Wandering Spleen is a rare condition characterized by the abnormal mobility of the spleen due to the absence or weakening of its supporting ligaments. It is more commonly observed in women of reproductive age. The exact prevalence of this condition is not well-established, but it is considered extremely rare. Wandering Spleen is often diagnosed incidentally during imaging studies or may present with symptoms such as abdominal pain, nausea, or a palpable mass. Surgical intervention is typically required to prevent complications associated with torsion or infarction of the spleen.
Wandering Spleen is a rare condition characterized by the abnormal mobility of the spleen due to the absence or weakening of its supporting ligaments. This allows the spleen to move freely within the abdomen, potentially leading to torsion or twisting of its blood vessels, which can be life-threatening.
Although wandering spleen is considered a rare condition, its exact prevalence is not well-established. It primarily affects children and young adults, with a slightly higher incidence in females. The condition is often associated with congenital abnormalities or conditions that weaken the ligaments supporting the spleen, such as trauma, pregnancy, or connective tissue disorders.
Due to its rarity and varied clinical presentation, wandering spleen can be challenging to diagnose. Symptoms may include abdominal pain, a palpable mass, or intermittent torsion leading to acute abdomen. Imaging techniques like ultrasound, CT scan, or MRI are typically used to confirm the diagnosis.
Treatment for wandering spleen usually involves surgical intervention to reposition and secure the spleen, or in severe cases, splenectomy may be necessary. Prompt diagnosis and appropriate management are crucial to prevent complications and preserve spleen function.