Background: The bronchopulmonary carcinoid tumor accounts for 1-2% of all adult malignancies of the lung and 20-30% of all carcinoid tumors. Cushing’s syndrome is the result of chronic exposure to increased concentration of exogenous or endo-genus cortisol hormone, and it is generally associated with central obesity, metabolic syndrome, and hypertension. Treatment is based on decreasing cortiso...

Abstract Carcinoid tumors are well differentiated neuroendocrine tumors with secretory components. These tumors are uncommon but the most common primary tumors of the distal small intestine. We present a rare terminal ileum carcinoid tumor presenting with a small bowel obstruction. A 65 years old man presented with intermittent, gen-eralized, dull and colicky abdominal pain accompanied with int...

abstract carcinoid tumors are well differentiated neuroendocrine tumors with secretory components. these tumors are uncommon but the most common primary tumors of the distal small intestine. we present a rare terminal ileum carcinoid tumor presenting with a small bowel obstruction. a 65 years old man presented with intermittent, gen-eralized, dull and colicky abdominal pain accompanied with int...

Background : Carcinoids are neuroendocrine tumors that typically occur in the gastrointestinal and respiratory systems. Carcinoid middle ear rare. Herein, we report a case of carcinoid developed spinal metastasis required decompression surgery more than 20 years after initial surgery.

carcinoid tumors of the bile duct are rare. despite cholangiocarcinoma, they grow more slowly and generally occur in younger patients and females. these tumors have a better prognosis and more disease-free survival. we present the case of a 25-year- old male with common bile duct (cbd) carcinoid tumor misdiagnosed as cholangiocarcinoma.

Carcinoid tumors are rare, slow-growing neuroendocrine neoplasms that often are indolent and may not become clinically apparent until there has been metastatic spread or evidence of carcinoid syndrome. Recent evidence has revealed that the overall incidence of carcinoid tumors has been steadily increasing, and although the disease was thought to be relatively benign, it is now considered one of...

BACKGROUND Pulmonary carcinoid tumors make up approximately one percent of all pulmonary tumors, and controversy exists regarding management and prognosis. We undertook a retrospective analysis of all patients who underwent surgical resection of pulmonary carcinoid tumors at our institution. METHODS From 1992 through 2014, 121 patients who underwent surgical resection of pulmonary carcinoid t...

Background: Carcinoid tumors usually originate from the enterochromaffin cells located in gastrointestinal tract and bronchopulmonary system. They may rarely arise in the urinary bladder, where this can be eventually miscued as any other commoner bladder neoplasms. The current study was conducted to connote an uncommon clinicopathological presentation by a carcinoid tu...

Primary ovarian carcinoid tumors of the ovary are rare and represent less than 0.1% of ovarian malignancy. One of its subtypes is the strumal carcinoid in which the thyroid tissue is seen in intimate association with carcinoid tumor. We here report a 47-year-old woman with strumal carcinoid of the right ovary presented with cessation of menstrual periods in the past 3 months and was referred du...

Lubarsch in 1888 first described the histology of carcinoid tumors (1) and the term carcinoid was proposed in 1907 by Oberndorfer (2) when described a submucosal tumor of the small intestine. Since then, carcinoid has been reported to develop in various organs, including gastrointestinal tract, liver, lung, breast, gall bladder, skin, trachea, parotid gland, and thymus (3). It is well known tha...