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1.
West Indian med. j ; 60(1): 99-101, Jan. 2011. ilus
Article in English | LILACS | ID: lil-672727

ABSTRACT

Yellow nail syndrome is a very rare clinical entity usually diagnosed from a combination of yellow dystrophic nails, lymphoedema and respiratory diseases. The aetiology is not known though dysfunctional hypoplastic lymphatics is speculated. Most cases occur sporadically but few cases may be associated with systemic diseases or may be inherited. This report documents another case in a 56-year old Caribbean female who presented with a six-year history of recurrent respiratory symptoms and later yellow dystrophic nails and lymphoedema. She responded well to vitamin E and oral fluconazole. We also did a short literature review of yellow nail syndrome.


El síndrome de las uñas amarillas es una entidad clínica muy rara, la cual usualmente se diagnostica a partir de una combinación de uñas amarillas distróficas, linfedemas, y enfermedades respiratorias. Se desconoce la etiología, aunque se especula que se debe a vasos linfáticos hipoplásticos disfuncionales. La mayoría de los casos ocurre esporádicamente pero pocos casos pueden asociarse con las enfermedades sistémicas o pueden ser heredados. Este informe documenta el caso de una mujer caribeña de 56 años, que se presentó con antecedentes de síntomas respiratorios recurrentes y más tarde con uñas amarillas distróficas y linfedemas. Durante el tratamiento, respondió bien a la vitamina E y al fluconazol oral. El trabajo también realiza una breve revisión de la literatura del síndrome de las uñas amarillas.


Subject(s)
Female , Humans , Middle Aged , Antifungal Agents/therapeutic use , Fluconazole/therapeutic use , Vitamin E/therapeutic use , Yellow Nail Syndrome/diagnosis , Yellow Nail Syndrome/drug therapy , Diagnosis, Differential
2.
West Indian med. j ; 49(4): 338-339, Dec. 2000.
Article in English | LILACS | ID: lil-333430

ABSTRACT

We present the case of a 30-year-old woman with HIV/AIDS who experienced a 47 weight gain over a period of a year after commencing treatment with highly active anti-retroviral therapy (HAART) and went on to develop benign intracranial hypertension (BIH). She was not on any other medication associated with BIH. Although weight gain has been reported in patients on treatment with protease inhibitors, such gains have been minimal to moderate. We are unaware of any previous report of this degree of weight gain or BIH in a patient on protease inhibitors.


Subject(s)
Humans , Female , Adult , Pseudotumor Cerebri , Weight Gain , Antiretroviral Therapy, Highly Active , Pseudotumor Cerebri , Acquired Immunodeficiency Syndrome/drug therapy
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