| Literature DB >> 27804244 |
Shohei Yamamoto1, Kosuke Akiyama2, Ryota Kaneko2, Mayumi Hayashi2, Daisuke Toyama2, Keiichi Isoyama2.
Abstract
Kasabach-Merritt syndrome (KMS) is characterized by hemangioma associated with life-threatening thrombocytopenia, and is a consumptive coagulopathy. Although treatments available include corticosteroids, α-interferon, vincristine, and surgery, response may be unsatisfactory, and the mortality rate remains at approximately 30%. Although radiotherapy has been used effectively for KMS, it may cause growth retardation and secondary malignancy. We report a case of KMS in which hemangioma of the left thigh was successfully treated with low-dose radiotherapy (6 Gy in six fractions, weekly) after failure of corticosteroid therapy. No significant late effects due to the radiotherapy were noted at 5 year follow up. Thus, low-dose radiotherapy remains an important treatment method for KMS when patients fail to respond to other treatments.Entities:
Keywords: Kasabach-Merritt syndrome; late effect; low-dose radiotherapy
Mesh:
Year: 2016 PMID: 27804244 DOI: 10.1111/ped.13083
Source DB: PubMed Journal: Pediatr Int ISSN: 1328-8067 Impact factor: 1.524