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This family of diseases contains 2 subgroups, largely based on clinical features: keratosis pilaris atrophicans (<jats:styled-content style=\"fixed-case\">KPA<\/jats:styled-content>; including keratosis pilaris atrophicans faciei\/ulerythema ophryogenes, atrophoderma vermiculatum, and keratosis follicularis spinulosa decalvans); and the lichen planopilaris (<jats:styled-content style=\"fixed-case\">LPP<\/jats:styled-content>) subgroup (including <jats:styled-content style=\"fixed-case\">LPP<\/jats:styled-content>, frontal fibrosing alopecia, Graham\u2010Little\u2010Piccardi\u2010Lassueur Syndrome and fibrosing alopecia in a pattern distribution). An interface dermatitis with lichenoid inflammation is characteristic of the <jats:styled-content style=\"fixed-case\">LPP<\/jats:styled-content> group of disorders, but the literature provides scant information about the histopathology of the <jats:styled-content style=\"fixed-case\">KPA<\/jats:styled-content> group. Our experience has been that the 2 subgroups show a unifying histologic similarity as well as considerable clinical overlap. Because these conditions overlap clinically and histologically, we propose that the term lichenoid folliculitis (<jats:styled-content style=\"fixed-case\">LF<\/jats:styled-content>) be used to refer to this group of diseases, thus simplifying cumbersome nomenclature and highlighting the possibility of shared pathogenesis and treatment options.<\/jats:p>","DOI":"10.1111\/cup.12938","type":"journal-article","created":{"date-parts":[[2017,3,27]],"date-time":"2017-03-27T01:56:38Z","timestamp":1490579798000},"page":"647-654","source":"Crossref","is-referenced-by-count":20,"title":["Lichenoid folliculitis: A unifying concept"],"prefix":"10.1111","volume":"44","author":[{"given":"Mamina M.","family":"Turegano","sequence":"first","affiliation":[{"name":"Department of Pathology and Laboratory Medicine, Division of Dermatopathology, David Geffen School of Medicine University of California Los Angeles  Los Angeles Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2587-8023","authenticated-orcid":false,"given":"Leonard C.","family":"Sperling","sequence":"additional","affiliation":[{"name":"Department of Dermatology Uniformed Services University of the Health Sciences  Los Angeles Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2017,5,5]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.1953.01540040004002"},{"issue":"1","key":"e_1_2_5_3_1","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1001\/archderm.1983.01650250026010","article-title":"Keratosis follicularis spinulosa decalvans. 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