Non-Small Cell Lung Carcinoma With Bilayered Architecture and TP53 Alteration: A Diagnostic Pitfall and a Potential Distinct Entity.

Thorac CancerNov 1, 2026

Yao Liu, Biao Zhang, Xiaobin Cui et al.

✦ AI-curated · Sources linked

Case in brief

A 75-year-old never-smoker had a 1.1-cm pulmonary nodule with an intact bilayered architecture, including a continuous basal cell layer. However, both luminal and basal cells showed marked high-grade atypia, diffuse strong P53 expression, and an increased Ki-67 index of approximately 10%. Sequencing identified a pathogenic TP53 mutation (p.A161T). The combined findings supported fully malignant carcinoma rather than benign bronchiolar adenoma/ciliated muconodular papillary tumor (BA/CMPT); the lesion was classified as non-small cell lung cancer, not otherwise specified, with a distinctive bilayered phenotype.

What made this case unusual

The lesion retained the basal cell layer usually regarded as a marker of BA/CMPT and benign behavior, yet showed high-grade atypia in both cell compartments and shared P53 expression, supporting malignancy.

Diagnostic / clinical pearl

An intact basal cell layer does not by itself establish benignity. In a bilayered pulmonary lesion, assess cytology alongside immunophenotypic and molecular findings before classifying it as BA/CMPT.

Why it matters

This morphology can mimic BA/CMPT and risk underdiagnosis; integrating cytologic, immunohistochemical, and sequencing findings supported correct classification in this case.

Source

Published in Thorac Cancer. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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