Rhabdomyoma laboratory findings: Difference between revisions
Nima Nasiri (talk | contribs) |
Nima Nasiri (talk | contribs) |
||
| (2 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Rhabdomyoma}} | {{Rhabdomyoma}} | ||
{{CMG}}; {{AE}} {{Nnasiri}} | |||
==Overview== | ==Overview== | ||
Rhabdomyoma is a [[benign]] [[tumor]] of [[Muscle|striated muscle]]. Rhabdomyomas are rare and can be classified into [[cardiac]] type and extracardiac type.The most common primary benign [[pediatric]] tumor of the heart is [[cardiac]] rhabdomyoma which can be seen mainly in [[fetal]] life and children, second most common primary [[benign]] cardiac tumor in children is [[fibroma]]. Most [[tumors]] regress spontaneously, [[prognosis]] depends on the location of [[tumor]] and size. [[Cardiac]] rhabdomyoma is strongly associated with [[tuberous sclerosis]]. | Rhabdomyoma is a [[benign]] [[tumor]] of [[Muscle|striated muscle]]. Rhabdomyomas are rare and can be classified into [[cardiac]] type and extracardiac type.The most common primary benign [[pediatric]] tumor of the heart is [[cardiac]] rhabdomyoma which can be seen mainly in [[fetal]] life and children, second most common primary [[benign]] cardiac tumor in children is [[fibroma]]. Most [[tumors]] regress spontaneously, [[prognosis]] depends on the location of [[tumor]] and size. [[Cardiac]] rhabdomyoma is strongly associated with [[tuberous sclerosis]]. | ||
== Laboratory Findings == | == Laboratory Findings == | ||
*There are no specific laboratory findings associated with rhabdomyoma. | *There are no specific laboratory findings associated with rhabdomyoma. | ||
*The following laboratory studies may be ordered to rule out additional conditions: | *The following laboratory studies may be ordered to rule out additional conditions:<ref name="pmid24959237">{{cite journal |vauthors=Zhu J, Zhang J, Tang G, Hu S, Zhou G, Liu Y, Dai L, Wang Z |title=Computed tomography and magnetic resonance imaging observations of rhabdomyosarcoma in the head and neck |journal=Oncol Lett |volume=8 |issue=1 |pages=155–160 |date=July 2014 |pmid=24959237 |pmc=4063592 |doi=10.3892/ol.2014.2094 |url=}}</ref> | ||
**[[Complete blood count]] (CBC) | **[[Complete blood count]] (CBC) | ||
**[[Hemoglobin]]/[[hematocrit]] | **[[Hemoglobin]]/[[hematocrit]] | ||
| Line 17: | Line 18: | ||
{{WS}} | {{WS}} | ||
[[Category: | [[Category:Oncology]] | ||
[[Category: | [[Category:Rhabdomyoma]] | ||
Latest revision as of 21:50, 10 January 2019
|
Rhabdomyoma Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Rhabdomyoma laboratory findings On the Web |
|
American Roentgen Ray Society Images of Rhabdomyoma laboratory findings |
|
Risk calculators and risk factors for Rhabdomyoma laboratory findings |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Nima Nasiri, M.D.[2]
Overview
Rhabdomyoma is a benign tumor of striated muscle. Rhabdomyomas are rare and can be classified into cardiac type and extracardiac type.The most common primary benign pediatric tumor of the heart is cardiac rhabdomyoma which can be seen mainly in fetal life and children, second most common primary benign cardiac tumor in children is fibroma. Most tumors regress spontaneously, prognosis depends on the location of tumor and size. Cardiac rhabdomyoma is strongly associated with tuberous sclerosis.
Laboratory Findings
- There are no specific laboratory findings associated with rhabdomyoma.
- The following laboratory studies may be ordered to rule out additional conditions:[1]
References
- ↑ Zhu J, Zhang J, Tang G, Hu S, Zhou G, Liu Y, Dai L, Wang Z (July 2014). "Computed tomography and magnetic resonance imaging observations of rhabdomyosarcoma in the head and neck". Oncol Lett. 8 (1): 155–160. doi:10.3892/ol.2014.2094. PMC 4063592. PMID 24959237.