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Article

Mucinous cells in type 1 pulmonary congenital cystic adenomatoid malformation as mucinous bronchioloalveolar carcinoma precursors.

The American journal of surgical pathology - 1 Jun 2007

Lantuejoul Sylvie, Nicholson Andrew G, Sartori Giuliana, Piolat Christian, Danel Claire, Brabencova Eva, Goldstraw Peter, Brambilla Elisabeth, Rossi Giulio

Abstract excerpt

Type 1 congenital cystic adenomatoid malformation (CCAM), the most frequent malformation of the lung, is the only type to present intracystic mucinous cell clusters, which may form beyond the cysts extracystic mucinous proliferation resembling mucinous bronchioloalveolar carcinomas (BACs). As muc...

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Share to Adenocarcinoma, Bronchiolo-Alveolar
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17527088
DOI: 10.1097/01.pas.0000249444.90594.27

Genes

CDX2
FHIT
MUC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17527088-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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