Incomplete resolution and followed by bronchiectasis later on. Delayed resolution.
Pleural Effusion,Empyema.
Lung Abscess,ARDS and respiratory failure.
A)Systemic sclerosis without Scleroderma:- i.e internal organ involvement without cutaneous scleroderma. B)Overlap syndrome:- scleroderma associated with other autoimmune disease. C)localized scleroderma:- scleroderma without internal organ involvement. Charachterized by Morphoea which are local patches of scleroderma. D)Limited scleroderma(CREST Syndrome):- There is minimal visceral involvement, positive anticentromere antibodies and good prognosis. Skin hardening is limited to face,feet and fingers. (Calcinosis,Raynaud's phenomenon,Esophageal dysfunction,Sclerodactly,Telangectasia.) E)Diffuse scleroderma:- Diffuse thickening of trunk,proximal and distal limbs with internal organ development and damage so it is life threatening.