Goblet Cell Carcinoid

نویسنده

  • Hanlin L. Wang
چکیده

Goblet cell carcinoid (GCC) is a unique type of mixed endocrine-exocrine neoplasm, almost exclusively seen in the appendix. Historically, it has been variably termed as adenocarcinoid, mucinous carcinoid, microglandular carcinoma, amphicrine neoplasm, mucin-producing neuroendocrine tumor or carcinoma, and crypt cell carcinoma. GCC is the preferred term in the current literature, but this remains debatable. Extraappendiceal GCC is exceedingly rare and has been reported to occur in the stomach, small bowel and colon [1]. This tumor was first described by Gagne and colleagues in 1969 and the name of GCC was coined by Subbuswamy and colleagues in 1974.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Goblet cell carcinoid of the appendix

been identified in appendiceal carcinoids: the argentaffin-positive carcinoid, the nonargentaffin carcinoid, and the mucinous, goblet cell carcinoid. Therapy for carcinoids in the first 2 classes traditionally depends on tumour size and location with respect to the base of the appendix. The third type is rarer and behaves more aggressively, hence the literature suggests that management should b...

متن کامل

Appendiceal Goblet Cell Carcinoid Tumour: A Case of Unexpected Lung Metastasis

Goblet cell carcinoid tumours are often considered a subset of appendiceal neuroendocrine tumours which behave more aggressively. They usually metastasize through transcoelomic/peritoneal invasion and common sites include the ovaries, peritoneum, and liver. Metastases may have goblet cell carcinoid, signet ring cell carcinoma or classic carcinoid histology. We report the first case in the liter...

متن کامل

Goblet Cell Carcinoid Tumors of the Appendix: A Report of Two Cases, Review of a Rare Clinical Entity, and Guidelines for Treatment

Goblet cell carcinoid tumor is a rare clinical entity which is usually diagnosed either as acute appendicitis or advanced cancer. Its main characteristic is that the histological findings are between those of adenocarcinoma and typical carcinoid tumor of the appendix. Goblet cell carcinoid tumors appear almost exclusively in the appendix, and prognosis depends mainly on the stage and the subtyp...

متن کامل

Intestinal goblet cell carcinoid presenting with recurrent sterile peritonitis in a patient on peritoneal dialysis: a case report

BACKGROUND Goblet cell carcinoid is a rare variant of appendiceal carcinoid with mixed endocrine and exocrine features. The most common symptom and signs are abdominal pain, acute appendicitis and palpable mass. Additionally, abdominal pain is common in patient on peritoneal dialysis, which may confound the diagnosis in such patient. CASE PRESENTATION We report a 71- years- old woman on perit...

متن کامل

Adenocarcinoma ex goblet cell carcinoid in a renal transplant patient: a case report and review of the literature.

Adenocarcinoma ex goblet cell carcinoid is a rare neoplasm of appendiceal origin that contains features of both carcinoid tumor and adenocarcinoma. We report on a case of a 45-year-old woman, post-renal transplant who presented with ovarian metastases from this tumor. This appears to be the first report of an adenocarcinoma ex goblet cell carcinoid in a renal transplant recipient.

متن کامل

Adenocarcinoma Ex Goblet Cell Carcinoid of Appendix: Two Case Reports

Adenocarcinoma ex goblet cell carcinoid is a rare tumor incidentally found in specimens of appendicitis. Most patients present with acute abdomen, similar to acute appendicitis. Here we present two cases, which were found incidentally after operation. We give a brief summary about clinical and biological behavior of this entity.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2017