2024 Volume 11 Pages 119-123
Rheumatoid meningitis (RM) is a rare but serious extra-articular manifestation of rheumatoid arthritis. Due to the absence of specific biomarkers, imaging findings, or guidelines for its detection, the diagnosis of RM is difficult. This report describes a patient of RM diagnosed with an open biopsy and discusses the utility of anticyclic citrullinated peptide antibodies (ACPA) levels in the serum and cerebrospinal fluid (CSF), and contrast-enhanced (CE) fluid-attenuated inversion recovery (FLAIR) images for screening and monitoring RM. A 65-year-old woman presented with a 2-month history of headaches. Imaging studies showed asymmetric meningeal and leptomeningeal involvement seen on brain magnetic resonance imaging (MRI). An open biopsy of the meninges and leptomeninges depicted palisaded and necrotizing granulomatous inflammation, which suggests rheumatoid nodules. Treatment with prednisolone and tocilizumab led to symptom improvement and reduced lesion intensity on follow-up MRI. Throughout the treatment, the ACPA index in her serum and CSF, and the findings of CE-FLAIR images, rather than the CE T1WI, reflected disease activity. For 6 months, the patient has been stable without symptom recurrence. The ACPA index and the CE-FLAIR images were useful for the diagnosis and monitoring of RM. To validate these findings, further studies are necessary.
Rheumatoid meningitis (RM) is a rare but serious extra-articular manifestation of rheumatoid arthritis (RA). This manifestation primarily can not only occur in patients with long-standing RA1) but also independently of the presence or severity of RA. At the time of RM onset, more than 30% of cases are not diagnosed with RA.2) Nevertheless, RM can take place even in patients with well-controlled RA. A definitive diagnosis is more challenging when laboratory data or imaging findings suggest other diseases. Despite that asymmetric meningeal or leptomeningeal involvement seen on brain magnetic resonance imaging (MRI) is a characteristic feature of this disease, along with other diseases, such as malignancies and IgG4-related pathologies,3-5) gadolinium (Gd) enhancement can be blunted because it leaks into the adjacent cerebrospinal fluid (CSF) through damaged tissues. Hence, contrast-enhanced (CE) T1-weighted images (T1WI) may not accurately reflect the distribution of meningeal and leptomeningeal lesions. Anti-cyclic citrullinated peptide antibodies (ACPA) have been reported as a potential marker of RM.2,6) This antibody is an immune protein produced by autoreactive B cells and serves as a diagnostic biomarker in patients with RA. ACPA can also be found in the CSF because of passive diffusion from the serum due to the blood-CSF barrier dysfunction and has been shown to decrease in titer following treatment in several reports of RM.6) Herein, we report a patient with RM, and demonstrate the utility of ACPA levels in the serum, CSF, and enhanced fluid-attenuated inversion recovery (FLAIR) images for screening and monitoring RM is demonstrated. The patient involved in this case report provided informed consent.
A 65-year-old woman presented with a 2-month history of headaches. She had a 26-year history of RA that was well-controlled with salazosulfapyridine, bucillamine, and iguratimod. Initial brain computed tomography (CT) showed less pronounced sulci on the right side than on the left (Fig. 1A). FLAIR and diffusion-weighted images (DWI) revealed hyperintensities in the right frontoparietal sulci (Fig. 1B, C). These lesions were negative for hemorrhage on T2* images (Fig. 1D). CE T1WI and CE FLAIR images showed meningeal and leptomeningeal enhancements on the same site (Fig. 1E, F), and the lesion distribution was clearer on CE FLAIR than on CE T1WI.
Brain computed tomography scan obtained on the day of admission showing effacement of the sulci at the right frontoparietal lobes (A). Magnetic resonance imaging (MRI), fluid-attenuated inversion recovery (FLAIR) (B), and diffusion-weighted images (DWI) (C) showing the hyperintensities on the right frontoparietal cortical sulci. These lesions demonstrate no evidence of hemorrhage on T2* images (D). Contrast-enhanced (CE) T1-weighted images (T1WI) (E) and CE-FLAIR images (F) showing the meningeal and leptomeningeal enhancement on the same site. Lesion distribution was more clearly depicted on CE FLAIR compared to CE T1WI.
On laboratory workup, serology exhibited elevated rheumatoid factor (RF) 33.5 IU/mL (0-15 IU/mL), ACPA 78.4 U/mL (0-4.5 U/mL), IgG 2,434 mg/dL (861-1,747 mg/dL), antinuclear antibody 80 times (0-39 times), soluble interleukin-2 receptor 490 U/mL (157-474 U/mL), and cancer antigen 15-3 (CA15-3) 25.3 U/mL (0-25.0 U/mL).
