Difference between revisions of "Glomus tumour"

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| Width      =
| Width      =
| Caption    = Glomus tumour. [[H&E stain]].
| Caption    = Glomus tumour. [[H&E stain]].
| Micro      = sheets of equally-spaced cells ("cookie cutter appearance"), polygonal cells with identifiable cellular borders, thin-walled blood vessels, moderate clear cytoplasm
| Micro      = sheets of equally-spaced cells ("cookie cutter appearance"), polygonal cells +/-identifiable cellular borders, thin-walled blood vessels, moderate clear cytoplasm
| Subtypes  =
| Subtypes  =
| LMDDx      =
| LMDDx      =
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| Clinicalhx =
| Clinicalhx =
| Signs      =
| Signs      =
| Symptoms  = [[painful skin lesion]]
| Symptoms  = [[painful skin lesion]], cold intolerance, point tenderness
| Prevalence = uncommon
| Prevalence = uncommon
| Bloodwork  =
| Bloodwork  =
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*Tumour derived from smooth muscle cell.<ref name=pmid18788860>{{cite journal |author=Gombos Z, Zhang PJ |title=Glomus tumor |journal=Arch. Pathol. Lab. Med. |volume=132 |issue=9 |pages=1448–52 |year=2008 |month=September |pmid=18788860 |doi=10.1043/1543-2165(2008)132[1448:GT]2.0.CO;2 |url=}}</ref>
*Tumour derived from smooth muscle cell.<ref name=pmid18788860>{{cite journal |author=Gombos Z, Zhang PJ |title=Glomus tumor |journal=Arch. Pathol. Lab. Med. |volume=132 |issue=9 |pages=1448–52 |year=2008 |month=September |pmid=18788860 |doi=10.1043/1543-2165(2008)132[1448:GT]2.0.CO;2 |url=}}</ref>
*Usually benign.
*Usually benign.
**Malignant variant exists - extremely rare.
**Malignant variant exists (known as ''glomangiosarcoma'') - extremely rare.<ref>{{cite journal |authors=Alhroub OA, Mahameed SA, Abdelhafez MO, Alhroub A, Hour H, Hasasna N, Kamal N |title=A case of malignant glomus tumor (glomangiosarcoma) of the nasal cavity |journal=J Surg Case Rep |volume=2022 |issue=1 |pages=rjab641 |date=January 2022 |pmid=35096369 |pmc=8791658 |doi=10.1093/jscr/rjab641 |url=}}</ref>
*May be associated with [[neurofibromatosis 1]].<ref name=pmid25426397>{{cite journal |authors=Harrison B, Sammer D |title=Glomus tumors and neurofibromatosis: a newly recognized association |journal=Plast Reconstr Surg Glob Open |volume=2 |issue=9 |pages=e214 |date=September 2014 |pmid=25426397 |pmc=4229273 |doi=10.1097/GOX.0000000000000144 |url=}}</ref><ref name=pmid24685357>{{cite journal |authors=Kumar MG, Emnett RJ, Bayliss SJ, Gutmann DH |title=Glomus tumors in individuals with neurofibromatosis type 1 |journal=J Am Acad Dermatol |volume=71 |issue=1 |pages=44–8 |date=July 2014 |pmid=24685357 |doi=10.1016/j.jaad.2014.01.913 |url=}}</ref>
*May be associated with [[neurofibromatosis 1]].<ref name=pmid25426397>{{cite journal |authors=Harrison B, Sammer D |title=Glomus tumors and neurofibromatosis: a newly recognized association |journal=Plast Reconstr Surg Glob Open |volume=2 |issue=9 |pages=e214 |date=September 2014 |pmid=25426397 |pmc=4229273 |doi=10.1097/GOX.0000000000000144 |url=}}</ref><ref name=pmid24685357>{{cite journal |authors=Kumar MG, Emnett RJ, Bayliss SJ, Gutmann DH |title=Glomus tumors in individuals with neurofibromatosis type 1 |journal=J Am Acad Dermatol |volume=71 |issue=1 |pages=44–8 |date=July 2014 |pmid=24685357 |doi=10.1016/j.jaad.2014.01.913 |url=}}</ref>


 
Clinical - classic triad:<ref name=pmid36590779>{{cite journal |authors=Dhingra M, Niraula BB, Regmi A, Bansal S, Singh V, Phulware RH |title=Glomus Tumour of Hand--A Commonly Misdiagnosed Pathology: A Case Series |journal=J West Afr Coll Surg |volume=12 |issue=4 |pages=39–45 |date=2022 |pmid=36590779 |pmc=9802603 |doi=10.4103/jwas.jwas_171_22 |url=}}</ref>
Clinical:
*Pain - see ''[[painful skin lesion]]s''.
*[[Painful skin lesion]].
*Point tenderness.
*Cold intolerance.


