Danforth Olivia M, Tamulonis Karen, Vavra Kimberly, Oh Caleb, Brickman Arlen, Ebersole John, Cameron James, Mahon Brett, Kent Paul
Family Medicine Residency Program, Samaritan Health Services, Corvalis, OR.
Rush University Medical Center.
J Pediatr Hematol Oncol. 2019 Jul;41(5):382-387. doi: 10.1097/MPH.0000000000001459.
Pseudomyogenic hemangioendothelioma (PMH) is a rare neoplasm with vascular and sarcomatous elements, unpredictable course, and uncommon metastatic or fatal potential. Although systemic chemotherapy has been reported with variable success, generally accepted treatment is aggressive surgery with wide margins. Evidence-based treatment options are lacking, and lack of clear prognostic features poses a risk of undertreatment or overtreatment with associated morbidity and mortality. We report the use of initial systemic therapy with oral sirolimus (SIR) and IV zoledronic acid (ZA) to induce a sustained clinical response and avoidance of amputation in a 6-year-old boy. At 37 months after diagnosis, our patient remains in sustained clinical remission as documented by x-ray, MRI, and PET-CT with return of normal mobility/activity and resolution of swelling and pain. Literature review identified 20 cases of pediatric and young adult patients with PMH, of which 7 received some form of systemic therapy. To the best of our knowledge, our patient represents the youngest reported case of PMH and the first successful and limb-sparing utilization of systemic chemotherapy as primary treatment for PMH.
假性肌源性血管内皮瘤(PMH)是一种罕见的肿瘤,兼具血管和肉瘤成分,病程难以预测,具有不常见的转移或致命风险。尽管已有全身化疗取得不同程度成功的报道,但普遍认可的治疗方法是进行广泛切缘的积极手术。目前缺乏基于证据的治疗方案,且缺乏明确的预后特征,这存在治疗不足或过度治疗的风险,进而带来相关的发病率和死亡率。我们报告了一名6岁男孩,采用口服西罗莫司(SIR)和静脉注射唑来膦酸(ZA)进行初始全身治疗,以诱导持续的临床反应并避免截肢。诊断后37个月,经X线、MRI和PET-CT证实,我们的患者仍处于持续临床缓解状态,活动恢复正常,肿胀和疼痛消退。文献回顾发现了20例儿童和年轻成人PMH患者,其中7例接受了某种形式的全身治疗。据我们所知,我们的患者是报道的最年轻的PMH病例,也是首例成功采用全身化疗作为PMH主要治疗方法并保留肢体的病例。