BACKGROUND:The 1991 Bethesda System for cervical/vaginal cytology reporting defined adequacy criteria for the unsatisfactory designation. Most laboratories have implemented these criteria, but clinical implications have not been established.

METHODS:Researchers at two university hospitals retrieved by computer search all unsatisfactory Papanicolaou (Pap) smears taken between January 1994 and July 1995. Of 71,872 total Pap smears, 208 (0.3%) were unsatisfactory (corresponding atypical rate of 9% and a dysplasia/carcinoma rate of 6.5%). Time interval to follow-up and clinicopathologic outcome were determined.

RESULTS:Approximately 26% of unsatisfactory Pap smears were from patients with a history of epithelial abnormalities. The majority (129 of 208 specimens; 62%) of follow-up Pap smears or biopsies occurred within 6 months, 5.7% within 6-12 months, and 1.4% in 12-18 months. Approximately 31% had no follow-up. The first repeat Pap smear or histologic specimen in 144 patients with follow-up was negative in 107 (74%), unsatisfactory in 6 (4%), atypical squamous cells of undetermined significance in 15 (10%), squamous intraepithelial lesion (SIL) in 13 (9%), and malignant in 3 (2%). Nonmalignant conditions contributing to the unsatisfactory smears on histologic specimens (12%) included cervicitis, endometritis, endometrial hyperplasia, and polyps. Progressive abnormalities after the first repeat specimen were noted in 7 patients (5%). A total of 23 of 144 initial unsatisfactory specimens (16% )were found to be from patients diagnosed with SIL or malignancy when all follow-up specimens were analyzed.

CONCLUSIONS:The majority of patients with unsatisfactory Pap smears had follow-up studies within 6 months. A significant number (16%) of those with follow-up had eventual diagnoses of SIL or neoplasia. Benign pathologic conditions also contributed to unsatisfactory smears. This patient subset was more likely to have a history of abnormalities, confirming the importance of peer/hierarchical review of unsatisfactory smears.

译文

背景 : 1991的Bethesda宫颈/阴道细胞学报告系统定义了不令人满意的指定的充分性标准。大多数实验室已经实施了这些标准,但尚未确定临床意义。
方法 : 两所大学医院的研究人员通过计算机搜索检索了1994年1月和1995年7月之间所有不满意的Papanicolaou (Pap) 涂片。在71,872的子宫颈抹片检查中,208 (0.3%) 不令人满意 (相应的非典型9% 率和不典型增生/癌率为6.5%)。确定了随访的时间间隔和临床病理结果。
结果 : 大约26% 的不满意的子宫颈抹片检查来自有上皮异常病史的患者。大多数 (208标本129; 62%) 的随访子宫颈抹片检查或活检发生在6个月内,5.7% 发生在6-12个月内,1.4% 发生在12-18个月内。大约31% 没有随访。144例随访患者的首次重复巴氏涂片或组织学标本阴性107例 (74% 例),不满意6例 (4%),非典型鳞状上皮细胞未明确意义15例 (10% 例),鳞状上皮内病变 (SIL) 13例 (9%),恶性3例 (2% 例)。导致组织学标本涂片不令人满意的非恶性疾病 (12%) 包括宫颈炎,子宫内膜炎,子宫内膜增生和息肉。在7例患者 (5%) 中发现了第一个重复标本后的进行性异常。在分析所有随访标本时,发现144例初始不满意标本中的23例 (16% 例) 来自诊断为SIL或恶性肿瘤的患者。
结论 : 大多数子宫颈抹片检查不满意的患者在6个月内进行了随访研究。大量 (16%) 随访的患者最终诊断为SIL或肿瘤。良性病理状况也导致涂片不令人满意。该患者子集更有可能有异常病史,这证实了对不满意的涂片进行同行/分级审查的重要性。

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