Department of Radiotherapy & Oncology, All India Institute of Medical Sciences, New Delhi, 110029, India.
Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.
J Egypt Natl Canc Inst. 2022 Nov 7;34(1):46. doi: 10.1186/s43046-022-00147-y.
The reported incidence of leptomeningeal carcinomatosis is 3-8% in patients with solid tumours. More commonly, it has been described in the setting of advanced cancers of the lung, breast and malignant melanoma.
A 50-year-old diabetic patient with recurrent unresectable squamous cell carcinoma (SCC) of the right retromolar trigone (rT4bN0M0) presented with severe low backache and weakness in bilateral lower limbs 20 days after the completion of concurrent chemoradiotherapy. Contrast-enhanced MRI of the spine showed multiple nodular enhancing leptomeningeal lesions at the lumbar level and an intramedullary T2/FLAIR-hyperintense longitudinal lesion involving the central cord from C2 to C7 vertebral levels, suggestive of leptomeningeal metastases. Cerebrospinal fluid (CSF) analysis revealed pleocytosis, elevated protein and markedly decreased glucose. The CSF cytology revealed scattered large atypical cells, suspicious for metastasis. Non-contrast MRI of the brain showed a T2/FLAIR-hyperintense lesion involving the right caudate nucleus suggestive of either an acute infarct with haemorrhagic transformation or a haemorrhagic brain metastasis. During assessment, he had high-grade fever and was started on empirical intravenous antibiotics (ceftriaxone, vancomycin and subsequently meropenem) in line with the management for acute bacterial meningitis. Gram staining of CSF did not demonstrate the presence of any bacteria and the specimen was sterile on culture. He did not respond to empirical antibiotics, had a progressive downhill course and eventually died due to aspiration pneumonia.
This brief report highlights the importance of awareness of leptomeningeal carcinomatosis as a possible cause of backache with sensorimotor deficit and autonomic dysfunction in a previously treated case of head and neck SCC.
在实体瘤患者中,软脑膜癌病的报告发病率为 3-8%。更常见的是,它在晚期肺癌、乳腺癌和恶性黑色素瘤患者中被描述。
一位 50 岁的糖尿病患者,右侧磨牙后三角区复发性不可切除的鳞状细胞癌(SCC)(rT4bN0M0),在同步放化疗完成后 20 天出现严重的腰痛和双侧下肢无力。脊柱增强 MRI 显示多个腰椎结节状增强软脑膜病变和从 C2 到 C7 椎体水平的中央脊髓内 T2/FLAIR 高信号的长节段病变,提示软脑膜转移。脑脊液(CSF)分析显示白细胞增多、蛋白升高和葡萄糖明显降低。CSF 细胞学显示散在的大异型细胞,可疑为转移。脑非增强 MRI 显示右尾状核 T2/FLAIR 高信号病变,提示急性梗死伴出血转化或出血性脑转移。在评估过程中,他出现高热,并根据急性细菌性脑膜炎的治疗方案开始经验性静脉注射抗生素(头孢曲松、万古霉素和随后的美罗培南)。CSF 的革兰氏染色未显示任何细菌的存在,且标本在培养时无菌。他对经验性抗生素没有反应,病情逐渐恶化,最终因吸入性肺炎死亡。
本简要报告强调了在先前治疗过的头颈部 SCC 患者中,出现腰痛伴感觉运动障碍和自主神经功能障碍时,要警惕软脑膜癌病可能是病因。