The other serology parameters were normal including beta2-microglobulin (β2MG), Aspergillus antigen, Cryptococcus neoformans antigen, cytoplasmic antineutrophil cytoplasmic antibodies (c-ANCA), perinuclear ANCA (p-ANCA), immunoglobulin G subclass IV (IgG4), angiotensin converting enzyme, anti-Sjogren's syndrome A (anti-SSA) /Ro antibody, anti-Sjogren's syndrome B (anti-SSB) /La antibody, anti-Sm antibody, and anti-ssDNA antibody, as well as tumor markers except CA15-3. Polymerase chain reaction (PCR) tests were negative for human immunodeficiency virus, Treponema pallidum, Epstein-Barr virus, varicella-zoster virus, herpes simplex virus, mumps virus, measles virus, and cytomegalovirus. QuantiFERON-TB and serum fungal testing were also negative.
CSF analysis revealed elevating opening pressure reaching 27 cm H2O, leukocyte count of 133/μL (~5/μL, 88% mononuclear cells and 12% polynuclear cells), protein level of 149 mg/dL (10-40 mg/dL), glucose level of 43 mg/dL (50-80 mg/dL), and interleukin-6 level of 349 pg/mL (0-4.0 pg/mL). The CSF PCR results for viral infections, as mentioned above, were negative. CSF cytology for malignancies and culture results were negative. CSF ACPA and CSF IgG were 12.1 U/mL (no reference values, higher than serum reference value) and 19.8 mg/dL (0.5-4.0 mg/dL), respectively. The ACPA index is obtained by dividing the CSF/serum ratio of ACPA by the CSF/serum ratio of IgG. A ratio of > 1.4 means that the ACPA is produced within the central nervous system.6) For antibodies other than ACPA, the antibody titer index using serum and CSF were calculated using the same formula, and an increase in this index indicated specific antibody production in the CSF.7) Based on this formula, the ACPA index was 19.25 in this case. Table 1 includes the time course of serological and CSF markers.
Time course of serological and cerebrospinal fluid markers
| RF (IU/mL) | Serum ACPA (U/mL) | CSF ACPA (U/mL) | Serum IgG (mg/dL) | CSF IgG (mg/dL) | ACPA index | |
|---|---|---|---|---|---|---|
| RF, rheumatoid factor; ACPA, anti-cyclic citrullinated peptide antibodies; CSF, cerebrospinal fluid; IgG, immunoglobulin G | ||||||
| Pre-treatment | 33.5 | 78.4 | 12.1 | 2434 | 19.8 | 19.25 |
| Post-treatment | 20.7 | 22.4 | <0.6 | 699 | 3 | <6 |
Whole-body CT revealed an enhanced lesion in the left breast. She had undergone surgery for left-sided breast cancer 2 years ago, and CT findings suggested breast cancer recurrence. As shown by breast ultrasound, the possibility of breast cancer recurrence cannot be ruled out.
We performed an open craniotomy and biopsy of the meninges and leptomeninges of the frontal convexity, which was enhanced on MRI, and a needle biopsy of the breast lesion. The meninges were thickened but did not adhere to the leptomeninges. In the leptomeninges, yellow white caseous necrosis was observed. These biopsies showed palisaded and necrotizing granulomatous inflammation, which indicates the presence of rheumatoid nodules (Fig. 2A, B). Tests for bacterial, fungal, Mycobacterium tuberculosis, and viral tissue infections were negative. A needle biopsy of the left breast exhibited no evidence of malignancy, and the enhanced lesion on body CT was considered a postoperative change. These findings showed that the patient was diagnosed with RM. Oral prednisolone was initiated at a dosage of 60 mg/day with gradual tapering. Her symptoms gradually improved, and she was discharged 1 month later.
(A) Meningeal and leptomeningeal biopsy demonstrating palisaded and necrotizing granulomatous inflammation. (B) Immunostaining revealing CD68-positive perivascular histiocytes. No evidence of bacterial, fungal, Mycobacterium tuberculosis, or viral infections was found, indicating the rheumatoid nodules.
Follow-up MRI 4 months later showed attenuation of the hyperintensities in the sulci on FLAIR and DWI (Fig. 3A, B). Enhancement on the T1WI and FLAIR images was also attenuated (Fig. 3C, D). Follow-up laboratory workup revealed decreasing RF 20.7 IU/mL, ACPA 22.4 U/mL, and IgG 699.0 mg/dL (Table 1). CSF analysis revealed opening pressure reaching 26 cmH2O, leukocyte count of 2/μL, protein level of 87 mg/dL, and glucose level of 115 mg/dL. CSF ACPA and CSF IgG were <0.6 U/mL and 3.0 mg/dL, respectively (Table 1). The ACPA index decreased to <6 with the actual value possibly being lower because of the CSF ACPA level being below the detection limit (Table 1). She stopped taking salazosulfapyridine, bucillamine, and iguratimod 10 days after the biopsy when the pathological diagnosis results arrived. She started taking prednisolone orally at 60 mg/day, tapered it down by 5 mg/week to 20 mg/day, and is now managed with subcutaneous injections of tocilizumab at a dose of 162 mg every 2 weeks, along with an oral intake of prednisolone at a dose of 20 mg/day, without symptom recurrence.
