Steatocystoma multiplex is a rare genetic disorder characterized by the presence
of hamartomatous malformations at the junction of the pilosebaceous duct. It
consists of encapsulated cystic lesions in the dermis, with adjacent sebaceous
gland. When associated with inflammation, resembling hidradenitis, it is called
steatocystoma multiplex suppurativa, a condition rarely reported. This is the
first case of steatocystoma multiplex suppurativa reported in the Brazilian
literature. Female patient, 23 years old, with papular and nodular cystic
lesions that started in the armpits and groin, later spreading to the trunk,
lower limbs, anticubital fossa, face and scalp. The presence of papular-nodular
lesions associated with disseminated hidradenitis-like lesions in flexural areas
and the histopathological diagnosis of steatocystoma defined the diagnosis of
steatocystoma multiplex suppurativa.