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Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: olgu sunumu

Year 2016, Volume: 6 Issue: 3, 214 - 217, 19.10.2016
https://doi.org/10.16899/ctd.51716

Abstract

Fox-Fordyce hastalığı (FFH), apokrin ter bezlerin kronik, nadir görülen, klinik olarak kaşıntılı papüllerle karakterize bir hastalığıdır. Kadınlarda daha sık görülür ve etyolojisi tam olarak net değildir. Bu makalede Stevens-Johnson Sendromu sonrasında dudaklarında FFD gelişen 17 yaşında bir erkek hasta sunuldu.

References

  • Odom RB, James WD, Berger TG. Diseases of the Skin Appendages. In Andrews’ diseases of the skin. 9. baskı. Philadelphia: Saunders Co, 2000: .975-6.
  • Ozcan A, Senol M, Aydin NE, Karaca S, Sener S. Fox-Fordyce disease. J Eur Acad Dermatol Venereol. 2003 Mar;17(2):244-5.
  • Kamada A, Saga K, Jimbow K. Apoeccrine sweat duct obstruction as a cause for Fox-Fordyce disease. J Am Acad Dermatol 2003; 48: 453–455.
  • Sandhu K, Gupta S, Kanwar AJ. Fox fordyce disease in a prepubertal girl. Pediatr Dermatol 2005;22:89-90.
  • Mayser P, Gründer K, Nilles M, Schill WB (1993) Fox–Fordyce disease (apocrine miliaria). Hautarzt 44:309–311.
  • Shelley WB, Levy EJ. Apocrine sweat retention in man. II: Fox-Fordyce disease (apocrine miliaria). Arch Dermatol 1956; 74: 38.
  • Gündüz K, Kandiloğlu AR, Köşk EE, Türel A, Türkdoğan P. A male patient with Fox-Fordyce disease. Turk J Dermatopathol 1998; 7: 63-5.
  • Stashower ME, Kriuda SJ, Turiansky GW. Fox-Fordyce disease:Diagnosis with transverse histologic sections. J Am Acad Dermatol 2000; 42: 89-91.
  • Roujeau JC: The spectrum of Stevens-Johnson syndrome and toxic epidermal necrolysis: a clinical classification. J Invest Dermatol 1994;102:28-30.
  • Assier H, Bastuji-Garin S, Revuz J, Roujeau JC: Erythema multiforme with mucous membrane involvement and Stevens-Johnson syndrome are clinically different disorders with distinct causes. Arch Dermatol 1995;131:539-43.
  • Roujeau JC, Stern RS: Severe adverse cutaneous reactions to drugs. N Engl J Med 1994;331:1272-85.
  • Leaute-Labreze C, Lamireau T, Chawki D, Maleville J, Taieb A: Diagnosis, classification, and management of erythema multiforme and Stevens-Johnson syndrome. Arch Dis Child 2000;83:347-52.
  • Ranalli DN, Elliott MA, Whaley TM, Campagna Jr ED. Stevens–Johnson syndrome: report of case with abnormal root development. ASDC J Dent Child 1984;51(4):298–301.
  • Gaultier F, Rochefort J, Landru MM, Allanore L, Naveau A, Roujeau JC, et al. Severe and unrecognized dental abnormalities after drug-induced epidermal necrolysis. Arch Dermatol 2009;145(11):1332–3.
  • Koseki M, Maki Y, Matsukubo T, Ohashi Y, Tsubota K. Salivary flow and its relationship to oral signs and symptoms in patients with dry eyes. Oral Dis 2004;10(2):75–80.
Year 2016, Volume: 6 Issue: 3, 214 - 217, 19.10.2016
https://doi.org/10.16899/ctd.51716

