Abstract
“Rhupus” syndrome is a rare condition that describes the coexistence of systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), which prevalence among patients with SLE varies from 0.01% to 9.7%. There are few reported cases of the association between autoimmune hemolytic anemia and rheumatoid arthritis with systemic lupus erythematosus (rhupus). We report a rare case of rhupus in a 29-year-old woman, associated with autoimmune hemolytic anemia.
1. Introduction
The term “rhupus” describes a syndrome that comprises the coexistence of systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA). Lupus arthropathy is a nonerosive process and is relatively a common manifestation of SLE; however, approximately 1% of patients with SLE will develop erosive arthropathy, which is difficult to differentiate from AR arthropathy. Autoimmune hemolytic anemia (AHA) presents in approximately 1/10 patients with SLE, but is a very uncommon process in RA. The presence of rhupus and AHA is an extremely uncommon condition, with only a few cases previously reported [1–3].
2. Case Presentation
A 29-year-old woman, with no previous medical history, started 2 years before her presentation to our center with pain and 30–60 minutes morning stiffness in both hands, symmetric polyarticular pain, and swelling at both glenohumeral joints, all metacarpophalangeal, all proximal interphalangeal joints, both wrist and hip joints with pain improvement after movement. The signs and symptoms remitted partially with ketorolac, and she had also improvement while pregnancy 1 year ago. She denied other symptoms including fever, dry mouth or dry eye, muscular weakness, hair loss, oral ulcers, or dermal lesions.
Two weeks before admission, she presented dyspnea (mMRC 3). At arrival, she had a heart rate of 105 beats per minute, and other vital signs were within normal range. On physical examination, there was pain and palpable synovial thickening at both glenohumeral, all metacarpophalangeal, all proximal interphalangeal joints and both wrist joints. No other abnormal findings were found.
Biochemical data showed severe anemia with elevated reticulocyte count and slightly elevated DHL, total bilirubin, and indirect bilirubin. Immunological tests were positive antinuclear antibody 1 : 2520 in an AC-1 pattern, anti-dsDNA antibody titer of 479.23 UI/ml, and anticitrullinated peptide antibody titer of 188.50 U/ml, with negative anti-Smith and antiphospholipid antibodies; other laboratory results at admission are shown in Table 1. Peripheral blood smear showed macrocytosis and punctate basophilia. Urinary sediment was not active, and no proteinuria was found. After suspected autoimmune hemolytic anemia, specific antibodies were requested, which were positive for IgG Ab directed to C3b and C3d. The plain radiograph of both hands showed juxta-articular osteopenia and joint space narrowing without bone erosions, and these findings were consistent with the articular ultrasonography of both hands, as nonerosive inflammatory arthropathy (Figure 1).
Dexamethasone was started at a dose of 40 mg for autoimmune hemolytic anemia. After two days, the patient reported significant improvement, and hemoglobin levels remained stable. She was discharged after a blood transfusion.
Diagnosis of ruphus was based on new SLE classification criteria by EULAR/ACR 2019 and on RA classification criteria revised by the EULAR/ACR. After four weeks of oral prednisone, chloroquine, and azathioprine, all symptoms and laboratory findings improved (Table 1). Initial SDAI (Simple Disease Activity Index) was 70.3, and one month after treatment, it was 0. The initial Systemic Lupus Erythematous Disease Activity Index (SLEDAI) was 8 points, and, also, after one month of treatment, it was 0 points.
3. Discussion
The cumulative number of globally reported rhupus cases is about 140 [1]. Among patients with SLE, rhupus syndrome has a variable prevalence from 0.01% a 9.7%; this variation is likely due to different classification and selection criteria [1–5].
The syndrome can present initially as either of both diseases, SLE or RA. The exact median onset age is not established, and the interval between RA diagnosis and development of SLE varies from 4 to 11 years [2–4]. However, Tani et al. reported a case series in which SLE features preceded arthritis onset in 50% of the patients [4].
In a cohort of Mexican population, the reported median onset age was 45.5 ± 10.7 years, and RA was the initial diagnosis in 68% of patients; it preceded rhupus for up to four years. Both were simultaneously diagnosed in the rest 32%, and no single patient was first diagnosed with SLE. In this cohort, hematologic manifestations were reported in 78%. However, AHA was seen only in one patient who initially responded to prednisone, but later, in the course of the disease, the patient developed alveolar hemorrhage and died [5]. In another study, among 56 patients with rhupus, the prevalence of AHA was just 5%, versus 21% in SLE patients [6]. Other series report no cases of rhupus and AHA [7].
Patients with rhupus tend to show a lower incidence of malar rash, renal disease, and neurological disorders. This rare condition has a lesser visceral organ involvement as compared with SLE patients without RA [5–8].
The incidence of autoimmune hemolytic anemia in RA is uncertain, but it has been described in 2.1–2.5% with 8 cases reported [9, 10].
4. Conclusions
Rhupus syndrome is an unusual overlap between RA and SLE. Characteristically, this syndrome shows more RA-associated manifestations and less SLE-associated damage. Autoimmune hemolytic anemia is not a common finding on RA patients, neither on rhupus cases.
We report an overlap syndrome case with an atypical initial presentation due to the presence of autoimmune hemolytic anemia, no erosive arthritis, and elevated titles of anti-CCP antibody.
Data Availability
The data used to support the findings of this study are available from the corresponding author upon request.
Conflicts of Interest
The authors declare no conflicts of interest.
Acknowledgments
The authors acknowledge all the health workers who participated in the care of this patient. The study was performed in Department of Internal Medicine, Hospital de Especialidades. “Dr. Bernardo Sepulveda Gutiérrez,” Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Ciudad de México.