# Salmonella Brain Abscess in Sickle Cell Disease Patient: Case Report

## TL;DR

This case report describes a rare brain abscess caused by Salmonella in a sickle cell disease patient, highlighting the need for broader diagnostic considerations in immunocompromised individuals.

## Contribution

The paper presents the second documented case of Salmonella-induced brain abscess in a sickle cell disease patient, adding to the limited literature on this rare condition.

## Key findings

- Salmonella can cause brain abscesses in patients with sickle cell disease, despite being more commonly associated with other infections.
- A multidisciplinary approach is essential for managing complex infections in immunocompromised individuals.
- Early diagnosis and treatment can lead to recovery, as seen in the patient's improved condition after surgical drainage and antibiotics.

## Abstract

Background and Clinical Significance: A brain abscess, defined as a localized intracranial infection that evolves into a purulent collection encased by a vascularized capsule, has higher prevalence among immunocompromised populations. Patients with sickle cell disease (SCD) are particularly vulnerable to bacterial infections due to their compromised immune systems, increasing their susceptibility to pathogens like Salmonella. While Salmonella is typically associated with gastroenteritis, osteomyelitis, and septicemia, its involvement in brain abscesses is exceedingly rare. There are few documented cases of Salmonella brain abscesses in the general population, and among patients with SCD, only one such case has been reported to date. In this report, we describe the second known case of a brain abscess caused by Salmonella infection in a patient with sickle cell disease, contributing to the limited literature on this rare and life-threatening condition. Case Presentation: A 32-year-old African American woman with sickle cell disease presented to the ER after a generalized seizure, reporting two weeks of worsening headaches, fevers, and left upper extremity weakness. Imaging revealed a right frontoparietal brain abscess, which was surgically drained, and cultures identified Salmonella enterica. After antibiotic treatment and a 23-day hospital stay, she was discharged. Four months later, she returned with another seizure during a sickle cell crisis, but follow-up MRI showed only minor scarring, and she was discharged on anticonvulsant therapy. Conclusions: This case emphasizes that Salmonella infections, though typically linked to osteomyelitis and sepsis, can also cause brain abscesses in immunocompromised patients like those with sickle cell disease. It highlights the need to consider infections alongside vascular causes in acute neurological cases and underscores the value of a multidisciplinary approach in managing such complex conditions.