Follow-up MRI conducted four months later (A, B, C, and D). FLAIR (A) and DWI (B) demonstrating the regression of the leptomeningeal involvement. CE-T1WI (C) and CE-FLAIR (D) demonstrating the attenuating of the enhancement.
The incidence of RA is estimated to be 1% of the population. RM is rarer in clinical practice, and its true prevalence is unknown.8,9) No specific biomarkers or guidelines for detecting RM are available; hence, the diagnosis is based on a combination of clinical presentation, hematological CSF parameters, imaging findings, and the exclusion of other etiologies.8)
RM exhibits diverse MRI features, with asymmetric meningeal or leptomeningeal involvement being relatively common;4,10) nevertheless, MRI findings alone cannot reliably differentiate between the RM and meningeal metastasis because some RM cases present with diffuse or bilateral lesions on MRI.11) In meningeal and leptomeningeal lesions, the concentration of Gd is lower than that in intra-axial brain lesions considering that Gd concentration is reduced as it leaks into the adjacent CSF through damaged vessels.12,13) CE FLAIR is more sensitive to low concentrations of Gd than CE T1WI, and this sequence is suitable for the diagnosis of inflammatory meningeal and leptomeningeal disease.12,14-16) Conversely, the diagnostic accuracy of meningitis with FLAIR is highly likely to depend on the amount of CSF protein concentration.15) Even in case reports wherein imaging findings improved after treatment17-19) including the present case, the narrowness of the cerebral sulcus remains and has not completely disappeared. These imaging findings may be attributed to a combination of inflammatory exudates with necrotizing granulomatous inflammation and leakage of Gd from the capillaries to the surrounding area. In the present case, CE FLAIR is the most accurate sequence for depicting the distribution of lesions, and it should be considered for detecting the meningeal and leptomeningeal lesions.
RM exhibits diverse laboratory findings and may mimic several neurological diseases, infections, and malignancies.6) ACPA is an autoantibody directed against cyclic citrullinated peptides found in the joints and blood of patients with RA and is useful for early diagnosis of RA because it presents prior to the appearance of the symptoms of joint inflammation.20) The ACPA index, which is calculated by dividing the ACPA CSF/serum ratio by the IgG CSF/serum ratio, is considered to be more useful than serum ACPA alone6) for diagnosing and monitoring RM. This may be because the underlying disease results in higher baseline inflammatory cytokine levels.21) Screening for serum ACPA in patients with asymmetric meningeal or leptomeningeal involvement seen on brain MRI is acceptable. If serum ACPA levels are increased, testing for CSF ACPA and CSF IgG may reduce repeat testing and minimize a missed diagnosis.
In this case, the patient developed RM while receiving salazosulfapyridine, bucillamine, and iguratimod. If RM develops while taking medications for RA, there is no consensus on the next treatment option. Although a certain number of RM case reports are believed to include drug-induced meningitis,18) its diagnosis is difficult in cases wherein the same medication has been employed for a long period, and the pathogenesis of which is not well understood.22) Considering that she had previously developed interstitial pneumonia, she was unable to use methotrexate (MTX), which is the first choice for RA. She also had to discontinue anti-tumor necrosis factor (TNF) alpha agents, which were previously utilized for cases where MTX could not be employed or was not sufficiently effective, due to liver dysfunction. Rituximab, a monoclonal antibody against the CD20 surface marker expressed on B cells, is often utilized in patients who are resistant to treatment with the two drugs mentioned above; nevertheless, rituximab is not covered by health insurance in Japan and cannot be utilized. She is now receiving tocilizumab subcutaneously and prednisolone orally. Tocilizumab is a recombinant humanized anti-interleukin-6 receptor monoclonal antibody and treats multiple autoimmune diseases effectively. It is effective for RA and is especially more potent than anti-TNF alpha agents in the absence of MTX.23) Reportedly, tocilizumab is more effective than rituximab in RA patients with low or absent B-cell lineage expression signatures in synovial tissue.24) Nevertheless, tocilizumab is not believed to cross the blood-brain barrier because of its high molecular weight.25) Hence, these findings cannot be directly applied to CNS diseases. The immunohistochemical findings obtained by biopsy may be reflected in future treatments.
In conclusion, even in patients with well-controlled RA, RM is a rare but must be critically considered. Despite that biopsy is still the gold standard for definitive diagnosis, MRI findings on CE-FLAIR images and ACPA titers may help screen and monitor treatment responses in patients with RM. However, to validate these findings, larger studies are required.
All authors declare that there are no conflicts of interest (COIs) concerning this article according to the criteria of The Japan Neurosurgical Society (JNS). The authors (TS, YA, SS, and SO) who are members of JNS have registered online self-reported COI disclosure statement forms through the website for JNS members.
