Papillary immature metaplasia (immature condyloma) of the uterine cervix: A report of three cases in postmenopausal women and review of the literature

IF 0.5
Human Pathology Reports Pub Date : 2026-03-01 Epub Date: 2026-02-19 DOI:10.1016/j.hpr.2026.300827
Jiqing Ye , Layla Hatem , Fadi Hatem , Sajeena Geevarghese , Dijana Poljak , Xi Wang , Huina Zhang
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Abstract

Objective

Papillary immature metaplasia (PIM) of the uterine cervix is an uncommon low-grade exophytic papillary squamous intraepithelial lesion characterized by immature metaplastic morphology. It typically involves the proximal transformation zone, often extending into the endocervical canal, and has been reported almost exclusively in premenopausal women. PIM is poorly recognized, partly because it is not included as a distinct entity in the current WHO classification of tumors. Because of its proximal location, papillary architecture, and morphologic immaturity, PIM can pose significant diagnostic challenges, particularly in postmenopausal patients.

Methods

Three cases of PIM occurring in postmenopausal women were described, and a review of the literature was performed.

Key findings

All three cases showed typical histopathologic features of PIM; notably, two patients presented with postmenopausal bleeding and underwent repeated endometrial sampling. Among these three cases, only one case tested positive for low-risk HPV infection based on the available testing panels. Immunohistochemically, all three lesions showed diffuse GATA3 expression, suggesting its potential utility as an adjunctive marker for PIM. Review of literature shows it occurs almost exclusively in premenopausal women presenting with abnormal screening cytology or a cervical mass. Most cases (77%) are associated with low-risk HPV, predominantly types 6 and 11, and demonstrate a low Ki-67 proliferation index.

Conclusion

PIM is a poorly recognized, low-grade papillary proliferative lesion of the uterine cervix associated with low-risk HPV infection. We report three cases of PIM in postmenopausal patients to increase awareness and improve recognition of this entity, thereby helping prevent both overdiagnosis and underdiagnosis.
宫颈乳头状未成熟皮化生(未成熟尖锐湿疣):绝经后妇女报告3例并复习文献
目的宫颈乳头状未成熟化生(PIM)是一种罕见的低级别外生性乳头状鳞状上皮内病变,其特征为未成熟的化生形态。它通常涉及近端转化区,经常延伸到宫颈内管,并且几乎只在绝经前妇女中报道。PIM未被充分认识,部分原因是它未被列入目前世卫组织肿瘤分类的一个独特实体。由于其近端位置,乳头状结构和形态不成熟,PIM可带来重大的诊断挑战,特别是绝经后患者。方法对3例绝经后妇女发生PIM的病例进行分析,并复习相关文献。主要发现3例均表现出典型的PIM组织病理特征;值得注意的是,两名患者出现绝经后出血,并进行了反复的子宫内膜取样。在这三个病例中,根据现有的检测小组,只有一个病例的低风险HPV感染检测呈阳性。免疫组织化学结果显示,所有3个病变均弥漫性表达GATA3,提示其作为PIM辅助标志物的潜在用途。文献回顾显示,它几乎只发生在绝经前妇女,表现为异常筛查细胞学或宫颈肿块。大多数病例(77%)与低风险HPV相关,主要是6型和11型,并表现出低Ki-67增殖指数。结论pim是一种与低危HPV感染相关的低级别宫颈乳头状增生性病变。我们报告三例绝经后患者的PIM,以提高对这一实体的认识和认识,从而有助于防止过度诊断和诊断不足。
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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