量、延长生存期和稳定神经功能恶化很重要。