Leprosy presents diversely, making diagnosis challenging. Histoid leprosy is a rare variant with atypical features. We present a case of a 40-year-old Filipino male with multiple erythematous to flesh colored, well demarcated hypoesthetic nodules primarily on his back and abdomen. Dermoscopy revealed features of granulomatous disease. Fite-Faraco stain showed globi formation. Skin biopsy showed epidermal atrophy, dense histiocyte infiltrates and collagen trapping. While histoid leprosy is uncommon in patients without a prior history of leprosy and treatment, this case highlights the importance of maintaining a high index of suspicion, especially in endemic regions. Early diagnosis and prompt multidrug therapy are crucial for preventing transmission and improving patient outcomes.