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. 2024 Mar 6;16(3):e55647. doi: 10.7759/cureus.55647

Table 1. Clinical information to help differentiate between angioleiomyoma and leiomyosarcomas.

Diagnostic considerations Angioleiomyoma Leiomyosarcoma
Clinical Appearance Typically under 2 cm and rarely over 4 cm. Typically encapsulated [2,10]. Median size of 6 cm with a large range: 0.3-45 cm. Typically not encapsulated [10,15].
Age The average age is 47 years [2]. The average age is 57 years [15].
Gender distribution More common in females (roughly 2:1) [2,10]. Roughly even distribution with a slight male preference [16].
Locality 67% in the lower extremity (83% for women) [2]. Disregarding uterine cases, 48% occur in the extremities (more common in the lower extremities), 41% in abdominal or retroperitoneal, and 11% in the trunk [14,15,17].
Recurrence following excision Less than 1% of cases [2]. Up to 60% of cases [18].
Pain Up to 70% of cases for the solid subtype [2]. Often presents without pain [10,14].
Imaging Generally, smaller but small size and non-aggressive lesion features do not exclude sarcoma. Isointense signal to muscle is seen on T1-weighted images and intermediate-high signal on T2-weighted images. T2 hypointense rim may be predictive of angioleiomyoma diagnosis [19]. Areas of internal necrosis or hemorrhage, with masses visible with computed tomography. Isointense signal to the muscle is seen on T1-weighted images and intermediate-high signal on T2-weighted images. Aggressive features, such as surrounding soft tissue invasion, larger size, and peritumoral edema/enhancement [20].
Histology Three main subtypes [1]: solid, closely compacted smooth muscle with small vascular channels; cavernous, dilated vascular channels and less smooth muscle; venous, thick muscular walls and less compact smooth muscle bundles. Well-defined intersecting bundles of spindle cells with increased eosinophilic cytoplasm and elongated/hyperchromatic nuclei. Increased mitotic activity may suggest a malignant character [16].