Pulmonary papillary adenoma with malignant transformation: report of one case and review of the literature.

C-myc FDG Pulmonary cancer development papillary adenoma

Journal

International journal of clinical and experimental pathology
ISSN: 1936-2625
Titre abrégé: Int J Clin Exp Pathol
Pays: United States
ID NLM: 101480565

Informations de publication

Date de publication:
2020
Historique:
received: 30 01 2020
accepted: 06 03 2020
entrez: 2 5 2020
pubmed: 2 5 2020
medline: 2 5 2020
Statut: epublish

Résumé

Pulmonary papillary adenoma is a rare tumor. A total of 32 cases was studied, include 31 cases in the literature. Most of the patients were asymptomatic, and tumor was usually discovered during a routine chest roentgenogram or with other disease. Most cases demonstrated benign behavior and there have been no recurrent cases after the operation or biopsy with the follow up of 6 to 120 months. However, there was some evidence indicating it can be locally aggressive or potentially malignant. We present the first case report of cancer development in a pulmonary papillary adenoma. In our case, the imaging findings progressed from initial well-defined border, without 18F-FDG accumulation, to one side rough edge after two years of follow up. Postoperative pathology revealed a partly well-defined tumor, without a fibrous capsule, but focally infiltrated the alveoli. Our case had definite areas of papillary adenoma, with focal acinar and micropapillary adenocarcinoma area near the central fibrosis. The papillary adenoma cells were with polarity and low expression of Ki67 and C-myc, without atypia or mitosis. But the adenocarcinoma cells were obviously different from them, with high expression of Ki67 and C-myc, indicating cancer development. MYC activation may play a role in tumorigenesis, and further investigation was needed. There was no EGFR mutation in both of the components.

Identifiants

pubmed: 32355529
pmc: PMC7191156

Types de publication

Case Reports

Langues

eng

Pagination

792-798

Informations de copyright

IJCEP Copyright © 2020.

Déclaration de conflit d'intérêts

None.

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Auteurs

Hongfei Ma (H)

Department of Thoracic Surgery, Qingdao Tumor Hospital, Qingdao Central Hospital Qingdao, China.

Yanli Wang (Y)

Department of PET/CT, Qingdao Central Hospital Qingdao, China.

Peng Chen (P)

Department of Thoracic Surgery, Qingdao Tumor Hospital, Qingdao Central Hospital Qingdao, China.

Zhixue Zhang (Z)

Department of Thoracic Surgery, Qingdao Tumor Hospital, Qingdao Central Hospital Qingdao, China.

Jing Xu (J)

Department of Pathology, The Second Affiliated Hospital of Medical College Qingdao University, Qingdao Central Hospital Qingdao, China.

Classifications MeSH