# Role of 18 F-FDG-PET/CT in an AML-M5a Subtype Patient with Rare Constellation of Hemophagocytic Lymphohistiocytosis & Bilateral Multiple Breast Chloromas

**Authors:** Yuvan Shrinivas, Shanmuga Sundaram Palaniswamy, Padma Subramanyam

PMC · DOI: 10.1055/s-0044-1779280 · 2024-02-13

## TL;DR

This case study shows how PET/CT imaging helped diagnose and monitor a rare combination of AML-M5a, HLH, and breast chloromas in a single patient.

## Contribution

Highlights the role of 18F-FDG-PET/CT in diagnosing and monitoring a rare coexistence of AML-M5a, HLH, and chloromas.

## Key findings

- 18F-FDG-PET/CT identified multiple lymph nodal and marrow lesions and later detected bilateral breast chloromas.
- PET/CT guided biopsy sites and monitored treatment response for both HLH and AML.
- The case emphasizes the importance of nuclear medicine physicians recognizing complications in AML with poor prognostic factors.

## Abstract

We report a treated case of acute myeloid leukemia (AML-M5a subtype) with monocytic differentiation (AMoL) presenting with fever and body pains. Initial
18
F-FDG-PET/CT (
18
F-flurodeoxyglucose positron emission tomography/computed tomography) identified multiple lymph nodal, and marrow lesions. Biopsy confirmed hemophagocytic lymphohistiocytosis (HLH). Post HLH treatment, follow-up PET/CT demonstrated unsuspected FDG avid bilateral breast lesions (
n
 = 5), which proved to be chloromas, that is, extranodal manifestation of AML.
18
F-FDG-PET/CT has helped not only in identifying the various sites of disease involvement but also in guiding the sites for biopsy. Finally,
18
F-FDG-PET/CT was useful in monitoring therapy response for both these coexisting pathologies, which are said to be resistant to treatment based on FLT3-ITD tyrosine kinase-3 internal tandem duplication mutation positivity and high-grade AML status. This case represents a rare constellation of different etiologies that needed to be differentiated. It also emphasizes the challenges in interpreting PET/CT findings, especially in difficult clinical scenarios. Disease distribution in HLH/presence of chloromas, etc., can mimic stage IV lymphoma in a known case of AML. So the nuclear medicine physician should be aware of the different complications in the background of AML, especially in patients with poor prognostic factors.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667), hemophagocytic lymphohistiocytosis (MONDO:0015540), AML (MONDO:0018874)

## Full-text entities

- **Genes:** FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322] {aka CD135, FLK-2, FLK2, STK1}, FER (FER tyrosine kinase) [NCBI Gene 2241] {aka PPP1R74, TYK3, p94-Fer}
- **Diseases:** stage IV lymphoma (MESH:D008223), body pains (MESH:D010146), differentiation (MESH:D012734), fever (MESH:D005334), chloromas (MESH:D023981), lymph nodal, and marrow lesions (MESH:D001855), HLH (MESH:D051359), Multiple Breast Chloromas (MESH:D061325), AML (MESH:D015470)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11001452/full.md

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Source: https://tomesphere.com/paper/PMC11001452