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2.
Indian J Dermatol Venereol Leprol ; 2015 Jul-Aug; 81(4): 389-390
Article in English | IMSEAR | ID: sea-160061
3.
Indian J Dermatol Venereol Leprol ; 2015 May-Jun; 81(3): 251-256
Article in English | IMSEAR | ID: sea-158306

ABSTRACT

Background: Azathioprine in daily doses has been shown to be effective and safe in the treatment of Parthenium dermatitis. Weekly pulses of azathioprine (WAP) are also effective, but there are no reports comparing the effectiveness and safety of these two regimens in this condition. Aims: To study the effi cacy and safety of WAP and daily azathioprine in Parthenium dermatitis. Methods: Sixty patients with Parthenium dermatitis were randomly assigned to treatment with azathioprine 300 mg weekly pulse or azathioprine 100 mg daily for 6 months. Patients were evaluated every month to assess the response to treatment and side effects. Results: The study included 32 patients in the weekly azathioprine group and 28 in the daily azathioprine group, of whom 25 and 22 patients respectively completed the study. Twenty-three (92%) patients on WAP and 21 (96%) on daily azathioprine had a good or excellent response. The mean pretreatment clinical severity score decreased from 26.4 ± 14.5 to 4.7 ± 5.1 in the WAP group, and from 36.1 ± 18.1 to 5.7 ± 6.0 in the daily azathioprine group, which was statistically signifi cant and comparable (P = 0.366). Patients on WAP had a higher incidence of adverse effects (P = 0.02). Limitations: The study had a small sample size and the amount of clobetasol propionate used in each patient was not determined, though it may not have affected the study outcome due to its comparable use in both groups. Conclusions: Azathioprine 300 mg weekly pulse and 100 mg daily dose are equally effective and safe in the treatment of Parthenium dermatitis.


Subject(s)
Adult , Aged , Azathioprine/administration & dosage , Azathioprine/therapeutic use , Dermatitis, Allergic Contact/drug therapy , Dermatitis, Allergic Contact/epidemiology , Dermatitis, Allergic Contact/etiology , Female , Humans , Male , Middle Aged , Pulse Therapy, Drug/methods , Tanacetum parthenium/adverse effects
4.
Rev. chil. pediatr ; 85(6): 720-723, dic. 2014. ilus
Article in Spanish | LILACS | ID: lil-734814

ABSTRACT

Black henna tattoos have paraphenylenediamine (PPD), which contains a product of herbal origin, which due to its molecular characteristics is capable of inducing, in susceptible individuals, a type IV hypersensitivity reaction. It clinically manifests as a contact dermatitis that usually when it disappears, scarring and hypopigmentation are left in the injured area. Objective: To describe the case of a patient with hypersensitivity to henna tattoo and to present the most relevant phenomena associated with this condition. Case report: The case of a 6 year-old patient with a black henna tattoo on his right leg, who was diagnosed with contact dermatitis probably attributed to PPD, is presented. Mometasone furoate and topical silicone gel treatment was started with good response. Conclusion: Mometasone furoate and silicone gel are a good possible therapeutic option for treating contact dermatitis caused by PPD as the dermatosis was resolved without residual lesions.


Los tatuajes de henna negra son aquellos que contienen parafenilendiamina (PPD), que contienen un producto de origen herbal, que por sus características moleculares es capaz de inducir, en individuos susceptibles, una reacción de hipersensibilidad tipo IV. Se manifiesta clínicamente como una dermatitis de contacto, que generalmente al desaparecer, persiste de manera residual una cicatriz hipertrófica e hipopigmentación en la zona lesionada. Objetivo: Describir el caso de un paciente con hipersensibilidad al tatuaje de henna, y presentar los fenómenos más relevantes asociados a esta patología. Caso clínico: Paciente de 6 años de edad, que se realizó un tatuaje con henna negra en la pierna derecha, en quien se diagnosticó posteriormente una dermatitis de contacto atribuida probablemente a la PPD. Se comenzó tratamiento con furoato de mometasona y gel de silicona con buena respuesta por vía tópica. Conclusión: El furoato de mometasona y gel de silicona son una posible opción terapéutica de utilidad para tratar la dermatitis de contacto causada por el PPD, debido a que la dermatosis se resolvió sin lesiones residuales.


Subject(s)
Child , Female , Humans , Mometasone Furoate/therapeutic use , Phenylenediamines/adverse effects , Silicone Gels/therapeutic use , Tattooing/adverse effects , Coloring Agents/administration & dosage , Coloring Agents/adverse effects , Drug Therapy, Combination , Dermatitis, Allergic Contact/drug therapy , Dermatitis, Allergic Contact/etiology , Hypersensitivity, Delayed/drug therapy , Hypersensitivity, Delayed/etiology , Mometasone Furoate/administration & dosage , Phenylenediamines/administration & dosage , Silicone Gels/administration & dosage , Treatment Outcome
5.
Rev. chil. dermatol ; 28(2): 173-175, 2012. ilus
Article in Spanish | LILACS | ID: lil-718978

ABSTRACT

En la actualidad los tatuajes de henna negra se utilizan en forma muy frecuente, por lo que el número de reportes sobre reacciones adversas asociadas a su uso se ha incrementado. La Parafenilendiamina o PPD es el químico que más se adiciona a la henna para intensificar y prolongar la duración del color del tatuaje. Posee un gran poder sensibilizante y se le atribuyen la mayoría de las reacciones, desde dermatitis leve hasta reacciones generalizadas tipo eritema multiforme-like. Se presenta el caso de un paciente de 7 años con lesiones cutáneas frente a segunda exposición a tatuaje de henna. Con diagnóstico de dermatitis de contacto se maneja con corticoidestópicos con excelente respuesta clínica. Como prevención primaria planteamos la necesidad de programas que permitan educar a la comunidad en relación a los riesgos asociados a la exposición a PPD, recomendando el NO uso de tatuajes de henna negra.


