year old child. JSCR 2012 9:3 Signet cell carcinomas of the colon are well documented in the adult population, but this cancer incidence is very low in the adolescent population. A 17 year old male child presented with one month of progressive abdominal pain. CT scan of the abdomen showed significant abnormality involving the ascending colon characterized as marked mural thickening. Biopsy results indicated signet ring cell carcinoma. Signet cell carcinoma is presumed to be caused by genetic mutations just like the other colorectal cancers. Treatment for signet cell carcinoma is the same as other colorectal cancer. Surgery is part of the standard management of patients with colon and rectal cancer stages I, II and III. Signet cell cancer ha...
Signet ring cell carcinoma is an epilethial malignancy characterized by the histologic appearance of...
Nine cases of signet-ring carcinoma have been observed from among 800 consecutive histologic cases d...
Lynch syndrome is an autosomal dominant disorder in which one's DNA mismatch repair mechanism is imp...
Signet ring cell carcinoma (SRCC), a variant of adenocarcinoma, is defined by the presence of more t...
Copyright © 2013 Özgül Pamukçu et al.This is an open access article distributed under the Creativ...
Introduction: Signet cell carcinoma (SRCC)of the rectum is a rare subtype of the rectum cancer which...
Background. Carcinoma of colon is rare in children and adolescents. The staging criteria of the carc...
Signet-ring cell carcinoma of the colon is a rare and aggressive form of colonic cancer which is ass...
Colorectal cancer (CRC) remains the second leading cause of cancer-related deaths in the United Stat...
Primary signet ring cell carcinoma (SRC) of colon at early stage is quite rare. Only 26 cases were r...
While colorectal carcinoma is a common gastrointestinal cancer in adults, it is rare in pediatrics w...
The incidence of colorectal cancer is increasing in patients younger than 50 years. In this populati...
Colorectal cancer is a common malignant neoplasm in adults, with a peak incidence of 60-79 years. Ab...
Background: Colorectal adenocarcinoma (CRC) is the third leading cause of death in the United States...
Carcinoma of the colon is usually associated with conditions such as familial adenomatous polyposis,...
Signet ring cell carcinoma is an epilethial malignancy characterized by the histologic appearance of...
Nine cases of signet-ring carcinoma have been observed from among 800 consecutive histologic cases d...
Lynch syndrome is an autosomal dominant disorder in which one's DNA mismatch repair mechanism is imp...
Signet ring cell carcinoma (SRCC), a variant of adenocarcinoma, is defined by the presence of more t...
Copyright © 2013 Özgül Pamukçu et al.This is an open access article distributed under the Creativ...
Introduction: Signet cell carcinoma (SRCC)of the rectum is a rare subtype of the rectum cancer which...
Background. Carcinoma of colon is rare in children and adolescents. The staging criteria of the carc...
Signet-ring cell carcinoma of the colon is a rare and aggressive form of colonic cancer which is ass...
Colorectal cancer (CRC) remains the second leading cause of cancer-related deaths in the United Stat...
Primary signet ring cell carcinoma (SRC) of colon at early stage is quite rare. Only 26 cases were r...
While colorectal carcinoma is a common gastrointestinal cancer in adults, it is rare in pediatrics w...
The incidence of colorectal cancer is increasing in patients younger than 50 years. In this populati...
Colorectal cancer is a common malignant neoplasm in adults, with a peak incidence of 60-79 years. Ab...
Background: Colorectal adenocarcinoma (CRC) is the third leading cause of death in the United States...
Carcinoma of the colon is usually associated with conditions such as familial adenomatous polyposis,...
Signet ring cell carcinoma is an epilethial malignancy characterized by the histologic appearance of...
Nine cases of signet-ring carcinoma have been observed from among 800 consecutive histologic cases d...
Lynch syndrome is an autosomal dominant disorder in which one's DNA mismatch repair mechanism is imp...