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. 2017 Sep 15;9(3):169–176. doi: 10.1159/000479922

Table 2.

The clinical and paraclinical characteristics of PPLD and the 4 most common differential diagnoses

Majocchi disease Schamberg disease PPLD Eczematoid-like purpura of Doucas and Kapetanakis Lichen purpuricus (aureus)
Sex Predominantly seen in females Predominantly seen in males Predominantly seen in males Predominantly seen in males Both sexes

Frequency Rare Most common type of PPD Rare Uncommon Rare

Peak incidence Children and young adults Adolescents and young adults Middle-aged Middle-aged Children and young adults

Skin distribution Begins on the lower limb symmetrically and then extends to the trunk and upper extremities Most frequently bilaterally on the tibial regions, but may be unilateral or involve the thighs, buttocks, trunk, or upper extremities Predilection for the legs, and rarely on the trunk and thighs Legs with progression to the thighs, trunk, and upper extremities Lesions frequently occur bilaterally on the lower limbs, although can be unilateral and may affect the trunk and upper limbs; unlike other forms of PPD, the lesions of lichen aureus may also occur in a dermatomal distribution, or can follow the distribution of veins or arteries

Clinical presentation Variable number of annular erythematous plaques and patches, often with central clearing and atrophy Discrete reddish-brown patches that are bordered from red to brown; nonpalpable, pinpoint puncta; Cayenne pepper- like lesions Minute, lichenoid papules that tend to fuse into plaques of various hues Lesions are extensive and patients typically complain of severe pruritus Presents with yellowish or red papules or patches which may either itch or be asymptomatic

Histology Perivascular and predominantly band-like infiltrate of lymphocytes that extend to the overlying epidermis, showing vacuolar alteration of the basal layer and spongiosis; hemosiderin-laden macrophages, and extravasation of red blood cells within the lichenoid infiltrate Perivascular infiltrate of mononuclear cells in the upper dermis, endothelial cell swelling, extravasated red blood cells, and hemosiderin-laden macrophages Perivascular infiltrate of lymphocytes which is lichenoid and macrophages centered on the superficial small blood vessels of the skin with endothelial cell swelling and narrowing of lumina Spongiosis with inflammation of the epidermis Perivascular lymphohistiocytic infiltrate in a band-like pattern; hemosiderin-laden macrophages, and extravasation of red blood cells; the epidermis is unaffected

Remission Common Common Often chronic course but spontaneous remission may occur Spontaneous remission may occur, but recurrences may occur Spontaneous remission may occur, but recurrences may occur

Treatment The disorder is benign and self-limiting; treatment is not effective and the lesions may last several months to years Systemic steroids have been reported to result in clearance; ascorbic acid and antihistamines have been used with limited success; PUVA therapy is beneficial; narrow band UVB Difficult; topical and systemic steroids, elastic stockings, antipruritic topical preparations, systemic antihistamines, PUVA, griseofulvin, cyclosporin A, bioflavonoids, and ascorbic acid have been suggested Topical corticosteroids and antihistamines Oral corticosteroids; may resolve spontaneously

Extracted from [2, 6, 9, 10, 11, 12]. PPLD, pigmented purpuric lichenoid dermatitis of Gougerot-Blum; PPD, pigmented purpuric dermatosis.