Am J Surg Pathol 2016 Oct;40(10):1360-7
*Research Unit Dermatopathology, Department of Dermatology, Medical University of Graz, Graz, Austria †Department of Dermatology, University of Modena and Reggio Emilia, Modena ‡Department of Dermatology, Galliera Hospital, Genoa §Division of Dermatology, San Gallicano Dermatological Institute, Rome, Italy.
Interstitial mycosis fungoides (IMF) is a rare histopathologic variant of mycosis fungoides (MF) that may mimic other inflammatory dermatoses, mainly interstitial granuloma annulare, inflammatory morphea, and interstitial granulomatous dermatitis. Only small series and sporadic case reports of IMF have been described in the literature. We reviewed 27 specimens from 21 patients with IMF (M:F=11:10, median age 60) to better characterize clinical, histopathologic, and immunohistochemical features of this disease. Read More