Invasive micropapillary carcinoma of the ampulla of Vater with extensive lymph node metastasis: Report of a case

Surgery Today ◽  
2010 ◽  
Vol 40 (12) ◽  
pp. 1197-1200 ◽  
Author(s):  
Takeo Fujita ◽  
Masaru Konishi ◽  
Naoto Gotohda ◽  
Shinichiro Takahashi ◽  
Toshio Nakagohri ◽  
...  
2014 ◽  
Vol 12 (1) ◽  
pp. 84 ◽  
Author(s):  
Kenji Taketani ◽  
Eriko Tokunaga ◽  
Nami Yamashita ◽  
Kimihiro Tanaka ◽  
Yoko Zaitsu ◽  
...  

2022 ◽  
Vol 13 (1) ◽  
Author(s):  
Qianqian Shi ◽  
Kang Shao ◽  
Hongqin Jia ◽  
Boyang Cao ◽  
Weidong Li ◽  
...  

AbstractInvasive micropapillary carcinoma (IMPC) has very high rates of lymphovascular invasion and lymph node metastasis and has been reported in several organs. However, the genomic mechanisms underlying its metastasis are unclear. Here, we perform whole-genome sequencing of tumor cell clusters from primary IMPC and paired axillary lymph node metastases. Cell clusters in multiple lymph node foci arise from a single subclone of the primary tumor. We find evidence that the monoclonal metastatic ancestor in primary IMPC shares high frequency copy-number loss of PRDM16 and IGSF9 and the copy number gain of ALDH2. Immunohistochemistry analysis further shows that low expression of IGSF9 and PRDM16 and high expression of ALDH2 are associated with lymph node metastasis and poor survival of patients with IMPC. We expect these genomic and evolutionary profiles to contribute to the accurate diagnosis of IMPC.


2021 ◽  
Vol 12 (12) ◽  
Author(s):  
Jianke Lv ◽  
Qianqian Shi ◽  
Yunwei Han ◽  
Weidong Li ◽  
Hanjiao Liu ◽  
...  

AbstractInvasive micropapillary carcinoma (IMPC) is a special histological subtype of breast cancer, featured with extremely high rates of lymphovascular invasion and lymph node metastasis. Based on a previous series of studies, our team proposed the hypothesis of “clustered metastasis of IMPC tumor cells”. However, the transcriptomics characteristics underlying its metastasis are unknown, especially in spatial transcriptomics (ST). In this paper, we perform ST sequencing on four freshly frozen IMPC samples. We draw the transcriptomic maps of IMPC for the first time and reveal its extensive heterogeneity, associated with metabolic reprogramming. We also find that IMPC subpopulations with abnormal metabolism are arranged in different spatial areas, and higher levels of lipid metabolism are observed in all IMPC hierarchical clusters. Moreover, we find that the stromal regions show varieties of gene expression programs, and this difference depends on their distance from IMPC regions. Furthermore, a total of seven IMPC hierarchical clusters of four samples share a common higher expression level of the SREBF1 gene. Immunohistochemistry results further show that high SREBF1 protein expression is associated with lymph node metastasis and poor survival in IMPC patients. Together, these findings provide a valuable resource for exploring the inter- and intra-tumoral heterogeneity of IMPC and identify a new marker, SREBF1, which may facilitate accurate diagnosis and treatment of this disease.


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