Spleen Flashcards
Name Spleen variations
4
- Accessory spleen (picture)
- 40% of patients
- arises from failure of fusion
- usually near hilum of spleen
- usual size <3cm
- round
- Lobulations
- normal
- Wandering spleen
- abnormal congenital development of the dorsal mesogastrium
- Normally the posterior leaft of the doral mesogastrium fuses with the parietal peritoneum anterior to the left kidy to form the lienorenal ligament, the most important stabiliser of splenic position
- Failure of complete fusion of these structures allows for abnormal mobility of the spleen with a long splenic vascular pedicle.
- therefore excessive intraperitoneal movement and torsion can occur
- laxity of suspensory ligements allws spleen to move in the abdomen
- Confirm with a TC-99m sulfur colloid scan.
- Polysplenia
- multiple splenic nodules
- left sided liver
- abseces of GB
- Cardiac anomalies
- incomplete development of the IVC
- Asplenia
- absence of the spleen
- exclude splenectomy
*
what is this syndrome?
Associations?
AKAs
Polysplenia syndrome
Polysplenia syndrome, also known as left isomerism, is a type of heterotaxy syndrome where there are multiple spleens congenitally as part of left-sided isomerism.
Epidemiology
- Polysplenia is seen predominantly in female patients.
- It is usually diagnosed in childhood or adulthood, later than asplenia syndrome, since associated congenital heart diseases tend to be less severe than those encountered in the latter.
- Aetiology
The exact cause of polysplenia is unknown. However it is suggested that it is caused by various factors 10:
- embryogenic
- genetic
- teratogenic
Pathology
- Polysplenia results from failure of development of the usual left-right asymmetry of organs and consists of situs ambiguus, with features of bilateral left-sidedness.
Radiographic features
General
- It is characterised by multiple splenules without a parent spleen.
- It occurs on the patient’s left side but may be bilateral.
- The most common associated feature is inferior vena cava interruption with azygos or hemiazygos continuation 3.
Other characteristic features include:
- bilateral hyparterial bronchi
- bilateral bilobed lungs
- bilateral pulmonary/left atria
- midline liver
Associations
- Cardiac
- congenital heart disease (>50%): especially non-cyanotic, and less complex/severe than in asplenia syndrome 3
- abnormal pulmonary venous return (70%, PAPVR/TAPVR)
- dextrocardia (37%)
- gastrointestinal
- semi-annular pancreas / congenitally short pancreas 4,6,8
- midgut malrotation (80%) 7,8
- gallbladder agenesis (50%) and biliary atresia
- mobile caecum
- tracheo-oesophageal fistula
- genitourinary
- renal cyst
- renal agenesis
- ovarian cyst
- vascular
- inferior vena cava anomalies 7,8
- intrahepatic IVC interruption with azygos/hemiazygos continuation
- portal vein anomalies 7,8
- preduodenal portal vein
There is inversion of some abdominal structures (liver, spleen and stomach) with thoracic structures in normal position. Multiple splenules are seen on right hypochondrium. The study protocol was made for chest CT.
Case Discussion
Situs inversus partialis refers to any kind of incomplete organs inversion, like in this case. Malformations associations are more frequent in situs inversus partialis than in situs inversus totalis.
Polysplenia refers to multiple small accessory spleens.
Wandering Spleen
Wandering spleen is a rare condition in which the spleen migrates from its usual anatomical position, commonly to the lower abdomen or pelvis.
Epidemiology
Wandering spleen is rare, with a reported incidence of <0.5%.
Diagnosis is most commonly made between ages 20 and 40 years and is more common in multiparous women 1,6.
Clinical presentation
Wandering spleen can be an elusive diagnosis as its presentation is greatly variable and intermittent torsion can cause non-specific signs and symptoms.
It can present as an asymptomatic or painful abdominal mass, intermittent abdominal pain, or as an acute abdomen (e.g. bowel obstruction, acute pancreatitis) 3,4,6.
Pathology
The abnormal mobility of the spleen is caused by an abnormality of its suspensory ligaments. There may be a congenital absence or underdevelopment of these ligaments, or an acquired laxity of the ligaments caused by various conditions, such as pregnancy or diseases causing splenomegaly. Due to these abnormal ligaments a long vascular pedicle may form, containing the splenic vessels, predisposing the spleen to torsion and consequently splenic infarction 4.
