A Rare Case of Subcutaneous Panniculitis-Like T Cell Lymphoma with Hemophagocytic Lymphohistiocytosis Mimicking Cellulitis

Aniket Mody; Daniel Cherry; Georgiana Georgescu; Cyenthia Koehler; Veenu Gill

doi:10.12659/AJCR.927142

11 January 2021 : Case report USA

A Rare Case of Subcutaneous Panniculitis-Like T Cell Lymphoma with Hemophagocytic Lymphohistiocytosis Mimicking Cellulitis

Challenging differential diagnosis, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)

Aniket Mody^1ABDEF*, Daniel Cherry^2EF, Georgiana Georgescu^3BD, Cyenthia Koehler^4B, Veenu Gill^5ADEF

DOI: 10.12659/AJCR.927142

Am J Case Rep 2021; 22:e927142

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Figure 5. CD8 immunohistochemical stain highlights the atypical lymphocytes with hyperchromic nuclei in a membranous distribution, also demonstrating T cell lineage (×400).

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A Rare Case of Subcutaneous Panniculitis-Like T Cell Lymphoma with Hemophagocytic Lymphohistiocytosis Mimicking Cellulitis

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