Leiomyosarcoma

Last revised by Liz Silverstone on 4 Feb 2025

Leiomyosarcomas are extremely rare malignant neoplasms that originate from smooth muscle cells and may be considered the malignant counterpart of a leiomyoma. They are classified as soft tissue tumours and account for ~8% of malignant soft tissue tumours 10.

Leiomyosarcomas can potentially occur anywhere there is smooth muscle. Commonly described sites include the following 14:

Less common sites include:

Morphological imaging features would be invariably dependent on the site (refer to individual articles). Generally, they tend to be large masses, especially in cases of abdominopelvic lesions ref.

  • generally heterogeneous ref

  • commonly demonstrate central low attenuation representing necrosis 12

  • calcification exceedingly rare ref

The tumour frequently demonstrates cystic foci. Signal characteristics include ref:

  • T1: isointense to muscle 

  • T2: intermediate to hypointense to neighbouring fat 

  • T2 FS: predominantly hyperintense 

For a meaningful differential, it is necessary to consider site-specific tumours.

Cases and figures

  • Case 1: uterine leiomyosarcoma
  • Case 2: uterine leiomyosarcoma
  • Case 3: of small bowel
  • Case 4 : lung metastases from a leiomyosarcoma
  • Case 5: uterine leiomyosarcoma
  • Case 6: XR, MRI, FDG PET-CT
  • Case 7: with tumour thrombus CT MR
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