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Diagnostic Ultrasound - Abdomen and Pelvis

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Cystic Renal Mass<br />

964<br />

Differential Diagnoses: Kidney<br />

DIFFERENTIAL DIAGNOSIS<br />

Common<br />

• Simple Renal Cyst<br />

• Complex Cysts: Hemorrhagic, Infected, or Proteinaceous<br />

• Renal Sinus Cysts<br />

• Hydronephrosis<br />

• Cystic Disease of Dialysis<br />

• Autosomal Dominant Polycystic Kidney Disease<br />

• Multicystic Dysplastic Kidney<br />

• Cystic Renal Cell Carcinoma<br />

• Localized Cystic Renal Disease<br />

• Renal Abscess<br />

• Renal Hematoma<br />

Less Common<br />

• Multilocular Cystic Nephroma<br />

• Mixed Epithelial <strong>and</strong> Stromal Tumor<br />

• Primary Renal Synovial Sarcoma<br />

• Lymphangioma<br />

• Perinephric Collection<br />

• Tuberous Sclerosis<br />

• von Hippel-Lindau Disease<br />

• Arteriovenous Fistula/Malformation; Intrarenal Aneurysm<br />

• Congenital Megacalyces<br />

• Renal Lymphoma or Metastases<br />

• Hydatid Cyst<br />

ESSENTIAL INFORMATION<br />

Key Differential Diagnosis Issues<br />

• Cystic renal masses run the gamut from simple cyst to cystic<br />

renal carcinoma<br />

• Simple cysts are benign <strong>and</strong> require no follow-up<br />

• Ensure that the lesion is truly a simple cyst<br />

• Beware of technical artifacts producing internal echoes<br />

within cysts such as<br />

○ Reverberation from skin-transducer interfaces superficial<br />

to cyst<br />

○ High gain settings<br />

○ Side lobe artifacts from adjacent tissue<br />

• Posterior acoustic enhancement typically occurs with larger<br />

lesions<br />

○ May not be seen if cyst is very small<br />

• Multiple tiny cysts may not be resolved<br />

○ Instead may appear as an echogenic lesion due to<br />

multiple reflective surfaces<br />

• Complex cysts may represent complicated benign cysts or<br />

cystic neoplasms including renal cell carcinoma<br />

• Therefore, it is imperative to detect features that indicate<br />

further imaging or follow-up<br />

○ Look for solid components or mural nodules<br />

○ Evaluate the entire wall of large cysts<br />

○ Evaluate septa<br />

○ CECT: CEMR or CEUS for further evaluation<br />

○ Bosniak classification helps in guiding management<br />

• May difficult to confirm origin of exophytic or large renal<br />

cysts<br />

• Cysts in upper pole of kidney may be difficult to<br />

differentiate from suprarenal, hepatic (right), or splenic<br />

(left) cysts<br />

○ Try to delineate relationship during real-time imaging<br />

• Determine if single cystic lesion or multiple lesions<br />

• Consider syndromes with cysts if multiple bilateral renal<br />

cysts in young patients<br />

Helpful Clues for Common Diagnoses<br />

• Simple Renal Cyst<br />

○ Extremely common; increases with age<br />

○ Well-defined, round or oval, smooth, <strong>and</strong> thin walled<br />

○ Entirely echo free with posterior acoustic enhancement<br />

○ No septum or solid component; no color Doppler flow<br />

○ May exert mass effect on calyces if large<br />

○ Location: Renal cortex, deep or superficial<br />

• Complex Cysts: Hemorrhagic, Infected, or Proteinaceous<br />

○ Thin, smooth internal septa<br />

○ Internal echoes from hemorrhage, infection, or<br />

proteinaceous debris<br />

○ Calcified wall or septa<br />

• Renal Sinus Cysts<br />

○ Include peripelvic cysts <strong>and</strong> lymphangiectasia<br />

○ Located in renal hilum<br />

○ Surround <strong>and</strong> may compress renal pelvis but do not<br />

communicate with collecting system<br />

○ Can mimic hydronephrosis<br />

○ Most are asymptomatic; rarely associated with<br />

hematuria or hypertension<br />

• Hydronephrosis<br />

○ Dilated calyces connecting to dilated pelvis<br />

○ Use color Doppler to distinguish from prominent vessels<br />

• Cystic Disease of Dialysis<br />

○ 3 or more cysts per kidney in patient with chronic kidney<br />

disease <strong>and</strong> no history of hereditary cystic disease<br />

○ May precede dialysis, almost inevitable after long-term<br />

dialysis<br />

○ Atrophic echogenic kidneys with loss of corticomedullary<br />

differentiation<br />

○ Cysts in both renal cortex <strong>and</strong> medulla, especially at site<br />

of renal scars<br />

○ Renal size may be enlarged due to multiple large cysts<br />

– May resemble polycystic kidney disease, clinical<br />

correlation needed<br />

○ Increased risk of renal cell carcinoma (RCC): 3-7%<br />

• Autosomal Dominant Polycystic Kidney Disease<br />

○ Autosomal dominant inheritance, spontaneous mutation<br />

in 10%<br />

○ Massively enlarged, echogenic kidneys with lack of<br />

corticomedullary differentiation<br />

○ Multiple bilateral cysts of varying size<br />

○ Intracystic hemorrhage/infection/milk of calcium<br />

○ Mural calcification<br />

○ Associated with cysts of other organs: Liver (75%),<br />

pancreas (10%), spleen (5%)<br />

• Multicystic Dysplastic Kidney<br />

○ Congenital lesion discovered on prenatal ultrasound or<br />

incidental finding<br />

○ Multiple noncommunicating cysts of varying size<br />

○ No communication to ureter<br />

○ Usually unilateral, may be complete or segmental

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