CASE 10589 Published on 22.02.2013

Glomus tumour of pulp of 3rd toe

Section

Musculoskeletal system

Case Type

Clinical Cases

Authors

Chary Duraikannu

VRR Diagnostics, Radiology;
No 10, HABIBULLAH ROAD,
T.NAGAR 600017 Chennai, India;
Email:charyrad@gmail.com
Patient

21 years, male

Categories
Area of Interest Musculoskeletal soft tissue ; Imaging Technique Ultrasound, MR
Clinical History
21-year-old male patient with severe pain and tenderness and cold hypersensitivity in base of distal phalanx of right 3rd toe for 4 years. On examination no obvious swelling was seen and the overlying skin was normal.
Imaging Findings
Ultrasonography showed a small hypoechoic lesion in plantar aspect of distal phalanx. No significant vascularity could be demonstrated within the lesion.
MRI showed a small globular lesion noted abutting the plantar surface of distal phalanx of 3rd toe measuring 5 x 4 mm. The lesion had T1 hypointense and PD hyperintense signal.
Dynamic contrast study showed intense enhancement of the lesion in arterial phase. Arterial feeders noted from the corresponding digital arteries. The adjacent bone showed no erosion or marrow oedema.
Discussion
Glomus tumours are benign tumours arising from glomus bodies of fingers and toes. These glomus bodies are specialized neuromyoarterial receptors containing arteriovenous anastomosis regulating the body temperature. Glomus tumour was first described clinically in 1812 by Wood [1, 2]. These tumours predominantly occur in the subungual region of fingers. Glomus tumour involving pulp region is rare, about 10% [2, 3, 4]. Even rarer is the occurrence in pulp of the toe.
The average age of occurrence is 30 -50 yrs with female predominance [1, 4]. Although most cases can be diagnosed clinically, some of them may not be detected for years. The typical clinical triad of symptoms are pain, tenderness and cold hypersensitivity [1-4].
Glomus tumour can occur either sporadically or multifocally if associated with neurofibromatosis. Several cases of neurofibromatosis 1 with multifocal glomus tumour have been reported [5, 6, 7].
Imaging plays an important role in establishing the diagnosis. Radiographs may show erosion of the adjacent phalanx. The lesion appears hypoechoic in ultrasonography with significant vascularity on Doppler. In MRI the glomus tumour shows T1 hypointense and T2 hyperintense signal intensity. On dynamic MR contrast angiogram, the lesion shows intense enhancement in arterial phase with tumour blush. Treatment is complete surgical resection by transungual or lateral incision depending on the tumour location [2]. The typical clinical presentation and imaging findings together help to make an accurate diagnosis.
Differential Diagnosis List
Glomus tumour
Haemangioma
Neurofibroma
Melanoma
Lipoma
Final Diagnosis
Glomus tumour
Case information
URL: https://www.eurorad.org/case/10589
DOI: 10.1594/EURORAD/CASE.10589
ISSN: 1563-4086