“…It was first classified into the following four types by Starink: solitary, multiple ESFA associated with hidrotic ED-like Schopf–Schulz–Passarge syndrome (eyelid cysts, hypotrichosis, hypodontia, nail hypoplasia) or Clouston syndrome (palmoplantar keratoderma, patchy alopecia, nail dystrophy), multiple ESFA without associated cutaneous findings, and nonfamilial unilateral linear ESFA. [ 1 2 3 ] In 1997, the fifth type was recognized as reactive ESFA by French as a ductal hyperplastic or hamartomatous process initiated by repeated damage to the eccrine structures by chronic inflammatory or neoplastic dermatoses such as diabetic foot ulcer, leprous neuropathy, venous stasis or insufficiency, burn scar, BP, EB, naevus sebaceous, stoma of ileostomy, palmoplantar erosive LP, trauma, chronic plaque type psoriasis, epithelioid haemangioendothelioma, and squamous cell carcinoma. [ 4 5 6 ] Reactive ESFA is usually single and acrally located, but if multiple sites are involved, it is termed as “eccrine syringofibroadenomatosis.” Apart from these five types, another clear cell variant was also reported by Hu et al .…”