An edition of Systemic lupus erythematosus (2012)

Systemic lupus erythematosus

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Last edited by ImportBot
September 17, 2024 | History
An edition of Systemic lupus erythematosus (2012)

Systemic lupus erythematosus

Patients that present with a connective tissue disease are often a challenge to diagnose and treat. A connective tissue disease is a disorder in which the tissues of the body consisting of the cells and the matrix which holds them together are disrupted. This guide will describe several multi system conditions that result from the inflammatory and immune-mediated disorder systemic lupus erythematosus and the related condition of Sjogren's syndrome. These diseases affect various tissues of the body; details of their management are discussed within, including presentation, investigation, differential diagnosis, and treatment. These diseases are multifactorial conditions associated with a complex genetic predisposition and various, not well understood, environmental triggers that induce inflammatory and immune-mediated responses directed against components of the person's own body. As a result these diseases fall under the umbrella term known as the systemic autoimmune diseases. Patients with a systemic autoimmune connective tissue disease can present with clinical symptoms and signs in one or more often, several, systems of the body. Some of these diseases affect people of certain ages and gender more often than others, including children, but this guide will focus on the management of adult patients. These diseases are more common than is generally realized, cannot be cured, are associated with considerable morbidity and still cause significant mortality. Appropriate investigations are critical to making the correct diagnosis so that treatment can be tailored to the patient's condition. It is important not only to recognize and treat the current disease activity, but also to prevent death and the development of chronic damage due to complications of the disease and the immuno-suppressive drugs used to treat it. Principles of drug treatment are discussed, but the final choice of drug and exact dosages to be used will depend on the details of the patient's condition and should be planned by a physician with relevant experience of these conditions and responsible for the management of the patient. Due to the variable severity of these diseases and their multisystem nature, patients with an autoimmune connective tissue disease may present to general practitioners, general physicians or internal medicine specialists, obstetricians, intensive care or any medical or surgical specialist. The majority of patients with these conditions are cared for long term by dermatologists, rheumatologists, and/or nephrologists, as it is the skin, joints and kidneys that are most often involved. However, it should be noted that many patients develop cardio-respiratory or infectious complications, including accelerated atherosclerosis, due to the disease and/or its treatment. Multidisciplinary care is important and should involve the full range of allied health professionals, as well as the relevant clinical specialists depending on the organs and systems involved.

Publish Date
Publisher
Clinical Pub.
Language
English
Pages
56

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Previews available in: English

Edition Availability
Cover of: Systemic lupus erythematosus
Systemic lupus erythematosus
2012, Clinical Pub.
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Book Details


Table of Contents

General approach to the assessment of patients with a suspected connective tissue disease / Ariane L. Herrick
Systemic lupus erythematosus / Caroline Gordon, Julia U. Holle, Wolfgang L. Gross
Sjögren's syndrome / Iona Meryon [and others].

Edition Notes

Content originally published in 2011 as part of Connective tissue diseases : an atlas of investigation and management (Oxford : Clinical Publishing).

Includes bibliographical references and index.

Published in
Oxford
Series
Visual guide for clinicians, Visual guide for clinicians

Classifications

Dewey Decimal Class
616.772
Library of Congress
RC924.5.L85 G67 2012

The Physical Object

Pagination
viii, 56 pages
Number of pages
56

ID Numbers

Open Library
OL37080738M
Internet Archive
systemiclupusery0000unse_e6o1
ISBN 10
1846921007, 1846926432
ISBN 13
9781846921001, 9781846926433
OCLC/WorldCat
764366062

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September 17, 2024 Edited by ImportBot import existing book
February 25, 2022 Created by ImportBot import new book