Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
Anticancer Res. 2024 Nov;44(11):4969-4981. doi: 10.21873/anticanres.17322.
BACKGROUND/AIM: Human papillomavirus-independent (HPVI) squamous cell carcinoma (SCC) and adenosquamous carcinoma (ASC) of the uterine cervix are extremely rare. The aim of this study was to comprehensively describe the clinicopathological features, patient outcomes, and immunophenotypes of HPVI SCC and ASC.
We found four and two patients with HPVI SCC and ASC, respectively, and reviewed their electronic medical records and pathology slides. We also performed immunostaining for p16 and p53.
All except one patient underwent surgery. Two, one, and one patients with HPVI SCC were diagnosed as having IIIC1, IVA, and IVB diseases, respectively. Two patients with HPVI SCC experienced recurrences, and died of disease within nine months after treatment initiation. Both patients with HPVI ASC developed lung metastasis at four months post-operatively. HPVI SCCs and the squamous component of HPVI ASCs showed keratinizing, condylomatous, or poorly differentiated morphology. The glandular component of HPVI ASCs was gastric-type endocervical adenocarcinoma. None of the six tumors exhibited block positivity for p16. Two HPVI SCCs and one HPVI ASC displayed aberrant p53 expression.
HPVI SCC is a rare and aggressive cervical malignancy that presents initially as advanced-stage disease with poor prognosis. Although the patients with initial stage I and II HPVI ASC were treated with curative intent, distant metastases appeared in the lungs during the early course of treatment. Further investigations are necessary to clarify the association between histological features and clinical behavior of HPVI ASC.
背景/目的:人乳头瘤病毒(HPV)非依赖型(HPVI)宫颈鳞状细胞癌(SCC)和腺鳞癌(ASC)极其罕见。本研究旨在全面描述 HPVI SCC 和 ASC 的临床病理特征、患者结局和免疫表型。
我们分别发现了 4 例和 2 例 HPVI SCC 和 ASC 患者,并查阅了他们的电子病历和病理切片。我们还对 p16 和 p53 进行了免疫组化染色。
除了 1 例患者外,其余所有患者均接受了手术治疗。2 例、1 例和 1 例 HPVI SCC 患者分别被诊断为 IIIC1 期、IVA 期和 IVB 期疾病。2 例 HPVI SCC 患者复发,并在治疗开始后 9 个月内死于疾病。2 例 HPVI ASC 患者在术后 4 个月均发生肺部转移。HPVI SCC 和 HPVI ASC 的鳞状成分表现为角化、湿疣样或低分化形态。HPVI ASC 的腺成分表现为胃型宫颈内膜腺癌。这 6 个肿瘤均无 p16 弥漫阳性。2 例 HPVI SCC 和 1 例 HPVI ASC 显示异常的 p53 表达。
HPVI SCC 是一种罕见且侵袭性的宫颈恶性肿瘤,最初表现为晚期疾病,预后较差。尽管有初始 I 期和 II 期 HPVI ASC 患者接受了治愈性治疗,但在治疗早期肺部就出现了远处转移。需要进一步研究来阐明 HPVI ASC 的组织学特征与临床行为之间的关联。