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 2. Computed tomography (axial plane) of the abdomen shows hepatosplenomegaly. Enlargement of the liver up to 23 cm and spleen up to 23 cm with the presence of a subcapsular rupture in the lower pole of about 13 mm, with numerous retroperitoneal enlarged lymph nodes. (Alteris ver. 1.0.9.97 DicomVision).

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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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