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Diagnostic Ultrasound - Abdomen and Pelvis

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Splenic Cyst<br />

406<br />

Diagnoses: Spleen<br />

Neoplastic<br />

• Benign: e.g., hemangioma & lymphangioma<br />

○ Hemangioma<br />

– Variable size <strong>and</strong> echogenicity, solid ± cystic areas,<br />

rarely solitary large lesion involving entire spleen<br />

○ Lymphangioma<br />

– Heterogeneous/multicystic appearance, intracystic<br />

echoes: Proteinaceous material<br />

• Malignant: e.g., lymphoma & metastases<br />

○ Lymphoma<br />

– Hypoechoic/anechoic type of lymphomatous nodules:<br />

May resemble cysts, however reveal "indistinct<br />

boundary" echo pattern<br />

– Posterior acoustic enhancement absent<br />

○ Metastases: Necrotic/cystic<br />

– Relatively common; e.g., malignant melanoma,<br />

adenocarcinoma of breast, pancreas, ovaries, <strong>and</strong><br />

endometrium may cause "cystic" splenic metastases<br />

– Multiple focal, cystic lesions of variable size<br />

Vascular<br />

• Hematoma or laceration<br />

○ Hypo-/iso-/hyperechoic, blood-filled cleft; nonspherical<br />

shape<br />

○ Hematoma echogenicity depends on stage of bleed;<br />

fresh blood echo-free initially, later becomes echogenic<br />

○ End stage: Cystic degeneration →pseudocyst<br />

• Infarction (arterial or venous)<br />

○ Acute phase: Well-defined, wedge-shaped areas of<br />

decreased echogenicity<br />

○ Subacute & chronic phases: Anechoic (due to liquefactive<br />

necrosis)<br />

• Peliosis<br />

○ Rare; usually with liver findings; multiple indistinct areas<br />

of hypo-/hyperechogenicity that may involve entire<br />

spleen<br />

• Intrasplenic pseudoaneurysm<br />

○ Post-traumatic; anechoic on grayscale, fills with color<br />

Doppler<br />

Intrasplenic Pancreatic Pseudocyst<br />

• In 1-5% of patients with pancreatitis<br />

• Direct extension of pancreatic pseudocyst; pancreatic<br />

secretions extend along splenic vessels to hilum, pancreatic<br />

enzymes cause erosion into spleen<br />

• Well-defined, rounded, cystic splenic lesion; associated<br />

inflammatory changes of pancreas<br />

PATHOLOGY<br />

General Features<br />

• Etiology<br />

○ Congenital: Genetic defect of mesothelial migration<br />

○ Acquired: Most often post-traumatic, end-stage of<br />

splenic hematoma/infarction<br />

– Pathogenesis: Liquefactive necrosis, cystic change<br />

Gross Pathologic & Surgical Features<br />

• Congenital cyst<br />

○ Usually large, glistening, smooth walls<br />

• Acquired cyst<br />

○ Smaller than true cysts, debris, wall calcification<br />

○ Parasitic: Hydatid (Echinococcus granulosus most<br />

common form to affect spleen), Taenia solium<br />

Microscopic Features<br />

• True cyst: Epithelial lining present<br />

○ Epidermoid (stratified, nonkeratinizing squamous<br />

epithelium), mesothelial (low cuboidal to low columnar),<br />

dermoid (squamous lining with dermal structures)<br />

○ Epidermoid most common<br />

• False cyst: No epithelial lining, may have fibrous capsule<br />

CLINICAL ISSUES<br />

Presentation<br />

• Most common signs/symptoms<br />

○ Depends on etiology, acuity<br />

○ Often asymptomatic<br />

○ Mild pain or tenderness, palpable mass in LUQ,<br />

splenomegaly<br />

Demographics<br />

• Age<br />

○ 2/3 < 40 years old<br />

• Gender<br />

○ M:F = 2:3<br />

Natural History & Prognosis<br />

• Complications: Hemorrhage, rupture, infection<br />

• Prognosis<br />

○ Good: Uncomplicated cases; after surgical removal<br />

○ Poor: Complicated cases<br />

Treatment<br />

• Symptomatic: Surgery (total cystectomy, marsupialization,<br />

cyst decapsulation, or partial/total splenectomy)<br />

• Asymptomatic<br />

○ Small: No treatment<br />

○ Large (> 5-6 cm): Surgical removal (controversial)<br />

• <strong>Ultrasound</strong>-guided drainage ± injection of sclerosing agent<br />

is alternative option<br />

DIAGNOSTIC CHECKLIST<br />

Consider<br />

• Rule out infectious, vascular, <strong>and</strong> neoplastic cystic lesions<br />

Image Interpretation Pearls<br />

• Congenital: Larger, well defined, anechoic, thin wall; ±<br />

calcification <strong>and</strong> debris (less common)<br />

• Acquired: Usually smaller, well defined; often anechoic with<br />

thicker wall; ± calcification, ± debris<br />

• Often impossible to distinguish primary vs. secondary (or<br />

true vs. false) cysts by imaging<br />

SELECTED REFERENCES<br />

1. Gaetke-Udager K et al: Multimodality imaging of splenic lesions <strong>and</strong> the role<br />

of non-vascular, image-guided intervention. Abdom Imaging. 39(3):570-87,<br />

2014<br />

2. Li W et al: Real-time contrast enhanced ultrasound imaging of focal splenic<br />

lesions. Eur J Radiol. 83(4):646-53, 2014<br />

3. Caremani M et al: Focal splenic lesions: US findings. J <strong>Ultrasound</strong>. 16(2):65-<br />

74, 2013

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