Last edited by Branos
Tuesday, July 21, 2020 | History

5 edition of Systemic Sclerosis found in the catalog.

Systemic Sclerosis

by Philip J Clements

  • 48 Want to read
  • 20 Currently reading

Published by Lippincott Williams & Wilkins .
Written in English

    Subjects:
  • Rheumatology,
  • Internal Medicine,
  • Medical,
  • Medical / Nursing,
  • Scleroderma, Systemic,
  • Diseases - Musculoskeletal,
  • Medical / Rheumatology,
  • Dermatology,
  • Systemic scleroderma

  • The Physical Object
    FormatHardcover
    Number of Pages417
    ID Numbers
    Open LibraryOL9874245M
    ISBN 100781737443
    ISBN 109780781737449

      Systemic scleroderma is an autoimmune disorder that affects the skin and internal is characterized by the buildup of scar tissue (fibrosis) in the skin and other organs. The fibrosis is caused by the body's production of too much collagen, which normally strengthens and supports connective tissues. Scleroderma, also known as systemic sclerosis, is an autoimmune connective tissue disorder characterised by multisystem fibrosis and soft tissue such, it affects many separate organ systems, which are discussed separately: musculoskeletal manifestations of scleroderma; thoracic manifestations of scleroderma.

      Systemic scleroderma is an autoimmune disorder that affects the skin and internal organs. Autoimmune disorders occur when the immune system malfunctions and attacks the body's own tissues and organs. The word "scleroderma" means hard skin in Greek, and the condition is characterized by the buildup of scar tissue (fibrosis) in the skin and other organs. This book presents a wide variety of cutaneous features of systemic sclerosis under one cover as cutaneous manifestations are often the first to appear and help in diagnosing this condition early. It has a multidisciplinary approach as systemic sclerosis is a multi-system disorder which comes under.

    Tea. Modulation of fibrosis in systemic sclerosis by nitric oxide and antioxidants. The dietary antioxidant epigallocatechingallate (EGCG), with its long history of safe beverage consumption in green tea, is a good candidate for therapeutic treatment targeting oxidative stress and fibrogenesis in patients with systemic sclerosis (SSc). The term scleroderma literally means hard skin. But scleroderma (also known as systemic sclerosis, or SSc) is much more than a skin disorder. While nearly all persons with systemic sclerosis have issues with their skin, particularly excessive scarring, swollen, tight, or hard skin on their fingers, they also have organ system involvement.


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Systemic Sclerosis by Philip J Clements Download PDF EPUB FB2

Systemic Sclerosis is a comprehensive, standard reference on sclerosis written by well-known experts in the field. The book presents a concise overview of the causes of scleroderma, as well as the latest information on the development and diagnosis of the disease.

Problems in affected organs are discussed along with treatment options.4/5(1). Systemic Sclerosis is a comprehensive, standard reference on sclerosis written by well-known experts in the field. The book presents a concise overview of the causes of scleroderma, as well as the latest information on the development and diagnosis of the disease.

Problems in affected organs are discussed along with treatment : Systemic Sclerosis (SSc) is a chronic disease of the connective tissue (CT), of unknown etiology, and variable severity/course.

The CT supports, connects, or separates different types of tissues and organs of the body. It is one of the four general classes of biological tissues, the others of which are epithelial, muscular, and nervous tissues. Systemic sclerosis (scleroderma), like other chronic diseases, is the consequence of a disruption of normal body functions.

The human body works by an incredibly complex array of biological interactions that are delicately balanced and closely linked.

Similar to a healthy and functional society, the human body is dependent on eachFile Size: KB. “This book takes a novel approach to systemic sclerosis, using case studies to highlight many different clinical findings in scleroderma.

The cases are practical and make the information from each chapter more memorable. it is clear that this book is most appropriate for rheumatologists, from fellow to /5(2). A comprehensive, standard reference on sclerosis written by well-known experts in the field.

The book presents a concise overview of the causes of scleroderma, as well as the latest information on the development and diagnosis of the disease. Problems in affected organs are discussed along with treatment options. Systemic sclerosis. [Philip J Clements; Daniel E Furst;] Home.

WorldCat Home About WorldCat Help. Search. Search for Library Items Search for Lists Search for Book: All Authors / Contributors: Philip J Clements; Daniel E Furst.

