Hemophagocytic Lymphohistiocytosis Secondary to Peripheral T Cell Lymphoma with Rapid Onset and Fatal Progression in a Young Patient: A Case Report and Review of the Literature

Patrycja Paluszkiewicz; Adrian Martuszewski; Maciej Majcherek; Marta Kucharska; Aleksandra Bogucka-Fedorczuk; Tomasz Wróbel; Anna Czyż

doi:10.12659/AJCR.932765

30 September 2021 : Case report Poland

Hemophagocytic Lymphohistiocytosis Secondary to Peripheral T Cell Lymphoma with Rapid Onset and Fatal Progression in a Young Patient: A Case Report and Review of the Literature

Challenging differential diagnosis, Rare disease

Patrycja Paluszkiewicz^1CDEF, Adrian Martuszewski^2CDEF, Maciej Majcherek^3ABCDE*, Marta Kucharska^4BC, Aleksandra Bogucka-Fedorczuk^3CDE, Tomasz Wróbel^3EFG, Anna Czyż^3ABCDEF

DOI: 10.12659/AJCR.932765

Am J Case Rep 2021; 22:e932765

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Figure 3. (A–D) Bone marrow smear reveals activated macrophages with phagocytosis of red blood cells marked by red arrows (May-Grunwald-Giemsa; Microsoft Paint ver. 10.0.19041.746).

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Hemophagocytic Lymphohistiocytosis Secondary to Peripheral T Cell Lymphoma with Rapid Onset and Fatal Progression in a Young Patient: A Case Report and Review of the Literature

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