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LETTER TO THE EDITOR
Year : 2013  |  Volume : 61  |  Issue : 1  |  Page : 43-44

Chondroid syringoma: A rare lid tumor


Department of Ophthalmology, Mahatma Gandhi Medical College and Research Institute, Puducherry, India

Date of Web Publication26-Dec-2012

Correspondence Address:
M Ashok Kumar
Department of Ophthalmology, Mahatma Gandhi Medical College and Research Institute, Pillayarkupam, Puducherry
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.105060

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How to cite this article:
Kumar M A, Srikanth K, Vathsalya R. Chondroid syringoma: A rare lid tumor. Indian J Ophthalmol 2013;61:43-4

How to cite this URL:
Kumar M A, Srikanth K, Vathsalya R. Chondroid syringoma: A rare lid tumor. Indian J Ophthalmol [serial online] 2013 [cited 2020 Jun 2];61:43-4. Available from: http://www.ijo.in/text.asp?2013/61/1/43/105060

Sir,

Chondroid syringoma is a rare primary skin tumor (0.01% to 0.1% of primary skin tumors). [1] Though its very common occurrence is in head and the neck region, involvement of eyelids is extremely rare. In English literature we found 27 reported cases of chondroid syringoma involving ocular adnexa. [1],[2] We are reporting a case of recurrent chondroid syringoma of upper eyelid in a young male.

A 27-year-old male present with a slow growing painless mass in right upper lid since past 6 months duration. The mass was 1.5 cm × 1.5 cm firm, non-tender, sub-cutaneous and not fixed to underlying tissues [Figure 1]. This was a recurrence of a lesion that had been removed by lamellar excision in the same site 2 years back. The recurrent mass was removed this time by pentagonal full thickness lid excision with re-construction by advancement eyelid flap. Histopathological examination showed tumor with variegated appearance. The epithelial component composed of round to oval cells with large nucleoli with scanty cytoplasm and the cells were arranged in nests and acinar pattern. The coating for epithelium of the glandular elements was two layered. The intervening stroma showed fibrosis and myxoid areas. No evidence of lacrimal gland tissue was noted in multiple sections [Figure 2].
Figure 1: 1.5 cm × 1.5 cm mass involving the right upper lid

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Figure 2: Histopathology showing glandular elements with two layered lining epithelium in myxoid matrix

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Chondroid syringoma is a tumor arising from the sweat glands which can be apocrine (found throughout the surface of lid) or eccrine (glands of Moll in association with eyelash follicles) with a mean age of 50 years (22-73 years). [1] Ozdal et al. in a study of 228 benign ocular adnexal tumors reported apocrine/eccrine hydrocystoma as very common and no case of Chondroid Syringoma was found in that series. [3] Tyagi et al. in their study of 207 eyelid tumors had one case of Chondroid syringoma with an incidence of 0.48% in their series. [4]

This tumor was first described by Billroth [5] and the term chondroid syringoma was coined by Hirsh and Helwig to characterize the origin from sweat glands [6] though the appearance is like pleomorphic adenoma of lacrimal gland. A proper histopathological examination to rule out presence of normal lacrimal gland tissue external to the tumor capsule helps to differentiate chondroid syringoma. [1] The case being reported had tubular and cystic branching lumina with 2 layered epithelium showing an apocrine origin. [1]

Chondroid syringoma is a benign tumor but incomplete excision can undergo malignant transformation. [1] Hence complete excision is advised.

This case is being reported for its rarity (this is the 28 th case in literature involving ocular adnexa), its occurrence in a young patient and the need to keep this rare entity as a differential diagnosis of eyelid tumors.

 
  References Top

1.
Gunduz K, Demirel S, Heper AO, Gunalp I. A Rare case of atypical chondroid syringoma of the lower eyelid and review of the literature. Surv Ophthalmol 2006;51:280-5.  Back to cited text no. 1
    
2.
Huerva V, Sanchez MC, Egido RM, Matías-Guiu X. Pleomorphic adenoma with extensive myoepithelial component of the lower eyelid. Ophthal Plast Reconstr Surg 2008;24:223-5.  Back to cited text no. 2
    
3.
Ozdal PC, Callejo SA, Codere F, Burnier MN Jr. Benign ocular adnexal tumours of apocrine, eccrine or hair follicle origin. Can J Ophthalmol 2003;38:357-63.  Back to cited text no. 3
    
4.
Tyagi NN, Abdi UU, Tyagi SP, Maheshwari VV, Gogi RR. Pleomorphic adenoma of skin (chondroid syringoma) involving the eyelid. J Postgrad Med 1996;42:125-6.  Back to cited text no. 4
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5.
Billroth T. Beobachtungen uber geschwulste der speichel-drusen. Virchows Arch Pathol Anat 17:357-75, 1859. Cited by: Mandville JT, Roh JH, Woog JJ, Gonnering RS, Levin PS, Mazzoli RA, et al. Cutaneous benign mixed tumor chondroid syringoma of the eyelid: Clinical presentation and management. Ophthal Plast Reconstr Surg 2004;20:110-6.  Back to cited text no. 5
    
6.
Hirsch P, Helwig EB. Chondroid syringoma: Mixed tumor of skin, salivary gland type. Arch Dermatol 1961;84:835-47.  Back to cited text no. 6
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