Cervical cytology in endometrial cancer patients with Lynch syndrome: opportunities for early detection and limitations

Q2 Medicine
Yongsang Park MD , Megan E. Dibbern MD , Kari L. Ring MD , Anne M. Mills MD
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引用次数: 0

Abstract

Introduction

Timely detection of endometrial carcinoma in Lynch syndrome patients ensures prompt treatment and appropriate cancer screening for the patient and impacted family members. While cervical cytology is utilized primarily in cervical cancer screening, endometrial glandular abnormalities can be identified as part of routine cervical cancer screening or during work-up for abnormal uterine bleeding.

Materials and Methods

We retrospectively evaluated cervical cytology samples from Lynch syndrome patients with endometrial carcinoma to determine how often atypical/malignant glandular cells were identified on prior/concurrent cytology.

Results

We identified 14 Lynch syndrome patients with cervical cytology available within a year of endometrial carcinoma diagnosis. The average patient age was 55 years (36-73). Cervical cytology preceded diagnostic biopsy in 57% and was concurrent in 43%. A glandular abnormality was identified on original diagnosis in 43% and ranged from atypical glandular cells (AGC), not otherwise specified to adenocarcinoma consistent with endometrial primary. In 4 cases, abnormal cervical cytology triggered the subsequent biopsy. Evaluation of 8 cases with accessible cytology slides revealed 2 previously unrecognized glandular abnormalities, leading to an abnormal rate of 63% among cases reviewed retrospectively and a final glandular abnormality detection rate of 57% based on either original or review diagnosis.

Conclusions

In summary, abnormal glandular cells were commonly identified in endometrial cancer patients with Lynch syndrome and led to endometrial cancer work-up and diagnosis in a subset. These results suggest that cervical cytology may have utility in endometrial cancer screening in this population and indicate that awareness of the patient’s familial cancer risk is important for maximizing sensitivity of this test. They also caution against primary human papillomavirus screening in the Lynch syndrome population, as this may result in missed opportunities for early endometrial carcinoma detection among these high-risk individuals.
林奇综合征子宫内膜癌患者的宫颈细胞学检查:早期检测的机会和局限性。
导言:及时发现林奇综合征患者的子宫内膜癌可以确保及时治疗,并为患者和受影响的家庭成员提供适当的癌症筛查。宫颈细胞学检查主要用于宫颈癌筛查,而子宫内膜腺体异常可在常规宫颈癌筛查或异常子宫出血检查中发现:我们对林奇综合征子宫内膜癌患者的宫颈细胞学样本进行了回顾性评估,以确定先前/当前细胞学检查中发现非典型/恶性腺细胞的频率:我们发现14名林奇综合征患者在确诊子宫内膜癌后一年内进行了宫颈细胞学检查。患者平均年龄为 55 岁(36-73 岁)。57%的患者在诊断性活组织检查前进行了宫颈细胞学检查,43%的患者同时进行了宫颈细胞学检查。43%的患者在最初诊断时就发现了腺体异常,范围从未作其他说明的非典型腺细胞(AGC)到与子宫内膜原发癌一致的腺癌。在 4 个病例中,宫颈细胞学异常引发了随后的活组织检查。对 8 例可获取细胞学切片的病例进行评估后,发现了 2 例之前未被发现的腺体异常,导致回顾性复查病例的异常率为 63%,根据原始诊断或复查诊断,最终腺体异常检出率为 57%:总之,在林奇综合征子宫内膜癌患者中,腺体细胞异常很常见,并导致了一部分患者的子宫内膜癌检查和诊断。这些结果表明,宫颈细胞学检查在这一人群的子宫内膜癌筛查中可能具有实用性,同时也表明,了解患者的家族性癌症风险对于最大限度地提高该检查的灵敏度非常重要。他们还提醒不要在林奇综合征人群中进行人类乳头瘤病毒初筛,因为这可能会导致这些高危人群错失早期子宫内膜癌检测的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of the American Society of Cytopathology
Journal of the American Society of Cytopathology Medicine-Pathology and Forensic Medicine
CiteScore
4.30
自引率
0.00%
发文量
226
审稿时长
40 days
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