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Glomus tumor of finger pulp – An unusual
presentation
Dr.N.Mariappan
Dr.M.Srivignesh
Department of Hand surgery,
Sri Ramachandra Institute of Higher Education
and Research, Porur
Introduction
• Glomus tumours – A.K.A Barré–Masson
syndrome
• Rare benign hamartomas that arise from the
normal glomus apparatus, located in
subcutaneous tissue.
• They are either solitary or multiple.
• Solitary tumours are more common.
• Multiple types develop in young children or in
males in an autosomal dominant fashion.
History
• Wood described the condition as a painful
subcutaneous tubercle (1812)
• Masson coined the term “glomus” (Latin for
“ball”) and with histopathological study
recognised their neuromyoarterial origin.
(1924)
• Touraine first described multiple hereditary
glomangiomas.(1936)
• Glomus body consists of
– Afferent arteriole
– Anastomotic Sucquet–
Hoyer canal
– Efferent venule
– Intraglomerular reticulum
– Capsule.
The Sucquet–Hoyer canals are lined by
endothelial cells which are surrounded by smooth
muscle cells and large cuboid glomus cells are
interspersed in the smooth muscle.
Common presentation
• Glomus tumour is classified as digital and
extra-digital.
• Multiple glomus tumours are most often are
painless, pink or purple appearance with a
nodal shape
• Rettig and Strickland : Solitary variant mostly
found hand, with 25%–75% occurring in the
subungual region are more common in
women of age group 25- 40
Subungual tumor
Classical histological features
• Glomus tumours are typically composed of 3
components: glomus cells, smooth muscle
cells and vasculature.
3 variants : Solid form/Glomangioma/
Glomangiomyoma and Malignant form.
angiocentric uniform sheets of cells with oval
nuclei, forming a perivascular “collar” around
vessels.
INCIDENCE
Toes
8%
Arm
29%
Leg
27%
Trunk
11%
Back
8%
Others
17%
INCIDENCE
Mechanism of pain
• The capsule of the tumours are more sensitive to
pressure changes.
• Abundant mast cells in the glomus tumours
release substances such as heparin, 5-hydroxy-
tryptamin, and histamine. This results in
receptors sensitive to pressure / cold stimulation
• Excessive dominance over the nerve of numerous
non-myelinated nerve fibers that penetrate into
glomus tumours.
Case Presentation
• 73 year/Male
• Right handed individual
• Security guard
History of:
• Pain in the pulp of his right mid finger- 6 years
• Lancinating type, more in dependent position.
• Cold intolerance.
• No history of trauma.
• No co-morbid illness
Clinical Examination
• No visible swelling Right middle
finger
• Severe tenderness on palpation of
pulp of finger
• Tenderness localised on ulnar side
of the finger
• On deep palpation diffuse tender
Differential Diagnosis
• Vascular or melanocytic lesions
• Lipoma
• Angioma
• Fibroma
• Neuroma
• Leiomyoma,
• Pyogenic granuloma
• Spiradenoma.
Clinical tests
• Love test: Eliciting pain by applying precise
pressure with the tip of a pencil (Love test)
helps locate the lesion.
• Hildreth’s test: Elevate patients’ arm,
exsanguinate it and a tourniquet is inflated to
250 mm Hg. Pain and tenderness are reduced
on palpation of the tumour. Positive test is
sudden onset of pain and tenderness in the
area of tumour when the cuff is released.
Clinical tests
• Provocation test shows impact of cold on
pain. The cold-sensitivity test is positive when
hand immersion in cold water elicits severe
pain in and around the lesion.
• Transillumination test recently introduced by
EKIN et al. has been found useful in the
diagnosis and location of sub-ungual tumours.
X-Ray – Right Hand
Operative Procedure
• Excision biopsy under digital block
anaesthesia.
• Under tourniquet control
• Under Loupe magnification
• Curvilinear incision with
convexity to the ulnar side of TPX
region
Operative Procedure
• On exploration a pink, ovoid glistening lesion,
was found deep along the ulnar border of pulp
of TPX region.
• Tumor was surrounded by fat along with
dilated vessels.
• Tumor was lying above the periosteum of TPX
• Tumor along with surrounding fat was excised.
Underlying TPX was curetted.
• Wound closed after irrigation.
Intra-operative
Excised specimen
Post-operative period
• Uneventful.
• His wounds healed well
• Sutures removed on 7thPOD
• Significant relief from symptoms of local and
paroxysmal pain.
• Has not experienced intolerance to cold.
Histopathological diagnosis of Glomus tumour
• Multiple fragments of fibro-adipose and fibro-
collagenous tissue shows well circum-scribed
tumour composed of predominantly glomus
cells, blood vessels and smooth muscle cells.
• Glomus cells arranged in sheets interspersed
with myxoid stroma.
Histopathological diagnosis
• Round sharply punched out nucleus with
indistinct border
• Eosinophilic cytoplasm and homogenous
nuclear chromatin and few of them showing
prominent nucleoli.
