INTRODUCTION

Atopic dermatitis (AD) is a highly pruritic recurring inflammatory skin disease. It can be ex­acerbated by bacterial, viral, and fungal infections. In fact, many AD patients suffered from recurrent infections of skin lesions. Especially, Staphylococcus aureus (S. aureus) is found in more than 90% of AD skin lesions, but in only 5% of normal subjects. The high frequency of skin infection in AD may be due to impairment of immune system, such as am- timicrobial lipids, peptides, toll-like receptors and chemokines. Among them, Ong and co-workers have shown that the levels of AMPs were dramatically suppressed in AD’. AMPs are small peptides produced by keratinocytes in the hostskin. A number of endogenous AMPs have been shown to play an integral part in innate immunity. They exhibit potent killing of a broad range of micro-organisms, including gram-negative and gram- positive bacteria, fungi, and viruses. The lowered AMPs may explain the susceptibility of patients in AD to skin infections.

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Papular elastorrhexis (PE) is a rare condition, characterized by asymptomatic papules and fragmen­tation of dermal elastic fibers. In 1987 Bordas et al. described the first case of papular elastorrhexis which consisted of several small yellowish papules on the trunk. It was thought to be a variant of nevus an- elasticus due to the reduction and fragmentation of elastic tissue. Sears et al. suggested that this disorder represented a variant of a connective tissue nevi.

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A healthy 21-year-old woman presented with a 1- year history of multiple skin-colored papules on the upper back. The history of trauma to the lesions was unremarkable, except for excoriation due to an itching sensation. However, the papules had already been present several months before excoriation. She had no past history of acne and no family history of similar lesions or other skin diseases. The physical examination revealed multiple, white- colored papules dominantly on the upper back (Fig. 1). The lesions were nonfollicular and did not coalesce to form plaques.

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Papular Elastorrhexis

12 Jan
2011

Papular Elastorrhexis

INTRODUCTION

Papular elastorrhexis (PE) was first described in 1987 by Bordasl as multiple, discrete, nonfolli­cular, 1 to 5 mm diameter-sized white papules evenly distributed over the back, chest, shoulders, and upper extremities. It usually occurs in females, first appearing during the second decade of life. It histologically characterizes as decreased and fragmented elastic fibers, with or without changes to the collagen bundles in the reticular dermis.

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IV infusion

This study showed that peripheral intravenous KCl infusion caused significantly more pain at the infusion site when administered in sterile water than in saline. The exact mechanism of infusion-related pain and phlebitis is not known. Irritation, inflammation, and damage to the venous endothelium can be caused by the inherent chemical property, pH, or osmolality of the infusate.

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After 36 of the intended 60 patients had been enrolled, an interim analysis was conducted. At that time, 7 patients had discontinued the infusion prematurely because of pain. The interim analysis revealed significant differences in pain severity at the end of all 3 infusion periods between the groups (first infusion p = 0.002, second infusion p = 0.002, and third infusion p = 0.042). Based on these results, the study was halted and the remaining 24 patients were not recruited.

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Consecutive inpatients with hypokalemia requiring intravenous potassium replacement were enrolled in the study after they gave informed consent. This consent was given while they were in a combined medical and surgical ward. The study protocol was reviewed and approved by the Hamilton Health Sciences/McMaster University Research Ethics Review Board.
Patients who had been prescribed one or more intravenous mini-infusions of KCl (10 mmol in 100 mL) through the peripheral vein were randomized into 3 groups: (i)10 mmol KCl in 100 mL sterile water, (ii) 10 mmol KCL in 100 mL 0.9% sodium chloride (NaCl), and (iii) 10 mmol KCl in 100 mL 0.45% NaCl. The KCl solutions for all 3 groups were prepared by the hospital pharmacy (Hamilton Health Sciences, McMaster University Medical Centre Site, Hamilton, Ontario) in identical mini-infusion bags. The randomization code was available in the pharmacy in case of infusion- related problems.

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