# Pyogenic Splenic Abscess With Concurrent Active Plasmodium falciparum Malaria and Sickle Cell Trait: A Case Report

**Authors:** Shamon Gumbs, Winnie Gikunda, Herlyne Das, Jeremiah Douchee, Cameron A Wilkinson

PMC · DOI: 10.7759/cureus.102272 · Cureus · 2026-01-25

## TL;DR

A rare case of splenic abscess in a patient with malaria and sickle cell trait highlights the complex interaction between parasitic infection, hemoglobinopathy, and bacterial infection.

## Contribution

This case report documents a rare concurrent occurrence of Plasmodium falciparum malaria, sickle cell trait, and a pyogenic splenic abscess caused by Fusobacterium.

## Key findings

- The patient had a pyogenic splenic abscess caused by Fusobacterium species.
- The case involved concurrent active Plasmodium falciparum malaria and sickle cell trait.
- Successful treatment required antimalarial therapy and broad-spectrum antibiotics with anaerobic coverage.

## Abstract

Splenic abscess is a rare but life-threatening condition with poorly understood links to malaria and hemoglobinopathies. We present the case of a young male from West Africa who developed a pyogenic splenic abscess with concurrent Plasmodium falciparum malaria and sickle cell trait. Clinical data were collected through retrospective chart review, and a literature review was conducted focusing on splenic abscess in the context of malaria and hemoglobinopathies. The patient presented with abdominal pain and fever after initiating antimalarial treatment. Imaging revealed a large splenic abscess. Percutaneous drainage yielded purulent fluid, and cultures identified Fusobacterium species. Laboratory findings confirmed sickle cell trait and active malaria. Treatment included antimalarial therapy and broad-spectrum antibiotics with anaerobic coverage. The patient recovered completely after drainage and antimicrobial therapy. This case highlights the importance of considering anaerobic bacterial pathogens, particularly Fusobacterium species, in splenic abscesses among patients from malaria-endemic regions. The concurrent presentation of bacterial infection, active malaria, and sickle cell trait represents a rare scenario demonstrating complex interplay between parasitic infection, hemoglobinopathies, and bacterial superinfection. Healthcare providers should maintain high suspicion for bacterial splenic infections in travelers with splenic complications, even when malaria is diagnosed.

## Linked entities

- **Diseases:** malaria (MONDO:0005136), splenic abscess (MONDO:0002333)
- **Species:** Plasmodium falciparum (taxon 5833)

## Full-text entities

- **Genes:** KRT90P (keratin 90, pseudogene) [NCBI Gene 85340] {aka HBA, KRT124P, KRTHBP1}, HBA2 (hemoglobin subunit alpha 2) [NCBI Gene 3040] {aka ECYT7, HBA-T2, HBH}, TCN1 (transcobalamin 1) [NCBI Gene 6947] {aka HC, TC-1, TC1, TCI}
- **Diseases:** necrosis (MESH:D009336), Pyogenic Splenic Abscess (MESH:D001922), thrombophlebitis (MESH:D013924), periodontal disease (MESH:D010510), SCT (MESH:D012805), hyperplasia (MESH:D006965), septic (MESH:D001170), Malaria (MESH:D008288), immune dysregulation (OMIM:614878), HIV infection (MESH:D015658), infectious diseases (MESH:D003141), Fusobacterium infections (MESH:D005674), mucosal injuries (MESH:D052016), endocarditis (MESH:D004696), renal complications (MESH:D007674), abdominal tenderness (MESH:D000007), infarction (MESH:D007238), lymphoma (MESH:D008223), bacterial (MESH:D001424), parasitic infection (MESH:D010272), constipation (MESH:D003248), Sickle cell (MESH:D000755), systemic (MESH:D015619), costovertebral tenderness (MESH:D063806), splenic complications (MESH:D013158), chills (MESH:D023341), bacteremia (MESH:D016470), Infections (MESH:D007239), P. falciparum or P. vivax infection (MESH:D016720), cerebral malaria (MESH:D016779), weight loss (MESH:D015431), dehydration (MESH:D003681), translocation (MESH:D014178), microvascular occlusion (MESH:D017566), anemia (MESH:D000740), myeloproliferative disorders (MESH:D009196), pyogenic (MESH:D017789), leukemia (MESH:D007938), deaths (MESH:D003643), brain involvement (MESH:D001927), hematologic disorders (MESH:D006402), emboli (MESH:D020766), Acute (MESH:D000208), hematologic malignancies (MESH:D019337), acute respiratory distress syndrome (MESH:D012128), fever (MESH:D005334), acute leukemia (MESH:D015470), ischemia (MESH:D007511), hypoxia (MESH:D000860), Lemierre's syndrome (MESH:D057831), hemolysis (MESH:D006461), bacterial superinfection (MESH:D015163), malarial splenomegaly (MESH:D013163), multi-organ dysfunction (MESH:D009102), lung failure (MESH:D012131), vitamin B12 deficiency (MESH:D014806), jaundice (MESH:D007565), malignancy (MESH:D009369), intra-abdominal infections (MESH:D059413), rupture (MESH:D012421)
- **Chemicals:** albendazole (MESH:D015766), imipenem (MESH:D015378), vitamin B12 (MESH:D014805), lipopolysaccharide (MESH:D008070), piperacillin-tazobactam (MESH:D000077725), cephalosporin (MESH:D002511), Beta-lactam/beta-lactamase inhibitor (-), Clindamycin (MESH:D002981), B12 (MESH:C034730), meropenem (MESH:D000077731), iron (MESH:D007501), carbapenems (MESH:D015780), amoxicillin-clavulanate (MESH:D019980), Metronidazole (MESH:D008795), oxygen (MESH:D010100), atovaquone-proguanil (MESH:C109496)
- **Species:** Fusobacterium mortiferum (species) [taxon 850], Entamoeba histolytica (species) [taxon 5759], Fusobacterium nucleatum (species) [taxon 851], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Fusobacterium necrophorum (species) [taxon 859], Streptococcus (genus) [taxon 1301], Human immunodeficiency virus 1 (no rank) [taxon 11676], Klebsiella (genus) [taxon 570], Human immunodeficiency virus 2 (no rank) [taxon 11709], Escherichia coli (E. coli, species) [taxon 562]

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932075/full.md

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Source: https://tomesphere.com/paper/PMC12932075