# Cerebral myeloid sarcoma (Chloroma): Report of a rare entity

**Authors:** Mohamed Aziz Hermassi, Khalil Ghedira, Kais Bouzouita, Alia Zehani, Sofiene Bouali, Khansa Abderrahmen

PMC · DOI: 10.1016/j.ijscr.2025.111233 · International Journal of Surgery Case Reports · 2025-03-28

## TL;DR

This paper reports a rare case of cerebral myeloid sarcoma in a 28-year-old man with a history of acute myeloid leukemia, emphasizing the challenges in diagnosis and the role of surgery.

## Contribution

The paper presents a rare case of cerebral myeloid sarcoma, highlighting its diagnosis and surgical treatment in a patient with a history of AML.

## Key findings

- Cerebral myeloid sarcoma is a rare condition, often associated with acute myeloid leukemia.
- Immunohistochemistry is essential for confirming the diagnosis of cerebral myeloid sarcoma.
- Surgical excision can successfully remove the lesion and alleviate symptoms in cerebral myeloid sarcoma cases.

## Abstract

Myeloid sarcoma is a rare, malignant solid tumor composed of the progenitor cells of the myeloid lineage. Often associated with acute myeloid leukemia. Intracranial localization is very rare and diagnosis is confirmed by immunohistochemistry. The purpose of this case is to highlight the diagnostic and surgical treatment of a pathologically confirmed case of cerebral myeloid sarcoma.

We present the case of a 28-year-old Tunisian man who was diagnosed with AML in 2019, went into remission and was admitted to hospital with headaches and visual disturbances. Cranial MRI revealed an intra-axial parieto-occipital lesion on the left side. The patient underwent a successful surgical removal of the tumor. Immunohistochemistry confirms a cerebral myeloid sarcoma.

Myeloid sarcoma is a rare condition. It is mainly found on skin and soft tissue. Intracranial localization is very rare. The clinical presentation of myeloid sarcoma varies depending on the location of the lesion. Histochemistry studies are essential for accurate diagnosis. There is no consensus on the treatment of myeloid sarcoma and different treatment strategies have been used. Surgery plays a key role in alleviating the symptoms of the mass effect, in confirming the diagnosis and in removing the major lesions before initiating systemic therapy.

Cerebral myeloid sarcomas are uncommon. Intracranial mass should be strongly considered in acute myeloid leukemia patients. Conventional chemotherapy for AML is still the primary treatment for myeloid sarcomas, followed by surgery and possibly radiation.

•Cerebral myeloid sarcoma is a rare extramedullary malignant solid tumor composed of myeloid progenitor cells.•Diagnosis of this extremely rare disease is still challenging and is typically confirmed by immunohistochemical analysis•We are presenting a very rare case of cerebral myeloid sarcoma in a 28-year-old Tunisian man diagnosed with acute myeloid leukemia.•The patient underwent successful surgical excision of the lesion.

Cerebral myeloid sarcoma is a rare extramedullary malignant solid tumor composed of myeloid progenitor cells.

Diagnosis of this extremely rare disease is still challenging and is typically confirmed by immunohistochemical analysis

We are presenting a very rare case of cerebral myeloid sarcoma in a 28-year-old Tunisian man diagnosed with acute myeloid leukemia.

The patient underwent successful surgical excision of the lesion.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667), myeloid sarcoma (MONDO:0006861)

## Full-text entities

- **Diseases:** solid tumor (MESH:D009369), AML (MESH:D015470), Cerebral myeloid sarcoma (MESH:D023981), headaches (MESH:D006261), lesion (MESH:D009059), Intracranial mass (MESH:C536030), visual disturbances (MESH:D014786)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11997360/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11997360/full.md

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Source: https://tomesphere.com/paper/PMC11997360