【南方日报】“怪脸女孩”在广州成功“换脸”,8年后她带着男友来见救命恩人

发布日期:2018-10-30

YUANWENLIANJIE:http://static.nfapp.southcn.com/content/201810/23/c1594925.html?colID=1374


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2010年做手术前的小燕

2010年做手术前的小燕

脸部肿物“蚕食”了她的整张脸

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中山大学附属口腔医院口腔颌面外科主任廖贵清教授推翻了以前的诊断。原来,小燕患的是“骨纤维异常增殖症”,这是一种骨发育异常疾病,原本应该发育成骨头的骨纤维异常增殖,形成巨大的肿瘤“蚕食”了她的面部。

手术8个月后复诊,她基本恢复了正常人的容貌

手术8个月后复诊,她基本恢复了正常人的容貌

一场惊心动魄的手术,医生为她重造了一张脸

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“当初我也是凭借着初生牛犊的勇气,如今可能会有更多顾虑。”回忆起8年前这场惊心动魄的手术,廖贵清感慨,要是今天,自己可能也不敢做这台手术。

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手术过程甚至比预判的更加凶险。廖贵清说,肿物如同海沙一样,软绵绵的没有边界。手术中,鲜血便像是海沙里涌出来的喷泉,凶猛难以止住。

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“医护人员急得脸都青了,我有一刻觉得她救不回来了,甚至质疑自己到底为什么会决定做这台手术。”廖贵清回忆。

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如今的小燕和男友,脖子上的围巾是她亲手织了送给帮助过自己的医护人员

如今的小燕和男友,脖子上的围巾是她亲手织了送给帮助过自己的医护人员

“怪脸”女孩最后也收获了爱情

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给廖教授送上锦旗

给廖教授送上锦旗

她可以带着残余肿瘤一直正常生存

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廖贵清介绍,当初手术,大约切除了小燕面部肿瘤的90%,重达两公斤多。位于颅内的肿块没有强行取尽,因为全部切除的话手术风险实在太大,小燕很可能撑不过去。而且,因为这不是恶性肿瘤,全部取出后会留下一个大的缺损,颅底反而会失去支撑。

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事实上,“骨纤维异常增殖症”并不罕见,只是严重程度不等,小燕的情况实属罕见。廖贵清说,医院还曾接诊一家父子三人全部患有此病的案例,因此该病或有遗传倾向,但具体病因仍不明。

“最早这一肿瘤生长在视神经位置,压迫视神经导致了失明。”廖贵清说,如果小燕当初发现视力下降后就能及时找出病因,不仅视力可以保留,容貌也不会到后来的地步。他提醒,患者如发现类似异常,一定要及时到正规医院就医。

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