A 62-year-old man with a long-standing history (>40 years) of Hailey-Hailey disease was admitted from an outside hospital due to anemia (hemoglobin, 8.6 g/dL [reference range, 14.0-17.5 g/dL]), thrombocytopenia (platelets, 7×10 3 /µL [reference range, 150-350×10 3 /µL]), and worsening skin rash. The patient reported that his Hailey-Hailey disease worsened abruptly 1 month prior to admission and had progressed steadily since then. He described the rash as painful, especially with movement. Over the preceding month, he had been treated with topical triamcinolone, topical diphenhydramine, oral prednisone, fluconazole, and oral clindamycin, all without improvement. The skin lesions continued to worsen and persistently bled; he then presented to our institution for further care. Physical examination demonstrated widespread shallow erosions with hemorrhagic drainage and crusting located on the lower back, chest, abdomen (top), axillae (bottom), groin, arms, and legs. No vesicles or pustules were noted. The patient had no cognitive dysfunction or focal neurologic deficits. A punch biopsy was performed. WHAT'S THE DIAGNOSIS? a. Hailey-Hailey disease flare b. impetigo c. Kaposi varicelliform eruption (eczema herpeticum) d. multiple myeloma e. tinea corporis