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Texte intégral de l'article
 
  Version imprimable

Digitate dermatosis


European Journal of Dermatology. Volume 9, Numéro 2, 135-6, March 1999, Votre diagnostic !


Summary  

Auteur(s) : Thilo Gambichler, .

Illustrations

ARTICLE

A 76-year-old man presented with a long history of asymptomatic erythematous skin changes. On examination, erythematous, finger-shaped plaques with a marked tendency to palisading were found on the trunk and on the proximal aspects of the limbs (Fig. 1) A skin biopsy specimen revealed superficial, perivascular, lymphocytic infiltrates as well as spongiosis and parakeratosis. General physical and laboratory examinations were unremarkable.

Digitate dermatosis

Since Brocq first proposed the term parapsoriasis in 1902 many synonyms and classifications of the parapsoriasis group have been used. Nowadays, parapsoriasis is clinically divided into three entities, with subtypes as follows: pityriasis lichenoides, small plaque parapsoriasis and large plaque parapsoriasis. Benign small plaque parapsoriasis (chronic superficial dermatitis), usually appearing with lesions smaller than 5 cm in diameter, is clinically and prognostically distinguished from large plaque parapsoriasis, which is known to progress to cutaneous lymphoma in about 10% of cases [1-3]. Digitate dermatosis has a chronic course and is generally described as a clinical variant of small plaque parapsoriasis, however, there are authors who consider digitate dermatosis and small plaque parapsoriasis to be synonymous [4, 5]. Characteristically in digitate dermatosis, pink or erythematous, elongated plaques occur along the tension lines. In rare cases, finger-shaped lesions show a marked tendency to palisading as shown in the present case. This clinical picture of digitate dermatosis has occasionally been described as fingerprint parapsoriasis [1, 6, 7]. The histological findings in digitate dermatosis are predominantly nonspecific, similar to those seen in chronic dermatitis. Although digitate dermatosis has been suggested to be an abortive lymphoma, without conversion into systemic lymphoma, the pathogenesis of this skin disease remains uncertain [4]. Following four weeks of balneophototherapy, combining salt water baths and subsequent UVB/UVA irradiation, extensive clearing of the lesions was seen in our patient.

REFERENCES

1. Lambert WC, Everett MA. The nosology of parapsoriasis. J Am Acad Dermatol 1981; 5: 373-95.

2. Kikuchi A, Naka W, Harada T, et al. Parapsoriasis en plaques: its potential for progression to malignant lymphoma. J Am Acad Dermatol 1993; 29: 419-22.

3. Mueller KK, Yeager JK. Clinical considerations in digitate dermatosis. Int J Dermatol 1997; 36: 764-78.

4. Burg G, Dummer R. Small plaque (digitate) parapsoriasis is an abortive cutaneous T cell lymphoma and is not mycosis fungoides. Arch Dermatol 1995; 131: 336-8.

5. King-Ismael D, Ackermann AB. Guttate parapsoriasis/digitate dermatosis (small plaque parapsoriasis) is mycosis fungoides. Am J Dermatopathol 1992; 14: 518-30.

6. Hu C, Winkelmann RK. Digitate dermatosis: a new look at symmetrical, small plaque parapsoriasis. Arch Dermatol 1973; 107: 65-9.

7. Lambert WC. Premycotic eruptions. Dermatol Clin 1985; 3: 629-45.


 

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