Buradasınız

Anasayfa » Content

Laugier-Hunziker sendromu: bir olgu sunumu

Laugier-Hunziker sendromu: bir olgu sunumu

Journal Name:

  • Gülhane Tıp Dergisi

Publication Year:

  • 2006

Key Words:

Keywords (Original Language):

Author Name
Abstract (2. Language): 
Laugier-Hunziker syndrome is an idiopathic, macular hyperpigmentation of the oral mucous membranes and the lips, with frequent pigmentation of the nails in a longitudinal pattern. Laugier-Hunziker syndrome is a rare disease with approximately 100 cases reported in the literature. The clinical features consist of dark brown to bluish-black macules mainly located on the buccal mucosa and lips. Involvement of the tongue is exceedingly rare. Herein we report a 25-year-old woman diagnosed as Laugier-Hunziker syndrome, with confluent, hyperpigmented lesions of the tongue, that responded to cryosurgery.
Bookmark/Search this post with
Abstract (Original Language): 
Laugier-Hunziker sendromu, idiyopatik, sıklıkla tırnaklarda longitudinal pigmentasyonun gözlendiği, oral müköz membran ve dudaklarda hiperpigmente maküler lezyonlarla klinik seyir gösteren bir hastalıktır. Laugier-Hunziker sendromu, literatürde yaklaşık 100 olgunun yer aldığı ender bir hastalıktır. Klinik bulgular çoğunlukla yanak mukozası ve dudaklarda, koyu kahverengiden mavimsisiyaha kadar değişen renklerde maküler lezyonlardan oluşmaktadır. Dil tutulumuna ender olarak rastlanmaktadır. Bu makalede, dil mukozasında birleşik, hiperpigmente maküllerin saptandığı, Laugier-Hunziker sendromu tanısı alan ve kriyoterapiye yanıt aldığımız 25 yaşındaki kadın olgu sunulmuştur.
FULL TEXT (PDF): 
PDF icon arastirmax-laugier-hunziker-sendromu-bir-olgu-sunumu.pdf
  • 2
104-106
  • Turkish

REFERENCES

References: 

1. Moore RT, Chae KA, Rhodes AR.
Laugier and Hunziker pigmentation:
a lentiginous proliferation of melanocytes. J Am Acad Dermatol 2004; 50:
70-74.
2. Fisher D, Field EA, Welsh S. LaugierHunziker syndrome. Clin Exp
Dermatol 2004; 29: 312-313.
3. Ayoub N, Barete S, Bouaziz JD, Le
Pelletier F, Frances C. Additional
conjunctival and penile pigmentation
in Laugier-Hunziker syndrome: a
report of two cases. Int J Dermatol
2004; 43: 571-574.
4. Lampe AK, Hampton PJ, WoodfordRichens K, Tomlinson I, Lawrence
CM, Douglas FS. Laugier-Hunziker
syndrome: an important differential
diagnosis for Peutz-Jeghers syndrome. J Med Genet 2003; 40: 77.
5. Laugier P, Hunziker H. Pigmentation
melaniques lenticulaire de la nuquese
jugale et des levres. Arch Belges
Dermatol Syph 1970; 26: 391-399.
6. Kanwar AJ, Kaur S, Kaur C, Thami
GP. Laugier-Hunziker syndrome. J
Dermatol 2001; 28: 54-57.
7. Lenane P, Sullivan DO, Keane CO,
Loughlint SO. The Laugier-Hunziker syndrome. J Eur Acad Dermatol
Venereol 2001; 15: 574-577.
8. Yamamato O, Yoshinaga K, Asahi M,
Murata I. A Laugier-Hunziker syndrome associated with esophageal
melanocytosis. Dermatology 1999;
199: 162-164.
9. Mowad CM, Shrager J, Elenitsas R.
Oral pigmentation representing
Laugier-Hunziker syndrome. Cutis
1997; 60: 37-39.
10. Makhoul EN, Ayoub NM, Helou JF,
Abadjian GA. Familial LaugierHunziker syndrome. J Am Acad
Dermatol 2003; 49 :143-145.
11. Baran R, Barriere H. Longitudinal
melanonychia with spreading pigmentation in Laugier-Hunziker syndrome: a report of two cases. Br J
Dermatol 1986; 115: 707-710.
12. Veraldi S, Cavicchini S, Benelli C,
Gasparini G. Laugier-Hunziker syndrome: a clinical, histopathologic, and
ultrastructural study of four cases and
review of the literature. J Am Acad
Dermatol 1991; 25: 632-636.
13. McGrath DR, Spigelman AD. Preventive measures in Peutz-Jeghers
syndrome. Fam Cancer 2001; 1: 121-
125.
14. Marzotti S, Falorni A. Addison's disease. Autoimmunity 2004; 37: 333-
336.
15. Papadavid E, Walker NP. Q-switched
Alexandrite laser in the treatment of
pigmented macules in LaugierHunziker syndrome. J Eur Acad
Dermatol Venereol 2001; 15: 468-
469.
16. Sheridan AT, Dawber RP. LaugierHunziker syndrome: treatment with
cryosurgery. J Eur Acad Dermatol
Venereol 1999; 13: 146-148.

Thank you for copying data from http://www.arastirmax.com