Adenoid cystic carcinoma is a rare, slow-growing neoplasm. It is most commonly located in the salivary glands, affects people older than 55 years of age, and has a predilection for women. These lesions may recur locally but have shown low metastatic potential. We present the unique case of a 71-year-old female with a nonraised hyperpigmented lesion isolated to the right heel. Confusion surrounded the clinical presentation of this dermatologic lesion, and many physicians postulated several differential diagnoses. The purpose of this case report is to bring further awareness to this rare dermatologic variant of adenoid cystic carcinoma, which has been rarely reported in the literature. (J Am Podiatr Med Assoc 107(5): [457][458][459][460] 2017) Adenoid cystic carcinoma (ACC) is an unusual adnexal skin tumor that may present in any glandular tissue. These lesions are usually located on the salivary glands, scalp, and neck; they rarely occur in the breast, lung, uterine cervix, or prostate. These lesions have unknown etiology; however, recent theories propose that they are derived from apocrine and modified apocrine glands.1 Cutaneous adenoid cystic carcinoma is a rare variant of ACC with unique histopathologic characteristics. Clinically, cutaneous ACC presents as a solitary, ulcerated, slow growing, and normal skin-colored lesion that measures between 0.5 and 10 cm. Histologically, cutaneous ACC tumor cells demonstrate neoplastic changes on the skin and subcutaneous tissue with a collection of basophilic cells in cribriform pattern. Perineural invasion is seen in 76% of cases and not only has prognostic features, but may also increase the risk of local recurrence twofold over lesions without neural changes. 1 Based on the nature of cutaneous ACC and the success rate of Mohs surgery in other cutaneous malignancies that exhibit perineural invasion, Mohs surgery is reported to be superior to wide local excision in achieving a more complete excision of this tumor and reducing the rate of local recurrence of the many primary skin tumors.
Case ReportWe present a case of a 71-year-old female who was admitted to our medical center with an altered mental status and an extensive past medical history for type 2 diabetes mellitus, hypertensive cardiovascular disease, dyslipidemia, stroke, dementia, and chronic renal insufficiency. Upon physical examination it was noted and documented by the primary care physician that the patient presented with a painful callus-like lesion on the plantarmedial aspect of the right heel that had been present for approximately 5 to 6 months. The patient denied any recent trauma to the area or active bleeding.Upon further examination of the lesion, it was revealed to be an asymmetrical raised nodule measuring 1.5 3 1.5 cm with irregular thickened borders and a satellite lesion at the 3 o'clock position measuring less than 1 cm (Fig. 1). Because *Podiatric Medicine and Surgery Residency Program,