Aetiology
There are various causes, mostly related to the splenomegaly.
sickle cell disease
heterotaxy syndrome
lymphoproliferative disease
trauma
mononucleosis
Radiographic features
The often non-specific clinical presentation of wandering spleen makes radiological evaluation invaluable in its diagnosis. Performing the radiological investigations in different positions allows identification of the wandering spleen’s inclination to wander.
Plain radiograph
A wandering spleen is not frequently diagnosed on plain film radiography, but findings on abdominal x-ray may include 3,6:
absence of splenic shadow in the left upper quadrant
space-occupying soft tissue mass in abnormal location
distended bowel loops
Asplenia syndrome
AKA
- right isomerism
- Ivemark syndrome
- A type of heterotaxy syndrome.
Epidemiology
- There is an increased male predilection. Asplenia syndrome is usually diagnosed in neonates 4.
Associations
- severe/complex congenital heart disease (50%), especially cyanotic congenital cardiac anomalies
- total anomalous pulmonary venous return (almost 100%)
- endocardial cushion defect (85%)
- transposition of the great arteries (72%)
- single ventricle (51%)
- double outlet right ventricle (DORV)
gastrointestinal
- gallbladder agenesis
- intestinal malrotation (up to 100% in small series) 3
- microgastria
- imperforate anus
genitourinary
- horseshoe kidney
- fused / horseshoe adrenal gland or absent left adrenal gland
- bicornuate uterus
- bilobed urinary bladder
vascular
- duplication of the superior vena cava
- absent coronary sinus
- juxtaposition of the IVC in front (usually) of the abdominal aorta (piggyback configuration)
Clinical presentation
- In contrast to polysplenia syndrome, most patients die before 1-year-old because of severe/complex congenital heart disease. Most patients are immunocompromised due to absent spleen.
Pathology
- Howell-Jolly and Heinz bodies are seen on H&E blood smear 6.
Radiographic features
- absence of spleen
- bilateral eparterial bronchi
- bilateral trilobed lungs
- bilateral right atria
- transverse liver
What are the common causes of Splenomegaly
what disease is demonstrated?
- Defined as splenic length >13cm longest diameter in longest dimention
- Causes
- Tumor
- infection
- Metabolic
- Vascular
- Causes
- Tumor
- leukaemia
- lymphoma
- infection
- AIDS related
- Infectious mononucleosis
- Metabolic
- Gauchers disease
- Vascular
- portal hypertension
- May be a/w Gamna Gandy bodies
- benign siderotic nodules
- hypointense by MRI
- Tumor
- Splenic siderotic nodules, also known as Gamna-Gandy bodies, of the spleen, are most commonly encountered in portal hypertension. The pathophysiological process is the result of microhaemorrhage resulting in haemosiderin and calcium deposition followed by fibroblastic reaction.
what is this?
- Splenic Epidermoid
- True cyst
- epithelial lining
- Splenic epithelial cysts, also known as splenic epidermoid cysts or primary splenic cysts, are unilocular fluid lesions with thin and smooth walls and no enhancement. They represent ~20% of cysts found in the spleen, and are usually an innocuous incidental imaging finding.
Note that most (~80%) simple-appearing cystic splenic lesions represent secondary cysts or pseudocysts (see Differential diagnosis section below).
- Terminology
In practice, both primary and secondary cysts are often described simply as “splenic cyst” for the sake of simplicity, as often the specific aetiology is not evident.
Epidemiology
They are thought to account for 20% of benign non-parasitic cysts of the spleen 5,8. There may be an increased female predilection.
DDx for a Splenic Cyst
- A number of splenic lesions may appear cystic, depending on the modality:
- True Splenic cyst 20% (ie epithelial lined)
- secondary cysts (~80% of all splenic cysts) splenic pseudocysts
- post-traumatic pseudocyst: the end-stage of splenic haematoma with resultant liquefactive necrosis and cystic changes
- post-infarction pseudocyst: also resultant from liquefactive necrosis
- intrasplenic pancreatic pseudocyst
- infection
- splenic hydatid cyst (image)
- other congenital cystic lesions (tend to be unilocular in a majority of cases)
- splenic lymphangioma
- splenic haemangioma
- splenic bacterial abscess
- cystic splenic metastases
- splenic lymphoma: although may appear nearly anechoic, hypoechoic lymphoma tends to have less distinct margins than a cyst 10
- splenic peliosis 11,12
asssociations of this finding
- splenic hamartoma
- Rare
- benign tumour primarily composed of vascular elements
- can be asymptomatic or anemia and thrombocytopenia may occur
- Usually hyper echoic on US
- Hypodense or isodense on CT
- Cystic and calcified elements may be present in large lesions.
