Splenic abscess is a rare disease. The spleen is a highly selective filter for microorganisms in the blood and a center for phagocytic activity, with immune capacity to resist local infections and is generally not prone to infection. Clinical manifestations are often atypical and often lack specific symptoms. The vast majority of patients have symptoms such as fever and abdominal pain. Early diagnosis is difficult and is often misdiagnosed as sepsis or septicemia. Various serious complications appear in the late stage.
Spleen abscesses are often caused by pathogenic emboli, so the abscesses formed may be multiple, secondary to traumatic hematoma and subsequent infection. Generally, they are solitary, but the structure of splenic abscesses is rarely seen in clinical practice and is no different from that of general abscesses. Only because the pus cavity contains fragmented spleen tissue, the pus is often brownish and thicker than general pus.
In the early stage of the abscess, the spleen is often not adherent to the surrounding tissues. In patients with a long course of disease, because the inflammation has reached the surface of the spleen, it often leads to dense adhesion between the spleen and the surrounding tissues. If the abscess involves the surface of the spleen, it may sometimes penetrate into the abdominal cavity or abdominal wall of other organs, causing various internal and external fistulas and peritonitis. Occasionally, it may perforate the diaphragm, causing empyema, but most splenic abscesses are still localized within the spleen. Moreover, as an infectious focus, it can also transport pathogenic emboli through the blood to other parts, causing metastatic abscesses.