Posttherapy imaging of musculoskeletal neoplasms.

Posttreatment imaging is important to ensure early detection of oncological complications, and appropriate timing and frequency is an important consideration, especially in high-risk patients. Focused magnetic resonance (MR) imaging is the preferred modality for detection of local recurrence of soft tissue tumors and is also used in high-risk osteosarcoma. Although posttreatment changes can mimic or obscure local recurrence on MR imaging, a systematic approach and knowledge of the features of recurrence versus therapeutic change allows differentiation in almost all cases. Positron emission tomography/computed tomography is also emerging as an important problem-solving tool in local recurrence and in metastatic surveillance.

Clinical utility of dual-energy CT for evaluation of tophaceous gout.

Although diagnosing gout generally is straightforward, atypical disease may present a challenge if it is associated with unusual symptoms or sites, discordant serum urate level, or mimics of gout. Dual-energy computed tomography (CT) may be used to differentiate urate crystals from calcium by using specific attenuation characteristics, which may help diagnose gout. In patients with known tophaceous gout, dual-energy CT may be used for serial volumetric quantification of subclinical tophi to evaluate response to treatment. Given the utility of dual-energy CT in challenging cases and its ability to provide an objective outcomes measure in patients with tophaceous gout, dual-energy CT promises to be a unique and clinically relevant modality in the diagnosis and management of gout.

Benign and malignant soft-tissue tumors: posttreatment MR imaging.

Soft-tissue sarcoma requires aggressive treatment, often with a combination of radiation therapy, chemotherapy, and surgical resection. Even after multimodality treatment, local recurrence is common, and regular follow-up imaging at short intervals is required. Interpretation of posttreatment magnetic resonance (MR) images may be complicated by changes in the surgical bed or treatment field. The challenge of distinguishing posttreatment change from recurrent tumor may be minimized by using an organized, systematic approach to imaging, with emphasis on the patient's clinical and surgical history and a review of pretreatment images. Common changes that result from radiation therapy include soft-tissue trabeculation, increased fatty marrow, and focal marrow abnormalities. Rarely, radiation-induced malignancies may develop within the treatment field. Chemotherapy also influences posttreatment imaging appearance. Occasionally, it causes a substantial increase in tumor size that is a result of chemotherapy-induced hemorrhage. Although myocutaneous flaps used in reconstructive surgery may mimic a mass, they demonstrate time-dependent changes in size, signal intensity, and enhancement on MR images. Recurrent tumor is characterized by the presence of a discrete nodule or mass with signal characteristics that typically mirror those of the original tumor. MR imaging sequences such as unenhanced T1-weighted fat-suppressed and gradient-echo sequences may help differentiate posttreatment hemorrhage from local tumor recurrence. A consistent imaging approach combined with a detailed knowledge of the patient's history, familiarity with pretreatment images, and an understanding of the various posttreatment changes enables optimal monitoring of the treatment bed and maximizes accuracy in the detection of recurrence.