Evidence map›Paper›PMID 38690654›Full record

ArticleThoracic cancer2024

Pulmonary pleomorphic carcinoma arising in mixed squamous and glandular papilloma: A case report.

Hiroyuki Nitanda, Taku Homma, Ryo Taguchi, Tetsuya Umesaki, Yoshinobu Ichiki, Hirozo Sakaguchi, Hironori Ishida

Abstract readCase Reports
In one paragraph

Article in Thoracic cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hiroyuki NitandaDepartment of General Thoracic Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.ORCID 0009-0003-7164-0769
Taku HommaDepartment of Pathology, Saitama Medical University International Medical Center, Hidaka, Japan.
Ryo TaguchiDepartment of General Thoracic Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.
Tetsuya UmesakiDepartment of General Thoracic Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.
Yoshinobu IchikiDepartment of General Thoracic Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.
Hirozo SakaguchiDepartment of General Thoracic Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.
Hironori IshidaDepartment of General Thoracic Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.ORCID 0000-0002-7325-1623

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solitary pulmonary papillomas (SPPs) are rare lung neoplasms. Histologically, SPP is classified into three subtypes, and mixed squamous and glandular papilloma (MP) is the rarest subtype. Although SPPs are considered benign tumors, there have been several reports on the synchronous malignant transformation in SPPs. An 82-year-old asymptomatic man was referred to our hospital for further examination of a 2.2 cm-sized left lung tumor. Pathology of bronchoscopic specimens showed the possibility of pulmonary papilloma but did not reveal any malignancy. The patient complained of bloody sputum during the eighth month after the initial visit. The size of the lesion had increased to 4.3 cm. These data suggested the existence of malignancy, and the patient underwent an operation. Histologically, the tumor was composed of fibrovascular cores and papillomatous fronds lined by pseudostratified columnar cells and mucin-filled goblet cells. Keratinizing squamous epithelium was also observed. Overall, the diagnosis of MP was obtained by fundamental histology. In addition, a solid part beneath mild atypical squamous epithelia, which was composed of malignant-appearing squamous cells and spindle-shaped atypical cells, was observed. The spindle portion was positive for cytokeratin AE1/AE3 and vimentin, and focally positive for alpha-smooth muscle actin (αSMA). The final diagnosis was pulmonary pleomorphic carcinoma (PPC) arising in the MP. Only two cases have been reported for atypical spindle tumor cells that are found in MP or bronchiolar adenoma/ciliated muconodular papillary tumor (BA/CMPT), which has histologically similar features to MP. This is the second case report of PPC arising in MP.

Indexed as

Lung NeoplasmsPapillomaAged, 80 and overCarcinoma, Squamous CellHumansMalemixed squamous and glandular papillomapulmonary pleomorphic carcinomasolitary papillomasurgical resection

Identifiers

PMID38690654
PMCPMC11168906

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