What Other Conditions Can Look Like Scleroderma?
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Symptoms similar to symptoms of scleroderma can occur
with a number of other diseases. Here are some of the most common
scleroderma lookalikes:
- Eosinophilic fasciitis (EF) (EE-oh-SIN-oh-FIL-ik
fa-shi-EYE-tis): a disease that involves the fascia (FA-shuh), the
thin connective tissue around the muscles, particularly those of the
forearms, arms, legs, and trunk. EF causes the muscles to become
encased in collagen, the fibrous protein that makes up tissue such as
the skin and tendons. Permanent shortening of the muscles and tendons,
called contractures, may develop, sometimes causing disfigurement and
problems with joint motion and function. EF may begin after hard
physical exertion. The disease usually fades away after several years,
but people sometimes have relapses. Although the upper layers of the
skin are not thickened in EF, the thickened fascia may cause the skin
to look somewhat like the tight, hard skin of scleroderma. A skin
biopsy easily distinguishes between the two.
- Undifferentiated connective tissue disease (UCTD): a
diagnosis for patients who have some signs and symptoms of various
related diseases, but not enough symptoms of any one disease to make a
definite diagnosis. In other words, their condition hasn't
"differentiated" into a particular connective tissue disease. In time,
UCTD can go in one of three directions: it can change into a systemic
disease such as systemic sclerosis, systemic lupus erythematosus, or
rheumatoid arthritis; it can remain undifferentiated; or it can
improve spontaneously.
- Overlap syndromes: a disease combination in which patients
have symptoms and lab findings characteristic of two or more
conditions.
At other times, symptoms resembling those of scleroderma
can be the result of an unrelated disease or condition. For example:
- Skin thickening on the fingers and hands also appears with
diabetes, mycosis fungoides, amyloidosis, and adult celiac disease. It
can also result from hand trauma.
- Generalized skin thickening may occur with scleromyxedema,
graft-versus-host disease, porphyria cutanea tarda, and human adjuvant
disease.
- Internal organ damage, similar to that seen in systemic
sclerosis, may instead be related to primary pulmonary hypertension,
idiopathic pulmonary fibrosis, or collagenous colitis.
- Raynaud's phenomenon also appears with atherosclerosis or
systemic lupus erythematosus or in the absence of underlying
disease.
An explanation of most of these other diseases is beyond
the scope of this booklet (for brief definitions, see the glossary).
What's important to understand, however, is that scleroderma isn't
always easy to diagnose; it may take time for you and your doctor to
establish a diagnosis. And while having a definite diagnosis may be
helpful, knowing the precise form of your disease is not needed to
receive proper treatment.
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