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Jesús Fernández-Herrera, MD, PhD; Ruud Valks, MD; Carlos Feal, MD; Javier Fraga, MD, PhD; José F. Tomás, MD, PhD; Amaro Garcia-Díez, MD, PhD

Arch Dermatol. 1999;135:304-308.

Background  Infusions of leukocytes obtained from the original bone marrow donor is a new approach for treating patients who have a relapse of leukemia after allogeneic bone marrow transplantation. Up to 90% of patients who achieved remission developed graft-vs-host disease (GVHD). However, any description of the clinical and histologic features in these cases is lacking.

Observations  We describe 2 patients in whom a severe, peculiar, hyperacute, fatal GVHD developed after treatment with donor leukocyte infusions and interferon alfa. The patients had not received any additional chemotherapy or GVHD prophylaxis. In both patients, the eruption started with the appearance of erythematous plaques at the interferon alfa injection sites, and a generalized maculopapular eruption subsequently developed. The clinical lesions evolved from acute to lichenoid within several days. The histologic examination also demonstrated unusual findings and showed features of both acute and chronic lichenoid GVHD.

Conclusions  Donor leukocyte infusions without GVHD prophylaxis may provoke a severe fatal hyperacute GVHD. In the cases presented herein, we discuss the significance of the rapid clinical evolution from acute to lichenoid and the combination of histologic features of both acute and chronic GVHD in the biopsy specimens.

From the Departments of Dermatology (Drs Fernández-Herrera, Valks, Feal, and Garcia-Díez), Pathology (Dr Fraga), and Hematology (Dr Tomás), Hospital Universitario de la Princesa, Madrid, Spain.

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