Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/16675
Citations
Scopus Web of ScienceĀ® Altmetric
?
?
Type: Journal article
Title: Malignant fibrous histiocytoma of the eyelid: Differential diagnosis and management
Author: Khong, J.
Chen, C.
James, C.
Huilgol, S.
O'Donnell, B.
Sullivan, T.
Selva-Nayagam, D.
Citation: Ophthalmic Plastic and Reconstructive Surgery, 2005; 21(2):103-108
Publisher: Lippincott Williams & Wilkins
Issue Date: 2005
ISSN: 0740-9303
1537-2677
Abstract: <h4>Purpose</h4>Malignant fibrous histiocytoma (MFH) is a pleomorphic soft tissue sarcoma that occurs rarely in the periocular region. The purpose of this study was to present a case series of periocular MFH and to discuss the differential diagnosis and management.<h4>Methods</h4>This is a retrospective case review of patients diagnosed with periocular MFH from tertiary hospitals and private practices.<h4>Results</h4>Four patients, two women and two men with periocular MFH, had a mean age of 81 years (range, 72 to 85 years). All tumors were <5 cm in diameter and of storiform pleomorphic histologic subtype. One was located deep and 3 presented superficially. The initial diagnoses were sarcomatoid carcinoma, atypical fibroxanthoma, and leiomyosarcoma that were subsequently reclassified as MFH. One patient had a frozen section, 1 had fast track paraffin section margin control, and 2 had no frozen section margins at the initial excisions. Histology showed 2 negative margins, 1 close margin, and 1 positive margin that were cleared with wide local excision. Local recurrence occurred in 3 cases, and of these, 1 required orbital exenteration. Adjuvant radiotherapy was given to 3 patients. One had regional node metastases. There were no distant metastases or tumor-related deaths. Mean follow-up period was 36 +/- 35 months (median, 30; range, 1 to 84 months).<h4>Conclusions</h4>This study highlights the difficulties in the clinicopathologic diagnosis of periocular MFH and in particular the distinction of more superficial tumors from atypical fibroxanthoma. The mainstay of treatment is complete surgical excision with wide margins, and consideration should be given to histologic margin control in addition to adjuvant radiotherapy.
Keywords: Humans; Eyelid Neoplasms; Lymphatic Metastasis; Neoplasm Recurrence, Local; Diagnosis, Differential; Combined Modality Therapy; Radiotherapy, Adjuvant; Ophthalmologic Surgical Procedures; Retrospective Studies; Aged; Aged, 80 and over; Female; Male; Histiocytoma, Benign Fibrous
RMID: 0020050220
DOI: 10.1097/01.IOP.0000155858.52464.6F
Appears in Collections:Surgery publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.