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Agostino Gemelli Hospital Rome 00168, Italy
A 75-year-old woman came to our institution for observation in March 2002 with a history of nausea, melena, and loose stools. She had undergone left radical nephrectomy and splenectomy for renal cell carcinoma in January 2000, with resultant renal insufficiency. Rectal examination showed bloody stool. Esophagogastroduodenoscopy and colonoscopy showed normal findings. The referring surgeon proposed small-bowel examination; MR enteroclysis was performed.
Nasojejunal intubation was performed under fluoroscopy guidance using a 13-French catheterguidewire device. After intubation, the patient was transferred to the MRI suite and placed on the MR device table in the prone position to distend the loops and to avoid gastric reflux and vomiting.
MR enteroclysis was performed with a torso phased array coil on a 1.5-T magnet. The images revealed a 5-cm oval soft-tissue mass involving a distal ileal loop, slightly hyperintense on T2-weighted images with a strong enhancement in the arterial phase of contrast administration (Fig. 3A, 3B, 3C, 3D). The mass was multilobulated with smooth borders and no extraserosal invasion, suggesting a hypervascular submucosal lesion. No evidence of other lesions or lymphadenopathy was observed.
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At surgery, a 5-cm endoluminal mass was found in a distal ileal loop without serosal infiltration; no other abdominal lesions were detected. Diagnosis of ileal metastasis from renal cell carcinoma was established. Small-bowel secondary lesions are usually multiple; solitary metastases from renal carcinoma are rare [1].
MR enteroclysis was only recently introduced in clinical practice; it offers adequate image quality coupled with the benefits of volume challenge [2]. MR enteroclysis allowed the identification and local staging of the ileal lesion, combining the advantages of cross-sectional MRI to evaluate the local neoplastic staging [3] with those of conventional enteroclysis for intraluminal evaluation.
MRI examination of the small intestine includes T1- and T2-weighted sequences in the axial and coronal planes. We use single-shot fast spin-echo heavily T2-weighted sequences (slab thickness, 710 cm; TR/TE, infinite/950) to monitor the infusion process and the functional assessment, followed by single-shot fast spin-echo T2-weighted sequences (TE, 90 msec) to visualize the lumen, bowel walls, and mesenteries. T1-weighted sequences are acquired with fast-spoiled gradient-echo sequences, fat saturation, and IV administration of gadolinium chelates 3D acquisition. This technique allowed our surgeons to assess the small-bowel lesion before potential surgery with high-quality images while avoiding the use of multiple radiation examinations.
References
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