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Diagnostic Ultrasound - Abdomen and Pelvis

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Cystic Disease of Dialysis<br />

TERMINOLOGY<br />

Abbreviations<br />

• Acquired cystic kidney disease (ACKD)<br />

Synonyms<br />

• Acquired cystic disease of uremia<br />

Definitions<br />

• Presence of 3 or more renal cysts per kidney in patients<br />

with chronic kidney disease (CKD) who do not have<br />

hereditary cystic disease<br />

• Occurs predominantly in patients on long-term dialysis<br />

(peritoneal or hemodialysis)<br />

IMAGING<br />

General Features<br />

• Best diagnostic clue<br />

○ Small kidneys with multiple small cysts bilaterally<br />

○ Advanced stage: Large kidneys as cysts increase in size<br />

<strong>and</strong> number<br />

• Location<br />

○ Bilateral; in areas of scarring throughout cortex <strong>and</strong><br />

medulla<br />

• Size<br />

○ Usually < 1 cm, up to 3 cm<br />

• Morphology<br />

○ Simple cyst: Round, fluid-filled lesion with imperceptible<br />

walls<br />

○ Complex cyst: Internal debris, septations, calcifications,<br />

wall thickening<br />

Ultrasonographic Findings<br />

• Grayscale ultrasound<br />

○ Multiple bilateral small cysts in normal size or atrophic,<br />

echogenic kidneys<br />

○ Cysts scattered in both renal cortex <strong>and</strong> medulla<br />

○ Renal size may be enlarged due to increase in size <strong>and</strong><br />

number of cysts<br />

– In advanced stage, appearance may resemble adult<br />

polycystic kidney disease (ADPKD)<br />

○ Simple cysts:Well-defined round lesions with posterior<br />

acoustic enhancement, distinct echogenic posterior wall,<br />

lack of internal echoes<br />

○ Hemorrhagic cysts: May contain internal echoes or<br />

nodular debris<br />

– Distinction from neoplasm not always possible<br />

○ Cyst rupture: May bleed into renal pelvis or<br />

retroperitoneum resulting in hematuria or<br />

retroperitoneal hematoma, respectively<br />

○ Malignant transformation of cysts typically manifests as<br />

papillary growth within the cyst<br />

• Color Doppler<br />

○ Presence of internal flow signal distinguishes tumor<br />

from hemorrhagic cyst<br />

○ Power Doppler more sensitive than color Doppler to<br />

detect slow flow<br />

• Contrast enhanced ultrasound (CEUS)<br />

○ Increased sensitivity for detecting malignancy compared<br />

to unenhanced US <strong>and</strong> CECT<br />

○ Not nephrotoxic, can be used in end-stage renal disease<br />

○ No internal enhancement in simple <strong>and</strong> complex cysts<br />

(other than thin smooth septa)<br />

○ Contrast uptake within cystic lesion is suspicious for<br />

malignancy<br />

CT Findings<br />

• Well-defined, thin-walled, nonenhancing lesions, < 20 HU<br />

• ± cyst wall calcifications, ± luminal high density from crystal<br />

deposition<br />

• Superior to ultrasound for detection of small tumors<br />

○ Neoplasms enhance with contrast, typically more<br />

heterogeneous<br />

○ Hyperdense cysts may be difficult to distinguish from<br />

solid lesions unless contrast is administered<br />

MR Findings<br />

• Best imaging test to evaluate for enhancing lesions, but<br />

contrast use may be limited secondary to risk of<br />

nephrogenic systemic fibrosis (NSF)<br />

• Simple cyst:T1 hypointense, T2 hyperintense,<br />

homogeneous<br />

• Hemorrhagic cyst: Variable T1 <strong>and</strong> T2 signal dependent<br />

upon age of hemorrhage<br />

• CEMR: No enhancement<br />

Imaging Recommendations<br />

• Best imaging tool<br />

○ <strong>Ultrasound</strong> as initial investigation for establishing<br />

diagnosis in patients on dialysis<br />

○ CEUS, CECT, or CEMR to evaluate complex cysts <strong>and</strong><br />

distinguish from renal cell carcinoma (RCC)<br />

• Protocol advice<br />

○ No widely accepted guidelines for screening of dialysis<br />

patients for ACKD or RCC<br />

DIFFERENTIAL DIAGNOSIS<br />

Multiple Simple Cysts<br />

• Rarely as numerous as in ACKD<br />

• Normal size kidneys with normal echogenicity<br />

• Renal function not impaired<br />

• Incidence increases with increasing age<br />

Adult Polycystic Kidney Disease (ADPKD)<br />

• Hereditary disorder characterized by multiple renal cysts<br />

<strong>and</strong> various systemic manifestations<br />

• Cysts <strong>and</strong> kidneys are larger in size than in ACKD<br />

• Differential features favoring ADPKD<br />

○ Family history; presence of renal failure<br />

○ Cysts in other organs: Liver (75%), pancreas (10%),<br />

spleen, ovaries<br />

○ Intracranial aneurysms<br />

von Hippel-Lindau Disease<br />

• Autosomal dominant multisystemic disorder<br />

• Multiple renal cysts, cysts in other organs<br />

• Kidneys are normal in size <strong>and</strong> functional<br />

• Hemangioblastomas: Cerebellar, spinal, <strong>and</strong> retinal<br />

• Multifocal renal cell carcinomas, pheochromocytomas<br />

Tuberous Sclerosis (TS)<br />

• Multiple bilateral renal cysts<br />

• Multiple small fat-containing renal angiomyolipomas<br />

Diagnoses: Urinary Tract<br />

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