RESUMEN
BACKGROUND: Fractional ablative laser resurfacing has been shown to improve the final cosmetic appearance of surgical scars, but optimal timing is unknown. OBJECTIVE: To compare surgical scars treated with fractional carbon dioxide (CO 2 ) laser performed on Day 0 and Day 14. METHODS: Prospective, randomized, split-scar, physician-blinded study of 30 surgical scars on the limbs. Scars halves received fractional CO 2 laser on either Day 0 or Day 14. Scar assessment at 6 months evaluated patient preference, physician modified Manchester Scar Scale (MMSS) score, and quantitative scar analysis on histology (fractal dimension [F D ] and lacunarity [L] analysis). RESULTS: There was no significant difference in patient assessment (54% preferred Day 0 side, 46% preferred Day 14 side, p = .58) or physician assessment (mean MMSS 8.4 for Day 0 vs 8.7 for Day 14, p = .28). Fractal dimensions were similar for both interventions (mean 1.778 for Day 0 vs 1.781 for Day 14, p = .80). Lacunarity was similar for both interventions (mean 0.368 for Day 0 vs 0.345 for Day 14, p = .44). LIMITATIONS: Single-center study with wounds limited to limbs of skin Phototype I-II subjects; 4 of whom were lost to follow-up. CONCLUSION: Intraoperative CO 2 laser is noninferior to Day 14 laser resurfacing for surgical scar treatment.
Asunto(s)
Terapia por Láser , Láseres de Gas , Neoplasias Cutáneas , Humanos , Cicatriz/etiología , Cicatriz/cirugía , Cicatriz/patología , Terapia por Láser/efectos adversos , Terapia por Láser/métodos , Láseres de Gas/uso terapéutico , Estudios Prospectivos , Neoplasias Cutáneas/cirugía , Resultado del TratamientoRESUMEN
Cholinergic urticaria (CU) is triggered by a rise in body temperature and can be complicated by bronchial hyperresponsiveness and anaphylaxis. It primarily affects young adults who actively engage in strenuous exercise, such as servicemen and servicewomen. If the patient reports a history of wheezing or difficulty breathing with urticaria, a water challenge test in a warm bath can be performed to confirm the presence of anaphylaxis. The test should be conducted in an environment in which the patient's airway can be secured and epinephrine can be administered if necessary. Nonsedating antihistamines commonly are used to treat CU, but few other treatments have been thoroughly evaluated for cases that are refractory to antihistamines. We present the case of a 27-year-old US Marine with CU and anaphylaxis confirmed by a water challenge test in a warm bath.
Asunto(s)
Anafilaxia/etiología , Temperatura Corporal , Ejercicio Físico , Calor/efectos adversos , Personal Militar , Urticaria/etiología , Adulto , Humanos , MasculinoAsunto(s)
Antineoplásicos/efectos adversos , Erupciones por Medicamentos/patología , Indoles/efectos adversos , Sulfonamidas/efectos adversos , Neoplasias de las Glándulas Sudoríparas/patología , Siringoma/patología , Anciano , Dermis/patología , Erupciones por Medicamentos/etiología , Glándulas Ecrinas/patología , Eritema/inducido químicamente , Eritema/patología , Femenino , Humanos , Indoles/uso terapéutico , Melanoma/tratamiento farmacológico , Metaplasia , Neoplasias Cutáneas/tratamiento farmacológico , Sulfonamidas/uso terapéutico , VemurafenibRESUMEN
Voriconazole, a second-generation triazole, has recently been approved by the Food and Drug Administration (FDA) to treat invasive aspergillosis and refractory infections with Scedosporium apiospermum or Fusarium spp. The reported side-effects of voriconazole include visual changes, headaches, elevated hepatic enzymes, Steven-Johnson syndrome, toxic epidermal necrolysis, chelitis, photosensitivity, discoid lupus erythematosus and anaphylactoid infusion reactions. Pseudoporphyria was first described in association with nalidixic acid. It has the same clinical and histologic features as porphyria cutanea tarda (PCT) but is distinguished by normal porphyrin levels in the serum, urine and stool. We present the case of a patient who developed pseudoporphyria after receiving treatment with voriconazole.
Asunto(s)
Antifúngicos/efectos adversos , Erupciones por Medicamentos/diagnóstico , Enfermedades Pulmonares Fúngicas/tratamiento farmacológico , Micetoma/tratamiento farmacológico , Porfiria Intermitente Aguda/diagnóstico , Pirimidinas/efectos adversos , Scedosporium , Triazoles/efectos adversos , Anciano , Antifúngicos/administración & dosificación , Diagnóstico Diferencial , Erupciones por Medicamentos/etiología , Erupciones por Medicamentos/patología , Humanos , Masculino , Porfiria Intermitente Aguda/etiología , Porfiria Intermitente Aguda/patología , Pirimidinas/administración & dosificación , Triazoles/administración & dosificación , VoriconazolRESUMEN
This report describes an HIV-1-positive patient who presented to the dermatology clinic with a 2-year history of secondary erythermalgia. A review of salient clinical features, disease classification, associated diseases, pathogenesis, and treatment of this disorder is presented.