To the Editor: A 45-year-old African American man with a 3-year history of oral pemphigus vulgaris (PV) presented with new-onset smooth, broad-based, well-defined, red, ulcerated nodules on the right buccal mucosa, right lateral border of the tongue, and left back aspect of the tongue developing during a 5-week period (Fig 1). The patient's oral pemphigus, which had initially led to a 60-lb weight loss, has been refractory to a number of aggressive combination immunosuppressive therapies of oral prednisone, azathioprine, cyclophosphamide, cyclosporine, mycophenolate mofetil, and intravenous immunoglobulin and methylprednisolone, with concomitant use of several topical corticosteroids, tacrolimus, and antihistamine-anesthetic rinses. At the time of the development of the oral nodules, the patient was taking prednisone and mycophenolate mofetil. The excisional biopsy specimen of the lesions showed a peculiar histologic picture–the nodule was a combination of a vasoformative tissue proliferation of a pyogenic granuloma (PG) with overlying epithelial changes of PV (Fig 2). After a year of follow-up, the patient has not experienced recurrence of the excised nodules.