Thymoma history and symptoms: Difference between revisions
No edit summary |
Amr Marawan (talk | contribs) No edit summary |
||
Line 1: | Line 1: | ||
__NOTOC__ | |||
{{Thymoma}} | {{Thymoma}} | ||
{{CMG}} | {{CMG}} {{AE}} {{AM}} | ||
Please help WikiDoc by adding more content here. It's easy! Click [[Help:How_to_Edit_a_Page|here]] to learn about editing. | Please help WikiDoc by adding more content here. It's easy! Click [[Help:How_to_Edit_a_Page|here]] to learn about editing. | ||
==Overview== | ==Overview== | ||
One-third of patients have their tumors discovered because they have an associated autoimmune disorder. The most common of those conditions is [[myasthenia gravis]] (MG); 10–15% of patients with MG have a [[thymoma]] and, conversely, 30–45% of patients with thymomas have MG. | |||
==Signs and symptoms== | |||
A third of all people with a thymoma have symptoms caused by compression of the surrounding organs by an expansive mass. These problems may take the form of (compression of the [[vena cava superior|upper caval vein]]), [[dysphagia]] (difficulty swallowing), [[cough]] or [[chest pain]].<ref name="pmid10561285">{{cite journal |author=Thomas CR, Wright CD, Loehrer PJ |title=Thymoma: state of the art |journal=[[Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology]] |volume=17 |issue=7 |pages=2280–9 |year=1999 |month=July |pmid=10561285 |doi= |url=http://www.jco.org/cgi/pmidlookup?view=long&pmid=10561285 |accessdate=2012-01-18}}</ref> | |||
As mentioned earlier,one-third of patients have their tumors discovered because they have an associated autoimmune disorder the most common of those conditions is [[myasthenia gravis]] (MG). Additional associated autoimmune conditions include [[pure red cell aplasia]] and [[Good's syndrome]] (thymoma with [[combined immunodeficiency]] and [[hypogammaglobulinemia]]). Other reported disease associations are with acute [[pericarditis]], [[Addison's disease]], [[agranulocytosis]], [[alopecia areata]], [[ulcerative colitis]], [[Cushing's disease]], [[hemolytic anemia]], [[limbic encephalopathy]], [[myocarditis]], [[nephrotic syndrome]], [[panhypopituitarism]], [[pernicious anemia]], [[polymyositis]], [[rheumatoid arthritis]], [[sarcoidosis]], [[scleroderma]], [[sensorimotor radiculopathy]], [[stiff person syndrome]], [[systemic lupus erythematosus]] and [[thyroiditis]]. | |||
One-third to one-half of all persons with thymoma have no symptoms at all, and the mass is identified on a [[chest X-ray]] or [[CT]]/[[CAT scan]] performed for an unrelated problem. | |||
A third to half of all people with a thymoma have no symptoms at all, and the mass is identified on a [[chest X-ray]] performed for an unrelated problem.<ref name="pmid10561285">{{cite journal |author=Thomas CR, Wright CD, Loehrer PJ |title=Thymoma: state of the art |journal=[[Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology]] |volume=17 |issue=7 |pages=2280–9 |year=1999 |month=July |pmid=10561285 |doi= |url=http://www.jco.org/cgi/pmidlookup?view=long&pmid=10561285 |accessdate=2012-01-18}}</ref> | A third to half of all people with a thymoma have no symptoms at all, and the mass is identified on a [[chest X-ray]] performed for an unrelated problem.<ref name="pmid10561285">{{cite journal |author=Thomas CR, Wright CD, Loehrer PJ |title=Thymoma: state of the art |journal=[[Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology]] |volume=17 |issue=7 |pages=2280–9 |year=1999 |month=July |pmid=10561285 |doi= |url=http://www.jco.org/cgi/pmidlookup?view=long&pmid=10561285 |accessdate=2012-01-18}}</ref> |
Revision as of 16:05, 19 February 2014
Thymoma Microchapters |
Diagnosis |
---|
Case Studies |
Thymoma history and symptoms On the Web |
American Roentgen Ray Society Images of Thymoma history and symptoms |
Risk calculators and risk factors for Thymoma history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Amr Marawan, M.D. [2]
Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.
Overview
One-third of patients have their tumors discovered because they have an associated autoimmune disorder. The most common of those conditions is myasthenia gravis (MG); 10–15% of patients with MG have a thymoma and, conversely, 30–45% of patients with thymomas have MG.
Signs and symptoms
A third of all people with a thymoma have symptoms caused by compression of the surrounding organs by an expansive mass. These problems may take the form of (compression of the upper caval vein), dysphagia (difficulty swallowing), cough or chest pain.[1]
As mentioned earlier,one-third of patients have their tumors discovered because they have an associated autoimmune disorder the most common of those conditions is myasthenia gravis (MG). Additional associated autoimmune conditions include pure red cell aplasia and Good's syndrome (thymoma with combined immunodeficiency and hypogammaglobulinemia). Other reported disease associations are with acute pericarditis, Addison's disease, agranulocytosis, alopecia areata, ulcerative colitis, Cushing's disease, hemolytic anemia, limbic encephalopathy, myocarditis, nephrotic syndrome, panhypopituitarism, pernicious anemia, polymyositis, rheumatoid arthritis, sarcoidosis, scleroderma, sensorimotor radiculopathy, stiff person syndrome, systemic lupus erythematosus and thyroiditis.
One-third to one-half of all persons with thymoma have no symptoms at all, and the mass is identified on a chest X-ray or CT/CAT scan performed for an unrelated problem.
A third to half of all people with a thymoma have no symptoms at all, and the mass is identified on a chest X-ray performed for an unrelated problem.[1]
References
- ↑ 1.0 1.1 Thomas CR, Wright CD, Loehrer PJ (1999). "Thymoma: state of the art". Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 17 (7): 2280–9. PMID 10561285. Retrieved 2012-01-18. Unknown parameter
|month=
ignored (help)