• No nuclear atypia or mitosis seen
Immunohistochemistry
• Positive for SMA and Vimentin.
• Ki67 labelling Index was 1%.
Glomus
tumor
• Section showing a well circumscribed lesion with thin walled
blood vessels surrounded by uniform cells (100 X H&E).
Glomus
tumor
• High Power showing glomus cells
with uniform round to oval cells,
moderate amount of eosinophilic
cytoplasm and homogenous
chromatin 200 X H&E
IHC for Smooth muscle Actin (SMA) showing strong postivity in the glomus cells X100.
Take home messages
• Patients with unexplained paroxysmal shooting
pain, sensitivity to cold, and localized tenderness
in the finger must be investigated to rule out
glomus tumour.
• The standard treatment of choice is surgical
removal.
• Recurrence of glomus tumour generally resulted
from incomplete excision.
• Rare presentation of glomus tumours at different
locations must always be kept in mind.
Take home messages
• A high index of suspicion of glomus tumour is
essential for clinical diagnosis.
• Imaging studies like ultrasonography and
magnetic resonance imaging are needed for
confirmation.
• Incision should be planned to avoid scars on the
contact areas of the fingers.
• Immunohistochemistry(IHC) studies are essential
to confirm diagnosis and also to rule out the
possibility of malignant transformation, which is
extremely rare.
Reference
• Kim DH. Glomus tumour of the fingertip and MRI appearance. Iowa Orthop J 1999;19:136-8.
• Shin DK, Kim MS, Kim SW, et al. A painful glomus tumor on the pulp of the distal phalanx. J
Korean Neurosurg Soc 2010;48:185-7.
• Lin YC, Hsiao PF, Wu YH, et al. Recurrent digital glomus tumor: analysis of 75 cases. Dermatol
Surg 2010;36:1396-400.
• Van Geertruyden J, Lorea P, Goldschmidt D, de Fontaine S, Schuind F, Kinnen L, et al. : Glomus
tumours of the hand. A retrospective study of 51 cases. J Hand Surg Br 21 : 257-260, 1996
• Venkatachalam MA, Greally JG. Fine structure of glomus tumor: Similarity of glomus cells to
smooth muscle. Cancer 1969;23:1176-84.
• Takei TR, Nalebuff EA. Extradigital glomus tumour. J Hand Surg Br 1995;20:409-12.
• 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 (http://dx.doi.org/10.1111%2Fj.1468-3083.2011.03 979.x). PMID
21371130 (http://www.ncbi.nlm.nih.gov/pubmed/21371130).
• Gombos Z, Zhang PJ. Glomus tumor. Arch Pathol Lab Med 2008; 132: 1448-52
Thank you
This Photo by Unknown Author is licensed under CC BY

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Ppt Glomus tumor of pulp of right middle finger

  • 1. Glomus tumor of finger pulp – An unusual presentation Dr.N.Mariappan Dr.M.Srivignesh Department of Hand surgery, Sri Ramachandra Institute of Higher Education and Research, Porur
  • 2. Introduction • Glomus tumours – A.K.A Barré–Masson syndrome • Rare benign hamartomas that arise from the normal glomus apparatus, located in subcutaneous tissue. • They are either solitary or multiple. • Solitary tumours are more common. • Multiple types develop in young children or in males in an autosomal dominant fashion.
  • 3. History • Wood described the condition as a painful subcutaneous tubercle (1812) • Masson coined the term “glomus” (Latin for “ball”) and with histopathological study recognised their neuromyoarterial origin. (1924) • Touraine first described multiple hereditary glomangiomas.(1936)
  • 4. • Glomus body consists of – Afferent arteriole – Anastomotic Sucquet– Hoyer canal – Efferent venule – Intraglomerular reticulum – Capsule. The Sucquet–Hoyer canals are lined by endothelial cells which are surrounded by smooth muscle cells and large cuboid glomus cells are interspersed in the smooth muscle.
  • 5. Common presentation • Glomus tumour is classified as digital and extra-digital. • Multiple glomus tumours are most often are painless, pink or purple appearance with a nodal shape • Rettig and Strickland : Solitary variant mostly found hand, with 25%–75% occurring in the subungual region are more common in women of age group 25- 40
  • 7. Classical histological features • Glomus tumours are typically composed of 3 components: glomus cells, smooth muscle cells and vasculature. 3 variants : Solid form/Glomangioma/ Glomangiomyoma and Malignant form. angiocentric uniform sheets of cells with oval nuclei, forming a perivascular “collar” around vessels.
  • 9. Mechanism of pain • The capsule of the tumours are more sensitive to pressure changes. • Abundant mast cells in the glomus tumours release substances such as heparin, 5-hydroxy- tryptamin, and histamine. This results in receptors sensitive to pressure / cold stimulation • Excessive dominance over the nerve of numerous non-myelinated nerve fibers that penetrate into glomus tumours.
