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Erythrokeratoderma en cocardes.

B Rajagopalan1, S Pulimood, S George

  • 1Department of Dermatology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.

Clinical and Experimental Dermatology
|June 3, 1999
PubMed
Summary
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Erythrokeratodermas are rare genetic skin disorders with red, thickened lesions. This study describes a case of Erythrokeratoderma en cocardes, a specific type with target-like plaques.

Area of Science:

  • Dermatology
  • Genetics
  • Rare Diseases

Background:

  • Erythrokeratodermas are a group of rare genodermatoses defined by erythematous and hyperkeratotic skin lesions.
  • Classification has historically relied on clinical and morphological criteria.

Observation:

  • Erythrokeratoderma en cocardes (Degos' syndrome) presents with distinctive target-shaped plaques.
  • These plaques exhibit concentric erythema and scaling, with periods of remission and recurrence.

Findings:

  • The study details a clinical case of this rare genodermatosis.
  • The observed case aligns with the characteristic presentation of Erythrokeratoderma en cocardes, including features of Erythrokeratoderma variabilis.

Implications:

Related Experiment Videos

  • This case contributes to the understanding of rare genodermatoses.
  • Further research may refine classification and management strategies for erythrokeratodermas.