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Dermoscopy of Pilonidal Cyst Disease: A Case-series.
Uzuncakmak TK, Oba MC, Sar M, Serdaroğlu S. Uzuncakmak TK, et al. Acta Dermatovenerol Croat. 2022 Nov;30(3):194-196. Acta Dermatovenerol Croat. 2022. PMID: 36812282
A peripheral brown rim, linear vessels, and yellow homogenous background of the entire lesion have been reported as dermoscopic features of steatocystoma multiplex as well as milias (5). Of note, other cystic lesions mentioned above are typified by linear vessels, w …
A peripheral brown rim, linear vessels, and yellow homogenous background of the entire lesion have been reported as dermoscopic features of …
A simple modified surgical technique combined with tissue adhesive for steatocystoma multiplex.
Jiang L, Yan J, Chen X, Chen Y, Tang Y. Jiang L, et al. J Cosmet Dermatol. 2021 Jan;20(1):218-221. doi: 10.1111/jocd.13438. Epub 2020 May 10. J Cosmet Dermatol. 2021. PMID: 32390282
BACKGROUND: Steatocystoma multiplex (SM) is a disorder of the pilosebaceous unit characterized by multiple sebum-containing dermal cysts. ...AIMS: To provide a facile and practical surgical technique combined with tissue adhesive for the treatment of steatocystom …
BACKGROUND: Steatocystoma multiplex (SM) is a disorder of the pilosebaceous unit characterized by multiple sebum-containing de …
Natal teeth and steatocystoma multiplex: a newly recognized syndrome.
King NM, Lee AM. King NM, et al. J Craniofac Genet Dev Biol. 1987;7(3):311-7. J Craniofac Genet Dev Biol. 1987. PMID: 3429608
This autosomal dominant condition is not similar to the two reported types of pachyonychia congenita, because nail lesions, palmoplantar keratosis and hyperhidrosis, follicular keratosis, and oral leukokeratosis were not observed. Therefore, it is suggested that this famil …
This autosomal dominant condition is not similar to the two reported types of pachyonychia congenita, because nail lesions, palmoplantar ker …
A simple surgical technique for the treatment of steatocystoma multiplex.
Kaya TI, Ikizoglu G, Kokturk A, Tursen U. Kaya TI, et al. Int J Dermatol. 2001 Dec;40(12):785-8. doi: 10.1046/j.1365-4362.2001.01325.x. Int J Dermatol. 2001. PMID: 11903679
BACKGROUND: Since steatocystoma multiplex is an uncommon disorder, its treatment has not been discussed in detail in the textbooks and surgical excision is the most commonly mentioned method. ...We believe that it must be considered as the treatment of choice for …
BACKGROUND: Since steatocystoma multiplex is an uncommon disorder, its treatment has not been discussed in detail in the textb …
Association of copeptin and cortisol in newly diagnosed multiple sclerosis patients.
Baranowska-Bik A, Kochanowski J, Uchman D, Litwiniuk A, Kalisz M, Martynska L, Wolinska-Witort E, Baranowska B, Bik W. Baranowska-Bik A, et al. J Neuroimmunol. 2015 May 15;282:21-4. doi: 10.1016/j.jneuroim.2015.03.011. Epub 2015 Mar 11. J Neuroimmunol. 2015. PMID: 25903724
We report that copeptin and cortisol were higher in overweight/obese MS patients. Positive correlations were observed between the two parameters. We conclude that alterations of copeptin and cortisol levels in multiple sclerosis patients may be related to adiposity. ...
We report that copeptin and cortisol were higher in overweight/obese MS patients. Positive correlations were observed between the two …
Mammographic demonstration of steatocystoma multiplex.
Apesteguía L, Mellado MT, Inchusta MI, Cordero JL. Apesteguía L, et al. Eur Radiol. 1998;8(4):647-8. doi: 10.1007/s003300050453. Eur Radiol. 1998. PMID: 9569341
Steatocystoma multiplex (SM) is a rare inherited cutaneous disorder characterised by multiple subcutaneous oil cysts. ...Many lipid-containing intradermal cysts of different sizes were also observed at sonography, scattered over both breasts, axillae, sternal …
Steatocystoma multiplex (SM) is a rare inherited cutaneous disorder characterised by multiple subcutaneous oil cysts. ...Many …
Pachyonychia congenita associated with steatocystoma multiplex.
Kim JU, Nogita T, Terajima S, Kawashima M. Kim JU, et al. J Dermatol. 1998 Jul;25(7):479-81. doi: 10.1111/j.1346-8138.1998.tb02439.x. J Dermatol. 1998. PMID: 9714984
We present an unique case of pachyonychia congenita associated with steatocystoma multiplex. A 33-year-old Japanese man had thickening and gray-brown dicoloration of all nails and a large number of nodules or tumors over his entire skin. No palmar and plantar hyperk …
We present an unique case of pachyonychia congenita associated with steatocystoma multiplex. A 33-year-old Japanese man had th …
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex.
Smith FJ, Corden LD, Rugg EL, Ratnavel R, Leigh IM, Moss C, Tidman MJ, Hohl D, Huber M, Kunkeler L, Munro CS, Lane EB, McLean WH. Smith FJ, et al. J Invest Dermatol. 1997 Feb;108(2):220-3. doi: 10.1111/1523-1747.ep12335315. J Invest Dermatol. 1997. PMID: 9008238 Free article.
We also show heterozygous missense mutations in K17 (N92H and R94H) in two families diagnosed as steatocystoma multiplex. Mild nail defects were observed in some but not all of these patients on clinical re-evaluation of these families. All the K17 mutations …
We also show heterozygous missense mutations in K17 (N92H and R94H) in two families diagnosed as steatocystoma multiplex. Mild …