Glomus tumor history and symptoms: Difference between revisions
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==History== | ==History== | ||
*A detailed history from the patient may be helpful. A positive history of trauma may be present.<ref name="pmid20322052">{{cite journal| author=Blanchard AJ| title=The Pathology of Glomus Tumours. | journal=Can Med Assoc J | year= 1941 | volume= 44 | issue= 4 | pages= 357-60 | pmid=20322052 | doi= | pmc=PMC1827043 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20322052 }} </ref> | *A detailed history from the patient may be helpful. A positive history of trauma may be present.<ref name="pmid20322052">{{cite journal| author=Blanchard AJ| title=The Pathology of Glomus Tumours. | journal=Can Med Assoc J | year= 1941 | volume= 44 | issue= 4 | pages= 357-60 | pmid=20322052 | doi= | pmc=PMC1827043 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20322052 }} </ref> | ||
**There is a delay in diagnosis of the lesions (sometimes up to 15 years) that was apparent both in several cases described in the literature. | |||
*A positive family history may be present in patients with multiple glomus tumors ([[autosomal dominant]]).<ref name="pmid20322052">{{cite journal| author=Blanchard AJ| title=The Pathology of Glomus Tumours. | journal=Can Med Assoc J | year= 1941 | volume= 44 | issue= 4 | pages= 357-60 | pmid=20322052 | doi= | pmc=PMC1827043 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20322052 }} </ref> | *A positive family history may be present in patients with multiple glomus tumors ([[autosomal dominant]]).<ref name="pmid20322052">{{cite journal| author=Blanchard AJ| title=The Pathology of Glomus Tumours. | journal=Can Med Assoc J | year= 1941 | volume= 44 | issue= 4 | pages= 357-60 | pmid=20322052 | doi= | pmc=PMC1827043 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20322052 }} </ref> | ||
Revision as of 01:31, 9 May 2019
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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]
- There is a delay in diagnosis of the lesions (sometimes up to 15 years) that was apparent both in several cases described in the literature.
- A positive family history may be present in patients with multiple glomus tumors (autosomal dominant).[1]
Symptoms
- Symptoms of solitary glomus tumor include:[2][3]
- Pain
- Paroxysmal
- Cold sensitivity
- Reproduced when the lesion is placed in cold water
- May worsen at night
- Extreme point tenderness in the region of the tumor
- Disappears when a tourniquet is applied
- Subungual glomus tumors are particularly painful
- Multiple glomus tumors are usually painless.
- Pain
References
- ↑ 1.0 1.1 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.
- ↑ Samaniego E, Crespo A, Sanz A (2009). "[Key diagnostic features and treatment of subungual glomus tumor]". Actas Dermosifiliogr. 100 (10): 875–82. PMID 20038364.