This case involves a 63-year-old woman with rheumatoid arthritis who developed severe breathing difficulties and heart failure symptoms. After extensive testing, doctors discovered abnormal soft tissue surrounding her heart, major blood vessels, and kidneys. The medical team considered several rare conditions before identifying the most likely diagnosis through careful analysis of her symptoms, lab results, and imaging studies.
A Complex Case: Understanding Unexplained Heart Failure in a Patient with Rheumatoid Arthritis
Table of Contents
- Case Presentation
- Medical History and Background
- Diagnostic Testing and Results
- Imaging Findings
- Differential Diagnosis
- Clinical Impressions
- What This Means for Patients
- Source Information
Case Presentation
A 63-year-old woman arrived at Massachusetts General Hospital with concerning breathing difficulties that had persisted for two months. The patient first noticed she was "struggling" during hikes with friends, which was unusual since she had typically been the first to reach the end of trails. Over the following two weeks, she developed a dry cough, and her breathing problems progressed to the point where she needed to rest after just 10 minutes of routine treadmill and elliptical exercises.
Her symptoms became severe enough that she started using three pillows to sleep due to breathing discomfort. She also experienced abdominal distention, loss of appetite, and nausea after eating. These symptoms developed approximately one year after she had been diagnosed with rheumatoid arthritis, an autoimmune condition that causes joint inflammation and pain.
Medical History and Background
Fifteen months before her current symptoms began, the patient received a diagnosis of rheumatoid arthritis at another hospital's rheumatology clinic. She had presented with a six-month history of hand joint swelling and stiffness, along with skin tightening on several fingers. Her examination revealed swan-neck deformities in both hands, and X-rays showed marginal erosion of the hand bones.
Her initial laboratory testing showed normal white blood cell counts, thyroid function, and various other blood markers. Importantly, multiple antibody tests came back negative, including those for various autoimmune conditions and infections like Lyme disease and hepatitis. Her erythrocyte sedimentation rate (a marker of inflammation) was elevated at 55 mm/hr (normal 0-20), and C-reactive protein (another inflammation marker) was high at 25.2 mg/liter (normal <8.0).
She tested positive for rheumatoid factor and anti-citrullinated cyclic peptide antibodies, both markers consistent with rheumatoid arthritis. Treatment with methotrexate (a medication that suppresses the immune system) was started, and her joint swelling improved over the next two months.
The patient had other medical conditions including hypertension, diabetes mellitus, dyslipidemia (high cholesterol), a history of meningioma (a type of brain tumor) surgery, and a positive tuberculin skin test (though a more specific test for tuberculosis was negative).
Diagnostic Testing and Results
When her breathing symptoms developed, the patient underwent extensive testing. Her laboratory results showed progressively worsening inflammation markers and anemia:
- Erythrocyte sedimentation rate increased from 55 to 70 mm/hr
- C-reactive protein increased from 25.2 to 47.1 mg/liter
- Hemoglobin decreased from 12.5 to 9.8 g/dl (normal 12.0-16.0), indicating anemia
- N-terminal pro-B-type natriuretic peptide (a heart failure marker) was elevated at 389 pg/ml initially and rose to 672 pg/ml (normal <900)
Other tests included normal thyroid function, kidney function, and liver enzymes. She tested negative for COVID-19 infection. An electrocardiogram (ECG or EKG, a test that measures electrical activity of the heart) showed an abnormal heart rhythm, T-wave inversions (which can indicate heart strain), and prolongation of the corrected QT interval (QTc) to 509 milliseconds (a potential risk for abnormal heart rhythms).
Imaging Findings
The patient underwent multiple imaging studies that revealed concerning abnormalities:
Chest X-ray showed diffuse reticular interstitial markings (abnormal lung patterns) and an enlarged cardiac silhouette. Abdominal ultrasound revealed hepatic cysts, pleural fluid (fluid around the lungs), and hydronephrosis (swelling of the kidneys) on both sides.
Computed tomography (CT) scans of the chest and abdomen showed:
- Pericardial fluid and thickening (around the heart)
- Pleural fluid on the left side
- Pararenal fluid on both sides (around the kidneys)
- Infiltrative changes in the mediastinal fat (the area between the lungs)
- Extensive abnormal soft-tissue thickening in the retroperitoneal space surrounding both kidneys and the aorta
Echocardiography (ultrasound of the heart) showed normal heart size and pumping function but revealed an irregular echogenic structure approximately 2 cm thick adjacent to the aortic root, plus echogenic material within the pericardial space.
