Fibroma of the Medial Canthal Tendon: a Case Report

PURPOSE: To report a case of medial canthal tendon fibroma, a rarely observed tumor at the eye or ocular adnexa. CASE SUMMARY: A 47-year-old female visited our clinic with a two-year history of a hard mass in the medial canthal region. On examination, a 7 x 5 mm2 sized, hard and unmovable subcutaneous mass was palpated. The mass was slowly enlarging and the patient had no symptoms including tearing or pain. To confirm the diagnosis, a total excision of the mass was performed under local anesthesia. The tumor was a well-demarcated, 7 x 5 x 2 mm3 sized, white oval mass. The histopathologic examination of the specimen revealed dense collagen bundles with scattered fibroblasts. Based on these findings, the lesion was diagnosed as a fibroma. Although rare, fibromas should be included in the differential diagnosis of medial canthal tumors.

Surgical Correction of the Blepharophimosis Syndorome

During the past decade the syndorome of blepharoptosis, blepharophimosis, epicanthus inversus and telecanthus(blepharophimosis syndrome)have become recognized as a distinct tetrad based upon clinical and hereditary characteristics. Early surgery is recommended to minimize being teased at school altough the final results surgical correction may be better in older children and in adults. We treated nine patients with epicanthus by Mustarde's quadrilateral flap or Y to V flap Medial canthal tendon is shortened by tucking for telecanthus. Blepharoptosis is corrected by frontalis suspension using preserved dura or preserved fascia lata as a sling material. We experience satisfactory results in nine patients by this technique without serious postoperative complications.