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Lymphocytes in Sweet syndrome: A potential diagnostic pitfall
Author(s) -
Kazlouskaya Viktoryia,
JunkinsHopkins Jacqueline M.
Publication year - 2018
Publication title -
journal of cutaneous pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 75
eISSN - 1600-0560
pISSN - 0303-6987
DOI - 10.1111/cup.13096
Subject(s) - pathology , dermis , medicine , histopathology , immunophenotyping , atypical lymphocyte , immunohistochemistry , cd20 , lymphocyte , vasculitis , population , reticular dermis , sweet syndrome , immunology , lymphoma , antigen , disease , environmental health
Background Patients with Sweet syndrome (SS) have acute onset of cutaneous lesions with characteristic histopathology (dense and diffuse neutrophilic infiltrate, dermal edema, leukocytoclasis and no vasculitis) accompanied by systemic symptoms. Sometimes, only skin lesions with classic histopathologic features are seen. Although SS is considered to be a “neutrophilic dermatosis,” lymphocytes are also seen on histological examination. Methods We evaluated the cellular infiltrate in 9 biopsies from SS lesions with routine staining and immunohistochemistry. Results Lymphocytes were present in all biopsies in variable amounts, often exceeding the number of intact neutrophils. Prominent fragmentation of neutrophils rendered some biopsies “lymphocyte‐rich” on routine histologic evaluation. Myeloperoxidase was helpful in highlighting the inconspicuous neutrophilic fragments in these cases. Lymphocytes were highlighted with immunohistochemistry, and had a CD3+, CD4+, CD20(−) immunophenotype, with rare CD8+ lymphocytes. Conclusion Awareness of the lymphocytic component of SS is important to avoid diagnostic errors, especially in subcutaneous lesions of SS, in which the lymphocytic infiltrate predominates in the upper parts of the dermis, while the typical neutrophilic infiltrate may be seen only in the deeper dermis and subcutis. The lymphocytic component may potentially help to differentiate lesions of SS from neutrophilic urticarial dermatosis, which has not been reported to contain a significant lymphocytic population.