Cardiac magnetic resonance imaging (MRI) showed abnormal gadolinium enhancement (indicating inflammation or scarring) in the pericardium and soft-tissue edema in the mediastinum, but no involvement of the heart muscle itself.
Differential Diagnosis
The medical team considered several possible explanations for her symptoms and findings:
Infection: Given her immunosuppressive medication (methotrexate), doctors considered infections like tuberculosis or Lyme disease. However, previous testing for these conditions was negative, and she lacked typical infection symptoms like fever.
Cancer: The widespread soft-tissue abnormalities could suggest lymphoma or metastatic cancer. However, she had no weight loss, night sweats, or lymph node enlargement typically seen with cancers.
Inflammatory Diseases: Given her rheumatoid arthritis, doctors considered whether this might represent an unusual manifestation of her autoimmune disease. However, the extensive soft-tissue involvement would be atypical for rheumatoid vasculitis (inflammation of blood vessels related to rheumatoid arthritis).
IgG4-Related Disease: This immune-mediated fibroinflammatory condition can affect multiple organs. It typically shows elevated IgG4 levels (though normal levels don't rule it out) and specific patterns on tissue biopsy. The patient's retroperitoneal fibrosis and possible pancreatic involvement were consistent with this condition.
Erdheim-Chester Disease: This rare non-Langerhans cell histiocytic disorder affects multiple systems. Cardiovascular involvement occurs in about one-third of patients, with manifestations including pericardial disease (13% of cases), aortic and vascular disease (17%), and myocardial infiltration (25%). The imaging findings of periaortic involvement and circumferential soft-tissue coating of the thoracic and abdominal aorta were highly suggestive of this diagnosis.
Clinical Impressions
The medical team determined that the patient's presentation was most consistent with Erdheim-Chester disease, a rare disorder involving abnormal white blood cells (histiocytes) accumulating in tissues throughout the body. Key supporting evidence included:
- Soft-tissue thickening surrounding the aorta, kidneys, and heart
- Pericardial involvement causing heart failure symptoms
- Elevated inflammatory markers
- Lack of evidence for infection or cancer
The team recommended a biopsy of the affected tissue to confirm the diagnosis, as this would be necessary before starting appropriate treatment.
What This Means for Patients
This case illustrates several important points for patients with autoimmune conditions:
First, new symptoms like breathing difficulties in someone with rheumatoid arthritis should never be dismissed as simply part of the existing condition. This patient's exercise intolerance progressed over weeks to the point where she couldn't sleep lying down—clear red flags that warranted thorough investigation.
Second, autoimmune conditions can sometimes involve unexpected parts of the body. While rheumatoid arthritis typically affects joints, it can rarely involve other systems, or patients can develop additional autoimmune conditions that affect organs like the heart, lungs, or kidneys.
Third, diagnosis often requires multiple types of testing. This patient underwent blood tests, imaging studies (X-ray, CT, MRI, ultrasound), and heart tests (ECG, echocardiogram) to piece together the complete picture. Sometimes, a tissue biopsy is necessary for definitive diagnosis.
Finally, rare diseases require careful consideration by specialists. The doctors in this case considered multiple rare conditions before identifying the most likely diagnosis. Patients with complex medical situations often benefit from evaluation at specialized medical centers with experience diagnosing unusual conditions.
If you have an autoimmune condition and develop new symptoms—especially breathing difficulties, unexplained swelling, or exercise intolerance—it's important to communicate these changes to your healthcare team promptly. Early recognition and diagnosis of unusual complications can lead to more effective treatment and better outcomes.
Source Information
Original Article Title: Case 18-2025: A 63-Year-Old Woman with Dyspnea on Exertion
Authors: Malissa J. Wood, Carola A. Maraboto Gonzalez, Reece J. Goiffon, Eric D. Jacobsen, Bailey M. Hutchison, Dennis C. Sgroi, Eric S. Rosenberg
Publication: The New England Journal of Medicine, June 26, 2025
DOI: 10.1056/NEJMcpc2300897
This patient-friendly article is based on peer-reviewed research from the Case Records of the Massachusetts General Hospital series.