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.2022 Dec;49(12):1051-1059.
doi: 10.1111/cup.14306. Epub 2022 Aug 18.

The mixed spongiotic and interface reaction pattern: A study of clinical and histopathologic findings

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The mixed spongiotic and interface reaction pattern: A study of clinical and histopathologic findings

Madison Ernst et al. J Cutan Pathol.2022 Dec.

Abstract

Background: Categorization of biopsy specimens into inflammatory reaction patterns is central to dermatopathologic assessment. Mixed inflammatory patterns are poorly characterized and may represent clinicopathologic challenges. The purpose of this study was to identify clinical and histopathologic findings associated with the mixed spongiotic-interface dermatitis (SID) histopathologic pattern.

Methods: Fifty-one institutional biopsy specimens of SID were identified over a 2-year period by retrospective natural language search. Histopathologic and clinical features were identified.

Results: The most common histopathologic features associated with SID were mild spongiosis (51%), focal vacuolar interface change (72%), lymphocytic exocytosis (92%), and superficial-dermal lymphocytic infiltrate (94%) with variable eosinophils (61%). Clinically, 80% of subjects presented with a symmetric morbilliform eruption. Polypharmacy (94%), immunosuppression (47%), and history of malignancy (47%) were common. The most common diagnoses were drug reaction (37%), possible drug reaction (12%), and viral exanthem (12%). Drug reaction with eosinophilia and systemic symptoms represented 25% of all confirmed cutaneous adverse drug reactions (CADR). Average time from drug initiation to symptom initiation was 20 days (SD: 22.3, range: 0-90); median disease duration was 25.5 days. Spongiotic vesicles and Langerhans cells were less common in patients with a strong clinicopathologic diagnosis of drug reaction compared to non-drug eruptions (p = 0.04).

Conclusions: The mixed SID pattern is commonly encountered in CADR but may represent a more subacute course, implying consideration for inciting medication(s) started before the typical 7- to 14-day window.

Keywords: dermatopathology; drug eruptions; drug reaction with eosinophilia and systemic symptoms; interface; maculopapular eruption; spongiotic.

© 2022 The Authors. Journal of Cutaneous Pathology published by John Wiley & Sons Ltd.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

FIGURE 1
FIGURE 1
Representative examples of spongiotic‐interface dermatitis with characteristic histopathologic features, stained with H&E, at original magnification ×100. (A) This case presented with acanthosis, mild spongiosis and subtle interface changes; dyskeratotic keratinocytes (arrow in epidermis) are noted within the spinous layer; a moderate perivascular lymphocytic infiltrate with rare eosinophils (arrows in dermis) is noted. (B) Here, there is scattered parakeratosis above epidermal hyperplasia with mild spongiosis, interface changes and dyskeratotic keratinocytes (arrows in epidermis); the inflammatory infiltrate contains sparse eosinophils (arrows in dermis). (C) In this case acanthosis is mild with mild spongiosis, interface changes with a dyskeratotic keratinocyte (arrow in the spinous layer), lymphocytic exocytosis, and a mild perivascular lymphocytic inflammatory infiltrate with rare eosinophils and neutrophils (arrow in dermis)
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