Croteau Stacy E, Gupta Deepti
Division of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts, USA.
Department of Pediatrics, Division of Dermatology, Seattle Children's Hospital/University of Washington School of Medicine, Seattle, Washington, USA.
Semin Cutan Med Surg. 2016 Sep;35(3):147-52. doi: 10.12788/j.sder.2016.048.
Kasposiform hemoangioendothelioma (KHE) and tufted angioma (TA) are classifed as vascular tumors with locally aggressive and benign growth potential, respectively, within the classification schema proposed by the International Society for the Study of Vascular Anomalies. A unique feature of these vascular tumors is the risk of Kasabach-Merritt phenomenon (KMP), a severe thrombocytopenia with mild to moderate coagulopathy resulting from intralesional platelet trapping. As with many vascular anomalies, accurate description of clinical course, responses to therapy, and long-term outcomes have been hindered by lesion misidentification, imprecise nomenclature, and lack of prospective, randomized clinical trials to assess therapeutic efficacy. The classic dermatologic features of these lesions can facilitate diagnosis for the astute provider; however, the absence of or unusual integumentary involvement or presentation in a less common age group (adolescents/adults) poses a diagnostic challenge. Current approaches to the management of KHE/TA are often informed by lesion features such as presence of KMP, extent and location of the tumor, and symptomatology. Evidence-based treatment guidelines are limited. Corticosteroids, vincristine, interferon, multi-agent regimens and newer therapies, such as sirolimus, have demonstrated efficacy in patient series. The use of surgical excision and interventional radiology guided therapies have been described with mixed clinical benefit. Collaboration among emerging vascular anomaly centers and an increasing number of providers across subspecialties with interest in this field are facilitating the development of standardized approaches to diagnosis and management. The rarity of KHE-spectrum lesions and the heterogeneity of clinical manifestations necessitate rationally designed, multisite clinical trials to investigate risk stratification schemas and formally evaluate the short and long-term efficacy of available and novel therapies.
卡波西样血管内皮瘤(KHE)和簇状血管瘤(TA)在国际血管异常研究学会提出的分类方案中,分别被归类为具有局部侵袭性和良性生长潜能的血管肿瘤。这些血管肿瘤的一个独特特征是存在卡萨巴赫-梅里特现象(KMP)的风险,即由于病灶内血小板滞留导致的严重血小板减少伴轻度至中度凝血病。与许多血管异常一样,临床病程、治疗反应和长期预后的准确描述一直受到病变误诊、命名不精确以及缺乏评估治疗效果的前瞻性随机临床试验的阻碍。这些病变的典型皮肤特征有助于经验丰富的医生进行诊断;然而,在不太常见的年龄组(青少年/成人)中缺乏或出现不寻常的皮肤受累或表现则构成诊断挑战。目前KHE/TA的治疗方法通常依据病变特征,如KMP的存在、肿瘤的范围和位置以及症状学。基于证据的治疗指南有限。皮质类固醇、长春新碱、干扰素、多药联合方案以及西罗莫司等较新的疗法在患者系列研究中已显示出疗效。手术切除和介入放射学引导治疗的应用已被描述,但临床获益不一。新兴的血管异常中心与越来越多对该领域感兴趣的各亚专业医生之间的合作,正在促进标准化诊断和管理方法的发展。KHE谱系病变的罕见性和临床表现的异质性使得有必要进行合理设计的多中心临床试验,以研究风险分层方案并正式评估现有和新型疗法的短期和长期疗效。