Abstract

References

  • Odom RB, James WD, Berger TG. Diseases of the Skin Appendages. In Andrews’ diseases of the skin. 9. baskı. Philadelphia: Saunders Co, 2000: .975-6.
  • Ozcan A, Senol M, Aydin NE, Karaca S, Sener S. Fox-Fordyce disease. J Eur Acad Dermatol Venereol. 2003 Mar;17(2):244-5.
  • Kamada A, Saga K, Jimbow K. Apoeccrine sweat duct obstruction as a cause for Fox-Fordyce disease. J Am Acad Dermatol 2003; 48: 453–455.
  • Sandhu K, Gupta S, Kanwar AJ. Fox fordyce disease in a prepubertal girl. Pediatr Dermatol 2005;22:89-90.
  • Mayser P, Gründer K, Nilles M, Schill WB (1993) Fox–Fordyce disease (apocrine miliaria). Hautarzt 44:309–311.
  • Shelley WB, Levy EJ. Apocrine sweat retention in man. II: Fox-Fordyce disease (apocrine miliaria). Arch Dermatol 1956; 74: 38.
  • Gündüz K, Kandiloğlu AR, Köşk EE, Türel A, Türkdoğan P. A male patient with Fox-Fordyce disease. Turk J Dermatopathol 1998; 7: 63-5.
  • Stashower ME, Kriuda SJ, Turiansky GW. Fox-Fordyce disease:Diagnosis with transverse histologic sections. J Am Acad Dermatol 2000; 42: 89-91.
  • Roujeau JC: The spectrum of Stevens-Johnson syndrome and toxic epidermal necrolysis: a clinical classification. J Invest Dermatol 1994;102:28-30.
  • Assier H, Bastuji-Garin S, Revuz J, Roujeau JC: Erythema multiforme with mucous membrane involvement and Stevens-Johnson syndrome are clinically different disorders with distinct causes. Arch Dermatol 1995;131:539-43.
  • Roujeau JC, Stern RS: Severe adverse cutaneous reactions to drugs. N Engl J Med 1994;331:1272-85.
  • Leaute-Labreze C, Lamireau T, Chawki D, Maleville J, Taieb A: Diagnosis, classification, and management of erythema multiforme and Stevens-Johnson syndrome. Arch Dis Child 2000;83:347-52.
  • Ranalli DN, Elliott MA, Whaley TM, Campagna Jr ED. Stevens–Johnson syndrome: report of case with abnormal root development. ASDC J Dent Child 1984;51(4):298–301.
  • Gaultier F, Rochefort J, Landru MM, Allanore L, Naveau A, Roujeau JC, et al. Severe and unrecognized dental abnormalities after drug-induced epidermal necrolysis. Arch Dermatol 2009;145(11):1332–3.
  • Koseki M, Maki Y, Matsukubo T, Ohashi Y, Tsubota K. Salivary flow and its relationship to oral signs and symptoms in patients with dry eyes. Oral Dis 2004;10(2):75–80.
There are 15 citations in total.

Details

Subjects Health Care Administration
Journal Section Case Report
Authors

Havva Yıldız Seçkin This is me

Yalçın Baş This is me

Akgül Arıcı This is me

Zennure Takçı This is me

Srecan Sezgin This is me

Publication Date October 19, 2016
Published in Issue Year 2016 Volume: 6 Issue: 3

Cite

APA Seçkin, H. Y., Baş, Y., Arıcı, A., Takçı, Z., et al. (2016). Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: olgu sunumu. Çağdaş Tıp Dergisi, 6(3), 214-217. https://doi.org/10.16899/ctd.51716
AMA Seçkin HY, Baş Y, Arıcı A, Takçı Z, Sezgin S. Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: olgu sunumu. J Contemp Med. September 2016;6(3):214-217. doi:10.16899/ctd.51716
Chicago Seçkin, Havva Yıldız, Yalçın Baş, Akgül Arıcı, Zennure Takçı, and Srecan Sezgin. “Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: Olgu Sunumu”. Çağdaş Tıp Dergisi 6, no. 3 (September 2016): 214-17. https://doi.org/10.16899/ctd.51716.
EndNote Seçkin HY, Baş Y, Arıcı A, Takçı Z, Sezgin S (September 1, 2016) Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: olgu sunumu. Çağdaş Tıp Dergisi 6 3 214–217.
IEEE H. Y. Seçkin, Y. Baş, A. Arıcı, Z. Takçı, and S. Sezgin, “Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: olgu sunumu”, J Contemp Med, vol. 6, no. 3, pp. 214–217, 2016, doi: 10.16899/ctd.51716.
ISNAD Seçkin, Havva Yıldız et al. “Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: Olgu Sunumu”. Çağdaş Tıp Dergisi 6/3 (September 2016), 214-217. https://doi.org/10.16899/ctd.51716.
JAMA Seçkin HY, Baş Y, Arıcı A, Takçı Z, Sezgin S. Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: olgu sunumu. J Contemp Med. 2016;6:214–217.
MLA Seçkin, Havva Yıldız et al. “Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: Olgu Sunumu”. Çağdaş Tıp Dergisi, vol. 6, no. 3, 2016, pp. 214-7, doi:10.16899/ctd.51716.
Vancouver Seçkin HY, Baş Y, Arıcı A, Takçı Z, Sezgin S. Stevens-Johnson Sendromu sonrasında gelişen Fox-Fordyce hastalığı: olgu sunumu. J Contemp Med. 2016;6(3):214-7.