Associations
- Tuberous sclerosis
- Wiskott-Aldrich syndrome
Splenic Hemangioma
- Most common benign splenic tumour
- 14% of autopsy series
- Hyperechoic on US
- well delineated
- small
- foci of calcification occasionally
Splenic haemangiomas, also known as splenic venous malformations, splenic cavernous malformations, or splenic slow flow venous malformations, while being rare lesions, are considered the second commonest focal lesion involving the spleen after simple splenic cysts 5,12 and the most common primary benign neoplasm of the spleen 6. They are usually found incidentally and have imaging appearances similar to hepatic haemangiomas.
What is this?
- Sclerosing angiomatoid nodular tumour
- benign vascular splenic lesion
- SANT
- imaging features
- early peripheral enhancement with lines radiating from the middle
- progressive enhancement of the vascular nodules
- delayed central scar enhancement
- T2 hypointense from hemosiderin
what are the most common metastases to the spleen?
- Breast
- lung
- Stomach
- melanoma
- end stage ovairan cancer
what is the most common malignancy of the spleen?
lymphoma. Metastases are less common.
Splenic lymphoma, also termed as lymphomatous involvement of the spleen, represents the most common malignancy to involve the spleen. They are commonly secondary, rarely being primary (referred as primary splenic lymphoma).
This article focuses on the location-specific primary and secondary lymphomas involving the spleen, for a broader and systemic discussion, please refer to the main article on lymphoma.
Epidemiology
The spleen is involved in about 30% of all Hodgkin lymphoma and 30-40% of patients with systemic non-Hodgkin lymphoma (NHL) 2,4. The primary splenic lymphoma is rarer, representing about 2% of all lymphomas 2.
Clinical presentation
Lymphoma can often present with B symptoms (fever, night sweats and weight loss 3), please refer to the main article for further discussion in the systemic presentation.
Both primary and secondary splenic lymphoma may cause left upper quadrant pain 3.
Pathology
Primary splenic lymphomas are in general due to diffuse large B-cell lymphoma (DLBCL) 4. Please refer to the main article on lymphoma for further discussion in the secondary involvement of the spleen.
- Seraut Spleen
- Innumerable small punctate extravasations in a traumatised spleen following motor vehicle accident. This angiographic appearance is often termed ‘Seurat spleen’ because of a likeness to the pointillistic artwork of French impressionist Georges Seurat (1859 - 1891).
“Gray weather, Grande Jatte” by Georges Seurat, painted 1888.
Case Discussion
Innumerable small punctate contrast extravasations in a traumatised spleen following motor vehicle accident. This angiographic appearance is often termed ‘Seurat spleen’ because of a likeness to the artwork of French impressionist Georges Seurat (1859 - 1891) who used a pointillistic technique to create an image out of tiny dots. Proximal splenic artery embolisation with coil was performed in this patient who went on to make an uneventful recovery from their splenic trauma.
What is the grading system for splenic Trauma?
- The American Association for the Surgery of Trauma (AAST) splenic injury scale
- grade I
- subcapsular haematoma <10% of surface area
- parenchymal laceration <1 cm depth
- capsular tear
- grade II
- subcapsular haematoma 10-50% of surface area
- intraparenchymal haematoma <5 cm
- parenchymal laceration 1-3 cm in depth
- grade III
- subcapsular haematoma >50% of surface area
- ruptured subcapsular or intraparenchymal haematoma ≥5 cm
- parenchymal laceration >3 cm in depth
- grade IV
- any injury in the presence of a splenic vascular injury* or active bleeding confined within splenic capsule
- parenchymal laceration involving segmental or hilar vessels producing >25% devascularisation
- grade V
- shattered spleen
- any injury in the presence of splenic vascular injury* with active bleeding extending beyond the spleen into the peritoneum
- Additional points
- advance one grade for multiple injuries, each up to grade III
- “vascular injury” (i.e. pseudoaneurysm or AV fistula) appears as a focal collection of vascular contrast which decreases in attenuation on delayed images
- “active bleeding” - focal or diffuse collection of vascular contrast which increases in size or attenuation on a delayed (i.e. later) phase
- Imaging technique
- The AAST guidelines recommend dual arterial/portal venous phase imaging for evaluation of a vascular injury of the liver, spleen, and kidney 4.
what grade trauma is this?
