scholarly journals Endoscopic features of early-stage signet-ring-cell carcinoma of the stomach

2015 ◽  
Vol 7 (7) ◽  
pp. 741 ◽  
Author(s):  
Chainarong Phalanusitthepha ◽  
Kevin L Grimes ◽  
Haruo Ikeda ◽  
Hiroki Sato ◽  
Chiaki Sato ◽  
...  
2015 ◽  
Vol 8 (3) ◽  
pp. 466-471 ◽  
Author(s):  
Peter Y. Park ◽  
Teresa Goldin ◽  
John Chang ◽  
Maurie Markman ◽  
Madappa N. Kundranda

Background: Colorectal adenocarcinoma (CRC) is the third leading cause of death in the United States. One of the histologic subtypes of CRC is signet-ring cell carcinoma (SRCC), which has a distinct molecular and tumor biology from that of adenocarcinoma. Primary SRCC diagnosed at an early stage is very rare as most cases are detected at an advanced stage. Therefore, overall prognosis of SRCC is poor. Case Presentation: A 36-year-old female presented to her primary care physician with new-onset progressive right lower quadrant pain without any significant past medical or family history. Computed tomography scan of the abdomen and pelvis with contrast showed a 4.9 × 3.5 × 3.1 cm, lobulated, septated cystic mass arising from the cecum. The mass demonstrated wall enhancement and contained focal areas of coarse calcification. There was nodal involvement either locally or distally. The patient underwent right hemicolectomy, and pathology revealed a high-grade mucinous carcinoma with signet-ring cell variant invading through the muscularis propria and into the subserosal adipose tissue. The margins were negative for tumor, and no lymphovascular or perineural invasion was noted. None of the 14 resected pericolonic lymph nodes was positive for malignancy. Hence, she was staged as pT3, pN0, pMx-stage IIA. The appendix was not involved. Microsatellite instability testing showed the preservation of MLH1, PMS2, MSH2 and MSH6 proteins by IHC and PCR. Carcinoembryonic antigen level was within normal limits. Due to the patient's young age, aggressive histology and microsatellite-stable status, adjuvant fluropyrimidine (5-FU)-based therapy with the single agent capecitabine was initiated. The patient completed 6 months of adjuvant therapy and has been disease free for approximately 18 months. Conclusion: Primary SRCC of the cecum is a rare disease. Given the poor prognosis of these patients, early-stage disease with microsatellite-stable patients should be considered for adjuvant 5-FU-based therapy in an attempt to prevent recurrence.


2019 ◽  
Vol 90 (3) ◽  
pp. 529-531
Author(s):  
Tatsunori Minamide ◽  
Kensuke Shinmura ◽  
Hiroaki Ikematsu ◽  
Tomonori Yano

2018 ◽  
Vol 50 (2) ◽  
pp. e130-e131
Author(s):  
V. De Re ◽  
L. Caggiari ◽  
G. Miolo ◽  
V. Canzonieri ◽  
M. Fornasarig ◽  
...  

2001 ◽  
Vol 59 (2) ◽  
pp. 90-91
Author(s):  
Wen San Ji ◽  
Koichiro Kumai ◽  
Hiroyuki Imaeda ◽  
Koichi Aiura ◽  
Haruhiko Ogata ◽  
...  

1994 ◽  
Vol 30 (2) ◽  
pp. 325
Author(s):  
Ki Nam Lee ◽  
Jong Cheol Choi ◽  
Kyung Jin Nam ◽  
Jae Ik Kim ◽  
Byeung Ho Park ◽  
...  

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