Vol 1 | Issue 2 | Oct-Dec 2015 | page:5-7 | Ashutosh Vikram[1], Swarnendu Samanta[2], Tapan Kumar Sarkar[2], Reena[3].
Authors : Ashutosh Vikram[1], Swarnendu Samanta[2], Tapan Kumar Sarkar[2], Reena[3].
[1] Department of Orthopaedics,Heritage Institute Of Medical Sciences,Varanasi, Uttar Pradesh, India-221011.
[2]Department of Orthopaedics, Peerless Hospital & B.K. Roy Research Centre, Kolkata.
[3]Department of Anaesthesiology, Heritage Institute of Medical Sciences, Varanasi, Uttar Pradesh, India-221011.
Address of Correspondence
Dr. Ashutosh Vikram
S/O Dr. Tarkeshwar rai, House no.- B32/32 A9-10
Saket nagar extension, P.O+P.S-Lanka. Distt.- Varanasi. Uttar Pradesh.Pincode-221005.
Email:- vikram_ashutosh@yahoo.co.in
Abstract
Introduction: Glomus tumor is a neuromyoarterial tumor arising from glomus bodies. It was first described by Wood & later named by Masson. Its a rare benign vascular tumor of the nail bed and are also difficult to diagnose. Most commonly found in the subungual space of the hand. They can either be solitary or multiple. Solitary glomus tumors are more common in women.
Case Report: We describe a case in a 24 years old female patient who presented to us with long standing severe pain in her left ring finger. Clinicoradiologically, patient was initially misdiagnosed as a case of chronic paronychia and was treated conservatively. However her symptoms persists and later surgical excision and biopsy proved it to be a solitary glomus tumor.
Conclusion: Glomus tumor is not so uncommon tumor but most of the time either it is misdiagnosed or overlooked by surgeons and physicians. So one should always rule out glomus tumor in a patient presented with unknown cause of nail bed pain. Early diagonosis and surgical excision is the key for successful treatment of the tumor.
Keywords: Glomus tumor, neuromyoarterial, Finger,Diagnosis, Surgical treatment.
Introduction
It is a rare benign vascular tumor, which presents with cold intolerance, intense paroxysmal pain, and well-defined site of pain at the origin of the tumor[2]. Most commonly occurs in the subungual region[1,3] and arises from glomus bodies which are highly concentrated in the finger and toe tip, especially beneath the nail which play a role in thermoregulation. Usually 75% are found in hands ,65% of which occur in finger tips[2,3]. The glomus tumor is very small and not easily palpable. May be misdiagnosed or diagnosed late. Plain radiograph does not show any bony involvement until late stage. Tumor can be diagonised clinically by various clinical tests[4]. Various other types of tumors that may affect the subungual space should always be ruled out such as subungual exostosis, soft-tissue chondroma, heman-gioma ,epidermal cysts,squamous cell carcinoma and malignant melanoma. However,MRI and histopathology remains the investigation of choice to confirm the diagnosis[5,6]. The treatment of choice is complete surgical excision of the tumor[8-11].
Case report
A 24 year old female patient, presented with pain and a small barely visible swelling over the fingertip of left ring finger(Fig.1a,b) for 9 months . The patient initially visited to many doctors and was treated conservatively for chronic paronychia in the form of analgesic and multiple courses of antibiotics and antifungals. But her symptoms persists and presented to our orthopaedic OPD. The patient had severe episodes of pain over her fingertip during same period . The pain was more excruciating during night and any stimulus to the fingertip would exacerbate the pain. The pain was localized. During episodes of pain, patient noticed erythema around the swelling. The pain had limited her daily activities. There was no history of trauma. No relevant past medical history. Systemic examinations was also normal.
The examination of fingertip revealed bluish discoloration and discrete swelling. Gentle touch exacerbated the pain. The plain radiograph (Fig. 2) and routine lab investigations were normal. The T1 weighted MRI images showed dark swelling in fingertip and MRI T2 images showed bright lesion. A localised mass at the subungual area with bony erosion was evident on MRI (Fig. 3a,3b and 3c).
In our case,under local anesthesia(digital block) a surgical incision was given over nail plate, part of it was removed and incision was extended proximally, the tumor was exposed (Fig. 4a –e) and removed with subsequent curettage of bony erosion. The wound was closed. The dimensions of tumor mass were approximately 5 mm x 5mm x 2.5 mm. The material obtained was sent for histopathological examination and it confirmed our diagnosis of Glomus Tumour (Fig. 5). The symptoms resolved after excision. There was no nail dystrophy. Patient resumed her daily activities on day seven after the procedure. There was no recurrence of tumor at one year follow up.
