Systemic sclerosis

Systemic sclerosis (SSc) is a generalized disorder of small arteries, microvessels and connective tissue, characterized by fibrosis and vascular obliteration in the skin and organs, particularly the lungs, heart, and digestive tract. There are two main subsets of SSc: diffuse cutaneous SSc (dcSSc) and limited cutaneous SSc (lcSSc) (see these terms). A third subset of SSc has also been observed, called limited Systemic Sclerosis (lSSc) or systemic sclerosis sine scleroderma (see these terms).

Keratoconjunctivitis sicca

Dryness of the eye related to deficiency of the tear film components (aqueous, mucin, or lipid), lid surface abnormalities, or epithelial abnormalities. Keratoconjunctivitis sicca often results in a scratchy or sandy sensation (foreign body sensation) in the eyes, and may also be associated with itching, inability to produce tears, photosensitivity, redness, pain, and difficulty in moving the eyelids.


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PMID (PMCID)
23323575
MALE Middle Aged
Anterior uveitis in a patient with scleroderma: a case report.
Bolad W.
Ocul Immunol Inflamm. 2013;21(1):11-2.
Clinical testing and investigation could not identify an underlying etiology other than systemic sclerosis.Ocular manifestations seen in association with scleroderma include eyelid skin changes, keratoconjunctivitis sicca, and retinal microvascular abnormalities.Only a small number of cases of uveitis have been reported in association with scleroderma.