  • 10. Case Presentation • 73 year/Male • Right handed individual • Security guard History of: • Pain in the pulp of his right mid finger- 6 years • Lancinating type, more in dependent position. • Cold intolerance. • No history of trauma. • No co-morbid illness
  • 11. Clinical Examination • No visible swelling Right middle finger • Severe tenderness on palpation of pulp of finger • Tenderness localised on ulnar side of the finger • On deep palpation diffuse tender
  • 12. Differential Diagnosis • Vascular or melanocytic lesions • Lipoma • Angioma • Fibroma • Neuroma • Leiomyoma, • Pyogenic granuloma • Spiradenoma.
  • 13. Clinical tests • Love test: Eliciting pain by applying precise pressure with the tip of a pencil (Love test) helps locate the lesion. • Hildreth’s test: Elevate patients’ arm, exsanguinate it and a tourniquet is inflated to 250 mm Hg. Pain and tenderness are reduced on palpation of the tumour. Positive test is sudden onset of pain and tenderness in the area of tumour when the cuff is released.
  • 14. Clinical tests • Provocation test shows impact of cold on pain. The cold-sensitivity test is positive when hand immersion in cold water elicits severe pain in and around the lesion. • Transillumination test recently introduced by EKIN et al. has been found useful in the diagnosis and location of sub-ungual tumours.
  • 16. Operative Procedure • Excision biopsy under digital block anaesthesia. • Under tourniquet control • Under Loupe magnification • Curvilinear incision with convexity to the ulnar side of TPX region
  • 17. Operative Procedure • On exploration a pink, ovoid glistening lesion, was found deep along the ulnar border of pulp of TPX region. • Tumor was surrounded by fat along with dilated vessels. • Tumor was lying above the periosteum of TPX • Tumor along with surrounding fat was excised. Underlying TPX was curetted. • Wound closed after irrigation.
  • 20. Post-operative period • Uneventful. • His wounds healed well • Sutures removed on 7thPOD • Significant relief from symptoms of local and paroxysmal pain. • Has not experienced intolerance to cold.
  • 21. Histopathological diagnosis of Glomus tumour • Multiple fragments of fibro-adipose and fibro- collagenous tissue shows well circum-scribed tumour composed of predominantly glomus cells, blood vessels and smooth muscle cells. • Glomus cells arranged in sheets interspersed with myxoid stroma.
  • 22. Histopathological diagnosis • Round sharply punched out nucleus with indistinct border • Eosinophilic cytoplasm and homogenous nuclear chromatin and few of them showing prominent nucleoli. • No nuclear atypia or mitosis seen
  • 23. Immunohistochemistry • Positive for SMA and Vimentin. • Ki67 labelling Index was 1%.
  • 24. Glomus tumor • Section showing a well circumscribed lesion with thin walled blood vessels surrounded by uniform cells (100 X H&E).
  • 25. Glomus tumor • High Power showing glomus cells with uniform round to oval cells, moderate amount of eosinophilic cytoplasm and homogenous chromatin 200 X H&E
  • 26. IHC for Smooth muscle Actin (SMA) showing strong postivity in the glomus cells X100.
  • 27. Take home messages • Patients with unexplained paroxysmal shooting pain, sensitivity to cold, and localized tenderness in the finger must be investigated to rule out glomus tumour. • The standard treatment of choice is surgical removal. • Recurrence of glomus tumour generally resulted from incomplete excision. • Rare presentation of glomus tumours at different locations must always be kept in mind.
  • 28. Take home messages • A high index of suspicion of glomus tumour is essential for clinical diagnosis. • Imaging studies like ultrasonography and magnetic resonance imaging are needed for confirmation. • Incision should be planned to avoid scars on the contact areas of the fingers. • Immunohistochemistry(IHC) studies are essential to confirm diagnosis and also to rule out the possibility of malignant transformation, which is extremely rare.
  • 29. Reference • Kim DH. Glomus tumour of the fingertip and MRI appearance. Iowa Orthop J 1999;19:136-8. • Shin DK, Kim MS, Kim SW, et al. A painful glomus tumor on the pulp of the distal phalanx. J Korean Neurosurg Soc 2010;48:185-7. • Lin YC, Hsiao PF, Wu YH, et al. Recurrent digital glomus tumor: analysis of 75 cases. Dermatol Surg 2010;36:1396-400. • Van Geertruyden J, Lorea P, Goldschmidt D, de Fontaine S, Schuind F, Kinnen L, et al. : Glomus tumours of the hand. A retrospective study of 51 cases. J Hand Surg Br 21 : 257-260, 1996 • Venkatachalam MA, Greally JG. Fine structure of glomus tumor: Similarity of glomus cells to smooth muscle. Cancer 1969;23:1176-84. • Takei TR, Nalebuff EA. Extradigital glomus tumour. J Hand Surg Br 1995;20:409-12. • 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 (http://dx.doi.org/10.1111%2Fj.1468-3083.2011.03 979.x). PMID 21371130 (http://www.ncbi.nlm.nih.gov/pubmed/21371130). • Gombos Z, Zhang PJ. Glomus tumor. Arch Pathol Lab Med 2008; 132: 1448-52
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