Ciliated Muconodular Papillary Tumors of the Lung Harboring Fusion: Case Report and Review of the Literature.
증례보고
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
2 patients presenting with CMPT as pulmonary nodules during clinical examinations.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Consequently, we conducted a review of relevant literature, summarizing the clinicopathological and molecular characteristics of CMPT to facilitate further research. Our insights enhance the understanding of this uncommon tumor and contribute to the expansion of its molecular alteration spectrum.
Ciliated muconodular papillary tumor (CMPT) is a rare pulmonary tumor, typically occurring in middle-aged and elderly individuals.
APA
Zhang X, Yuan W, et al. (2024). Ciliated Muconodular Papillary Tumors of the Lung Harboring Fusion: Case Report and Review of the Literature.. International journal of surgical pathology, 32(7), 1357-1363. https://doi.org/10.1177/10668969241226707
MLA
Zhang X, et al.. "Ciliated Muconodular Papillary Tumors of the Lung Harboring Fusion: Case Report and Review of the Literature.." International journal of surgical pathology, vol. 32, no. 7, 2024, pp. 1357-1363.
PMID
38321754 ↗
Abstract 한글 요약
Ciliated muconodular papillary tumor (CMPT) is a rare pulmonary tumor, typically occurring in middle-aged and elderly individuals. The molecular mutation spectrum of CMPT remains insufficiently explored. Commonly known driver gene alterations include , , , and rearrangement. This report details the clinicopathological features of 2 patients presenting with CMPT as pulmonary nodules during clinical examinations. Microscopic analysis revealed tumors with glandular or papillary structures, consisting of mucinous cells, ciliated columnar cells, and basal cells. Notably, both patients exhibited fusion, a finding not previously associated with CMPT. fusion serves as a target for therapy in various tumors, including non-small cell lung cancer, thyroid cancer, and colon cancer. Consequently, we conducted a review of relevant literature, summarizing the clinicopathological and molecular characteristics of CMPT to facilitate further research. Our insights enhance the understanding of this uncommon tumor and contribute to the expansion of its molecular alteration spectrum.
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