Today, black henna tattoos are very commonly used, so the number of reports on adverse reactions associated with its use has increased. The paraphenylenediamine or PPD is the chemical that is most commonly added to henna to intensify and prolong the duration of the color tattoo. PPD act as sensitizer of most of the reactions, from mild dermatitis to generalized reactions erythema multiforme-like. We show a case of a 7 year old patient with skin lesions that appears during the second exposure to henna tattoos. We made the diagnosis of a contact dermatitis and we manage it with topical corticosteroids with excellent clinical response. As primary prevention we suggest the need of educational programs for the community regarding the risks associated with the exposure of PPD, and avoiding the use of black henna tattoos.


Subject(s)
Humans , Male , Child , Coloring Agents/adverse effects , Dermatitis, Allergic Contact/etiology , Dermatitis, Allergic Contact/drug therapy , Phenylenediamines/adverse effects , Administration, Topical , Adrenal Cortex Hormones/administration & dosage , Dermatitis, Allergic Contact/prevention & control , Hypersensitivity , Naphthoquinones/adverse effects , Primary Prevention , Tattooing/adverse effects , Tattooing/methods
6.
Dermatol. argent ; 17(6): 474-476, nov.-dic.2011. ilus
Article in Spanish | LILACS | ID: lil-723467

ABSTRACT

El paintball es una actividad recreativa que ha cobrado gran auge en la actualidad. A partir de su difusión, se han descripto diversas lesiones asociadas al mismo. Presentamos a un paciente de 23 años con una dermatitis por contacto generada como consecuencia directa del juego.


Subject(s)
Humans , Male , Adult , Dermatitis, Allergic Contact/diagnosis , Dermatitis, Allergic Contact/etiology , Dermatitis, Allergic Contact/drug therapy
7.
Arq. neuropsiquiatr ; 65(3b): 822-825, set. 2007. ilus, tab
Article in English | LILACS | ID: lil-465187

ABSTRACT

BACKGROUND: Trigeminal sensory neuropathy (TSN) describes a heterogeneous group of disorders manifesting as facial numbness. OBJECTIVE: We report the case of a patient who had TSN associated with contact dermatitis due to Anthurium sp. METHOD/RESULTS: A 21-year-old female patient developed left hemifacial contact dermatitis after exposure to the anthurium plant. The patient had paresthesias and pain in the V2 and V3 divisions of the left trigeminal nerve. Eight days after its onset the dermatitis resolved, but numbness developed in the V2 and V3 divisions of the left trigeminal nerve. Cranial CT scan and MRI, as well as CSF and extensive work-up exams, were normal. After one month the symptoms disappeared completely. CONCLUSION: Anthurium sp, an indoor ornamental plant that contains calcium oxalate crystals, and can causes contact dermatitis. To our knowledge, this is the first report associating TSN with contact dermatitis due to Anthurium sp.


INTRODUÇÃO: A neuropatia trigeminal sensitiva (NTS) representa um grupo heterogêneo de doenças, cuja manifestação clínica é a presença de dormência na região facial. OBJETIVO: Relatamos o caso de paciente que apresenta NTS associada com dermatite de contato (DC) devido à planta Anthurium sp. MÉTODO/RESULTADOS: Uma paciente com 21 anos desenvolveu DC na região hemi-facial esquerda, após exposição à planta Anthurium sp. Após a resolução do quadro de dermatite, a referida paciente apresentou dormência e parestesias no território do segundo e terceiro ramos do nervo trigêmeo esquerdo. Um mês após o início do quadro houve resolução completa dos sintomas. CONCLUSÃO: O Anthurium é uma planta ornamental que contém cristas de oxalato de cálcio, que podem causar DC. Para o nosso conhecimento este é o primeiro relato associando NTS e dermatite de contato devido à exposição ao Anthurium sp.


Subject(s)
Adult , Female , Humans , Araceae/adverse effects , Dermatitis, Allergic Contact/etiology , Facial Dermatoses/etiology , Hypesthesia/etiology , Trigeminal Nerve Diseases/etiology , Analgesics, Non-Narcotic/therapeutic use , Araceae/chemistry , Carbamazepine/therapeutic use , Dermatitis, Allergic Contact/diagnosis , Dermatitis, Allergic Contact/drug therapy , Facial Dermatoses/diagnosis , Facial Dermatoses/drug therapy , Hypesthesia/diagnosis , Hypesthesia/drug therapy , Trigeminal Nerve Diseases/diagnosis , Trigeminal Nerve Diseases/drug therapy , Trigeminal Neuralgia/diagnosis , Trigeminal Neuralgia/drug therapy , Trigeminal Neuralgia/etiology
11.
In. Sociedad Médica de Santiago. Comité Científico; Chile. Ministerio de Salud. Curso 1995: problemas frecuentes en la atención primaria del adulto. Santiago de Chile, Sociedad Médica de Santiago, 1995. p.174-9.
Monography in Spanish | LILACS | ID: lil-156907
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