Discussion
One case was reported by Rijal et al [5], where a female patient was treated for paronychia of great toe, but the patient was actually having glomus tumor. Similarly our case was also misdiagnosed by clinicians as a case of swelling of infective origin and was treated several times with analgesic and multiple courses of antibiotics and antifungals. Glomus tumors arise from neuromyoarterial glomus bodies and it accounts for 1 to 5% of hand tumors out of which 20 to 75% occurs in subungual area[1,2]. The patient usually present with visible or palpable subungual tender mass and even slight touch to finger pulp would precipitate an excruciating pain[2,3]. Subungual glomus tumor results in nail deformity, change of color beneath the nail, and intolerance to cold[1]. Basically divided into two types – solitary and multiple. Of these, solitory are more common and mainly found in adults[1,2].The glomus tumor is very small and is not easily palpable. That is why most of the time either it is missed or misdiagnosed by the clinician. Plain X-rays remains irrelevant unless large & long standing cases where it might show some soft tssue changes and cortical erosion[1,6]. We stress the role of MRI in cases of unexplained pain, to rule out glomus tumor. MRI of glomus tumor is isointense with dermis of nail bed in T1 weighted images and homogenous hyperintense in T2 weighted images[6].Excision of tumor is easy, as it is located over the tip of finger, but Subungal glomus tumors are more difficult to treat, because they are small, and require meticulous surgery for nail preservation. Incomplete excision is the cause for recurrence of pain. Incorrect diagnosis and late diagnosis can result in destruction of nail. Glomus tumors are usually solitary lesions characterized by reddish purple discoloration of the area, paroxysmal pain, tenderness, and cold sensitivity. Multiple glomus tumors, also known as glomangiomas, are inherited by autosomal-dominant pattern with incomplete penetrance[1,3]. Histologically, the glomus tumor shows numerous small, vascular lumina, lined with a single layer of flattened endothelial cells. The vascular spaces are surrounded by clusters of cells characterized by a faintly eosinophilic cytoplasm and a large pale nucleolus[4,5]. Two clinical findings, Hildreth’s sign and Love’s test, have been described for painful subungal solitary tumors[3,4]. Hildreth’s sign is disappearance of pain after application of a tourniquet proximally. Love’s test consists of eliciting pain by applying pressure to a point area, with the tip of a pencil. Hildreth’s sign, Love’s test, and cold sensitivity, all were positive in our case. The treatment of choice for solitary glomus tumor is complete surgical excision[8-11]. Nail deformity can be avoided by adopting periungal approach or transungal approach followed by meticulous repair of nail bed[10-11].
Conclusion
Glomus tumor is not so uncommon tumor but most of the time either it is misdiagnosed or overlooked by surgeons or physicians [1-3]. So one should always rule out a case of glomus tumor in a patient presented with unknown cause of nail bed pain. Early diagnosis and surgical excision is the key for successful treatment of the tumor [8-11].
Clinical Message
By reporting this case our aim is that any case of chronic fingertip pain should be evaluated for Glomus tumour, to avoid unnecessary delay in the diagnosis, causing the increase in the suffering of the patient due to pain and cosmetic nail deformities.
References
1. Samaniego E, Crespo A, Sanz A. Key Diagnostic Features and Treatment of Subungual Glomus Tumor. Actas Dermosifiliogr; 2009;100:875-82.
2. Caroll RE, Berman AT. Glomus Tumours of hand: Review of the literature and report on twenty eight cases. J Bone Joint Surg Am, 1975; 54:691-703.
3. Bhaskaranand K, Navadgi BC. Glomus tumour of the hand. J Hand Surg Br, 2002; 27: 229-31.
4. Giele H. Hildreths test is a reliable clinical sign for the diagnosis of glomus tumours. J Hand Surg , 2002; 27:1578.
5. Rijal L, Nepal P, Sagar G, Vaidya S, Joshi A. It is a glomus tumor! Not at all a paronychia. Eur J Orthop Surg Traumatol , 2011; 1-4.
6. Takemura N, Fujii N, Tanaka T. Subungal Glomus tumor diagnosis based on imaging. B J Dermatol , 2006; 33:389-93.
7. Tada H, Hirayama T, Takemitsu Y. Prevention of postoperative nail deformity after subungual glomus resection. J Hand Surg 1994; 19:5003.
8. Rohrich RJ, Hochstein LM, Millwee RH. Subungual glomus tumors: an algorithmic approach. Ann Plast Surg, 1994; 33:3004.
9. Abraham GT, Benjamin B, Mamman KG. Glomus tumour of the hands: A review of presentations and outcomes. Brunei Int Med J, 2012; 8 (2): 66-70.
10. Fujioka H, Kokabu T, Akisue T, Nagura I, Toyokawa N, Inui A et al.Treatment of subungual glomus tumor. Kobe J Med Sci, 2009; 55 (1):1-4.
11. Takata H, Ikuta Y, Ishida O, Kimori K. Treatment of subungual glomus tumor. Hand Surg, 2001; 6: 25-7.
How to Cite this Article:Vikram A, Samanta S, Sarkar T K, Reena. GLOMUS TUMOR- Commonly missed tumour of the nail bed. International Journal of Surgical Cases 2015 Oct-Dec;1(2): 5-7. |