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1.
Indian J Dermatol Venereol Leprol ; 2017 Jan-Feb; 83(1): 108-112
Artigo em Inglês | IMSEAR | ID: sea-183425
2.
Indian J Dermatol Venereol Leprol ; 2016 May-June; 82(3): 343-345
Artigo em Inglês | IMSEAR | ID: sea-178217
4.
Indian J Dermatol Venereol Leprol ; 2014 Spt-Oct ; 80 (5): 483
Artigo em Inglês | IMSEAR | ID: sea-154964
5.
Artigo em Inglês | IMSEAR | ID: sea-182516

RESUMO

Background: Beetle dermatitis is a common condition seen in regions with warm and tropical climate. The condition causes significant morbidity and can be misdiagnosed. Aim: The study was conducted to know the clinical profile of beetle dermatitis and to increase awareness among nondermatologist physicians about this condition. Methods: All clinically diagnosed cases of beetle dermatitis were included in the study. Detailed history was taken and a thorough clinical examination was conducted in all the cases. Clinical photographs were taken in all the cases. Results: A total of 70 cases comprising of 46 males and 24 females were studied. The age of the patients ranged from 5 to 60 years. Majority of the cases presented during the post monsoon months (September-November), indicating a distinct seasonal trend. Morphology of lesions was mainly linear, but kissing and bizarre lesions were also observed. Head, neck and upper extremities were the most commonly involved sites. Fever and malaise was observed in a few cases. Conclusion: Beetle dermatitis should be included in differential diagnosis while examining erythematous vesicular lesions of sudden onset, especially on exposed parts during rainy and post rainy season. Awareness of this condition and its clinical features among the physicians will prevent misdiagnosis. Preventive measures can be undertaken based on the behavioral pattern of this beetle.

6.
Indian J Dermatol Venereol Leprol ; 2013 Jan-Feb; 79(1): 107-109
Artigo em Inglês | IMSEAR | ID: sea-147406
7.
Indian J Dermatol Venereol Leprol ; 2010 Sept-Oct; 76(5): 591
Artigo em Inglês | IMSEAR | ID: sea-140712

RESUMO

Progeria is a rare genetic disorder characterized by premature aging, involving the skin, bones, heart, and blood vessels. We report a 4-year-old boy who presented with clinical manifestations of progeria. He had characteristic facies, prominent eyes, scalp and leg veins, senile look, loss of scalp hair, eyebrows and eyelashes, stunted growth, and sclerodermatous changes. The present case is reported due to its rarity.

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