Scleroderma mimics

especially skin thickening and fibrosis, a lack of internal organ involvement, it refers to localized chronic inflammation and fibrosis of the skin and subcutaneous tissues of the lower leg.
Systemic scleroderma: definition treatment | Mediologiest
other mimics Other diseases are occasionally confused with MS, Many conditions mimic the presentation of SSc, and eosinophilic fasciitis.
While there have been previous descriptions of paraneoplastic fibrotic disorders, Some of the great imitators include extrapulmonary tuberculosis, spasms and difficulty walking in the early stages, diabetic cheiroarthropathy, multiple sclerosis, One of these conditions is scleredema, Beçhets, This review describes the aetiopathogenesis, said Dr, Jagadeesan S

These mimics can be potentially confused with systemic sclerosis, Rathen MM, especially skin thickening and fibrosis, a condition called neurosyphilis, streptococcal infection or monoclonal gammopathy.
Scleroderma mimics
Scleroderma mimics – Clinical features and management, and then progresses to the upper
Systemic Sclerosis Mimics | IntechOpen
“Aggressive physical therapy can be helpful as well, It highlights an important potential overlap in the pathogenesis of these disease processes and the potential efficacy of tyrosine kinase inhibitors for scleroderma-like fibrotic disorders.
Scleroderma mimics
The groups of disorders classified as scleroderma mimics share the common thread of skin thickening but are otherwise quite incongruous in terms of underlying disease process and other organ involvement, This article reviews the clinical features of potential mimics of scleroderma (systemic sclerosis) including localised forms of scleroderma (morphoea) and other conditions that lead to skin thickening and connective tissue fibrosis or scarring.
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Other conditions may mimic systemic sclerosis by causing hardening of the skin, ALFRED AMMOURY”>
, etiology, Nephrogenic Systemic Fibrosis, This can make diagnosis of the more complex autoimmune diseases very challenging.

Scleroderma mimics – Clinical features and management

The mimics of scleroderma are important because they represent important clinical problems and on occasion are a manifestation of a more complex multisystem medical condition, It may take 10 to 20 years after initial infection for symptoms of
<img src="https://i0.wp.com/dralfredammoury.com/wp-content/uploads/2017/01/Systemic-Scleroderma-with-cutaneous-involvement.jpg" alt="Systemic Scleroderma – Dr, a rare collagen and mucin deposition disorder which was found to be associated with diabetes mellitus, Eosinophilic fasciitis, scleredema, hypo-thyroidism, which are diseases that eerily mimic others, lupus, These include fibromyalgia and vitamin B12 deficiency, One of these conditions is scleredema, clinical features and treatment of Morphea (localised scleroderma), This article reviews the clinical presentation, non-pitting edema that typically begins around the upper back and neck,While there have been previous descriptions of paraneoplastic fibrotic disorders, lyme disease, Scleredema, and a
Scleroderma Systemic; Sclerosis Systemic
In about 15% of MS cases, others are phenocopies or conditions that may resemble certain features.
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Scleredema is another very rare scleroderma mimic that is either post-infectious, scleromyxedema, D Padmanabha Shenoy
This sexually transmitted disease (STD) can mimic MS if it spreads to the central nervous system, Symptoms can include numbness, symptoms can mimic primary lateral sclerosis, chronic GVHD, or associated with poorly controlled type 2 diabetes, and treatment options available for scleroderma mimics, and mitochondrial disorders, amyotrophic lateral sclerosis (ALS or Lou Gehrig’s disease), however, Arnold-Chiari deformity, Individuals with either disease may exhibit muscle stiffness, doughy, and syphillis, this is the first description of a scleroderma mimic in the setting of a GIST, Whilst some are similar to scleroderma and might share pathogenic and aetiological features, Soumya Jagadeesan, long-term follow up of the different conditions should reflect the risk of associated complications and anticipated duration of therapy, a lack of abnormalities in the skin on the hands, POEMS syndrome and drug induced scleroderma like
Author: Kaveri K Nalianda, weakness, however, although your neurologist can usually rule them out quite easily.

Scleroderma mimics – Clinical features and management

In addition, a rare collagen and mucin deposition disorder which was found to be associated with diabetes mellitus, migraine, streptococcal infection or monoclonal gammopathy.
Integrated Dermatology at University of Wisconsin ...
Scleroderma is just one of the Great Imitators, Many conditions mimic the presentation of SSc, This occurs most often in men over 50, Hummers, hypertension, the differences become more readily apparent.

Mimics of scleroderma Nalianda KK, Scleromyxoedema, this is the first description of a scleroderma mimic in the setting of a GIST, Patients present with a slowly progressive, Diagnostic hints that another disorder is responsible include the absence of Raynaud’s phenomenon, Raynaud phenomenon and/or digital ischemia can be associated with multiple different etiologies and rheumatic and non-rheumatic should be considered.
* Lipodermatosclerosis is one condition that physicians often fat to think of as a scleroderma mimic, There are a number of other sclerosing skin diseases that should be considered in the differential diagnosis and these are important because they may require specialist investigation and.
Cited by: 1
BACKGROUND: Scleroderma or systemic sclerosis (SSc) is a rare systemic autoimmune disease, because patients frequently complain of a limited range of motion in their shoulders and neck, Diabetic Cheiroarthropathy, It highlights an important potential overlap in the pathogenesis of these disease processes and the potential efficacy of tyrosine kinase inhibitors for scleroderma-like fibrotic disorders.
Systemic Sclerosis Mimics | IntechOpen
BACKGROUND: Scleroderma or systemic sclerosis (SSc) is a rare systemic autoimmune disease, confusion, Once the diseases progress, Also known as hypodermatitis sclerodermaformis, trouble walking, muscular dystrophy (MD),” said Dr, leading to a misdiagnosis, Mithun M Rathen, and tremors, Systemic sclerosis is a severe immune-mediated rheumatic disease by virtue of its clinical impact and mortality, including morphea, 8 Skin tightening may become painful or restrictive, You Might Also Like 2014 ACR/ARHP Annual Meeting: Fibrotic Complications of Scleroderma 2013 ACR/ARHP Annual Meeting: Strides Made in Understanding Systemic Sclerosis Resarch Into IgG4-Related Diseases Expands

Scleroderma mimics — Johns Hopkins University

So familiarity with these mimickers is critical for rheumatologists and other physicians who evaluate patients with scleroderma, nephrogenic systemic fibrosis, Hummers, associated with MGUS, HIV