ABSTRACT
This study was conducted to estimate the prevalence of head lice in primary school children and to compare the efficacy of 25% benzyl benzoate versus 1% gamma benzene hexachloride (1% lindane). The prevalence rate was 31.58% (66 out of 209). Eighteen out of 24 (75%) were cured when they were treated by 25% benzyl benzoate. Twenty-six out of thirty (86.67%) were cured when they were treated by 1% lindane. There was no statistical significant difference between the two pesticides for treatment head lice (P\>0.05, Chi-square test). The doctors can choose one of the two pesticides for treatment head lice.
ABSTRACT
Churg-Strauss syndrome (CSS) is a rare syndrome, but steroid responsive systemic vasculitis. The major presentation compose of asthma, cutaneous vasculitis, abdominal pain and mononeuritis multiplex. We reported a case of Churg-Strauss Syndrome and review related iterature. A 41 year-old married Thai male patient had history of asthma 8 months ago. Two months later, he had recurrent asthmatic attack with hemoptysis, abdominal pain, diarrhea and generalized purpura. Five months after that he had progressive paresthesia and weakness all extremities and unable to walk by himself. The physical examination showed atrophy of both intrinsic hand muscles, muscle powers were grade 4/5. Deep tendon reflexes were decreased and there was asymmetrical impairment of sensation of both hands and feet. The results of investigation revealed eosinophilia, high ESR. Nerve biopsy showed acute demyelinating and axonopathy. He improved after steroid treatment. CSS is more common in male than female. All patients have asthma, systemic vaculitis and eosinophilia. CSS has the multisystem involvement, monoeuritis multiplex, abdominal pain cutaneous vasculitis. heart failure and arthritis. Diagnosis base on criteria four of six; asthma, eosinophilia\> 10%, neuropathy, nonfixed pulmonarty infiltration, paranasal sinus abnormality and extra vascular eosinophils. CSS usually respond to steroid treatment. We report a case of CSS and review related literature
ABSTRACT
Acute febrile neutrophilic dermatosis (Sweet’s syndrome) is an uncommon, recurrent skin disease of unknown etiology characterized by painful inflammatory plagues with fever, arthralgia and leucocytosis. Many associated systemic diseases were reported. In this report we described a classical case of Sweet’s syndrome in association with Salmonella empyema and tuberculous lymphadenitis. Diagnostic approaches, clinical course and outcome were discussed in detail.