Accessory spleen
Accessory Spleen[edit | edit source]
An accessory spleen is a small nodule of splenic tissue that is separate from the main body of the spleen. It is a common congenital anomaly, occurring in approximately 10-30% of the population. Accessory spleens are usually asymptomatic and are often discovered incidentally during imaging studies or surgical procedures.
Anatomy and Location[edit | edit source]
Accessory spleens are typically found near the hilum of the spleen, but they can also be located in other areas of the abdominal cavity, such as the pancreas, omentum, or mesentery. They are usually small, ranging from a few millimeters to a few centimeters in diameter.
Development[edit | edit source]
Accessory spleens develop during embryogenesis when splenic tissue becomes separated from the main body of the spleen. This can occur due to incomplete fusion of the splenic anlage or due to the presence of multiple splenic nodules during development.
Clinical Significance[edit | edit source]
While accessory spleens are generally benign and asymptomatic, they can become clinically significant in certain situations. For example, in patients undergoing splenectomy for conditions such as idiopathic thrombocytopenic purpura (ITP), an accessory spleen can continue to produce platelets, potentially leading to a recurrence of symptoms. In such cases, identification and removal of the accessory spleen may be necessary.
Diagnosis[edit | edit source]
Accessory spleens are often identified through imaging studies such as computed tomography (CT) scans, magnetic resonance imaging (MRI), or ultrasound. On imaging, they appear as well-defined, homogeneous nodules with similar characteristics to the main spleen.
Treatment[edit | edit source]
In most cases, accessory spleens do not require treatment. However, if they cause symptoms or complications, surgical removal may be indicated. This is typically done laparoscopically.
Related Pages[edit | edit source]
Gallery[edit | edit source]
Accessory spleen[edit | edit source]
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