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1.
Dermatol Online J ; 29(5)2023 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-38478649

RESUMEN

Phytophotodermatitis is a condition caused by contamination of the skin with phototoxic plant substances, followed by exposure to ultraviolet rays. Ficus carica L 1753, belonging to the Moraceae family, can be responsible for acute photodermatitis. We present five cases of photodermatitis caused by contact with Ficus carica L and subsequent exposure to sunlight. A histopathologic study and review of the literature are included.


Asunto(s)
Dermatitis Fototóxica , Ficus , Humanos , Dermatitis Fototóxica/diagnóstico , Dermatitis Fototóxica/etiología , Dermatitis Fototóxica/patología , Extractos Vegetales
2.
J Infect Dev Ctries ; 14(3): 321-322, 2020 03 31.
Artículo en Inglés | MEDLINE | ID: mdl-32235095

RESUMEN

Endolimax nana is a commensal protozoan of the colon. We report a case of chronic urticaria associated with E. nana in a 34-year-old Italian woman. The patient suffered from abdominal pain, diarrhoea and weight loss. The disease appeared after a trip to Vietnam. Laboratory examinations showed mild blood eosinophilia. Three coproparasitological examinations were positive for cysts of E. nana. The patient was successfully treated with two courses of metronidazole (2 g/day for 10 days each). No antihistamines were used. Three coproparasitological examinations, carried out at the end of the therapy, were negative. Follow up (six months) was negative. E. nana can be responsible for very rare cases of abdominal pain, diarrhoea, polyarthritis and urticaria.


Asunto(s)
Disentería Amebiana/diagnóstico , Endolimax/aislamiento & purificación , Viaje , Dolor Abdominal/etiología , Adulto , Antiprotozoarios/administración & dosificación , Antiprotozoarios/uso terapéutico , Disentería Amebiana/complicaciones , Disentería Amebiana/tratamiento farmacológico , Heces/parasitología , Femenino , Humanos , Italia , Metronidazol/administración & dosificación , Metronidazol/uso terapéutico , Urticaria/etiología
3.
J Dermatolog Treat ; 31(2): 183-185, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30897011

RESUMEN

Background: Paclitaxel has recently been approved for AIDS-related Kaposi's sarcoma (KS) and there is much interest also in HIV-negative KS.Objective: To assess the safety and effectiveness of intravenous paclitaxel in the treatment of non-HIV-associated KS.Method: A retrospective database analysis of our departmental database in histologically proven, HIV-negative KS.Results: Fifty-eight patients treated with intravenous paclitaxel 100 mg weekly were identified. Among these patients, 11 patients underwent paclitaxel as first-line treatment, whereas 47 received paclitaxel after other types of systemic chemotherapy. Fifty-three (94.6%) patients achieved a partial or a complete remission after a mean of 13.5 infusions. Disease progression was observed in two patients and one patient had a stable disease. Thirty-one (58.5%) of 53 responding patients are still stable after a mean of 19.1 months of follow-up, while 22 (41.5%) patients relapsed after a mean of 14 months. Paclitaxel was repeated in relapsed patients obtaining PR/CR in all cases. Tolerance was good except for one patient who discontinued the treatment because of a severe allergic reaction.Conclusion: Paclitaxel is effective for the treatment of non-HIV-related KS, both as first- and as second-line treatment. It is well tolerated and can be repeated without loss of efficacy.


Asunto(s)
Antineoplásicos Fitogénicos/uso terapéutico , Paclitaxel/uso terapéutico , Sarcoma de Kaposi/tratamiento farmacológico , Administración Intravenosa , Anciano , Anciano de 80 o más Años , Progresión de la Enfermedad , Esquema de Medicación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Sarcoma de Kaposi/patología , Resultado del Tratamiento
4.
Case Rep Dermatol ; 8(1): 85-90, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27194976

RESUMEN

An uncommon type of epidermal nevus characterized by hyperpigmented hyperkeratotic bands following a Blaschko-linear pattern and generalized follicular hyperkeratosis were observed in a 17-year-old male patient who additionally showed tufted hair folliculitis on the scalp and clinodactyly of the fifth finger of both hands. The combination of epidermal nevus with skeletal abnormalities was first described by Gobello et al. [Dermatology 2000;201:51-55] as a new epidermal nevus syndrome that was named after the first author of this work. Our case shows identical clinical and histopathological features and represents the second case of this rare syndrome reported in the literature.

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