Hesselmann S, Micke O, Marquardt T, Baas S, Bramswig J H, Harms E, Willich N
Departments of Radiotherapy and Pediatrics, University Hospital Muenster, Albert-Schweitzer-Strasse 33, D-48149 Muenster, Germany.
Br J Radiol. 2002 Feb;75(890):180-4. doi: 10.1259/bjr.75.890.750180.
We describe the successful treatment of a neonate with Kasabach-Merritt syndrome who received local irradiation and interferon alpha therapy after failure of corticosteroid treatment. A male neonate, born after an uneventful pregnancy, had a huge haemangioma involving the upper right cervical region as well as severe thrombocytopenia. He was treated with corticosteroids, interferon alpha and radiotherapy. Prednisolone therapy (5 mg kg(-1) day(-1)) was started at 41 days of age. No therapeutic effect was observed after 2 weeks. At this time the tumour size had increased dramatically, platelet counts had decreased progressively and coagulation abnormalities had developed. Because corticosteroid therapy had been ineffective and the child was in a life-threatening condition, irradiation was delivered up to a total dose of 9.5 Gy in five fractions. Simultaneously, prednisolone therapy was slowly decreased and interferon alpha therapy (3 million U m(-2) day(-1)) was started and continued for 6 weeks. After irradiation with 9.5 Gy and beginning interferon alpha therapy, the tumour decreased in size and coagulation parameters normalized within 4 weeks. 6 months later, platelet counts and coagulation parameters were still normal. The tumour had further decreased in size. No acute severe side effects were observed. Radiation therapy combined with interferon alpha treatment is an alternative treatment modality when high dose corticoid steroid therapy has been ineffective in patients with Kasabach-Merritt syndrome, despite the risks of growth delay and secondary malignancy. In children showing no response to corticosteroids, radiotherapy and/or interferon alpha should be considered in Kasabach-Merritt syndrome.
我们描述了一名患有卡萨巴赫-梅里特综合征的新生儿的成功治疗案例,该患儿在皮质类固醇治疗失败后接受了局部照射和α干扰素治疗。一名男性新生儿,孕期正常,出生时右上颈部有一个巨大血管瘤,并伴有严重血小板减少症。他接受了皮质类固醇、α干扰素和放射治疗。泼尼松龙治疗(5 mg·kg⁻¹·d⁻¹)于41日龄开始。2周后未观察到治疗效果。此时肿瘤大小急剧增加,血小板计数逐渐下降,凝血异常也已出现。由于皮质类固醇治疗无效且患儿处于危及生命的状态,遂给予总剂量达9.5 Gy的分次照射,共5次。同时,泼尼松龙治疗逐渐减量,开始α干扰素治疗(300万U·m⁻²·d⁻¹)并持续6周。在给予9.5 Gy照射并开始α干扰素治疗后,肿瘤大小在4周内减小,凝血参数恢复正常。6个月后,血小板计数和凝血参数仍正常,肿瘤进一步缩小,未观察到急性严重副作用。当高剂量皮质类固醇治疗对卡萨巴赫-梅里特综合征患者无效时,尽管存在生长发育迟缓及继发恶性肿瘤的风险,放射治疗联合α干扰素治疗仍是一种替代治疗方式。对于对皮质类固醇无反应的儿童,卡萨巴赫-梅里特综合征应考虑放射治疗和/或α干扰素治疗。