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Red Nodules (red + nodule)

Distribution by Scientific Domains

Medical Sciences	100%

Selected Abstracts

Eccrine poroma of the heel

INTERNATIONAL JOURNAL OF DERMATOLOGY, Issue 6 2000
Harvey Lemont
A 67-year-old African,American woman had a tender red nodule on the posterior aspect of her left heel of 20 years' duration. The lesion had initially grown quickly to its present size, but subsequently remained unchanged through the years. No previous history of trauma to the area could be elicited. The lesion was not tender or painful, although the patient related some recent discomfort when wearing shoes with high heel counters. Examination revealed a soft, multilobulated, skin-colored nodule, measuring approximately 1.1 cm at its greatest diameter ( Fig. 1), with a rim space or moat ( Fig. 2) surrounding the lesion. Biopsy of the lesion demonstrated a uniform proliferation of basaloid cells exhibiting a sharp demarcation between the adjacent normal epidermis ( Fig. 3). No horn cysts were present. The papillary dermis demonstrated multiple ectatic blood vessels ( Fig. 4) which may be responsible for its reddish appearance. Figure 1 Multilobulated,. red, granulating lesion on the posterior heel Figure 2 Note. the characteristic ,,moat'' surrounding the lesion Figure 3 Biopsy. reveals a proliferation of uniformly small cuboidal cells sharply demarcated from the adjacent normal epidermal cells Figure 4 Ectatic. vessel dilatation most likely responsible for the reddish color of the lesion [source]

Alpha-1-antitrypsin deficiency associated with panniculitis treated with plasma exchange therapy

INTERNATIONAL JOURNAL OF DERMATOLOGY, Issue 9 2004
Priscila De Oliveira MD
Background, Alpha-1-antitrypsin is the principal serum protease inhibitor. In addition to the well-recognized association with early-onset emphysema and cirrhosis, alpha-1-antitrypsin deficiency may be associated with panniculitis. The treatment of this type of panniculitis presents a significant challenge. Previous attempts using immunosuppressive, anti-inflammatory, and cytotoxic drugs have shown variable results. Aim, To report a case of alpha-1-antitrypsin deficiency-associated panniculitis treated with plasma exchange therapy. Methods, A 23-year-old patient developed painful red nodules on her thighs and buttocks with spontaneous ulceration and discharge of oily fluid. A skin biopsy specimen showed septal and lobular panniculitis. The serum alpha-1-antitrypsin level was 22 mg/dL. She was treated with plasma exchange therapy. Results, Treatment of this patient with plasma exchange therapy led to the control of the cutaneous lesions. Conclusions, Plasma exchange therapy represents an alternative treatment which restores serum and tissue alpha-1-antitrypsin levels. This method is proposed because of its clinical benefits and greater availability. [source]

Acral pseudolymphomatous angiokeratoma of children: immunohistochemical and clonal analyses of the infiltrating cells

JOURNAL OF CUTANEOUS PATHOLOGY, Issue 5 2002
Yoshitaka Hagari
Background:, Acral pseudolymphomatous angiokeratoma of children (APACHE) is a disorder characterized clinically by red nodules and histopathologically by a massive subepidermal lymphohistiocytic infiltrate. Although it was initially thought to be a vascular nevus, it has never been regarded as a pseudolymphoma. Case report: We report a 7-year-old-girl with small red nodules on the dorsum of the right foot and a 73-year-old man with asymptomatic brown-red nodules on the lower extremities. Results:, Histopathologic examination revealed a massive lymphohistiocytic infiltrate with plasma cells, some eosinophils, or a multinucleated giant cell immediately beneath the epidermis. Thick-walled vessels were observed in the infiltrate. These characteristics are identical to those of acral pseudolymphomatous angiokeratoma of children. The infiltrate was composed mainly of equal numbers of CD4+ or CD8+ T cells and equal numbers of B cells stained for , or , light chains. PCR amplification of rearranged immunoglobulin heavy chain genes or T-cell receptor , genes showed no evidence of clonality, suggesting that these infiltrates were polyclonal both for B and T cells. Conclusions:, Our data support the idea that this disorder represents a reactive process. The modified term ,papular angiolymphoid hyperplasia' would define this disorder more appropriately. [source]