Find more information about: ISBN:. EULAR Textbook on Systemic Sclerosis – Second Edition () Order your copy now. This comprehensive textbook encompasses all aspects of scleroderma, from localized to systemic forms, and from pathophysiology to recent advances in evidence-based treatment.

Comprised of the authoritative work of international experts, this fully-updated second edition of Scleroderma builds upon the well-regarded approach in the first edition to provide integrated, concise, and up-to-date synthesis of current concepts of pathogenesis and modern approaches to management of systemic sclerosis (scleroderma).With a multidisciplinary approach to comprehensive care.

This book presents a wide variety of cutaneous features of systemic sclerosis under one cover as cutaneous manifestations are often the first to appear and help in diagnosing this condition early. It has a multidisciplinary approach as systemic sclerosis is Pages: Systemic sclerosis (SSc) is a chronic auto immune disease characterized by inflammation, vasculopathy and fibrosis of the skin and internal organs.

SSc can be subclassified in two major subtypes: limited cutaneous SSc (LcSSc) and diffuse cutaneous SSc (DcSSc), based on the extend of skin thickening. In LcSSc skin thickening is restricted to Author: Ruben L.

Smeets, Brigit E. Kersten, Irma Joosten, Charlotte Kaffa, Wynand Alkema, Hans Koenen, Madel. Systemic sclerosis Christopher P Denton, Dinesh Khanna Systemic sclerosis, also called scleroderma, is an immune-mediated rheumatic disease that is characterised by fibrosis of the skin and internal organs and vasculopathy.

Although systemic sclerosis is uncommon, it. A relationship exists between the extent of skin area affected and degree of internal organ/system involvement.

Systemic scleroderma can manifest itself in pulmonary fibrosis, Raynaud's syndrome, digestive system telangiectasias, renal hypertension and/or pulmonary hypertension. Definition (MSH) A chronic multi-system disorder of CONNECTIVE TISSUE.

Systemic sclerosis (SSc) is a chronic, autoimmune disease which can affect the blood vessels, the visceral organs, and the skin. SSc, most commonly, develops between the ages of 30 but it can be seen at any age.

In terms of skin involvement, SSc can be classified as limited or diffuse. Its etiopathogenesis is still unclear. Systemic sclerosis (SS) is an autoimmune disorder. This means it’s a condition in which the immune system attacks the body. Healthy tissue is destroyed because the immune system mistakenly.

This book provides a comprehensive review of the recent advances in the research of systemic sclerosis (scleroderma). Systemic sclerosis is a complex autoimmune disease characterized by vasculopathy, fibrosis, and immune activation.

This disease is also associated with certain susceptibility genes and is affected by epigenetic regulation. Systemic sclerosis is a complex autoimmune disease characterized by a chronic and frequently progressive course and by extensive patient-to-patient variability. Like other autoimmune diseases.

Systemic sclerosis is a rare, chronic autoimmune rheumatic disorder characterized by degenerative changes and scarring in the skin, joints, and internal organs and by blood vessel abnormalities. Systemic sclerosis causes an overproduction of collagen and other proteins in various tissues.

The cause. Product Information. This book consists of advanced information regarding the immunopathology and clinical aspects of systemic sclerosis (SSc).

Systemic sclerosis, often called as Scleroderma (tight skin) is a skin disorder characterized by excessive creation of. This book provides a comprehensive review of the recent advances in the research of systemic sclerosis (scleroderma). Systemic sclerosis is a complex autoimmune disease characterized by vasculopathy, fibrosis, and immune activation.

This disease is also associated with certain susceptibility genes and is affected by epigenetic : Springer Japan. Systemic sclerosis, also called scleroderma, is an immune-mediated rheumatic disease that is characterised by fibrosis of the skin and internal organs and vasculopathy.

Although systemic sclerosis is uncommon, it has a high morbidity and mortality. Improved understanding of systemic sclerosis has allowed better management of the disease, including improved classification and more systematic.Systemic sclerosis is a rare chronic disease of unknown cause characterized by diffuse fibrosis and vascular abnormalities in the skin, joints, and internal organs (especially the esophagus, lower gastrointestinal tract, lungs, heart, and kidneys).

Common symptoms include Raynaud phenomenon.Systemic scleroderma can manifest itself in pulmonary fibrosis, Raynaud's syndrome, digestive system telangiectasias, renal hypertension and/or pulmonary hypertension.

Definition (MSH) A chronic multi-system disorder of CONNECTIVE TISSUE.