Open Journal of Stomatology

Volume 13, Issue 11 (November 2023)

ISSN Print: 2160-8709   ISSN Online: 2160-8717

Google-based Impact Factor: 0.49  Citations  h5-index & Ranking

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

HTML  XML Download Download as PDF (Size: 552KB)  PP. 396-402  
DOI: 10.4236/ojst.2023.1311032    39 Downloads   242 Views  

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.

Share and Cite:

Ouattara, B. , Koffi, K. , Demisère, O. , Boka, K. , Kone, R. , Yapo, A. , Asseke, A. , Harding, M. and Breton, P. (2023) Primary Cutaneous Leiomyosarcoma of the Face: A Rare Tumor that Is Difficult to Diagnose. Open Journal of Stomatology, 13, 396-402. doi: 10.4236/ojst.2023.1311032.

Cited by

No relevant information.

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.