| Literature DB >> 33732635 |
Hyun Ee Yim1, Jang-Hee Kim1, Mi Sun Ahn2, Yongsik Jung3, Jin Roh1, So Hyun Park1, Tae-Gyu Kim1, Jin-Hyuk Choi2, Seok Yun Kang2.
Abstract
Pure mucinous breast carcinoma (PMBC) is characterized by clusters of tumor cells floating in abundant extracellular mucin and can be classified into paucicellular (Type A) and hypercellular (Type B) subtypes. However, the clinicopathological and genomic differences between these two subtypes have not been well characterized. We retrospectively investigated the clinicopathologic features of 45 cases of surgically removed PMBC (31 Type A and 14 Type B). We also performed whole-exome sequencing (WES) in eight cases of PMBC. We found that Type B PMBC occurs at an older age and shows more aggressive clinical behavior than Type A. WES analysis revealed that HYDIN was the most frequently mutated gene in both types of PMBC. Although Type B PMBC showed a tendency toward more frequent genetic alterations, there were no statistically significant differences between the two subtypes in single nucleotide variants or insertions or deletions of bases associated with moderate or high effects. Our results provide additional evidence that PMBCs are clinicopathologically and genetically heterogeneous and lack pathognomonic genetic alterations. Further, Type B PMBC is more frequently associated with lymph node metastasis than Type A.Entities:
Keywords: Immunohistochemistry; breast cancer; histological type; mucinous carcinoma; whole-exome sequencing
Year: 2021 PMID: 33732635 PMCID: PMC7956951 DOI: 10.3389/fonc.2020.558760
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244