==Gross==
==Gross==
Line 57: Line 58:
Features:<ref name=ouhsc>URL: [http://moon.ouhsc.edu/kfung/jty1/opaq/PathQuiz/Z0B003-PQ01-M.htm http://moon.ouhsc.edu/kfung/jty1/opaq/PathQuiz/Z0B003-PQ01-M.htm]. Accessed on: 19 October 2010.</ref>
Features:<ref name=ouhsc>URL: [http://moon.ouhsc.edu/kfung/jty1/opaq/PathQuiz/Z0B003-PQ01-M.htm http://moon.ouhsc.edu/kfung/jty1/opaq/PathQuiz/Z0B003-PQ01-M.htm]. Accessed on: 19 October 2010.</ref>
*Sheets of equally-spaced cells ("cookie cutter appearance") - '''key feature'''.
*Sheets of equally-spaced cells ("cookie cutter appearance") - '''key feature'''.
*Polygonal cells with identifiable cellular borders.
*Polygonal cells +/- identifiable cellular borders.
*Thin-walled blood vessels.
*Thin-walled blood vessels.
**May vaguely resemble antlers ([[staghorn vessels]]).  
**May vaguely resemble antlers ([[staghorn vessels]]).  

Latest revision as of 18:42, 26 January 2023

Glomus tumour
Diagnosis in short

Glomus tumour. H&E stain.
LM sheets of equally-spaced cells ("cookie cutter appearance"), polygonal cells +/-identifiable cellular borders, thin-walled blood vessels, moderate clear cytoplasm
IHC SMA +ve (100%), desmin usu. -ve, CD34 -ve, S-100 -ve
Site skin/soft tissue - classically subungal (under the nail)
Syndromes +/-neurofibromatosis 1
Symptoms painful skin lesion, cold intolerance, point tenderness
Prevalence uncommon
Prognosis usu. good (benign), rarely malignant
Treatment excision

Glomus tumours, also known as glomangioma, are painful, perivascular tumour that are classically periungual.

It should not be confused with paraganglioma, which were once called glomus tumour.

This tumour is classified as a perivascular tumour (also pericytic tumour) which is a subset of soft tissue tumours.

General

  • Tumour derived from smooth muscle cell.[1]
  • Usually benign.
    • Malignant variant exists (known as glomangiosarcoma) - extremely rare.[2]
  • May be associated with neurofibromatosis 1.[3][4]

Clinical - classic triad:[5]

Gross

Location:

  • Classically subungual (under the nail).[6]
    • Reported in almost very site imaginable.
    • Most common GI site: stomach.[7]

Appearance (extradigital tumours):[6]

  • Purplish papule.

Microscopic

Features:[8]

  • Sheets of equally-spaced cells ("cookie cutter appearance") - key feature.
  • Polygonal cells +/- identifiable cellular borders.
  • Thin-walled blood vessels.
  • Moderate clear cytoplasm.

Notes:

  • No significant nuclear atypia.
  • The regular cell spacing is called "cookie cutter appearance". It looks like the cells were created with a cookie cutter; the spacing between cell is equal and they all look very similar.
  • Should be perivascular - abut endothelial cells.
  • Myxoid matrix common.[9]

DDx - Why it is not a(n) ...[8]

  • Spiradenoma - also vascular and 'blue' but epithelial, often on the head (or at least chest and up).
  • Solid and cystic hidradenoma - epithelial and less 'blue'
  • Angiosarcoma - has nuclear atypia.
  • Dermatofibroma - spindle cell lesion.
  • Capillary hemangioma - no epithelioid cells, more blood vessels.

