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2.
Turk Arch Pediatr ; 57(5): 569-570, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-35866323
3.
J Low Genit Tract Dis ; 26(3): 276-282, 2022 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-35763612

RESUMO

OBJECTIVE: Nonvenereal genital dermatoses may be a reason for considerable concern to the patient and often pose diagnostic dilemma to the treating physicians. The objective of the present study was to find out the demographical and clinical profile of nonvenereal genital dermatoses including systemic comorbidities in a tertiary care hospital. MATERIALS AND METHODS: This was an observational study, carried out at the outpatient department of dermatology of a tertiary care hospital of Eastern India over a period of 12 months. Female patients with genital lesions were included in the study after excluding venereal disease. Results were tabulated and analyzed. RESULTS: A total of 189 female patients were evaluated having 39 different dermatoses. The age ranged from 2 months to 72 years with most patients belonged to the fourth decade and 70.4% patients were from reproductive age group. Most of the patients were literate (81%) and hailing from rural areas. Most of them were homemakers and belonged to lower socioeconomic status (42.3%). Itching (77.3%) was the most common presenting complaint followed by burning sensation (9.5%). Common dermatoses encountered were vulval candidiasis (40.7%), lichen sclerosus (15.3%), tinea cruris (13.8%), lichen planus (4.2%), vitiligo (3.2%), irritant contact dermatitis (2.6%), psoriasis (2.6%), lichen simplex chronicus (2.1%), among others. Most common associated comorbidity was diabetes mellitus. CONCLUSIONS: This study provides important data on the spectrum of vulvar diseases in Eastern Indian patients and emphasizes the importance of proper and timely diagnosing nonvenereal vulvar dermatoses.


Assuntos
Neurodermatite , Dermatopatias , Doenças da Vulva , Estudos Transversais , Feminino , Humanos , Lactente , Dermatopatias/epidemiologia , Dermatopatias/patologia , Vulva/patologia , Doenças da Vulva/diagnóstico
5.
Clin Exp Dermatol ; 47(5): 967-969, 2022 May.
Artigo em Inglês | MEDLINE | ID: mdl-34939220

RESUMO

In systemic sclerosis, vitiligo-like depigmentation of salt and pepper pigmentation usually spares the perifollicular areas. Pigmentation is also known to be preserved over the superficial veins. We describe a case series of salt and pepper pigmentation with some unusual features. We would like to emphasize that in about 40% of patients of the present series, the salt and pepper pigmentation spared the skin creases and folds, which appears to be a hitherto unreported finding.


Assuntos
Hipopigmentação , Transtornos da Pigmentação , Escleroderma Sistêmico , Vitiligo , Humanos , Pigmentação , Pigmentação da Pele , Vitiligo/etiologia
6.
Indian J Psychiatry ; 64(6): 599-604, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36714670

RESUMO

Dermatitis neglecta (DN), first described by Poskitt et al. in 1995, is a dermatosis resulting from insufficient frictional cleansing of the skin. Lesions result from self-neglect and may have several underlying etiologies, including psychiatric conditions. There is a dearth of any formal study or large case series on this subject. Moreover, the psychological aspects of DN mostly remain unexplored. We report here the clinical profile and psychiatric comorbidities of a group of patients with DN from eastern India. Sporadic cases of underlying psychological problems like cognitive deficit and executive dysfunction, schizophrenia, severe anxiety disorder, and depression have been reported in the existing literature. Associated psychiatric disorder was present in 72.7% of the patients of this case series that include several underlying psychiatric disorders like depression, schizophrenia, somatic symptom disorder, social anxiety disorder, intellectual disability, bipolar disorder, Alzheimer's disease, and alcohol dependence. In this article we would like to emphasize that DN is frequently associated with psychiatric disorder and management of the underlying psychiatric condition with psychotropic medications; psychotherapy is of immense importance.

10.
Pediatr Dermatol ; 37(3): 579-581, 2020 May.
Artigo em Inglês | MEDLINE | ID: mdl-32096881

RESUMO

Lupus erythematosus-lichen planus (LE-LP) overlap syndrome represents a rare disorder with clinical and histopathological features of both lichen planus and lupus erythematosus presenting in the same lesions. However, lichen planus and lupus erythematosus can also coexist in the same patient. Blaschkoid lichen planus in the setting of concurrent childhood-onset systemic lupus erythematosus has not been previously described.


Assuntos
Líquen Plano , Lúpus Eritematoso Sistêmico , Humanos , Líquen Plano/diagnóstico , Lúpus Eritematoso Sistêmico/complicações , Lúpus Eritematoso Sistêmico/diagnóstico , Síndrome
13.
J Paediatr Child Health ; 55(11): 1401-1402, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31691419
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