Coexistence of Hidradenitis Suppurativa and Steatocystoma Multiplex: Is It a New Variant of Hidradenitis Suppurativa?

1. Zouboulis, CC., Desai, N., Emtestam, L et al. European S1 guideline for the treatment of hidradenitis suppurativa/acne inversa. J Eur Acad Dermatol Venereol. 2015;29(4):619-644.doi:10.1111/jdv.12966 25640693
Google Scholar | Crossref | Medline | ISI2. Gasparic, J., Theut Riis, P., Jemec, GB. Recognizing syndromic hidradenitis suppurativa: a review of the literature. J Eur Acad Dermatol Venereol. 2017;31(11):1809-1816.doi:10.1111/jdv.14464 28696038
Google Scholar | Crossref | Medline3. Hollmig, T., Menter, A. Familial coincidence of hidradenitis suppurativa and steatocystoma multiplex. Clin Exp Dermatol. 2010;35(4):e151-e152.doi:10.1111/j.1365-2230.2009.03742.x 19886955
Google Scholar | Crossref | Medline4. Santana, CN., Pereira, DD., Lisboa, AP., Leal, JM., Obadia, DL., Silva, RS. Steatocystoma multiplex suppurativa: case report of a rare condition. An Bras Dermatol. 2016;91(5 suppl 1):51-53.doi:10.1590/abd1806-4841.20164539 28300893
Google Scholar | Crossref | Medline5. Zussino, M., Nazzaro, G., Moltrasio, C., Marzano, AV., Marzano, AV. Coexistence of steatocystoma multiplex and hidradenitis suppurativa: assessment of this unique association by means of ultrasonography and color Doppler. Skin Res Technol. 2019;25(6):1-4.doi:10.1111/srt.12751 31353757
Google Scholar | Medline6. Alotaibi, L., Alsaif, M., Alhumidi, A., Turkmani, M., Alsaif, F. Steatocystoma multiplex suppurativa: a case with unusual giant cysts over the scalp and neck. Case Rep Dermatol. 2019;11(1):71-76.doi:10.1159/000498882 31011316
Google Scholar | Crossref | Medline7. Adams, B., Shwayder, T. Steatocystoma multiplex suppurativum. Int J Dermatol. 2008;47(11):1155-1156.doi:10.1111/j.1365-4632.2008.03698.x 18986448
Google Scholar | Crossref | Medline8. Apaydin, R., Bilen, N., Bayramgürler, D., Başdaş, F., Harova, G., Dökmeci, S. Steatocystoma multiplex suppurativum: oral isotretinoin treatment combined with cryotherapy. Australas J Dermatol. 2000;41(2):98-100.doi:10.1046/j.1440-0960.2000.00403.x 10812703
Google Scholar | Crossref | Medline9. Monteiro, A., Rato, M., Tavares, E. Inherited steatocystoma multiplex suppurativa. J Am Acad Dermatol. 2018;6550. doi:10.1016/j.jaad.2018.05.689
Google Scholar10. Scheinfeld, N . Diseases associated with hidranitis suppurativa: Part 2 of a series on hidradenitis. Dermatol Online J. 2013;19(6):24011308
Google Scholar | Crossref | Medline11. McDonald, RM., Reed, WB. Natal teeth and steatocystoma multiplex complicated by hidradenitis suppurativa. A new syndrome. Arch Dermatol. 1976;112(8):1132-1139.doi:10.1001/archderm.1976.01630320038010 988984
Google Scholar | Crossref | Medline12. Pavlovsky, M., Sarig, O., Eskin-Schwartz, M et al. A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN. Br J Dermatol. 2018;178(2):502-508.doi:10.1111/bjd.16000 28922471
Google Scholar | Crossref | Medline13. McGarth, J . Concurrent hidradenitis suppurativa and dowling–degos disease taken down a ‘Notch’. Br J Dermatol. 2018;74:doi:10.1111/bjd.16068
Google Scholar14. Covello, S., Smith, F., Sillevis Smitt, J et al. Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2. Br J Dermatol. 1998;1:475-480.
Google Scholar | Crossref15. Agut-Busquet, E., de Gabriel, J., Pibernat, M., Gonzalez, A., Moreno, J. Dowling-Degos syndrome and hidradenitis suppurativa: An uncommon association with linked pathogenesis? Report of nien cases and review of the literature. J Am Acad Dermatol. 2017;4929 doi:10.1016/j.jaad.2017.04.416
Google Scholar16. Bedlow, AJ., Mortimer, PS., George, S., Road, B. Dowling-Degos disease associated with hidradenitis suppurativa. Clin Exp Dermatol. 1996;21(4):305-306.doi:10.1111/j.1365-2230.1996.tb00103.x 8959907
Google Scholar | Crossref | Medline17. Loo, WJ., Rytina, E., Todd, PM. Hidradenitis suppurativa, Dowling-Degos and multiple epidermal cysts: a new follicular occlusion triad. Clin Exp Dermatol. 2004;29(6):622-624.doi:10.1111/j.1365-2230.2004.01631.x 15550138
Google Scholar | Crossref | Medline18. Cho, S., Chang, S-E., Choi, J-H., Sung, K-J., Moon, K-C., Koh, J-K. Clinical and histologic features of 64 cases of steatocystoma multiplex. J Dermatol. 2002;29(3):152-156.doi:10.1111/j.1346-8138.2002.tb00238.x 11990250
Google Scholar | Crossref | Medline19. Goeteyn, M., Geerts, ML., Kint, A., De Weert, J., De, WJ. The Bazex-Dupré-Christol syndrome. Arch Dermatol. 1994;130(3):337-342.doi:10.1001/archderm.1994.01690030069011 8129412
Google Scholar | Crossref | Medline20. Kim, YC., Davis, MD., Schanbacher, CF., Su, WP., disease, D-D. Dowling-Degos disease (reticulate pigmented anomaly of the flexures): a clinical and histopathologic study of 6 cases. J Am Acad Dermatol. 1999;40(3):462-467.doi:10.1016/S0190-9622(99)70498-6 10071319
Google Scholar | Crossref | Medline21. Garg, A., Strunk, A., Midura, M., Papagermanos, V., Pomerantz, H. Prevalence of hidradenitis suppurativa among patients with Down syndrome: a population-based cross-sectional analysis. Br J Dermatol. 2018;178(3):697-703.doi:10.1111/bjd.15770 28662304
Google Scholar | Crossref | Medline22. Caceres-Rios, H., Tamayo-Sanchez, L., Duran-Mckinster, C., de la Luz Orozco, M., Ruiz-Maldonado, R., Keratitis, R-MR. Keratitis, ichthyosis, and deafness (kid syndrome): review of the literature and proposal of a new terminology. Pediatr Dermatol. 1996;13(2):105-113.doi:10.1111/j.1525-1470.1996.tb01414.x 9122065
Google Scholar | Crossref | Medline23. Vural, S., Gundogdu, M., Kundakci, N., Ruzicka, T. Familial Mediterranean fever patients with hidradenitis suppurativa. Int J Dermatol. 2017;56(6):660-663.doi:10.1111/ijd.13503 28194777
Google Scholar | Crossref | Medline

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