医学
朗格汉斯细胞组织细胞增多症
曲美替尼
MEK抑制剂
组织细胞增多症
肿瘤科
内科学
病理
MAPK/ERK通路
疾病
激酶
细胞生物学
生物
作者
Hong T Lin,Kathryn A. Wikenheiser‐Brokamp,Gavin Udstuen,Blaise V. Jones,Francis X. McCormack
出处
期刊:Chest
[Elsevier]
日期:2023-02-01
卷期号:163 (2): e53-e56
标识
DOI:10.1016/j.chest.2022.10.003
摘要
Multiple trials have demonstrated the efficacy of therapies targeting the RAS/MAPK pathway in children with Langerhans cell histiocytosis (LCH), but less is known about the success of this strategy in adults or in LCH that is the result of mutations other than BRAF V600E. A 53-year-old woman who has never smoked presented to our clinic with multisystem, multifocal LCH that resulted from an uncommon BRAF N486_P490del mutation. Low dose, and even intermittent, MEK inhibitor (trametinib) therapy was associated with rapid improvement in almost all of her disease manifestations, including regression of masses in her groin and neck, reduction in seizure frequency and intensity, improvement in white matter lesions on MRI, diabetes insipidus, dyspnea, and cognitive and memory functions. We conclude that MEK inhibitor therapy was effective for BRAF mutation-associated adult multisystem LCH, including CNS manifestations, in this patient.
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