| Literature DB >> 14602331 |
Hironori Ishibashi1, Takuya Moriya, Yasushi Matsuda, Tetsu Sado, Yasushi Hoshikawa, Masayuki Chida, Masami Sato, Hironobu Sasano, Takashi Kondo.
Abstract
A case of primary mucinous cystadenocarcinoma of the lung is presented. The patient was a 42-year-old woman with a 5-cm left lung mass. Left lower lobectomy was performed and analysis of a frozen section revealed mucinous cystadenocarcinoma. The tumor was a fibrous, walled cyst containing abundant mucinous material. Sparse groups of malignant cells were microscopically observed in pools of mucin; thus, the tumor resembled mucinous cystadenocarcinoma that occurs in the ovary, appendix, or pancreas. The tumor we found is a very rare intrapulmonary neoplasm that is differentiated from a metastatic lesion and mucinous bronchoalveolar carcinoma by its very different clinical course and prognosis.Entities:
Mesh:
Year: 2003 PMID: 14602331 DOI: 10.1016/s0003-4975(03)00657-x
Source DB: PubMed Journal: Ann Thorac Surg ISSN: 0003-4975 Impact factor: 4.330