Differential Diagnosis for a 55-year-old Woman with Optic Neuritis and Subsequent ARDS
Single Most Likely Diagnosis
- Neuromyelitis Optica Spectrum Disorder (NMOSD): This condition is characterized by optic neuritis and can also involve the spinal cord. The response to steroids followed by a relapse (in this case, with ARDS, which could be a manifestation of a severe relapse or a complication) is consistent with NMOSD, especially if there are other systemic symptoms or if the patient has antibodies against aquaporin-4.
Other Likely Diagnoses
- Multiple Sclerosis (MS): Although MS is a primary consideration for optic neuritis, the development of ARDS is less typical. However, MS can have a wide range of presentations, and in rare cases, it might be associated with systemic complications that could lead to ARDS.
- Systemic Lupus Erythematosus (SLE): SLE can cause optic neuritis and is known for its potential to affect multiple organ systems, including the lungs, which could result in ARDS. The response to steroids is also consistent with SLE.
Do Not Miss Diagnoses
- Sarcoidosis: This condition can cause optic neuritis and has the potential to affect the lungs severely, leading to ARDS. Sarcoidosis can respond to steroids but requires a high index of suspicion for diagnosis.
- Wegener's Granulomatosis (Granulomatosis with Polyangiitis, GPA): GPA can cause optic neuritis and is known for its potential to cause severe lung disease, including ARDS. It is a diagnosis that should not be missed due to its potential for severe morbidity and mortality.
Rare Diagnoses
- Susac Syndrome: A rare condition characterized by microangiopathic changes affecting the brain, retina, and inner ear. While it could potentially explain optic neuritis, the development of ARDS would be unusual.
- Behçet's Disease: This is a form of vasculitis that can affect multiple parts of the body, including the eyes (causing optic neuritis) and lungs. However, ARDS as a direct complication is less common, making it a rare consideration in this context.