High ANA + Sm/RNP, but very few symptoms — lupus diagnosis and UCTD diagnosis
32M, trying to understand some recent abnormal autoimmune labs and joint symptoms.
Timeline: In Feb 2026, during Army training, I had feverish symptoms, body aches and severe sore throat and tested positive for Group C strep. I was given amoxicillin but stopped early because of severe bloating. My throat symptoms persisted/recurred. On April 29, I went to the ER and was again diagnosed with strep and given another antibiotic, which I also didn’t complete fully.
About 1–2 weeks after the strep infection, I developed progressive stiffness/aches in my fingers, elbows and other joints, especially morning finger stiffness. I’ve never had visible joint swelling, redness or warmth. Symptoms fluctuated and improved dramatically with prednisone 15 mg for 2 weeks. Some mild stiffness returned after stopping.
I currently run 1.5–3+ miles, train college soccer, sprint and lift weights without joint pain/discomfort. I’ve also had some knee popping with minimal discomfort.
I briefly had a smooth red spot on my neck/chest that lasted only ~2 days, wasn’t itchy/painful, and completely disappeared. I’m not sure it was autoimmune. My fingers sometimes become pale/white in the cold, possibly Raynaud’s.
Labs
Positive:
ANA ≥1:1280, speckled
RF 75
Sm/RNP >8.0
Negative/normal:
dsDNA 1
CCP <16
C3 121
C4 17
SSA/SSB negative
Scl-70 negative
Centromere B negative
ESR 11
CRP <3
Creatinine 0.96 / eGFR 108
CBC essentially normal
Hep B and Lyme negative
No kidney problems or other known organ involvement.
The first rheumatologist I saw had never seen me before and mainly reviewed my bloodwork, didn’t really examine my joints, and told me I have lupus. He prescribed Plaquenil (hydroxychloroquine) and prednisone.
Another rheumatologist was more cautious and said she wouldn’t diagnose lupus with 100% certainty and that UCTD is possible.
I’m especially wondering about the post-streptococcal possibility because my joint symptoms started only ~1–2 weeks after recurrent/incompletely treated Group C strep.
Could this be UCTD, early/mild lupus, MCTD/RNP-related disease, post-streptococcal/post-infectious arthritis, or something else entirely?
I’m not asking anyone to diagnose me—just curious how others would interpret this combination of strong antibodies but relatively few clinical symptoms, especially with the strep timeline.
High ANA + Sm/RNP, but very few symptoms — lupus, UCTD, or post-strep?