Primary Cutaneous Leiomyosarcoma of the Face: A Rare Tumor that Is Difficult to Diagnose

Ouattara, Bakary and Koffi, Konan Marc and Demisère, Ory Opokou Alexandre and Boka, Koffi Laurent and Kone, Rokiatou and Yapo, Aké Lucien Jonathan and Asseke, Assoumou Lucien and Harding, Mouan Beatrice and Breton, Pierre (2023) Primary Cutaneous Leiomyosarcoma of the Face: A Rare Tumor that Is Difficult to Diagnose. Open Journal of Stomatology, 13 (11). pp. 396-402. ISSN 2160-8709

[thumbnail of ojst_2023110315090018.pdf] Text
ojst_2023110315090018.pdf - Published Version

Download (565kB)

Abstract

Leiomyosarcoma is a rare malignant tumour of the lower limbs. Its differential histological diagnosis is difficult and is made in the presence of young scar tissue, leimyoma, dermatofibroma, melanoma, rabdomyosarcoma, sarcomatoid carcinoma, fibroxantoma, Darrier Ferrand dermatofibrosarcoma and myofibroblastic tumours. Treatment is essentially surgical, with margins of 3 to 5 centimetres. We report two observations of tumours localised to the face, including one case of a known leiomyosarcoma and another case initially diagnosed as a leiomyosarcoma which turned out to be a cellular myofibroma with no sign of malignancy after several readings. The aim of this work is to review the literature on this pathology while highlighting the diagnostic and therapeutic difficulties. Conclusion: A rare smooth muscle tumour with a high risk of local recurrence in the event of incomplete treatment, leiomyosarcoma in its dermal component is preferentially located in the head and neck. Its treatment is exclusively surgical and highly mutilating.

Item Type: Article
Subjects: STM Library > Medical Science
Depositing User: Managing Editor
Date Deposited: 07 Nov 2023 12:46
Last Modified: 07 Nov 2023 12:46
URI: http://open.journal4submit.com/id/eprint/3187

Actions (login required)

View Item
View Item