Predominantly Lymphocytic Group

Chapter

Abstract

In this chapter, lichen planopilaris, Graham Little syndrome, frontal fibrosing alopecia (FFA), pseudopelade (Brocq), and central centrifugal cicatricial alopecia are described. Two additional entities that are not primary cicatricial alopecias are included, namely chronic cutaneous lupus erythematosus (CCLE) and keratosis follicularis spinulosa decalvans (KFSD) because they are important to recognize and differentiate.

Keywords

Burning Flare Cyclosporin Ferritin Triad 

Suggested Reading

  1. Castori M, Covaciu C, Paradisi M, et al. Clinical and genetic heterogeneity in keratosis follicularis spinulosa decalvans. Eur J Med Genet. 2009;52:53–8.PubMedCrossRefGoogle Scholar
  2. Chui CT, Berger TG, Price VH, et al. Recalcitrant scarring follicular disorders treated by laser-assisted hair removal: a preliminary report. Dermatol Surg. 1999:25:34–7.PubMedCrossRefGoogle Scholar
  3. Hallai N, Thompson I, Williams P, et al. Folliculitis spinulosa decalvans: failure to respond to oral isotretinoin. J Eur Acad Dermatol Venereol. 2006;20:223–4.PubMedCrossRefGoogle Scholar
  4. Oosterwijk JC, Nelen M, van Zandvoort PM, et al. Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2. Am J Hum Genet. 1992;50:801–7.Google Scholar
  5. Oranje AP, van Osch LD, Oosterwijk JC. Keratosis pilaris atrophicans. One heterogeneous disease or a symptom in different clinical entities? Arch Dermatol. 1994;130:469–75.Google Scholar

Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  1. 1.Department of DermatologyUniversity of California, San FranciscoSan FranciscoUSA
  2. 2.Department of DermatologyCase Western Reserve UniversityClevelandUSA
  3. 3.Department of DermatologyThe Permanente Medical GroupVallejoUSA

Personalised recommendations