HPV-independent Squamous Cell Carcinoma With Choriocarcinomatous Differentiation in Uterine Cervix: Case Report With Molecular Characterization

This report pertains to a rare case of cervical squamous cell carcinoma (SCC) with choriocarcinomatous (CC) differentiation in a 77-yr-old woman. The patient developed lung and mediastinal metastases 3 mo after surgery and died at 5 mo. Histopathologically, the tumor shows a mixed pattern of SCC and CCs. Both SCC and CC components showed a mutant-type p53 immunostaining and no high-risk HPV mRNA signals by RNAscope. PD-L1 was positive in SCC and CC, with a combined positive score of 10 and 90, respectively. Short tandem repeat analysis indicated identical alleles among CC, SCC, and the normal tissues. Targeted next-generation sequencing demonstrated high tumor mutational burden (>10 mutations/Mb) and 2 common driver mutations [TP53 (c.853G>A) and TERT (c.-146C>T)]. This is the first report of an HPV-independent cervical SCC with choriocarcinomatous differentiation, supporting a clonal origin with divergent differentiation, and suggesting comprehensive therapies combining immunotherapy and pathway inhibitors for this aggressive cancer.

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Publication Details

Journal
International Journal of Gynecological Pathology
Published
2026-06-24
DOI
https://doi.org/10.1097/pgp.0000000000001180
Primary Topic
Gestational Trophoblastic Disease Studies
Type
article
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0.00
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article

HPV-independent Squamous Cell Carcinoma With Choriocarcinomatous Differentiation in Uterine Cervix: Case Report With Molecular Characterization

Bingjian Lü, Lei Y
International Journal of Gynecological Pathology
Gestational Trophoblastic Disease Studies
article

HPV-independent Squamous Cell Carcinoma With Choriocarcinomatous Differentiation in Uterine Cervix: Case Report With Molecular Characterization

Bingjian Lü, Lei Y
article en

Abstract

This report pertains to a rare case of cervical squamous cell carcinoma (SCC) with choriocarcinomatous (CC) differentiation in a 77-yr-old woman. The patient developed lung and mediastinal metastases 3 mo after surgery and died at 5 mo. Histopathologically, the tumor shows a mixed pattern of SCC and CCs. Both SCC and CC components showed a mutant-type p53 immunostaining and no high-risk HPV mRNA signals by RNAscope. PD-L1 was positive in SCC and CC, with a combined positive score of 10 and 90, respectively. Short tandem repeat analysis indicated identical alleles among CC, SCC, and the normal tissues. Targeted next-generation sequencing demonstrated high tumor mutational burden (>10 mutations/Mb) and 2 common driver mutations [TP53 (c.853G>A) and TERT (c.-146C>T)]. This is the first report of an HPV-independent cervical SCC with choriocarcinomatous differentiation, supporting a clonal origin with divergent differentiation, and suggesting comprehensive therapies combining immunotherapy and pathway inhibitors for this aggressive cancer.

International Journal of Gynecological Pathology
Women's Hospital, School of Medicine, Zhejiang University (CN)
Good health and well-being
Openalex Percentile: Top 6%
Gestational Trophoblastic Disease Studies
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