Literature DB >> 15083078

Cutaneous benign mixed tumor (chondroid syringoma) of the eyelid: clinical presentation and management.

John T H Mandeville1, Joo Heon Roh, John J Woog, Russell S Gonnering, Peter S Levin, Robert A Mazzoli, Darryl J Ainbinder, J Justin Older, Alexandre P Moulin, Ralf Kiel, Yoon-Duck Kim, Thaddeus P Dryja.   

Abstract

PURPOSE: To describe the clinical presentation of cutaneous benign mixed tumor of the eyelid and its management options.
METHODS: Periocular cases of cutaneous benign mixed tumor were gathered from members of an oculoplastics specialty Internet discussion group. A total of 9 patients are described in this retrospective, interventional case series. The clinical presentation, histopathology, and management of these lesions is reviewed.
RESULTS: Patients were typically asymptomatic, presenting with a slowly enlarging, nontender nodule of 2 to 8 years' duration. The lesions ranged from 4 mm to 17 mm in greatest dimension. Four of the lesions were on the eyelid margin, three in the sub-brow area of the upper eyelid, and two in the central lids. All six cases not involving the brow were fixed to the tarsus; one brow lesion was believed to be adherent to the skin. None of the lesions was associated with significant changes of the overlying epidermis, although one lesion showed overlying pigmentation. All patients underwent excisional biopsy for diagnostic or cosmetic reasons. On histopathologic examination, the tumors were biphasic, with an epithelial component exhibiting apocrine or hair follicle differentiation and a myxoid, adipocytic, chondroid, and/or fibrous stroma. The pathologic diagnoses were all consistent with cutaneous benign mixed tumor (chondroid syringoma, pleomorphic adenoma). Follow-up ranged from 2 weeks to 12 months, although several patients failed to keep scheduled follow-up appointments. No clinical recurrences were identified.
CONCLUSIONS: Cutaneous benign mixed tumor may occur in the eyelid, and, although uncommon, should be included in the differential diagnosis of firm, nodular eyelid tumors. The histopathologic features are similar to those seen in this tumor type arising in other areas of the body. Preoperative consideration of this diagnostic possibility may allow the surgeon to plan for complete excision, thereby reducing the possibility of recurrence or malignant transformation.

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Year:  2004        PMID: 15083078     DOI: 10.1097/01.iop.0000117337.65340.e5

Source DB:  PubMed          Journal:  Ophthalmic Plast Reconstr Surg        ISSN: 0740-9303            Impact factor:   1.746


  4 in total

Review 1.  Extra-major salivary gland pleomorphic adenoma of the head and neck: a 10-year experience and review of the literature.

Authors:  Yen-Ling Kuo; Tzong-Yang Tu; Chia-Fan Chang; Wing-Yin Li; Shyue-Yih Chang; An-Suey Shiao; Pen-Yuan Chu; Kee-Tak Chan; Shyh-Kuan Tai; Yi-Fen Wang; Shu-Ching Kao; Shou-Yen Kao; Wen-Liang Lo; Cheng-Hsien Wu; Wen-Hu Shu; Shu Ma; Tien-Hsiang Wang
Journal:  Eur Arch Otorhinolaryngol       Date:  2010-12-01       Impact factor: 2.503

2.  Eyebrow lesion: an unusual suspect.

Authors:  Andrew Marano; Alexis L Parcells; Stephen R Peters; Mark S Granick
Journal:  Eplasty       Date:  2015-01-08

3.  Pleomorphic Adenoma of the Eyelid with Apocrine Gland Origin; an Atypical Location.

Authors:  Renata T Rothwell; Sofia B Campelos; Sandra Prazeres
Journal:  J Ophthalmic Vis Res       Date:  2016 Oct-Dec

4.  Conjunctival myxoid stromal tumor of the palpebral conjunctiva: A case report.

Authors:  Pamela S Martin; Cooper D Rodgers; Aldo Fantin; Gulsun Erdag
Journal:  Am J Ophthalmol Case Rep       Date:  2022-02-18
  4 in total

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