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accessory spleen
congenital anomaly where a small, round island of splenic tissue is typically located near the splenic hilum or possibly near the tail of the pancreas
sonographic appearance of an accessory spleen:
will appear isoechoic to the spleen
splenic cleft
congenital anomaly where the spleen appears to be divided by a hyperechoic line
asplenia
congenital absence of the spleen
polysplenia
congenital anomaly that leads to the development of multiple masses of splenic tissue
asplenia and polysplenia have been associated with what other conditions?
some complex cardiac malformations and the abnormal location of other organs → heterotaxia syndromes
wandering spleen
extremely rare
the splenic ligaments are absent or underdeveloped, thus allowing the opportunity for the spleen to be highly mobile and often positioned well into the lower abdomen
can result in splenic torsion which can further lead to splenic infarction
what is the most common abnormality of the spleen?
splenomegaly
splenomegaly
enlargement of the spleen
normal measurement of the spleen:
should not exceed 12-13 cm in length and 6 cm in thickness in adults
as the spleen enlarges, what happens to its echogenicity?
it becomes more hypoechoic
what is the most common cause of splenomegaly?
portal HTN
other causes of splenomegaly include:
trauma
leukemia
lymphoma
a pediatric sickle cell anemia crisis
granulomatous disease
infections → endocarditis, AIDS and hepatitis
Epstein-Barr infection
massive splenomegaly can lead to what other condition?
splenic rupture which can further lead to splenosis
clinical findings of splenomegaly:
palpable, enlarged spleen
hemolytic abnormalities → sickle cell anemia
trauma
infection
hx of cirrhosis, trauma, leukemia, or lymphoma
leukocytosis and/or elevated RBC count
possible LUQ pain or discomfort
sonographic findings of splenomegaly:
enlargement of the spleen to greater than 12-13 cm in length or 6 cm in thickness
spleen extends beyond the inferior pole of the left kidney
true splenic cysts are also referred to as:
epithelial cysts
clinical findings of simple splenic cysts:
asymptomatic
pain can occur with hemorrhage
sonographic findings of simple splenic cysts:
round
smooth-walled mass
anechoic mass
posterior enhancement
splenic abscess
may be caused by staphylococcus aureus, streptococcus, or salmonella
a history of what condition increases the patient’s likelihood of developing a pyogenic abscess?
a history of bacteremia
disease processes that may lead to a splenic abscess include:
bacterial endocarditis
diverticulitis
osteomyelitis
pelvic infections
clinical findings of splenic abscesses:
fever
leukocytosis
LUQ tenderness
left flank or shoulder pain
splenomegaly
sonographic findings of splenic abscesses:
complex appearance
may contain debris or gas → produces dirty shadowing or ring down
can be completely hypoechoic
fungal abscess may appear as small solid masses or have a target or bull’s-eye appearance
color doppler will demonstrate increased flow around the mass but not within it
fungal splenic abscesses are often caused by:
Candida
a splenic infarct may be caused by:
sickle cell disease
bacterial endocarditis
tumor embolization
vasculitis
lymphoma
clinical findings of a splenic infarct:
sudden onset of LUQ pain
sonographic findings of a splenic infarct:
acute infarct → hypoechoic, wedge-shaped mass within the spleen
chronic infarct → hyperechoic, wedge-shaped mass within the spleen
clinical findings of splenic trauma:
blunt trauma to the LUQ
severe LUQ pain
decreased hematocrit level indicating active bleeding
sonographic findings of splenic trauma:
acute hemorrhage → complex or hypoechoic
middle stage → echogenic (with clot formation) or isoechoic
later stages of hemorrhage → anechoic or hypoechoic
chronic hematomas may have a complex appearance of calcified walls
a laceration may be noted as an echogenic line within the spleen immediately following trauma
what is the most common benign tumor of the spleen?
hemangioma
clinical findings of a splenic hemangioma:
asymptomatic
pain occurs with hemorrhage
sonographic findings of a splenic hemangioma:
well-defined, hyperechoic mass
clinical findings of granulomatous disease in the spleen:
asymptomatic
may have a hx of histoplasmosis, tuberculosis, or sarcoidosis
sonographic findings of granulomatous disease in the spleen:
small, echogenic foci that may shadow
splenic hamartoma
a benign mass that is associated with Beckwith-Wiedemann syndrome and tuberous sclerosis
clinical findings of splenic hamartoma:
asymptomatic
pain can occur with rupture
patient may have a hx of Beckwith-Wiedemann syndrome or tuberous sclerosis
sonographic findings of splenic hamartoma:
hypoechoic mass or masses → echotexture can vary however
color doppler may reveal hypervascularity
angiosarcoma
exceedingly rare primary malignant tumor of the spleen
what is the most common malignancy of the spleen?
lymphoma
the presence of what type of cells indicates Hodgkin lymphoma?
Reed-Sternberg cells
what type of lymphoma is more common?
non-Hodgkin lymphoma
the most common primary locations for metastatic disease to the spleen are:
breast
lung
skin → melanoma
ovary
clinical findings of splenic malignancy:
LUQ pain
fever
weight loss
malaise
sonographic findings of splenic malignancy:
diffuse → splenomegaly
focal → hypoechoic masses
what type of lymphoma has a better chance of recovery?
Hodgkin lymphoma
splenic lymphangioma (pediatric)
a benign lesion that is a congenital malformation of the lymphatic system
comprised of both lymphatic and blood vessels
most identified in children
clinical findings of splenic lymphangioma:
nausea
LUQ pain
abdominal distention
sonographic findings of splenic lymphangioma:
multicystic masses
masses may contain hypoechoic or anechoic locules and hyperechoic septations
sickle cell disease
a group of inherited blood disorders that affects hemoglobin
sickle cell anemia (pediatric)
patients have abnormal, crescent-shaped RBCs that tend to attach to each other and obstruct normal vascular channels, causing many clinical complications
enlarged spleen
occasionally, focal masses of normal splenic tissue may be noted
recurrent sickle cell crises leads to the spleen becoming fibrotic and atrophy
patients undergoing a sickle cell crisis may have:
decreased hematocrit
complain of bone pain
increased risk for gallstones, multiple organ damage, blindness, and stroke