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Rowell's Syndrome to ds-DNA Negative Lupus Nephritis: A Yet Unreported Progression
Mayur R Bhobe1, Swagata Tambe1, Saurabh Jindal1
1Department of Skin and VD, MGM Medical College, Navi Mumbai, India.
Rowell's syndrome, a lupus erythematosus subtype, can rarely progress to severe kidney disease (lupus nephritis) even without specific antibodies. This case highlights a unique progression to stage V lupus nephritis in a young female patient.
Area of Science:
- Rheumatology
- Nephrology
- Dermatology
Background:
- Rowell's syndrome is a rare subtype of subacute cutaneous lupus erythematosus.
- It presents with characteristic skin lesions, positive rheumatoid factor, anti-Ro/La antibodies, and speckled antinuclear antibodies.
- Lupus nephritis (LN) is a severe complication of lupus erythematosus, often drug-induced.
Purpose of the Study:
- To report a unique case of Rowell's syndrome.
- To describe its progression to non-drug-induced, ds-DNA negative lupus nephritis.
- To highlight the rarity of cutaneous involvement in such cases.
Main Methods:
- Case report of an 18-year-old female.
- Clinical evaluation including dermatological and renal assessments.
- Serological testing for ds-DNA, rheumatoid factor, anti-Ro/La antibodies, and antinuclear antibodies.
Main Results:
- The patient presented with Rowell's syndrome.
- She was negative for ds-DNA antibodies.
- Over four months, she progressed to stage V lupus nephritis, a rare occurrence for non-drug-induced LN with negative dsDNA and cutaneous involvement.
Conclusions:
- Rowell's syndrome can rarely progress to severe, non-drug-induced lupus nephritis.
- This case underscores the importance of monitoring for renal complications even in the absence of ds-DNA antibodies.
- The co-occurrence of Rowell's syndrome and ds-DNA negative LN with cutaneous manifestations is exceptionally rare.
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