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Multicenter case series of indolent small/medium-sized CD8+ lymphoid proliferations with predilection for the ear and
Janet Y Li1, Joan Guitart, Melissa P Pulitzer
1*Department of Medicine, Dermatology Service, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, NY; †Department of Dermatology, Northwestern University, Chicago, IL; ‡Department of Pathology, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, NY; §Department of Dermatology and Pathology, Yale University, New Haven, CT; Departments of ¶Pathology, and ‖Dermatology, Stanford University, Stanford, CA; and **Department of Medicine, Lymphoma Service, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, NY.
Abstract:
We report 7 cases of a CD8 lymphoid proliferation of the ear and face with a cytotoxic T-cell phenotype, but an indolent clinical course. All patients presented with stable or slowly growing asymptomatic lesions on the ear, nose, or lower eyelid. Histopathology showed a dense diffuse dermal infiltrate of small- to medium-sized atypical lymphocytes without destructive features. The lymphocytes were positive for CD3, CD8, β-F1, and TIA-1 and negative for CD4, CD30, CD56, granzyme B, and PD-1. Of note, the proliferation index was low in available cases. All patients remained in complete remission at median follow-up of 14 months regardless of treatment modality. Staging was negative for extracutaneous disease in all patients. The clinically indolent behavior and histopathologic phenotype together with a low proliferation index (10%-15%) emphasize the importance of accurate diagnosis and appropriate clinical management to avoid overtreatment and complications of therapy.
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