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2012, Number 3

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Rev Cent Dermatol Pascua 2012; 21 (3)

Dowling-Degos disease

Domínguez GMA, Ramos GA, Valencia ÁM
Full text How to cite this article

Language: Spanish
References: 14
Page: 99-103
PDF size: 95.63 Kb.


Key words:

Dowling-Degos disease, cytokeratins, hiperpigmented spots.

ABSTRACT

Dowling-Degos disease has an autosomal dominant variable penetrance. It is caused by a mutation in chromosome 17 that produces altered cytokeratins 5 and 14. Clinicaly it is characterized by reticulated hiperpigmented spots that prevails in folds and it is accompanied by perioral scars and injuries of pimple-like aspect. It’s more frequent in women of the fourth decade of the life. In this article we report the case of a 40 year old female patient with Dowling-Degos disease.


REFERENCES

  1. Kim YC, Mark D, Schanbacher C. Dowling-Degos disease (reticulate pigmented anomaly of the fl exures): A clinical and histopathologic study of 6 cases. J Am Acad Dermatol 1999; 40: 462-467.

  2. Batycka A, Baran W, Hryncewicz A, Burgdorf W. Dowling-Degos disease: case report and review of the literature. Dermatology 2010; 220: 254-258.

  3. Donelli E, Sardi J, Pérez L et al. Enfermedad de Dowling-Degos: Presentación de un caso y revisión de la literatura. Dermatología Venezolana 1996; 34: 75-79.

  4. Wu YH, Lin YC, Taipei T. Generalized Dowling-Degos disease. Dermatopathology. J Am Acad Dermatol 2007; 57: 327-334.

  5. Wenzel J, Tappe K, Gerdsen R, Uerlich M et al. Successful treatment of Dowling-Degos disease with Er:YAG laser. Dermatol Surg 2002; 28: 748-750.

  6. Betz R, Planko L, Eigelshoven S et al. Loss-of-function mutations in the keratin 5 gene led to Dowling-Degos disease. Am J Hum Genet 2006; 78: 510-519.

  7. Ujihara M, Kamakkyra T, Ikeda M, Kodama H. Dowling-Degos disease associated with squamous cell carcinomas on the dappled pigmentation. British Journal of Dermat 2002; 147: 568-571.

  8. Cammarata F, Caraballo Y, Reyes O et al. Enfermedad de Dowling- Degos asociada con carcinoma basocelular. Reporte de un caso con hallazgos clínicos inusuales. Dermatología Peruana 2004; 14: 208-210.

  9. Valdés F, Peteiro C, Toribio J. Enfermedad Dowling-Degos. Act Dermosifi liogr 2003; 94: 409-411.

  10. Shabrawi L, Rutten A, Kerl H et al. The expanding spectrum of Galli- Galli disease. J Am Acad Dermatol 2007; 56: 86-91.

  11. Sprecher E, Indelman M, Khamaysi Z et al. Galli-Galli disease is an acantholytic variant of Dowling-Degos disease. British Journal of Dermatology 2007; 156: 572-574.

  12. Hanneken S, Rutten, Pasternack S, Eigelshoven S et al. Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease. British Journal of Dermatology 2010; 163: 197-200.

  13. Braun-Falco M, Wolfgang V, Borelli S et al. Galli-Galli disease: An unrecognized entity or an acantholytic variant of Dowling-Degos disease? J Am Acad Dermatol 2001; 45: 760-763.

  14. Muller C, Pfohler C, Tilgen W. Changing a concept-controversy on the confusing spectrum of the reticulate pigmented disorders of the skin. J Cutan Pathol 2008; 10: 1-5.




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Rev Cent Dermatol Pascua. 2012;21