Images

  • Glomus tumour - intermed. mag. (WC)

  • Glomus tumour - high mag. (WC)

  • Glomus tumour - very high mag. (WC)

  • Glomus tumour - very high mag. (WC)

www:

IHC

Features:[10]

  • SMA +ve ~ 100%.
  • Desmin usu. -ve.
  • CD34 -ve.
    • Rarely +ve.

Others:

  • S100 -ve.
  • Calponin +ve.

Sign out

LESION, RIGHT RING FINGERNAIL, EXCISION:
- GLOMUS TUMOUR.

COMMENT:
The tumour cells are positive for SMA.

Micro

The sections show a tumour composed of polygonal cells with moderately distinct cellular borders and moderate cytoplasm. The tumour cell nuclei are round and have round nucleoli seen with the 10x objective. Thin-walled blood vessels with bland endothelial cells are found within the tumour. Tumour cells are identified immediately adjacent to the endothelial cells. No mitotic activity is apparent. Focal nuclear enlargement is present; however, no significant nuclear atypia is identified.

See also

References

  1. ↑ Gombos Z, Zhang PJ (September 2008). "Glomus tumor". Arch. Pathol. Lab. Med. 132 (9): 1448–52. doi:10.1043/1543-2165(2008)132[1448:GT]2.0.CO;2. PMID 18788860.
  2. ↑ Alhroub OA, Mahameed SA, Abdelhafez MO, Alhroub A, Hour H, Hasasna N, Kamal N (January 2022). "A case of malignant glomus tumor (glomangiosarcoma) of the nasal cavity". J Surg Case Rep 2022 (1): rjab641. doi:10.1093/jscr/rjab641. PMC 8791658. PMID 35096369. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791658/.
  3. ↑ Harrison B, Sammer D (September 2014). "Glomus tumors and neurofibromatosis: a newly recognized association". Plast Reconstr Surg Glob Open 2 (9): e214. doi:10.1097/GOX.0000000000000144. PMC 4229273. PMID 25426397. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229273/.
  4. ↑ Kumar MG, Emnett RJ, Bayliss SJ, Gutmann DH (July 2014). "Glomus tumors in individuals with neurofibromatosis type 1". J Am Acad Dermatol 71 (1): 44–8. doi:10.1016/j.jaad.2014.01.913. PMID 24685357.
  5. ↑ Dhingra M, Niraula BB, Regmi A, Bansal S, Singh V, Phulware RH (2022). "Glomus Tumour of Hand--A Commonly Misdiagnosed Pathology: A Case Series". J West Afr Coll Surg 12 (4): 39–45. doi:10.4103/jwas.jwas_171_22. PMC 9802603. PMID 36590779. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9802603/.
  6. ↑ 6.0 6.1 Lee, DW.; Yang, JH.; Chang, S.; Won, CH.; Lee, MW.; Choi, JH.; Moon, KC. (Dec 2011). "Clinical and pathological characteristics of extradigital and digital glomus tumours: a retrospective comparative study.". J Eur Acad Dermatol Venereol 25 (12): 1392-7. doi:10.1111/j.1468-3083.2011.03979.x. PMID 21371130.
  7. ↑ Miettinen, M.; Paal, E.; Lasota, J.; Sobin, LH. (Mar 2002). "Gastrointestinal glomus tumors: a clinicopathologic, immunohistochemical, and molecular genetic study of 32 cases.". Am J Surg Pathol 26 (3): 301-11. PMID 11859201.
  8. ↑ 8.0 8.1 URL: http://moon.ouhsc.edu/kfung/jty1/opaq/PathQuiz/Z0B003-PQ01-M.htm. Accessed on: 19 October 2010.
  9. ↑ Mravic M, LaChaud G, Nguyen A, Scott MA, Dry SM, James AW (May 2015). "Clinical and histopathological diagnosis of glomus tumor: an institutional experience of 138 cases". Int J Surg Pathol 23 (3): 181–8. doi:10.1177/1066896914567330. PMC 4498398. PMID 25614464. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498398/.
  10. ↑ Hatori M, Aiba S, Kato M, Kamiya N, Kokubun S (July 1997). "Expression of CD34 in glomus tumors". Tohoku J. Exp. Med. 182 (3): 241–7. PMID 9362106.
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