Flaitz C M, Nichols C M, Adler-Storthz K, Hicks M J
Department of Stomatology, University of Texas Health Science Center-Houston, USA.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995 Jul;80(1):55-62. doi: 10.1016/s1079-2104(95)80016-6.
The purpose of this study was to characterize the clinical and histological features of intraoral squamous cell carcinoma in men who were seropositive for the human immunodeficiency virus and to evaluate viral cofactors (human papillomavirus, herpes simplex virus, Epstein-Barr virus), proliferative index (proliferating cell nuclear antigen), a factor associated with invasion (cathepsin D), and mutated tumor suppressor gene and proto-oncogene products (mutated p53, c-erbB-2). Four men who were seropositive for the human immunodeficiency virus and had acquired immunodeficiency syndrome presented with painful oral lesions of variable duration. Oral cancer risk factors included heavy tobacco use (four of four), heavy alcohol use (three of four), and previous radiotherapy (one of four). The lesions consisted of ulcers (two of four), a fungating mass (one of four), and papillary erythroplakia (one of four). Incisional biopsy specimens were obtained. High-stringency in situ hybridization was performed with DNA probes to the human papillomavirus (types 6/11; 16/18; 31/33/35) and Epstein-Barr virus: Immunocytochemical studies for the herpes simplex virus, proliferating cell nuclear antigen, cathepsin D, mutated p53, and c-erbB-2 were performed. Two lesions were moderately differentiated squamous cell carcinoma, one lesion was a basaloid squamous cell carcinoma, and one was carcinoma in situ. Stage of disease at diagnosis was II (one of four), III (two of four), and IV (one of four). Three cases were positive for the human papillomavirus, one case was positive for Epstein-Barr virus, and three cases were positive for the herpes simplex virus. C-erbB-2 was focally positive in one case, and mutated p53 was positive in a separate case.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究的目的是描述人类免疫缺陷病毒血清学阳性男性口腔鳞状细胞癌的临床和组织学特征,并评估病毒辅助因子(人乳头瘤病毒、单纯疱疹病毒、爱泼斯坦 - 巴尔病毒)、增殖指数(增殖细胞核抗原)、一种与侵袭相关的因子(组织蛋白酶D)以及突变的肿瘤抑制基因和原癌基因产物(突变型p53、c-erbB-2)。四名人类免疫缺陷病毒血清学阳性且患有获得性免疫缺陷综合征的男性出现了持续时间不等的口腔疼痛性病变。口腔癌危险因素包括大量吸烟(4例均有)、大量饮酒(4例中的3例)和既往放疗史(4例中的1例)。病变包括溃疡(4例中的2例)、蕈样肿物(4例中的1例)和乳头状红斑(4例中的1例)。获取了切取活检标本。使用针对人乳头瘤病毒(6/11型;16/18型;31/33/35型)和爱泼斯坦 - 巴尔病毒的DNA探针进行了高严谨度原位杂交:对单纯疱疹病毒、增殖细胞核抗原、组织蛋白酶D、突变型p53和c-erbB-2进行了免疫细胞化学研究。2例病变为中分化鳞状细胞癌,1例病变为基底样鳞状细胞癌,1例为原位癌。诊断时疾病分期为II期(4例中的1例)、III期(4例中的2例)和IV期(4例中的1例)。3例人乳头瘤病毒阳性,1例爱泼斯坦 - 巴尔病毒阳性,3例单纯疱疹病毒阳性。c-erbB-2在1例中局灶性阳性,突变型p53在另一例中阳性。(摘要截短于250字)