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α-2b干扰素成功治疗婴幼儿血管瘤

Successful treatment of infantile hemangiomas with interferon-alpha-2b.

作者信息

Chang E, Boyd A, Nelson C C, Crowley D, Law T, Keough K M, Folkman J, Ezekowitz R A, Castle V P

机构信息

Departments of Pediatrica, University of Michigan Medical Center, Ann Arbor, USA.

出版信息

J Pediatr Hematol Oncol. 1997 May-Jun;19(3):237-44. doi: 10.1097/00043426-199705000-00011.

Abstract

PURPOSE

Hemangiomas are benign tumors occurring in 10% of infants. A small percentage are complicated by blockage of vital structures, consumptive coagulopathy, or heart failure, resulting in a mortality of -20% of patients with complications. Here, we describe four infants with complicated hemangiomas responding to interferon-alpha-2b therapy.

PATIENTS AND METHODS

Four children with hemangiomas were treated with interferon-alpha-2b for complicating heart failure (1), visual impairment (2), or coagulopathy (1). Patients received interferon-alpha-2b alone or in conjunction with corticosteroid therapy over 2 to 9 months. Imaging studies and urinary basic fibroblast growth factor (bFGF) levels were used to monitor treatment response.

RESULTS

Three of four patients demonstrated involution of the hemangiomas with improvement in their coagulopathy or visual impairment. The fourth patient expired due to cardiac complications despite radiologic evidence of hemangioma involution. Side effects associated with interferon-alpha-2b treatment included elevated transaminases (2) and leukocytosis (2), which resolved upon completion of therapy. One patient developed mild gross motor delay (1), which improved after cessation of therapy. Decreased urinary bFGF levels correlated with hemangioma involution.

CONCLUSION

Interferon-alpha-2b therapy is an effective, well-tolerated treatment for complicated hemangiomas. Measurement of urinary bFGF levels may provide an objective method for monitoring treatment response.

摘要

目的

血管瘤是一种发生于10%婴儿的良性肿瘤。一小部分血管瘤会并发重要结构阻塞、消耗性凝血病或心力衰竭,导致并发症患者的死亡率约为20%。在此,我们描述了4例患有复杂性血管瘤且对α-2b干扰素治疗有反应的婴儿。

患者与方法

4例患有血管瘤的儿童因并发心力衰竭(1例)、视力损害(2例)或凝血病(1例)而接受α-2b干扰素治疗。患者在2至9个月内单独接受α-2b干扰素治疗或联合皮质类固醇治疗。采用影像学研究和尿碱性成纤维细胞生长因子(bFGF)水平监测治疗反应。

结果

4例患者中有3例血管瘤消退,凝血病或视力损害有所改善。第4例患者尽管影像学显示血管瘤消退,但因心脏并发症死亡。与α-2b干扰素治疗相关的副作用包括转氨酶升高(2例)和白细胞增多(2例),治疗结束后这些症状消失。1例患者出现轻度大运动发育迟缓,治疗停止后有所改善。尿bFGF水平降低与血管瘤消退相关。

结论

α-2b干扰素治疗是一种治疗复杂性血管瘤有效且耐受性良好的方法。测量尿bFGF水平可为监测治疗反应提供一种客观方法。

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