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  • 1
    Electronic Resource
    Electronic Resource
    Copenhagen : Munksgaard International Publishers
    Journal of cutaneous pathology 27 (2000), S. 0 
    ISSN: 1600-0560
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Multiple eruptive dermatofibromas have been reported in the setting of autoimmune diseases treated with immunosuppressive drugs and more recently in the course of human immunodeficiency virus (HIV) infection. We report herein the ninth case of multiple eruptive dermatofibromas associated with HIV infection. The relevant literature is reviewed and the differences of these lesions from “ordinary” dermatofibromas are discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    International journal of dermatology 38 (1999), S. 0 
    ISSN: 1365-4632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A 32-year-old man was seen in January 1997 for a skin eruption which had appeared 2 months earlier. He was in good health and was not taking any drugs. He had not left town and denied any other symptom except a short, flu-like episode 2 months earlier.On examination, he showed multiple, papular, scaly and necrotic lesions over the trunk, arms ( 〈link href="#f1"/〉), and thighs. The face and the mucosae were spared. No lymphadenopathy was evident, and the liver and spleen were not palpable.〈figure xml:id="f1"〉1〈mediaResource alt="image" href="urn:x-wiley:00119059:IJD670:IJD_670_f1"/〉Scaly and necrotic papules on the armRoutine laboratory tests were insignificant. Histopathology of a papular lesion of the arm showed a thick scaly crust overlying a necrotic epidermis and a lichenoid infiltrate of lymphocytes and neutrophils ( 〈link href="#f2"/〉). Extravasation of red blood cells and endothelial swelling of the small superficial vessels were also present.〈figure xml:id="f2"〉2〈mediaResource alt="image" href="urn:x-wiley:00119059:IJD670:IJD_670_f2"/〉Histopathology showing a lichenoid infiltrate of lymphocytes and neutrophils with a thick scaly crust and necrosis of the epidermis (hematoxylin and eosin, ×100)A diagnosis of subacute pityriasis lichenoides (PL) was made, and treatment with 500 mg/day azithromycin, 3 days a week for 1 month, was prescribed without any benefit. Enzyme-linked immunosorbent assay (ELISA) for Toxoplasma gondii showed immunoglobulin G (IgG) 150 (n.v. 〈10) and IgM 1.35 (n.v. 〈0.65). Diagnosis of recent toxoplasmosis prompted an ocular examination which excluded any eye involvement.A specific treatment with spiramycin, 3,000.000 U twice a day for 2 months, was given. The patient underwent a complete resolution of skin lesions which healed leaving atrophic and hyperpigmentary signs ( 〈link href="#f3"/〉). At the end of therapy, ELISA was still positive for both IgG and IgM. Spiramycin was changed to trimethoprim–sulfamethoxazole, 800–160 mg twice a day, which was continued for 2 months.〈figure xml:id="f3"〉3〈mediaResource alt="image" href="urn:x-wiley:00119059:IJD670:IJD_670_f3"/〉Clearing of the PL after specific anti-Toxoplasma therapyReactive serology persisted for both IgG and IgM for 8 months, but no new lesions developed.
    Type of Medium: Electronic Resource
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