Uterine leiomyoma

Last revised by Nicholas Verikios on 20 Oct 2024

Uterine leiomyomas, also known as uterine fibroids, are benign tumours of myometrial origin and are the most common solid benign uterine neoplasms. They are a common incidental finding on imaging and rarely cause diagnostic dilemma.

They are clinically apparent in ~25% of women of reproductive age and over 70% of women by menopause 21. Fibroids are responsive to hormones (e.g. stimulated by oestrogens). Being rare in prepubertal females, they commonly accelerate in growth during pregnancy and involute with menopause 1.

  • 2-3x increased incidence in Black women than in White women 20,21

  • increasing incidence with age: 10x more common between 41-60 years of age compared to 21-30 years of age, reaching a peak at 50-60 years 20,21

  • 3x increased incidence with a family history of uterine fibroids 21

They are often asymptomatic and discovered incidentally. Signs and symptoms associated with fibroids include:

Leiomyomas are benign monoclonal tumours 16 predominantly composed of smooth muscle cells with variable amounts of fibrous connective tissue. They are commonly multiple (~85% 8), and range significantly in size.

Any fibroid may undergo atrophy, internal haemorrhage, fibrosis, and calcification. They can also undergo several types of degeneration:

Fibroids may have a number of locations within or external to the uterus:

Histological subtypes include:

Popcorn calcification within the pelvis may suggest the diagnosis.

Ultrasound is used to diagnose the presence and monitor the growth of fibroids:

  • uncomplicated leiomyomas are usually hypoechoic, but can be isoechoic, or even hyperechoic compared to normal myometrium

  • calcification is seen as echogenic foci with shadowing

  • cystic areas of necrosis or degeneration may be seen

  • Venetian blind artifact may be seen but edge shadowing +/- dense posterior shadowing from calcification is also typically seen 17

  • fibroids are usually seen as soft tissue density lesions and may exhibit coarse peripheral or central calcification

  • they may distort the usually smooth uterine contour

  • enhancement pattern is variable

MRI is not generally required for diagnosis, except for complex or problem-solving cases. It is however more sensitive than ultrasound for detecting, localising, and characterising fibroids. Size, location, and signal intensity should be noted.

Signal characteristics are variable and include 1,2:

  • T1

    • non-degenerated fibroids and calcification appear as low to intermediate signal intensity compared with the normal myometrium

    • characteristic high T1 signal

    • an irregular, T1 hyperintense rim around a centrally located myoma suggests red degeneration, which is caused by venous thrombosis

  • T2

    • non-degenerated fibroids and calcification appear as low signal intensity

    • as they are usually hypervascular, flow voids are often observed around them 10

    • fibroids that have undergone cystic degeneration / necrosis can have a variable appearance, usually appearing as high T2 signal

    • hyaline degeneration is demonstrated as low T2 signal

    • cystic degeneration, which is an advanced stage of intratumoural oedema, also shows high T2 signal and does not enhance 10

  • T1 C+ (Gd)

    • variable enhancement is seen with contrast administration

    • the marked high signal intensity with gradual enhancement (albeit mild) suggests myxoid degeneration

MRI is of significant value in the symptomatic patient when surgery and uterine salvage therapy are considered. It is also of great value in differentiating a pedunculated fibroid from an adnexal mass 5.

There are various medical, surgical, and interventional treatment options:

  • invasion of adjacent venous channels leading to intravenous leiomyomatosis: rare 15

  • malignant degeneration into leiomyosarcomas: rare (0.1-0.5%)

  • benign metastasising leiomyoma: extremely rare 3

  • torsion of subserosal leiomyoma

  • pyomyoma 19

  • changes in pregnancy

    • around one-third of fibroids may grow in pregnancy (especially in the 1st trimester 18)

    • pregnancy may cause fibroid growth by 30%

  • intraperitoneal haemorrhage 24,25

    • a rare complication from rupture of a fibroid

    • usually secondary to an increase in abdominal pressure, which causes rupture of superficial veins

    • less often, bleeding can be arterial and associated with hypertension

    • trauma causing avulsion of a fibroid, torsion of a pedunculated fibroid, and pregnancy causing venous congestion

General imaging differential considerations include:

In occasional situations, it may be difficult to differentiate between uterine leiomyomas and:

Cases and figures

  • Figure 1: surgical specimen
  • Case 1: on angiogram
  • Case 2a: T2 MRI (annotated as F)
  • Case 2b: T1 MRI (annotated as F)
  • Case 3: calcified leiomyoma
  • Case 4
  •  Case 5
  • Case 6: prolapsing leiomyoma
  • Case 7: broad ligament leiomyoma
  • Case 8
  • Case 9: submucosal leiomyoma on HSG
  • Case 10
  • Case 11
  • Case 12: large subserosal leiomyoma
  • Case 13: giant calcific uterine leiomyoma
  • Case 14
  • Case 15: giant leiomyoma
  • Case 16
  • Case 17: embolisation
  • Case 18: with torsion
  • Case 19: with concurrent adenomyosis
  • Case 20: calcified leiomyoma
  • Case 21: calcified leiomyoma
  • Case 22
  • Case 23: with IUCD
  • Case 24: with red degeneration in pregnancy
  • Case 25: large bilobed
  • Case 26: with degeneration
  • Case 27: pyoleiomyoma
  • Case 28
  • Case 29
  • Case 30: calcified leiomyoma
  • Case 31: multiple
  • Case 32: with extensive intravenous leiomyomatosis
  • Case 33: large
  • Case 34: hysterosalpingogram
  • Case 35

Imaging differential diagnosis

  • Lipoleiomyoma
  • Leiomyosarcoma of the uterus
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