References
- Plewig G, Wolff HH, Braun-Falco O. Steatocystoma multiplex: anatomic reevaluation, electron microscopy, and autoradiography. Arch Dermatol Res 1982; 272: 363-80. https://doi.org/10.1007/BF00509068
- Sonnenblick EB, Buchness MR, Austin JH. CT demonstration of steatocystoma multiplex. J Comput Assist Tomogr 1986; 10: 357-9. https://doi.org/10.1097/00004728-198603000-00043
- Park YM, Cho SH, Kang H. Congenital linear steatocystoma multiplexof the nose. Pediatr Dermatol 2000; 17: 136-8. https://doi.org/10.1046/j.1525-1470.2000.01732.x
- Marzano AV, Tavecchio S, Balice Y, Polloni I, Veraldi S. Acral subcutaneous steatocystoma multiplex: a distinct subtype of the disease? Australas J Dermatol 2012; 53: 198-201. https://doi.org/10.1111/j.1440-0960.2011.00851.x
- Feinstein A, Friedman J, Schewach-Millet M. Pachyonychia congenita. J Am Acad Dermatol 1988; 19: 705-11. https://doi.org/10.1016/S0190-9622(88)70226-1
- Covello SP, Smith FJ, Sillevis Smitt JH, Paller AS, Munro CS, Jonkman MF, et al. Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2. Br J Dermatol 1998; 139: 475-80. https://doi.org/10.1046/j.1365-2133.1998.02413.x
- Jamieson WA. Case of numerous cutaneous cysts scattered over the body. Edinb Med J 1873; 19: 223-5.
- Olsen DB, Mostofi RS, Lagrotteria LB. Steatocystoma simplex in the oral cavity: a previously undescribed condition. Oral Surg Oral Med Oral Pathol 1988; 66: 605-7. https://doi.org/10.1016/0030-4220(88)90383-0
- Kim SJ, Park HJ, Oh ST, Lee JY, Cho BK. A case of steatocystoma multiplex limited to the scalp. Ann Dermatol 2009; 21: 106-9. https://doi.org/10.5021/ad.2009.21.1.106
- Ohtake N, Kubota Y, Takayama O, Shimada S, Tamaki K. Relationship between steatocystoma multiplex and eruptive vellus hair cysts. J Am Acad Dermatol 1992; 26: 876-8. https://doi.org/10.1016/0190-9622(92)70127-2
- Papakonstantinou E, Franke I, Gollnick H. Facial Steatocystoma multiplex combined with eruptive vellus hair cysts: a hybrid? J Eur Acad Dermatol Venereol 2015; 29: 2051-3. https://doi.org/10.1111/jdv.12588
- Xiao SX, Feng YG, Ren XR, Tan SS, Li L, Wang JM, et al. A novel mutation in the second half of the keratin 17 1A domain in a large pedigree with delayed-onset pachyonychia congenita type 2. J Invest Dermatol 2004; 122: 892-5. https://doi.org/10.1111/j.0022-202X.2004.22408.x
- Smith FJ, Corden LD, Rugg EL, Ratnavel R, Leigh IM, Moss C, et al. Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex. J Invest Dermatol 1997; 108: 220-3. https://doi.org/10.1111/1523-1747.ep12335315
- Moon SE, Lee YS, Youn JI. Eruptive vellus hair cyst and steatocystoma multiplex in a patient with pachyonychia congenita. J Am Acad Dermatol 1994; 30: 275-6. https://doi.org/10.1016/S0190-9622(08)81928-7
- Leachman SA, Kaspar RL, Fleckman P, Florell SR, Smith FJ, McLean WH, et al. Clinical and pathological features of pachyonychia congenita. J Investig Dermatol Symp Proc 2005; 10: 3-17. https://doi.org/10.1111/j.1087-0024.2005.10202.x
- Oh SW, Kim MY, Lee JS, Kim SC. Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity. J Dermatol 2006; 33: 161-4. https://doi.org/10.1111/j.1346-8138.2006.00037.x
- Zamiri M, McLean WH, Hodgins MB, Munro CS. Pachyonychia congenita type 2: abnormal dentition extending into adulthood. Br J Dermatol 2008; 159: 500-1. https://doi.org/10.1111/j.1365-2133.2008.08662.x
- Gass JK, Wilson NJ, Smith FJ, Lane EB, Mclean WH, Rytina E, et al. Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation. Br J Dermatol 2009; 161: 1396-8. https://doi.org/10.1111/j.1365-2133.2009.09383.x