# A Rare Case of Acute Myeloid Leukemia Initially Presenting With Fever of Unknown Origin and Rapidly Progressing Pericardial Effusion

**Authors:** Charity Iheagwara, Folasade Ajayi, Onyinye N Otaluka, Carlos Cantu Lopez, Jihad Slim, Hamid S Shaaban, Ala Muhanna, Bereket Tewoldemedhin, Maria Szabela, Jack Boghossian

PMC · DOI: 10.7759/cureus.51505 · 2024-01-02

## TL;DR

A rare case of acute myeloid leukemia presented with fever and pericardial effusion, highlighting the importance of recognizing unusual symptoms in leukemia diagnosis.

## Contribution

This case report emphasizes the rare but critical association between AML, fever of unknown origin, and pericardial effusion.

## Key findings

- AML can present with fever of unknown origin and rapidly progressing pericardial effusion.
- Fever in AML may result from inflammation, cytokine dysregulation, or bone marrow failure.
- Pericardial effusion and cardiac tamponade are rare but possible initial signs of AML.

## Abstract

This case report highlights a patient who had persistent fevers for weeks and rapidly progressing pericardial effusion following a positive test for coronavirus disease 2019 (COVID-19) two weeks before presentation to the hospital. The initial thought was that her fever was of infectious etiology, but relevant investigations led to the diagnosis of acute myeloid leukemia (AML). AML, which is characterized by clonal expansion of immature “blast cells” in the peripheral blood and bone marrow resulting in ineffective erythropoiesis and bone marrow failure, is the most prevalent form of leukemia. It is the most aggressive form of leukemia, which has varying prognoses determined by the subtypes. This report explores the association between AML, fever of unknown origin, and pericardial effusion, shedding light on a notable clinical aspect. Fever in AML may be attributed to underlying inflammatory processes, cytokine dysregulation, or bone marrow failure. Recognition of fever as a potential indicator of AML contributes to enhanced clinical vigilance. Pericardial effusions and cardiac tamponade, although rare, can be a presenting feature of AML, and can present side by side with fever of unknown origin as seen in this case report.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667), coronavirus disease 2019 (MONDO:0100096), pericardial effusion (MONDO:0001370)

## Full-text entities

- **Genes:** NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893] {aka ALPS4, CMNS, N-ras, NCMS, NRAS1, NS6}, CD34 (CD34 molecule) [NCBI Gene 947], MATN1 (matrilin 1) [NCBI Gene 4146] {aka CMP, CRTM}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, SDC1 (syndecan 1) [NCBI Gene 6382] {aka CD138, SDC, SYND1, syndecan}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}
- **Diseases:** blood dyscrasias (MESH:D006402), chest and back pain (MESH:D002637), dyspnea (MESH:D004417), hypertriglyceridemia (MESH:D015228), bone marrow failure (MESH:D000080983), thrombocytopenia (MESH:D013921), hematologic malignancy (MESH:D019337), leukocytopenia (MESH:D007970), genetic defect (MESH:D030342), cancer (MESH:D009369), COVID-19 (MESH:D000086382), atrial or ventricular collapse (MESH:D001261), soreness (MESH:D063806), effusion (MESH:D000080324), metastasis (MESH:D009362), febrile episodes (MESH:C580065), pain (MESH:D010146), acute infarct (MESH:D056989), infectious diseases (MESH:D003141), inflammation (MESH:D007249), pleural effusion (MESH:D010996), cardiac tamponade (MESH:D002305), MDS (MESH:D009190), type 2 diabetes mellitus (MESH:D003924), Pericardial Effusion (MESH:D010490), leukemia (MESH:D007938), microangiopathic hemolytic anemia (MESH:D000743), HLH (MESH:D051359), cardiomegaly (MESH:D006332), AML (MESH:D015470), ALL (MESH:D054198), hypertension (MESH:D006973), anemia (MESH:D000740), hypotension (MESH:D007022), FUO (MESH:D005335), Malaria (MESH:D008288), tachycardia (MESH:D013610), infarct (MESH:D007238), parasitic infections (MESH:D010272), fungal (MESH:D009181), leukocytosis (MESH:D007964), infection (MESH:D007239), constrictive pericarditis (MESH:D010494), hypercellular marrow (MESH:D001855), hemorrhagic (MESH:D006470), Pericardial involvement (MESH:D008476), back pain (MESH:D001416), Fever (MESH:D005334), adult leukemias (MESH:D015459), pallor (MESH:D010167), Mycobacterium tuberculosis infections (MESH:D014376), pulmonary embolism (MESH:D011655), Sinus tachycardia (MESH:D013616), granuloma (MESH:D006099)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Respiratory syncytial virus (no rank) [taxon 12814], Trypanosoma cruzi (species) [taxon 5693], Human rhinovirus sp. (species) [taxon 169066], Adenoviridae (family) [taxon 10508], Mycoplasma (genus) [taxon 2093]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10831924/full.md

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Source: https://tomesphere.com/paper/PMC10831924