-transparent.png){kind=logo}
Three patients with the unusual combinations of discoid lupus, systemic lupus erythematosus (SLE), and progressive systemic sclerosis (PSS) are reported. The first patient developed PSS eight years after a diagnosis of discoid lupus had been made and this was complicated by myositis six years later. The second patient developed PSS more than 20 years after being diagnosed as having SLE. The third patient developed SLE with predominant features of urticarial vasculitis six years after PSS. Mild myositis also ensued. There were no antibodies to U1RNP demonstrable in any of these patients. The clinical progression of SLE to PSS or vice versa in the absence of features of mixed connective tissue disease is distinctly uncommon.
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
February 1994,
The Journal of the Association of Physicians of India,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
January 2021,
Journal of oral and maxillofacial pathology : JOMFP,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
May 2024,
ACR open rheumatology,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
August 1983,
Arthritis and rheumatism,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
January 2011,
Reumatologia clinica,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
January 1997,
International ophthalmology clinics,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
February 1975,
Diseases of the nervous system,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
July 2008,
Mymensingh medical journal : MMJ,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
March 2024,
BMJ case reports,
R A Asherson, and
H Angus, and
J A Mathews, and
O Meyers, and
G R Hughes
January 2006,
The Journal of dermatology,
