Evidence map›Paper›PMID 38978975›Full record

ArticleMolecular and clinical oncology2024

Squamous cell carcinoma of uterine cervix with osteoclast‑like giant cells: A case report.

Ana Castillo, Cecília Perelló-Fabregat, Javier García-Gómez, Carolina Sanz, Lorena Valdivieso, Mireya Jimeno

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In one paragraph

Article in Molecular and clinical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ana CastilloDepartment of Pathology, Germans Trias i Pujol University Hospital, 08916 Barcelona, Spain.
Cecília Perelló-FabregatDepartment of Pathology, Germans Trias i Pujol University Hospital, 08916 Barcelona, Spain.
Javier García-GómezDepartment of Pathology, Germans Trias i Pujol University Hospital, 08916 Barcelona, Spain.
Carolina SanzDepartment of Pathology, Germans Trias i Pujol University Hospital, 08916 Barcelona, Spain.
Lorena ValdiviesoDepartment of Pathology, Germans Trias i Pujol University Hospital, 08916 Barcelona, Spain.
Mireya JimenoDepartment of Pathology, Germans Trias i Pujol University Hospital, 08916 Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Squamous cell carcinoma (SCC) is a common tumor of the uterine cervix, usually related to human papillomavirus (HPV). While osteoclast-like giant cells (OGCs) have been reported to be associated with tumors at various locations, to the best of our knowledge, only six cases have been reported in the cervix to date. The present study describes the case of a 38-year-old woman with a medical history of ectopic pregnancy and vaginal childbirth, who presented with coitorrhagia. On physical examination, a mass of ~4 cm was found in the uterine cervix. A biopsy of this lesion revealed infiltrating SCC, leading to a radical hysterectomy 2 months later. The surgical specimen displayed an exophytic lesion with a maximum diameter of 3.5 cm confined to the uterine cervix, histologically consistent with an infiltrating non-keratinizing SCC. There was a prominent intra- and peritumoral chronic inflammatory reaction, and a high number of OGCs. Immunohistochemically, tumoral cells were positive for cytokeratin βE12, epithelial membrane antigen, p40, p63 and p16, and negative for CD68, vimentin and CD163. OGCs exhibited an inverted expression pattern, with positivity only for histiocytic markers. PCR for HPV detection revealed a HPV 34 genotype (probable high oncogenic risk). This profile suggests the non-neoplastic nature of OGCs, i.e. they should be considered as part of the immune response to the tumor. To the best of our knowledge, this case is the seventh instance of SCC with OGCs in the uterine cervix. Similar findings in other organs, such as the breast, pancreas or stomach, have been associated with a favorable prognosis. While two of the three reported cases with poor outcomes in the uterine cervix had an associated sarcomatoid component, the limited number of cases described to date in this location does not yet allow for an accurate prediction of behavior.

Indexed as

case reportOGCsSCC of uterine cervixSCC with OGCs

Identifiers

PMID38978975
PMCPMC11228563

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