Primary leiomyosarcoma of bones – a rare entity in two different presentations

Authors

  • Withanage Don Duminda The National Hospital of Sri Lanka, Colombo, Sri Lanka https://orcid.org/0000-0002-9958-9534
  • Dishan Randika Samarathunga The National Hospital of Sri Lanka, Colombo, Sri Lanka https://orcid.org/0000-0002-4407-7021
  • Appu Arachchige Gayani Harindi Anupama The National Dental Hospital, Colombo, Sri Lanka https://orcid.org/0000-0003-0821-1286
  • Rukshan Sooriyarachchi The National Hospital of Sri Lanka, Colombo, Sri Lanka
  • Paththinikuttige Alexander Gamini Navarathna The National Dental Hospital, Colombo, Sri Lanka
  • Rathnayaka Mudiyanselage Ananda Sarath Rathnayaka The National Dental Hospital, Colombo, Sri Lanka
  • Rubasinha Liyanage Pemith Ranura Liyanage The National Dental Hospital, Colombo, Sri Lanka https://orcid.org/0000-0002-9003-8322
  • Ihala Wellala Gunawardena Arachchige Labandi Malhasi The National Hospital of Sri Lanka, Colombo, Sri Lanka

DOI:

https://doi.org/10.15584/ejcem.2021.4.9

Keywords:

bones, leiomyosarcoma, malignant neoplasms

Abstract

Introduction. Leiomyosarcomas (LMS) originate from smooth muscle cells. They are very rare malignant neoplasms. Bony Leiomyosarcoma is a variant of spindle cell sarcoma, primarily affecting long bones, predominantly the distal femur and the proximal tibia followed by craniofacial skeleton.

Aim. To describe clinical presentation and diagnostic approach of primary leiomyosarcoma of bones in two different patients.

Description of the cases.

Case 1. A 64-year-old male with a fracture of left distal femur after a fall was investigated and found to have a pathological fracture. An open biopsy of the fracture site confirms leiomyosarcoma.

Case 2. A 58-year-old previously healthy female presented with a swelling on right side mandibular region. Orthopantomogram radiograph (OPG) of mandible and Cone beam CT (CBCT) mandible was taken initially and revealed a large area of bone destruction of the right side of the mandible associated with a soft tissue mass. Initial incisional biopsy made the diagnosis of spindle cell sarcoma followed by excisional biopsy, which confirms the diagnosis of moderately differentiated leiomyosarcoma.

Conclusion. Primary leiomyosarcoma of bones is very rare. Imaging features are helpful in the evaluation of such conditions, but final diagnosis should be based on histopathologic and immunohistochemical features.

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Published

2021-12-30

How to Cite

Duminda, W. D., Samarathunga, D. R., Anupama, A. A. G. H., Sooriyarachchi, R., Navarathna, P. A. G., Rathnayaka, R. M. A. S., Liyanage, R. L. P. R., & Malhasi, I. W. G. A. L. (2021). Primary leiomyosarcoma of bones – a rare entity in two different presentations. European Journal of Clinical and Experimental Medicine, 19(4), 333–340. https://doi.org/10.15584/ejcem.2021.4.9

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CASUISTIC PAPERS