Carcinoid Lung Tumor
Medical Author:
George Schiffman, MD, FCCP
George Schiffman, MD, FCCPDr. Schiffman received his B.S. degree with High Honors in biology from Hobart College in 1976. He then moved to Chicago where he studied biochemistry at the University of Illinois, Chicago Circle. He attended Rush Medical College where he received his M.D. degree in 1982 and was elected to the Alpha Omega Alpha Medical Honor Society. He completed his Internal Medicine internship and residency at the University of California, Irvine. Medical Editor:
Melissa Conrad Stöppler, MD, Chief Medical Editor
Melissa Conrad Stöppler, MD, Chief Medical EditorMelissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology.
Carcinoid Lung Tumor OverviewThere are a few types of tumors that can neither be classified as benign (noncancerous) or malignant (cancerous). Their clinical behavior falls between the two classifications of benign and malignant, and they have sometimes been called "midway" tumors. They were so named in an attempt to designate these tumors as midway between cancers and benign tumors. Among these rare tumors are carcinoid tumors. Carcinoid tumors have also been called "cancers in slow motion." Even though they have the potential for being malignant, they mostly tend to grow so slowly that people with carcinoid tumors usually live for many years (sometimes for a normal lifetime). Carcinoid lung tumors are an uncommon group of lung tumors, developing from neuroendocrine cells. The neuroendocrine cells are in some respect like nerve cells and in other ways like cells of endocrine (hormone-producing) glands. These cells are scattered throughout the body and can be found in different organs, for instance, the lungs, stomach, and intestines. These neuroendocrine cells can form growths (tumors) in many different organs, but usually occur in other endocrine glands such as the adrenal or thyroid glands, or the intestinal tract. The uncontrolled growth of neuroendocrine cells leads to the development of carcinoid tumors. Most carcinoid tumors originate in the small intestine, but carcinoid lung tumors represent about 10% of all carcinoid tumors. Carcinoid lung tumors comprise 1%-6% of all lung tumors. There are two types of carcinoid lung tumors: typical and atypical.
Some carcinoid tumors produce hormone-like substances that can cause a number of endocrine syndromes. The term carcinoid syndrome has been used to refer to the collection of symptoms produced when a carcinoid tumor secretes hormone-like substances. These syndromes tend to reflect the excessive response of the body to the hormone-like substances produced. However, carcinoid syndrome occurs in only about 2% of people with carcinoid lung tumors. About 25% of lung carcinoid tumors are located within the airways and are referred to as bronchial carcinoids. These are not related to smoking or other environmental causes. While anyone can develop a carcinoid tumor of the lung, they may be slightly more common in African-American males. |
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Carcinoid Lung Tumor
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Carcinoid Lung Tumors »
Carcinoid tumors of the lung are a fascinating but uncommon group of pulmonary neoplasms.
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