Subdural Hematoma During Lorlatinib-Induced Regression of Leptomeningeal Carcinomatosis with Suspected Dural Involvement in ALK-Positive Lung Adenocarcinoma.

IF 1.1
Taiyo Kakefuda, Katsuyoshi Tomomatsu, Kaiki Suzuki, Kohei Umemoto, Yukihiro Horio, Jun Nishiyama, Naoki Hayama, Yoko Ito, Koichiro Asano, Tsuyoshi Oguma
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Abstract

Lorlatinib, a central nervous system (CNS)-penetrant anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitor, is effective in treating leptomeningeal carcinomatosis. A woman in her 30s with ALK-positive lung adenocarcinoma and leptomeningeal carcinomatosis developed an asymptomatic subdural hematoma (SDH) 7 weeks after starting lorlatinib, coinciding with the regression of leptomeningeal lesions. The posterior extent of the SDH appeared to be partially contiguous with the focal dural enhancement observed before treatment. Lorlatinib was continued under multidisciplinary supervision. The hematoma resolved without surgery and did not recur during the 6 years of treatment. SDH may occur during the rapid regression of leptomeningeal disease with suspected dural involvement under CNS-penetrant ALK inhibitor therapy.

lorlatinib诱导的alk阳性肺腺癌伴疑似硬脑膜受累的脑膜下血肿。
Lorlatinib是一种中枢神经系统(CNS)渗透性间变性淋巴瘤激酶(ALK)酪氨酸激酶抑制剂,可有效治疗轻脑膜癌。一名30多岁的alk阳性肺腺癌和脑膜轻脑癌患者在开始使用氯拉替尼7周后出现无症状硬膜下血肿(SDH),同时脑膜轻脑膜病变消退。SDH的后侧范围似乎与治疗前观察到的局灶性硬脑膜增强部分相邻。Lorlatinib继续在多学科监督下进行。在6年的治疗中,血肿没有手术解决,没有复发。SDH可能发生在疑似硬脑膜受累的轻脑膜疾病在中枢神经系统渗透ALK抑制剂治疗下的快速消退期间。
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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