McCord M L, Stovall T G, Summitt R L, Ling F W
Department of Obstetrics and Gynecology, University of Tennessee, Memphis.
Obstet Gynecol. 1991 May;77(5):715-9.
The purpose of this study was to determine whether diagnostic cervical conization is necessary in the patient with a discrepancy between the Papanicolaou smear and the colposcopically directed biopsy(s). Patients eligible for the study had at least a two-degree discrepancy, eg, CIN III cytology and CIN I or less on colposcopic biopsies, or CIN II cytology with biopsies showing no dysplasia. Of the 786 records reviewed, 87 (11.1%) had such a discrepancy. Twelve of 87 patients (13.8%) were pregnant and ten of 87 (11.5%) failed to return after their initial colposcopic evaluation, leaving 65 patients in the study group. Of these, 20 of 65 (30.8%) were treated medically, nine (13.8%) had cryotherapy, and 36 (55.4%) underwent diagnostic cervical conization. Of patients undergoing cervical conization, three had microinvasive carcinoma of the cervix. Following medical therapy, only two of 20 patients (10%) had negative cytology, two (10%) had CIN I, five (25%) received additional therapy, and 11 (55%) were lost to follow-up. Seven patients did not return for follow-up Papanicolaou smear after medical treatment, and four did not return after their initial posttreatment Papanicolaou smear revealed persistent dysplasia. Of the nine patients treated with cryotherapy, six (66.7%) had a negative Papanicolaou smear at the time of their initial follow-up. The results of this study emphasize the importance of proceeding with diagnostic or therapeutic conization if a two-stage or greater discrepancy exists between the colposcopically directed biopsies and the cervical cytology. The risk of not diagnosing a microinvasive or invasive cervical carcinoma far outweighs the risk of conization.
本研究的目的是确定在巴氏涂片结果与阴道镜指导下活检结果不一致的患者中,诊断性宫颈锥切术是否必要。符合研究条件的患者至少存在两级差异,例如,巴氏涂片为CIN III级,而阴道镜活检为CIN I级或更低级别,或者巴氏涂片为CIN II级,而活检显示无发育异常。在审查的786份记录中,87份(11.1%)存在这种差异。87例患者中有12例(13.8%)怀孕,87例中有10例(11.5%)在初次阴道镜评估后未复诊,研究组剩余65例患者。其中,65例中有20例(30.8%)接受了药物治疗,9例(13.8%)接受了冷冻治疗,36例(55.4%)接受了诊断性宫颈锥切术。在接受宫颈锥切术的患者中,有3例患有宫颈微浸润癌。药物治疗后,20例患者中只有2例(10%)细胞学检查为阴性,2例(10%)为CIN I级,5例(25%)接受了额外治疗,11例(55%)失访。7例患者在药物治疗后未返回进行随访巴氏涂片检查,4例在初次治疗后的巴氏涂片显示持续发育异常后未返回。在接受冷冻治疗的9例患者中,6例(66.7%)在初次随访时巴氏涂片检查为阴性。本研究结果强调,如果阴道镜指导下活检与宫颈细胞学检查之间存在两级或更大差异,进行诊断性或治疗性锥切术的重要性。未诊断出宫颈微浸润癌或浸润癌的风险远超过锥切术的风险。