M. Papi et al., PURPLE (ATROPHIC BLANCHE) - CLINICAL, HISTOLOGICAL AND IMMUNOLOGICAL STUDY OF 12 PATIENTS, JEADV. Journal of the European Academy of Dermatology and Venereology, 9(2), 1997, pp. 129-133
Objectives To investigate clinical, serologic, histopathologic and imm
unopathologic markers of PURPLE (painful purpuric ulcers with reticula
r pattern of lower extremities) or atrophie blanche. Design Twelve con
secutive patients affected with idiopathic PURPLE were studied in the
period 1992-1996. Patients with systemic diseases correlated to PURPLE
were excluded from the study. Subjects All twelve patients were hospi
talized at the Istituto Dermopatico Immacolata in Rome. Results Variou
s and dishomogeneous immunological alterations were detected, Circulat
ing immune complexes, increased serum levels of anticardiolipin and an
tinuclear antibodies, reduced serum complement levels, and deposition
of immunoreactants in dermal vessels, were found in a limited number o
f patients. The results were not statistically significant. All the pa
tients showed very similar histopathological aspects, characterized by
microvascular thromboses, endothelial swelling and segmental hyaliniz
ation of small dermal vessels. Conclusion PURPLE is a thrombogenic vas
culopathy in which unspecified immunological and laboratory changes ar
e present. The recently suggested pathogenetic role of anticardiolipin
and protein C deficiency in the disorder is not confirmed by this stu
dy. (C) 1997 Elsevier Science B.V.