Yang Haili, Wang Jun, Song Li, Zou Haixiao
Department of Stomatology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi.
Department of Stomatology, Huangshi Central Hospital, Huangshi, Hubei.
Medicine (Baltimore). 2019 Jul;98(30):e16572. doi: 10.1097/MD.0000000000016572.
Epithelioid haemangioendothelioma (EHE) is a rare vascular neoplasm that primarily occurs in the soft tissues of the extremities, with "intermediate" or "borderline" malignant biological characteristics and a propensity for recurrence and metastasis. Oral cavity involvement is extremely rare, with only 5 reported cases of intraosseous EHE of the mandible. Herein, we report an additional case and review the related literature.
A 44-year-old man was referred to our institution with a 2-month history of left lower lip numbness and a 2-week history of painful swelling of the left mandible. He had received antibiotic treatment, which failed to ameliorate his symptoms. His medical and family histories were not significant.
Enhanced computed tomography revealed a poorly defined, 4.5 × 3.5 × 1.0 cm osteolytic lesion in the angle and ramus of the mandible, as well as an eroded lingual cortex. Histopathological examination confirmed a diagnosis of EHE.
Surgical resection was performed via segmental mandibulectomy and the defect was reconstructed using a vascularized fibular flap.
The patient did not exhibit signs of locoregional recurrence after 3 years of follow-up.
Intraosseous EHE of the mandible is an unpredictable lesion with a relatively benign course; however, the few reported cases of this disease do not highlight any factors that can predict the risk of locoregional recurrence or metastasis. There is also no consensus regarding the optimal treatment for intraosseous EHE; however, we recommend extensive local excision with close clinical follow-up.
上皮样血管内皮瘤(EHE)是一种罕见的血管肿瘤,主要发生于四肢软组织,具有“中间型”或“交界性”恶性生物学特征,且有复发和转移倾向。口腔受累极为罕见,仅有5例下颌骨骨内EHE的报道。在此,我们报告1例新增病例并复习相关文献。
一名44岁男性因左下唇麻木2个月、左下颌骨疼痛性肿胀2周转诊至我院。他曾接受抗生素治疗,但症状未改善。其既往史和家族史无特殊。
增强计算机断层扫描显示下颌骨角部及升支有一4.5×3.5×1.0 cm边界不清的溶骨性病变,舌侧皮质有侵蚀。组织病理学检查确诊为EHE。
通过节段性下颌骨切除术进行手术切除,并采用带血管蒂腓骨瓣修复缺损。
随访3年,患者未出现局部复发迹象。
下颌骨骨内EHE是一种病程相对良性但难以预测的病变;然而,该疾病的少数报道病例未突出任何可预测局部复发或转移风险的因素。对于骨内EHE的最佳治疗方法也尚无共识;不过,我们建议广泛局部切除并密切临床随访。