Li Xiao, Wen Ming-Zhe, Su Li-Xin, Yang Xi-Tao, Han Yi-Feng, Fan Xin-Dong
Department of Interventional Therapy, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology and Shanghai Research Institute of Stomatology, Shanghai 200011, P.R. China.
Oncol Lett. 2019 Jan;17(1):981-989. doi: 10.3892/ol.2018.9661. Epub 2018 Nov 2.
Kaposiform haemangioendotheliomas (KHEs) complicated by the Kasabach-Merritt phenomenon (KMP) are rare and severe neoplastic lesions often associated with locally aggressive disease, consumption coagulopathy and high mortality rates. Current regimens have yet to achieve a satisfactory therapeutic effect. Thus, an effective and minimally invasive approach for treating complex KHE/KMP cases is necessary for clinical management. The present case series describes patients with KHE/KMP who underwent local suture ligation-assisted percutaneous sclerotherapy to minimise surgical trauma and ensure effective treatment. Between September 2015 and September 2017, 3 consecutive patients with KHE/KMP underwent staged local suture ligation-assisted percutaneous sclerotherapy. Of these patients, 2 presented with medical histories of corticosteroid treatment with unsatisfactory outcomes. The patients underwent a stepwise synthetic serial therapy programme consisting of percutaneous sclerotherapy and adjunctive pharmacotherapy accompanied by a suture ligation procedure. Clinical, radiological, pathological and laboratory data were analysed to evaluate the outcomes of the therapy. All patients were successfully managed with the proposed procedure. Significant relief of clinical symptoms and improvements in haematological indicators were achieved. No recurrence or complications were observed during regular follow-up (4, 19 and 28 months). In conclusion, local suture ligation-assisted percutaneous sclerotherapy was demonstrated to be a safe and effective treatment for KHE/KMP, being minimally invasive, involving simple manipulation and providing a clear treatment benefit in certain cases. Further studies involving larger sample sizes are required to thoroughly evaluate the procedure, which can potentially be used as a novel therapeutic option for KHE/KMP treatment.
卡波西型血管内皮瘤(KHEs)合并卡萨巴赫-梅里特现象(KMP)是罕见且严重的肿瘤性病变,常与局部侵袭性疾病、消耗性凝血病及高死亡率相关。目前的治疗方案尚未取得令人满意的治疗效果。因此,对于临床管理而言,一种有效且微创的方法来治疗复杂的KHE/KMP病例是必要的。本病例系列描述了接受局部缝合结扎辅助经皮硬化治疗的KHE/KMP患者,以尽量减少手术创伤并确保有效治疗。在2015年9月至2017年9月期间,连续3例KHE/KMP患者接受了分期局部缝合结扎辅助经皮硬化治疗。其中2例患者有皮质类固醇治疗病史但效果不佳。患者接受了由经皮硬化治疗和辅助药物治疗并伴有缝合结扎手术组成的逐步综合序贯治疗方案。分析临床、放射学、病理学和实验室数据以评估治疗效果。所有患者均通过所提议的手术成功治疗。临床症状得到显著缓解,血液学指标有所改善。在定期随访(4、19和28个月)期间未观察到复发或并发症。总之,局部缝合结扎辅助经皮硬化治疗被证明是一种安全有效的KHE/KMP治疗方法,具有微创性,操作简单,在某些情况下能带来明显的治疗益处。需要进一步开展更大样本量的研究以全面评估该手术,其有可能作为KHE/KMP治疗的一种新治疗选择。