| Literature DB >> 25047506 |
Hao-Wen Chuang1, Jia-Bin Liao, Huang-Chou Chang, Jyh-Seng Wang, Shong-Ling Lin, Pin-Pen Hsieh.
Abstract
We report the case of a 68-year-old man with a newly defined rare entity of a peripheral pulmonary tumor, consisting of a nodular papillary lesion with papillary structures containing ciliated columnar and goblet cells, as well as floating tumor cells in the mucin pool. The conspicuous mucin pool was observed to be mimicking colloid adenocarcinoma in a low-power view, particularly in a frozen section slide. We originally reported it as an adenocarcinoma during intraoperative consultation. Immunohistochemically, the tumor cells exhibited a similar immunophenotype to pulmonary adenocarcinoma, except for the presence of focal ciliated and basaloid cells, which we found using CK5/6 and P63 immunostaining. No KRAS or EGFR mutation was found. We revised the diagnosis to that of a ciliated muconodular papillary tumor (CMPT). Four years after a wedge resection, the patient remained free of tumors. Although the malignant potential of CMPT cannot be ignored, a wedge resection with a safe margin might be a treatment option for CMPT patients.Entities:
Keywords: ciliated muconodular papillary tumor; colloid adenocarcinoma; glandular papilloma; wedge resection
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Year: 2014 PMID: 25047506 DOI: 10.1111/pin.12179
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534