Glomus tumor history and symptoms: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
|||
Line 4: | Line 4: | ||
==Overview== | ==Overview== | ||
A detailed history from the patient may be helpful. A positive history of [[trauma]] may be present. | A detailed history from the patient may be helpful. A positive history of [[trauma]] may be present. A positive family history may be present in patients with multiple glomus tumors ([[autosomal dominant]]).Symptoms of glomus tumor include [[hypersensitivity]] to cold and paroxysmal pain at a well defined site. | ||
==History== | ==History== | ||
Line 11: | Line 11: | ||
==Symptoms== | ==Symptoms== | ||
*Symptoms of solitary glomus tumor include: | *Symptoms of solitary glomus tumor include:<ref name="pmid15689436">{{cite journal| author=Brouillard P, Ghassibé M, Penington A, Boon LM, Dompmartin A, Temple IK et al.| title=Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect. | journal=J Med Genet | year= 2005 | volume= 42 | issue= 2 | pages= e13 | pmid=15689436 | doi=10.1136/jmg.2004.024174 | pmc=1735996 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15689436 }}</ref> | ||
**Pain | **Pain | ||
***Paroxysmal | ***Paroxysmal |
Revision as of 01:22, 9 May 2019
Glomus tumor Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Glomus tumor history and symptoms On the Web |
American Roentgen Ray Society Images of Glomus tumor history and symptoms |
Risk calculators and risk factors for Glomus tumor history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Soujanya Thummathati, MBBS [2]
Overview
A detailed history from the patient may be helpful. A positive history of trauma may be present. A positive family history may be present in patients with multiple glomus tumors (autosomal dominant).Symptoms of glomus tumor include hypersensitivity to cold and paroxysmal pain at a well defined site.
History
- A detailed history from the patient may be helpful. A positive history of trauma may be present.[1]
- A positive family history may be present in patients with multiple glomus tumors (autosomal dominant).
Symptoms
- Symptoms of solitary glomus tumor include:[2]
- Pain
- Paroxysmal
- Cold sensitivity
- Reproduced when the lesion is placed in cold water
- May worsen at night
- Disappears when a tourniquet is applied
- Subungual glomus tumors are particularly painful
- Multiple glomus tumors are usually painless.
- Pain
References
- ↑ Blanchard AJ (1941). "The Pathology of Glomus Tumours". Can Med Assoc J. 44 (4): 357–60. PMC 1827043. PMID 20322052.
- ↑ Brouillard P, Ghassibé M, Penington A, Boon LM, Dompmartin A, Temple IK; et al. (2005). "Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect". J Med Genet. 42 (2): e13. doi:10.1136/jmg.2004.024174. PMC 1735996. PMID 15689436.