Cysticercus cellulosae is the larval form of Taenia solium, representing the second most common larval infection in humans produced by cestodes. It affects any tissue but is more common in skeletal muscle, CNS and eye. This infection has been known since 500 BC; in Guatemala it was first reported in 1877. It has no racial predilection but is rare in Jews and Moslems who do not eat pork. Humans are definitive hosts for Taenia solium ; pigs and wild hogs are intermediate hosts, but humans can manifest the sporadic larval form. Human cysticercosis is acquired by ingestion of infected pork or fecally contaminated foods. Cysticercosis is clinically characterized by the presence of solitary or multiple submucosal/cutaneous firm nodules, which are circumscribed, movable, usually asymptomatic, and measure 1-1.5 cms. Mature cysticerci are small translucent oval cysts containing the invaginated scolex with 4 sucking openings, each with a double crown of hooks. Macroscopic and microscopic features are both diagnostic. Living larvae with an intact membrane do not elicit an inflammatory reaction unless degenerated or dead. Anticysticercus serum titers are valuable for follow-up and should be first determined before or immediately after diagnosis. MRI and/or CT are mandatory to rule out CNS involvement. The affected head and neck sites in our series are buccal mucosa (3), lower lip (2), upper lip (1), tongue (2), and temporal muscle (1). All of our cases represented single lesions, 3 of them without active CNS compromise. Systemic treatment is mostly recommended for CNS cysticercosis, Praziquantel being the most accepted drug.