Volume 48, Issue 12 pp. 1480-1488
ORIGINAL ARTICLE

Histopathologic and immunophenotypic features of cutaneous solid organ transplant-associated graft-vs-host disease: Comparison with acute hematopoietic cell transplant-associated graft-vs-host disease and cutaneous drug eruption

Aaron J. Russell MD

Corresponding Author

Aaron J. Russell MD

Department of Medicine, Division of Dermatology, Washington University School of Medicine, St. Louis, Missouri, USA

Departments of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA

Correspondence

Aaron J. Russell, Department of Medicine, Division of Dermatology, Washington University School of Medicine, St. Louis, MO.

Email: [email protected]

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Amy C. Musiek MD

Amy C. Musiek MD

Department of Medicine, Division of Dermatology, Washington University School of Medicine, St. Louis, Missouri, USA

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Karl W. Staser MD, PhD

Karl W. Staser MD, PhD

Meramec Dermatology, Arnold, Missouri, USA

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Ilana S. Rosman MD

Ilana S. Rosman MD

Department of Medicine, Division of Dermatology, Washington University School of Medicine, St. Louis, Missouri, USA

Departments of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA

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First published: 26 June 2021

Funding information: Washington University in St. Louis

Abstract

Background

Although it is relatively common after hematopoietic cell transplant (HCT), graft-vs-host disease (GVHD) is a rare complication following solid organ transplantation (SOT).

Methods

This study evaluated skin biopsy specimens from five cases of SOT GVHD, 15 cases of HCT GVHD, and 15 cases of cutaneous drug eruption. Immunohistochemical staining for CD3, CD4, CD8, T-bet, and GATA-3 was performed to examine the density and immune phenotype of skin-infiltrating lymphocytes.

Results

Similar to HCT GVHD, the predominant histopathologic findings in skin biopsy specimens of SOT GVHD were widespread vacuolar interface dermatitis with scattered necrotic keratinocytes. However, the density of dermal inflammation was considerably higher in SOT GVHD. Features that were more predictive of a cutaneous drug eruption over GVHD included spongiosis, confluent parakeratosis, and many eosinophils. Involvement of the hair follicle epithelium was seen in all three disorders. Both forms of cutaneous GVHD showed a predominance of Th1 (CD3+/T-bet+) lymphocytes within the inflammatory infiltrates. This shift was more pronounced in SOT GVHD, particularly among intraepidermal T-cells.

Conclusions

SOT GVHD shares many histopathologic features with HCT GVHD. However, SOT GVHD has a greater tendency to develop brisk lichenoid inflammation.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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