Fernando Sánchez Martínez, Oscar Sebastian Salinas Rosas, Carlos Ronaldo Martínez Mateo, Alejandro Aguilar Sabori, Erik Ponce Graciano, David Alejandro Rodríguez Herrera, María Fernanda Vázquez Páez, Angeles Yasunari Cortes Garcia
{"title":"Splenic and Pancreatic Abscess Secondary to Chronic Corticosteroid Use: A Case Report and Literature Review.","authors":"Fernando Sánchez Martínez, Oscar Sebastian Salinas Rosas, Carlos Ronaldo Martínez Mateo, Alejandro Aguilar Sabori, Erik Ponce Graciano, David Alejandro Rodríguez Herrera, María Fernanda Vázquez Páez, Angeles Yasunari Cortes Garcia","doi":"10.7759/cureus.84325","DOIUrl":null,"url":null,"abstract":"<p><p>Splenic abscess is a rare but potentially life-threatening condition often associated with immunosuppressive states. We present the case of a 62-year-old man with a history of chronic corticosteroid use who developed fever, anorexia, weight loss, and left upper quadrant abdominal pain. Laboratory studies revealed leukocytosis and elevated inflammatory markers. Contrast-enhanced computed tomography identified multiloculated abscesses in the spleen and pancreatic tail. The patient underwent exploratory laparotomy, splenectomy, and distal pancreatectomy, with a favorable postoperative course complicated only by a superficial surgical site infection. Splenic abscess typically results from hematogenous spread, and its diagnosis is often delayed due to nonspecific symptoms. Imaging, particularly contrast-enhanced CT, is critical for early detection. Management strategies include percutaneous drainage or surgical intervention, depending on the patient's clinical status. Although corticosteroid-induced immunosuppression is a rare risk factor, it should be recognized as a potential cause. Early diagnosis, source control, and targeted antibiotic therapy are crucial for optimizing patient outcomes.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"17 5","pages":"e84325"},"PeriodicalIF":1.0000,"publicationDate":"2025-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12086024/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cureus","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7759/cureus.84325","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Splenic abscess is a rare but potentially life-threatening condition often associated with immunosuppressive states. We present the case of a 62-year-old man with a history of chronic corticosteroid use who developed fever, anorexia, weight loss, and left upper quadrant abdominal pain. Laboratory studies revealed leukocytosis and elevated inflammatory markers. Contrast-enhanced computed tomography identified multiloculated abscesses in the spleen and pancreatic tail. The patient underwent exploratory laparotomy, splenectomy, and distal pancreatectomy, with a favorable postoperative course complicated only by a superficial surgical site infection. Splenic abscess typically results from hematogenous spread, and its diagnosis is often delayed due to nonspecific symptoms. Imaging, particularly contrast-enhanced CT, is critical for early detection. Management strategies include percutaneous drainage or surgical intervention, depending on the patient's clinical status. Although corticosteroid-induced immunosuppression is a rare risk factor, it should be recognized as a potential cause. Early diagnosis, source control, and targeted antibiotic therapy are crucial for optimizing patient outcomes.