Grade I splenic trauma
Moderate volume of free intraperitoneal fluid, particularly around the spleen which has a small hypodense and superficial cleft posteriorly, suspicious for grade I laceration.
Patchy fat stranding and fluid is seen within the small bowel mesentery, in the region of mesenteric vessels. Small foci of higher density are seen within the fat stranding, immediately adjacent to vessels and suspicious for venous bleeding. The bowel loops themselves show no gross abnormality and there is no free gas.
Lap belt subcutaneous bruising overlies the epicentre of the mesenteric abnormality.
Case Discussion
Injuries demonstrated in this case:
mesenteric tear with (probable) active venous bleeding
grade 1 splenic laceration
What grade Splenic injury is this?
Grade II splenic Trauma
A hypodense laceration involves the posterior aspect of the spleen with intrasplenic haematoma. Right iliopsoas haematoma is noted from a fracture of the posterior right ilium and right side of sacral promontory. Mild free intraperitoneal fluid, mild bilateral basal pleural effusion and green stick fracture of left superior pubic ramus are also noted.
Diagnosis: Grade II splenic injury from blunt abdominal trauma
What grade Splenic injury is this?
There is an intraparenchymal haematoma/laceration measuring > 5 cm which extends to the splenic hilum. Further splenic laceration noted inferiorly. Trace of perisplenic haematoma and free fluid in the pelvis. The overall appearances are in keeping with a grade 3 splenic injury in accordance with the American Association for the Surgery of Trauma (AAST) splenic injury grading.
No bone fractures or injury to other organs. Chest was clear.
What grade Splenic injury is this?
Grade V spleen injury
Annotated images showing the active contrast extravastation from the splenic hilum on both arterial and portal venous phases.
Case Discussion
The spleen is ‘shattered’ into pieces, with active contrast extravasation at the splenic hilum, which extends across the midline towards the hepatic hilum.
High attenuation fluid in the upper abdomen and pelvis in keeping with haemoperitoneum.
This is the highest grade splenic injury (grade 5).
The patient proceeded to an emergency splenectomy, which confirmed the above, including 1.5 litres of blood in the peritoneum, and a bleeding vessel at the splenic hilum.
The concomitant left renal laceration managed conservatively.
Life lesson: motorbikes and alcohol are not sensible friends.
What grade Splenic injury is this?
Extensive splenic lacerations extending to the hilum with areas of devascularisation. No evidence of active bleeding or pseudo-aneurysm. There is extensive haemoperitoneum throughout the abdominopelvic cavity. Cholecystectomy clips are noted along with extrahepatic and first order intrahepatic duct dilatation. Liver is uninjured. Adrenal glands, kidneys and pancreas are uninjured. Bowel is unremarkable. Lung bases are clear. No bony injury identified.
Conclusion:
AAST grade IV splenic injury with extensive haemoperitoneum.
Case Discussion
Further history obtained (after the CT) revealed a fall from 1.5 metres. Patient proceeded to successful splenic embolisation.
what nuc med scan can be used to diagnose this condition?
Splenosis is one type of ectopic splenic tissue (the other being accessory spleen). It is an acquired condition and is defined as autoimplantation of one or more focal deposits of splenic tissue in various compartments of the body.
Abdominal splenosis is seen after abdominal trauma or surgery (e.g. splenectomy). It results from seeding of the peritoneal cavity with splenic tissue which recruits local blood supply. The ectopic splenic foci are typically small, sessile (as they grow on serosal/peritoneal surfaces) and multiple. They may grow over time to become quite sizeable. If located only intrahepatically, they can cause serious diagnostic problems.
A similar process occurring in the thorax is called thoracic splenosis. It is rare and presents as multiple pleurally-based nodules in the left hemithorax. It typically occurs following blunt trauma causing a combination of splenic injury and left diaphragmatic rupture 4.
