医学
朗格汉斯细胞组织细胞增多症
威罗菲尼
皮肤病科
耐火材料(行星科学)
疾病
组织细胞增多症
生活质量(医疗保健)
罕见病
重症监护医学
病理
内科学
癌症
转移性黑色素瘤
护理部
物理
天体生物学
作者
Norbert Neckel,Andrej Lissat,A von Stackelberg,Nadine Thieme,Mohemed-Salim Doueiri,Birgit Spors,Benedicta Beck‐Broichsitter,Max Heiland,Jan-Dirk Raguse
标识
DOI:10.1177/1758835919878013
摘要
Langerhans cell histiocytosis (LCH) is a diagnostic and therapeutic challenge. We report on a rare case of its primary oral manifestation that was treated successfully with the BRAF-specific agent, vemurafenib, after insufficient standard LCH treatment. This case underlines the importance of proper diagnosis and the evaluation of targeted therapy as a valuable tool in LCH treatment. Furthermore, the close collaboration of surgeons, oncologists, and dentists is mandatory to ensure adequate treatment, restore the stomatognathic system in debilitating post-treatment situations, improve quality of life, and ensure effective disease control in infants and young patients.
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