scholarly journals Metastatic Breast Signet-Ring Cell Carcinoma from a Colonic Primary: Review of a Rare Case Report

2021 ◽  
Vol 14 (12) ◽  
Author(s):  
Ghazaleh Shaker ◽  
Hayedeh Haeri ◽  
Behnaz Jahanbin

Introduction: Colonic signet-ring cell carcinoma is a distinctive rare subtype of adenocarcinoma with a predilection for early metastasis. Among the rare extramammary metastatic adenocarcinomas to the breast, colonic signet-ring cell carcinomas constitute a small percentage. The distinction of a primary from a secondary breast signet ring cell carcinoma is indispensable since it may result in different therapeutic approaches. Here we presented a rare case of metastatic breast signet-ring cell carcinoma from a rectal origin and review its distinctive histopathologic features. Case Presentation: A 37-year-old woman presented with a breast mass 3 months after undergoing low anterior resection surgery to remove a rectal mass, diagnosed as signet ring cell carcinoma. Histopathologic examination of the core needle breast mass biopsy revealed tumor cells with signet-ring cell cytomorphology. The performed immunohistochemistry confirmed carcinoma of colonic origin. Conclusions: Colorectal signet-ring cell carcinoma is a rare and aggressive tumor. Its metastatic spread is most seen in the intra-abdominal area, with seldom reported cases of breast metastasis. Histologically, it can mimic a primary breast carcinoma, especially if no prior history of colonic origin exists. Accurate diagnosis is important since these 2 entities carry different therapeutic management. Proper immunophenotyping, obtaining a thorough clinical history and imaging studies facilitate a correct diagnosis.

Gut and Liver ◽  
2012 ◽  
Vol 6 (1) ◽  
pp. 129-131 ◽  
Author(s):  
Sun Hyung Kang ◽  
Woo Suk Chung ◽  
Chang Lim Hyun ◽  
Hee Seok Moon ◽  
Eaum Seok Lee ◽  
...  

Urology ◽  
2020 ◽  
Vol 143 ◽  
pp. e17-e19
Author(s):  
Jasmine J. Park ◽  
Zachary A. Snow ◽  
Kelly L. Lurz ◽  
Daniel C. Edwards ◽  
Lawrence H. Belkoff ◽  
...  

2018 ◽  
Vol 50 (3) ◽  
pp. 609-612
Author(s):  
Takayuki Minami ◽  
Norihiro Yuasa ◽  
Eiji Takeuchi ◽  
Hideo Miyake ◽  
Hidemasa Nagai ◽  
...  

2017 ◽  
Vol 102 (3-4) ◽  
pp. 141-144 ◽  
Author(s):  
Kosuke Hirano ◽  
Yukinori Yamagata ◽  
Teppei Tatsuoka ◽  
Yawara Kubota ◽  
Kazuyuki Saito ◽  
...  

Duodenal cancers are rare. Histopathologically, most duodenal cancers are adenocarcinoma. Signet ring cell carcinoma (SRCC) is a rare tumor more commonly found in the stomach than at other sites in the digestive tract. SRCC is extremely uncommon in the duodenum, with most of these tumors occurring in the ampulla. Until now, there are few case reports of duodenal cancers with SRCC. To accumulate case reports, we report a rare case of nonampullary duodenal bulb SRCC. A 74-year-old man was admitted to our hospital with melena. Esophagogastroduodenoscopy (EGD) showed a duodenal bulb ulcer. He was treated with a proton pump inhibitor. However, 1 month later, he was readmitted to our hospital with epigastric pain and nausea. A second EGD examination showed an ulcer at the duodenal bulb. Biopsies taken from the ulcer showed SRCC. Distal gastrectomy and duodenal bulb resection were performed. Histologic examination of the specimen showed a type 4 lesion located from the duodenal bulb to the pyloric antrum. The tumor was composed of poorly differentiated adenocarcinoma (por) with SRCC. The distal margin of the duodenal bulb was invaded with tumor. Therefore, pancreatoduodenectomy was performed. One year after the initial operation, he is alive and had no relapse. We described a rare case of por with SRCC of the duodenal bulb. It is important to bear in mind that an ulcer following an abnormal clinical course should be biopsied, and we have to select a suitable operation in cases of duodenal bulb cancer.


2008 ◽  
Vol 14 (37) ◽  
pp. 5763 ◽  
Author(s):  
Yoon Ho Ko ◽  
Chan-Kwon Jung ◽  
Soon Nam Oh ◽  
Tae Hee Kim ◽  
Hye Sung Won ◽  
...  

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