carcinoma of the stomach
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2021 ◽  
Vol 48 (3) ◽  
pp. 38-40
Author(s):  
J. Ananiev ◽  
M. Hadzhi ◽  
K. Ivanova

Abstract Malignant tumors of the heart are rare. Even rarer, however, are metastases to the heart from cancers originating from the gastrointestinal tract. This case report involves a 63-year-old patient who presented into the clinic with a gastric ulcer and subsequent haemorrhage, and who died after sudden cardiac arrest. Autopsy revealed a metastatic involvement of the heart muscle from low-grade carcinoma of the stomach, as well as many other organ metastases.


Author(s):  
Vedant Chhibber

Gastric cancer growth is perhaps the most serious complex infection with high dismalness and mortality on the planet. This present sickness's sub-atomic components and hazard factors are hazy since various hereditary and ecological variables cause malignancy heterogeneity. With increasingly more articulation information gathered these days, an instance of essential squamous cell carcinoma of the stomach is accounted for, and the recently revealed cases are inspected. We can perform an integrative examination for this information to comprehend gastric disease's intricacy and distinguish agreement players for heterogeneous malignancy. In the current work, we screened the distributed cell articulation information and examined them with an integrative instrument joined with pathway and cell cosmology advancement examination. Thinking about the phase of the illness as well as patients' age and comorbidities. Trial approval is proposed to affirm this finding further.


2021 ◽  
Author(s):  
Shunsuke Uno ◽  
Yasuyuki Tanaka ◽  
Shinsuke Shibuya ◽  
Keijiro Okada ◽  
Shigehiko Fujii ◽  
...  

Author(s):  
Anais Jenvrin ◽  
Charles Lepine ◽  
Patrick-Yann Le Bozec ◽  
Julien Taieb ◽  
Claire Gallois

2021 ◽  
Vol 25 ◽  
pp. 200529
Author(s):  
Brian T Brinkerhoff ◽  
Mandy VanSandt ◽  
Skye C Mayo ◽  
Carol Beadling ◽  
Christopher L Corless

Medicine ◽  
2021 ◽  
Vol 100 (12) ◽  
pp. e24697
Author(s):  
Youpeng Li ◽  
Li Cui ◽  
Ying Chen ◽  
Furong Wang

2021 ◽  
pp. 1-3
Author(s):  
Edoardo Virgilio ◽  
Gian Luca Rampioni ◽  
Mariangela Lombardi ◽  
Genoveffa Balducci ◽  
Emanuela Pilozzi ◽  
...  

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Yuka Ooe ◽  
Kishichiro Watanabe ◽  
Isaya Hashimoto ◽  
Satoshi Takenaka ◽  
Toshihiko Ojima ◽  
...  

Abstract Background The majority of gastrointestinal tumors are adenocarcinomas. Rarely, there are other types of tumors, such as acinar cell carcinoma, and these are often called pancreatic-type acinar cell carcinomas. Among these tumors, some are differentiated into neuroendocrine components. A few of them are MiNENs. Case presentation The patient was an 80-year-old male who was referred to our hospital for treatment of a pedunculated gastric tumor. It was 5 cm in diameter and detected in the upper gastric body with upper GI endoscopy conducted to investigate anemia. In the biopsy, although hyperplasia of gastric gland cells was noted, no tumor cells were found. Retrospectively, the diagnosis was misdiagnosed. An operation was arranged because bleeding from the tumor was suspected as a cause of anemia and because surgical resection was considered to be desirable for accurate diagnosis. Hence, laparoscopic and endoscopic cooperative surgery was performed. In the pathological examination, several types of epithelial cells that proliferated in the area between the mucosa and deep inside the submucosa were observed. These consisted of acinar-glandular/trabecular patterns and solid. A diagnosis of pancreatic-type acinar cell carcinoma of the stomach with NET G2 and G3 was made based on characteristic cellular findings and the results of immunostaining tests. Each of them consisted of more than 30% of the lesion; a diagnosis of pancreatic-type mixed acinar neuroendocrine carcinoma (pancreatic-type MiNEN) of the stomach or a type of gastric MiNEN was obtained. Anemia was resolved after the operation, and the patient was discharged from the hospital without perioperative complications. Conclusions Pancreatic-type ACC of the stomach that is differentiated into neuroendocrine tumors is very rare. Hence, we report this case along with a literature review.


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