They are benign*, their greatest importance being the need to distinguish them from more sinister pathology.
*they are benign, but any pathology that can develop in the normal spleen can also arise within the splenic tissue foci
Radiographic features
CT
They are typically rounded or sessile nodules, and have density and enhancing characteristics similar to the rest of the spleen, or expected density of the spleen if there has been a splenectomy.
MRI
Signal characteristics are similar to normal spleen 2
T1: hypointense
T2: hyperintense
T1 C+ (Gd): heterogeneous enhancement
Nuclear medicine
Tc-99m sulfur colloid scan
The diagnosis can be confirmed with Tc-99m sulfur colloid scan which will demonstrate increased uptake as long as the splenunculus is at least 2 cm in diameter; improved sensitivity with hybrid imaging (SPECT-CT) is possible 7.
When Tc-99m sulfur colloid fails to confirm the presence of splenic tissue, Tc-99m-tagged heat-damaged RBC scan (Tc-99m-DRBC) with autologous erythrocytes remains the gold-standard of imaging, being capable of specifically proving splenic tissue 6,8.
Differential diagnosis
Splenosis should not be confused with polysplenia or accessory spleens (splenunculi), which are congenital in origin and retain arterial supply from the splenic artery. They are also composed of normal splenic tissue. Depending on their location they may appear to be arising from various organs, and thus mimic malignancy.
The differential diagnosis for soft tissue nodules includes
peritoneal metastases
enlarged lymph nodes (abdominal lymphadenopathy)
endometriosis
Tc-99m-tagged heat-damaged RBC scan (Tc-99m-DRBC) with autologous erythrocytes shows accumulation in the abdominal cavity, consistent with intra-abdominal splenosis.
Case Discussion
Main concern for intra-abdominal lesions found on CT scan was for metastatic disease. Using heat treated RBC confirmed the functioning splenosis at the various abdominal sites.
What are the causes of this condition?
- Splenic infarct
- Common cause of focal filling defects on contrast enhanced CT.
- Classically wedge-shaped and peripheral
- but more commonly rounded, irregularly shaped and random in distribution
- CAUSES
- Cardivascular
- bacterial endocarditis 50%
- artheroma
- valve vegetations
- mitral stenosis
- Tumor
- lymphoproliferative
- pancreas
- inflammatory
- pancreatitis
- other
- Sickle cell
- PCV
- Cardivascular
- The splenic enlargement and a wedge shaped infarct is confirmed. A rounded low density lesion in the adrenal gland on the right is noted, which in retrospect is visible on the noncontrast scans and has, on those scans, a density measurement of 5 HU, consistent with an incidental adrenal adenoma.
The liver is at the upper limit of normal in size and her main portal vein is enlarged measuring 17 mm in diameter. The splenic vein is also enlarged. Focal fatty change is again demonstrated. No focal lesions. The remainder of the upper abdominal solid viscera are unremarkable, with no other infarcts identified. No lymph node enlargement and no focal osseous lesion.
Conclusion
Splenic infarcts is confirmed and presumably accounts of the patient’s presentation. The cause of the patient’s splenomegaly is uncertain, although the main portal vein and splenic vein do appear enlarged as does the liver raising the possibility of portal hypertension. Incidental adrenal adenoma.
Case Discussion
This case highlights the need to remember the differential of regional pain when assessing CT KUB for nephrolithiasis.
what are the complications of this condition?
splenic infarct complications
Complications
Some complications are encountered, more frequently in patients with an embolic aetiology. These include:
- formation of a splenic pseudocyst(s)
- infected splenic infarction leading to the formation of a splenic abscess
- splenic haemorrhage
- splenic rupture
HIV and spleen related pathology
- Splenic involvement is commo nin AIDS
- CT has high sensitivity for detection >90% of splenic lesions and identification of associated findings in the retopertioneum, mesentery and bowel
- HIV associated splenic lesions
- Infection
- TB
- low density
- abnormal ileocecal region
- MAI
- LNs
- Jejunal wall thickening
- Fungus
- candidia
- aspergillus
- cryptococcus
- Bacteria
- staph
- strep
- E coli
- Protozoa
-
Pneumocystis jiroveci/carnii
- progressively enlarging lesions
- calcification in spleen liver and LNs
-
Pneumocystis jiroveci/carnii
- TB
- Tumour
- Infection
