Wang Zhaoling, Liu Ying, Yang Lu, Gu Ling, He Yuhong, Huang Diyan, Zhu Guoxiong
Department of Stomatology, General Hospital of Jinan Military Command Jinan 250031, Shandong, China.
Int J Clin Exp Pathol. 2015 Jan 1;8(1):1063-7. eCollection 2015.
Aggressive angiomyxoma, mostly originating in the female pelvis and peritoneum or in the male analogous sites, is a rare mesenchymal neoplasm characterized with infiltrative growth to adjacent tissue and local recurrence after primary excision. Herein, we report a case of aggressive angiomyxoma of maxilla in a 60-year-old male patient for its rarity. The patient presented with a one-year history of progressively enlarging maxillary mass on left side. Before referred to our hospital, he was given a biopsy and diagnosed as aggressive angiomyxoma by immunohistochemical staining. After that, he underwent 60 Gy radiotherapy. Unfortunately, CT scan showed bigger mass infiltrated to adjacent facial soft tissues and bones compared with that of before radiotherapy. Besides that, he began to suffer with ingravescent headache. The mass was surgically removed and the diagnosis was confirmed by immunohistology in our hospital. As a case of aggressive angiomyxoma occurred in a rare site and experienced an ongoing growth in spite of radiotherapy, its characteristics was discussed with a brief literature review, which may aid further understanding of aggressive angiomyoma.
侵袭性血管黏液瘤多起源于女性盆腔和腹膜或男性的类似部位,是一种罕见的间叶性肿瘤,其特征为向邻近组织浸润性生长且在初次切除后局部复发。在此,我们报告一例60岁男性上颌骨侵袭性血管黏液瘤病例,因其罕见性。该患者左侧上颌肿物渐进性增大1年。在转诊至我院之前,他接受了活检,并通过免疫组织化学染色诊断为侵袭性血管黏液瘤。之后,他接受了60 Gy的放射治疗。不幸的是,CT扫描显示与放疗前相比,肿物浸润至邻近面部软组织和骨骼且更大了。除此之外,他开始出现进行性加重的头痛。肿物在我院接受了手术切除,并通过免疫组织学确诊。作为一例发生在罕见部位且尽管接受了放疗仍持续生长的侵袭性血管黏液瘤病例,我们结合简短的文献复习讨论了其特征,这可能有助于进一步了解侵袭性血管黏液瘤。