out preceding bullous lesion and healed after oral corticosteroids (5, 6).In our patient the titre of circulating anti-ICS antibodies was low, which might indicate a prolonged initial phase of PV before generalized development of bullae. The massive plasma cell in®ltrate seen in the lesional upper dermis may be a factor for the localization of the lesions. Another possibility is that an unknown mechanism prevents the generalization of PV, resulting in the unique features described above. Since acanthosis was seen histologically, the diagnosis of pemphigus vegetans is also possible. 2. Jacyk WK, Simson IW. Pemphigus erythematosus resembling multiple seborrheic keratoses. Arch Dermatol 1990; 126: 543 ± 544. 3. Faber WR, Neumann HAM, Flinterman J. Persistent vegetating and keratotic lesions in patients with pemphigus vulgaris during immunosuppressive therapy. Br J Dermatol 1983; 109: 459 ± 463. 4. Yesudian PD, Krishnan SGS, Jayaraman M, Janaki VR, Yesudian P. Postpemphigus acanthomata: a sign of clinical activity? Int J Dermatol 1997; 36: 194 ± 196. 5. Bruckner N, Kats RA, Hood AF. Pemphigus foliaceus resembling eruptive seborrheic keratoses. Arch Dermatol 1980; 116: 815 ± 816. 6. Kahana M, Trau H, Schewach-Millet M, Sofer E. Pemphigus foliaceus presenting as multiple giant seborrheic keratoses.