VolumeVol. 53 • Number No. 3 • July - September 2015 Back

Case Report

​​​​​​​A Filipino with Systemic Lupus Erythematosus-Scleroderma Overlap Syndrome

Authors: Kristian Anteolin D. Punzalan, Patrick Y. Siy, Engelbert Simon S. Perillo, Lorielle Marie E.S. Galvez, Sandra Tankeh-Torres, Philip U. Chua

DOI: 10.65564/pjim.d7b2e62735

Date of Publication: September 2015

Abstract

Background: Overlap syndrome is a large group of condition that manifests with symptoms from two or more autoimmune conditions and satisfies the diagnostic criteria of at least two connective tissue diseases in the same patient. This condition might be unrecognized by the primary care physician and underreported.

Case: A 30-year-old female had a 10-week history of non-pruritic erythematous macules on her face that gradually spread to her trunk, and upper extremities which progressed to hyperpigmented macules and tightening of the skin. There was note of hair loss, anemia, ulcerating wounds on distal extremities and finger tips. She then developed generalized body weakness and easy fatigability. Physical and laboratory examinations were consistent with SLE and scleroderma. 2D-echocardiogram showed a large pericardial effusion and pulmonary hypertension. She was treated with prednisone and azathioprine which in less than a week, diminished significantly the pericardial effusion. Patient also complained of a few day history of unilateral blurring of vision which turned out to be central retinal artery occlusion.

Conclusion: Overlap syndrome is a disease entity to consider in patients with multiple symptoms that cannot be classified into one connective tissue disease. Treatment of this disease should be individualized and based on the connective tissue diseases involved.

Keywords: Systemic sclerosis, scleroderma, systemic lupus erythematosus, SLE, overlap syndrome

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