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Diagnostic Dilemma of Paraneoplastic Rheumatic Disorders: Case Series and Narrative Review
Youngmin Cho1, Erik W Anderson2, Sara J Guevara3
1Internal Medicine, Northeast Georgia Medical Center Gainesville, Gainesville, USA.
Paraneoplastic rheumatic disorders (RDs) mimic common rheumatic conditions, often resisting standard treatment. Early recognition of these cancer-related symptoms is crucial for effective management and improved patient outcomes.
Area of Science:
- Rheumatology
- Oncology
- Internal Medicine
Background:
- Paraneoplastic rheumatic disorders (RDs) manifest as rheumatic symptoms preceding, concurrent with, or following malignancy diagnosis.
- These disorders are clinical expressions of occult cancer, distinct from direct tumor effects or metastasis.
- Diagnosis is challenging due to symptom overlap with common rheumatic diseases, complicating treatment decisions.
Observation:
- Presents four diagnostic dilemma cases of RD: leukocytoclastic vasculitis/C3 glomerulopathy, scleroderma, Raynaud's syndrome/lupus-like syndrome, and inflammatory myositis.
- Highlights minimal or no responsiveness of paraneoplastic RDs to standard rheumatic treatments.
- Reviews literature on paraneoplastic rheumatoid arthritis and rheumatic presentations associated with immune checkpoint inhibitors (ICIs).
Findings:
- Paraneoplastic RDs present atypically, requiring careful consideration beyond common rheumatic disease diagnoses.
- Standard rheumatic treatments are often ineffective for paraneoplastic RDs, underscoring the need for underlying cancer identification.
- Interdisciplinary collaboration is essential for accurate diagnosis and management.
Implications:
- Clinicians must be aware of atypical paraneoplastic RD presentations to avoid diagnostic delays.
- