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痣样基底细胞综合征是基底细胞上皮瘤的一种罕见的类型,临床上很少见,现报道如下:患者孙××,男,32岁,湖北应城县人,农民,未婚,汉族。主诉:双侧面部反复肿胀瘘道溢脓10余年。现病史:自觉右下后磨牙疼痈,发烧、伴面部肿胀,张口受限。到当地公社卫生院穿刺有脓性分泌物,经右耳屏前切排以及静脉点滴青霉素伤口愈合。以后双侧面部及颌下反复肿胀,反复切排,遗留瘘道经久不愈达10余年。1983年12月又复发到本院口腔科
Mole-like basal cell syndrome is a rare type of basal cell epithelial tumor, clinically rare, are reported as follows: Patient Sun × ×, male, 32 years old, Hubei Yingcheng people, peasants, unmarried, Han nationality. Chief Complaint: bilateral repeated fistula overflowing the face more than 10 years. Current medical history: conscious right lower back after a molar pain, fever, with facial swelling, mouth restriction. To the local commune hospital puncture purulent secretions, cut through the right trash before the row and intravenous penicillin wound healing. After bilateral facial and submandibular repeated swelling, repeated cutting row, leaving the fistula unhealed for more than 10 years. In December 1983 it recurred to our department of dentistry