A woman in her fifties with diastolic congestive heart failure, diabetes mellitus type II, obstructive sleep apnea (on continuous positive airway pressure), and hypertension presented to our clinic for evaluation of lower extremity wounds refractory to treatment. Six months prior to presentation she noted increasing edema with severe pruritus and pain along the right anterior tibia resulting in the development of painful papules. Doppler ultrasound did not reveal venous insufficiency. Prior unsuccessful treatments included acetic acid soaks, sequential compression devices, compression stockings, massage, and elevation. Wound cultures were remarkable for polymicrobial growth, including Candida parapsilosis, methicillinresistant Staphylococcus aureus, Enterococcus, Streptococcus, Aerococcus, and Pseudomonas species. However, treatment with numerous antimicrobials did not result in improvement. She received hydrocodone-acetaminophen, pregabalin, and duloxetine for associated pain.Physical examination revealed weeping, flat-topped, pink papules coalescing into cobblestoned plaques on the right shin ( Figure 1A) and smaller papules on the left shin with surrounding significant woody edema. Repeat wound cultures were positive for Pseudomonas aeruginosa and Candida parapsilosis. Evaluation of a punch biopsy revealed parakeratotic, spongiotic epidermal, verruci form hyperplasia with prominent dermal edema, fibroplasia, and a superficial, mixed, perivascular infiltrate ( Figure 2) maintenance of the dermal papillae, eccrine glands and elastic fibers. The histopathologic picture supported the clinical diagnosis of erosive papulonodular dermatosis (EPD); however, arising in the setting of chronic lymphedema, elephantiasis nostra verrucosa (ENV) was also considered.EPD is considered an inflammatory cutaneous eruption secondary to a chronic, external irritant and includes the previously distinct entities of perianal pseudoverrucous papules and nodules, granuloma gluteale infantum, and Jacquet erosive dermatitis [1,2]. Papulonodules are classically found in the diaper area and at urostomy and colostomy sites following repeated leakage, encopresis or urinary incontinence [1]. However, striking cases have been reported in less common locations secondary to post-operative inflammation combined with an occlusive wound dressing [2], and following continuous wear of medical examination gloves due to an underlying delusion [4]. While presenting in atypical sites, both cases highlight occlusion as is common in EPD. In our case, the typical papules of EPD arose secondary to protein-rich lymphatic fluid in the setting of chronic lymphedema in the absence of occlusion. Elephantiasis nostra verrucosa is a more frequent complication of longstanding lymphedema and also demonstrates pseudoepitheliomatous hyperplasia on biopsy [5,6]. Our case is differentiated from ENV clinically by the presence of moist, red papules and nodules with erosions, and histopathologically by the absence of dermal and subcutaneous woody fibrosis, as well as by the...