Fig. 22.1
A 42-year-old woman with chronic cyclic groin pain during menstruation: Parietal endometrioid of the left rectus abdominis muscle. MRI shows recent hemorrhagic changes in the rectus abdominis (arrow) with high signal intensity on T1-weighted images (a), heterogeneous signal on T2-weighted (b) and STIR (c) images and significant enhancement after gadolinium injection (d).
Case 2
A 35-year-old woman with a parietal mass: Parietal endometrioid in the right rectus abdominis muscle.
MRI shows recent hemorrhagic changes in subcutaneous tissue and the abdominal wall (arrow) with low signal intensity on T1-weighted images (Fig. 22.2a), heterogeneous signal on T2-weighted images (Fig. 22.2b) and significant enhancement after gadolinium injection (Fig. 22.2c).
Fig. 22.2
A 35-year-old woman with a parietal mass: Parietal endometrioid in the right rectus abdominis muscle. MRI shows recent hemorrhagic changes in subcutaneous tissue and the abdominal wall (arrow) with low signal intensity on T1-weighted images (a), heterogeneous signal on T2-weighted images (b) and significant enhancement after gadolinium injection (c).
22.3 Discussion and Evaluation
Clinical examination is difficult with groin pain and endometriosis should always be considered if there is a history of chronic cyclic groin pain during menstruation. Painful nodules are due to destruction of the endometrial cells [4]. No nervous impingement has been described in the literature. Medical imaging, in particular MRI, may help in the diagnosis of extra-pelvic endometriosis in the groin muscles [7].
Ultrasound and CT are not specifically used for the diagnosis of muscular endometriosis in clinical practice. However, on CT signs of endometriosis are highly polymorphic, with generally a heterogeneous mass riding on muscle and the skin with or without hyperemia; or an isodense mass with or without contrast enhancement.
MRI allows the definitive diagnosis. On MRI, endometriosis lesions are also very polymorphic and are characterized by variable contents of hemorrhagic and/or fibrous lesions [8].
Hyperintense signal on T1-weighted sequences is noted if there is evidence of recent hemoglobin degradation; hypointense signal on T1-weighted sequences occurs in old bleeding lesions. With T2-weighted sequences, signal is quite variable, generally hypointense.