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Diagnostic Ultrasound - Abdomen and Pelvis

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Prostatic Carcinoma<br />

TERMINOLOGY<br />

Abbreviations<br />

• Prostate carcinoma (PCa)<br />

Synonyms<br />

• Prostate adenocarcinoma<br />

IMAGING<br />

General Features<br />

• Best diagnostic clue<br />

○ MR: Peripheral zone (PZ): T2 dark lesion with restricted<br />

diffusion; central gl<strong>and</strong>: "Erased charcoal" sign on T2WI<br />

• Location<br />

○ PZ 70-80%, transition zone (TZ) 20-25%, central zone<br />

(CZ) 1-5%<br />

• Targeted MR-guided <strong>and</strong> MR/ultrasound fusion-guided<br />

biopsy is promising for increasing detection of high-risk<br />

prostate cancer while reducing detection of low-risk cancer<br />

compared with st<strong>and</strong>ard biopsy<br />

Ultrasonographic Findings<br />

• Grayscale ultrasound<br />

○ Transrectal ultrasound (TRUS) is imaging modality of<br />

choice to guide biopsy but performs poorly in cancer<br />

detection <strong>and</strong> staging; also used to guide focal therapies<br />

– TRUS-guided biopsy considered "blind" or "r<strong>and</strong>om"<br />

since it is usually not targeted to specific abnormality<br />

○ Traditional description of PCa is hypoechoic PZ lesion;<br />

difficult to identify central gl<strong>and</strong> tumors due to<br />

heterogeneity from benign prostatic hyperplasia (BPH)<br />

– Now with earlier cancer detection with PSA, studies<br />

have shown that hypoechoic lesions are not<br />

pathognomonic for cancer, as was once thought<br />

– PCa can appear as hypoechoic (60-70%),<br />

isoechoic/invisible (30-40%), rarely hyperechoic ±<br />

asymmetric capsular bulging or irregularity<br />

– Probability of hypoechoic lesion being PCa is 17-57%<br />

• Color Doppler<br />

○ PCa may be hypervascular; however, absence does not<br />

exclude Ca, <strong>and</strong> other benign entities (e.g., prostatitis)<br />

may also be hypervascular<br />

• Power Doppler<br />

○ No advantages over color Doppler<br />

CT Findings<br />

• Not accurate in detection of cancer within prostate<br />

• Glazer et al showed mass-like PZ enhancement is predictive<br />

of higher-grade (≥ Gleason 4 + 3) cancer<br />

• Evaluate local/distant staging only among patients with<br />

intermediate- or high-risk disease<br />

○ Clinical stage ≥ T2b vs. 3 (differing guidelines), Gleason ≥<br />

8, PSA > 10 vs. 20, or chance of lymph node involvement<br />

> 20% (based on nomograms)<br />

MR Findings<br />

• MR is most sensitive imaging technique for prostate cancer<br />

diagnosis <strong>and</strong> staging: Prostate Imaging <strong>and</strong> Reporting <strong>and</strong><br />

Data System (PI-RADS) 1-5<br />

• Prostatic cancer is best seen on T2WI <strong>and</strong> DWI<br />

○ Abnormal low T2 signal in normally high signal PZ with<br />

corresponding reduced diffusion<br />

– Differential for T2 dark lesion in PZ: Biopsy-related<br />

hemorrhage, changes from hormone therapy,<br />

prostatitis, atrophy, fibrosis<br />

○ "Erased charcoal" sign in TZ: Focal, homogeneous low T2<br />

signal lesion with ill-defined margins<br />

• T1WI: Precontrast: Evaluate for post-biopsy hemorrhage;<br />

dynamic postcontrast: Hypervascular lesion corresponding<br />

to T2/DWI abnormality<br />

• MR useful for staging<br />

○ T stage: Organ confined (≤ T2 disease) vs. extending<br />

beyond gl<strong>and</strong> (≥ T3 disease); signs of extraprostatic<br />

extension: Bulging prostatic contour, irregular or<br />

spiculated margin, obliteration of rectoprostatic angle,<br />

asymmetry or invasion of neurovascular bundle, seminal<br />

vesicle or bladder wall invasion<br />

○ Pelvic <strong>and</strong> retroperitoneal lymph nodes<br />

○ Osteoblastic bone metastases: Low signal intensity on<br />

both T1WI <strong>and</strong> T2WI<br />

• Post-biopsy changes (e.g., hemorrhage, inflammation) may<br />

complicate interpretation of prostate MR for staging; at<br />

least 6 weeks interval between biopsy <strong>and</strong> MR should be<br />

considered for staging<br />

Nuclear Medicine Findings<br />

• Bone scan<br />

○ Tc-99m MDP planar bone scan is st<strong>and</strong>ard imaging<br />

modality for diagnosis of bone metastases: Sensitivity<br />

62-89%, specificity 57%; reflects osteoblastic response in<br />

cortex, misses early marrow disease<br />

○ Should only be performed in patients with high-risk<br />

disease or symptoms of bony involvement: Clinical stage<br />

≥ T2c vs. 3 (differing guidelines), Gleason ≥ 8, PSA > 10 vs.<br />

20, or bony symptoms<br />

○ Tc-99m MDP SPECT (single-photon emission CT)<br />

improves sensitivity (92%) <strong>and</strong> specificity (82%)<br />

• PET/CT<br />

○ Main role of PET/CT is in primary staging <strong>and</strong> evaluation<br />

for biochemically recurrent disease; not helpful in<br />

diagnosis or T staging<br />

○ 18F-FDG PET/CT: Limited utility due to relatively low<br />

glucose metabolism of most PCa<br />

○ 18F-NaF PET/CT: For bone metastases; higher diagnostic<br />

accuracy, but arguably more expensive than bone scan +<br />

SPECT<br />

○ 11C-choline PET/CT: Limited accessibility, requires on site<br />

cyclotron; may detect disease in nonenlarged nodes <strong>and</strong><br />

early marrow involvement; evaluation for suspected<br />

recurrent disease<br />

Imaging Recommendations<br />

• Best imaging tool<br />

○ MR is most sensitive imaging technique for prostate<br />

cancer diagnosis <strong>and</strong> staging<br />

○ TRUS is imaging modality of choice for prostate biopsy<br />

DIFFERENTIAL DIAGNOSIS<br />

Benign Prostatic Hyperplasia<br />

• Hyperplasia of TZ <strong>and</strong> periurethral gl<strong>and</strong>s; heterogeneous,<br />

nodular enlargement ± cystic degeneration, calcification<br />

Prostatitis<br />

• Acute <strong>and</strong> chronic prostatitis can mimic prostate cancer<br />

Diagnoses: Urinary Tract<br />

529

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