Department of Pediatrics, Gifu University, Gifu, Japan.
Head Neck. 2013 Aug;35(8):E258-61. doi: 10.1002/hed.23107. Epub 2012 Aug 21.
Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor of infancy and childhood. This tumor results in poor prognosis, and therefore, development of a more effective treatment is needed.
We describe an 11-year-old boy presenting with left facial palsy caused by aggressive KHE of the left temporomastoid region. He was treated with paclitaxel-based chemotherapy, because of the difficulty with complete surgical resection for anatomic factor, multiple lung metastases on diagnosis, and no response to conventional treatments. This treatment reduced the volume of primary tumor and lung metastatic lesions, but the efficacy was transitory.
Paclitaxel-based chemotherapy for aggressive KHE may be effective, therefore the multimodality therapy including paclitaxel of aggressive KHE, particularly in the head and neck, needs to be investigated in further studies.
卡波西样血管内皮细胞瘤(KHE)是一种罕见的婴儿和儿童期血管肿瘤。这种肿瘤的预后较差,因此需要开发更有效的治疗方法。
我们描述了一名 11 岁男孩,因左侧颞骨区域侵袭性 KHE 导致左侧面瘫。由于解剖因素导致完全手术切除困难、诊断时多发性肺转移和常规治疗无反应,他接受了紫杉醇为基础的化疗。这种治疗方法减少了原发性肿瘤和肺部转移病灶的体积,但疗效是暂时的。
紫杉醇为基础的化疗治疗侵袭性 KHE 可能有效,因此需要进一步研究包括紫杉醇在内的侵袭性 KHE 的多模式治疗,特别是在头颈部。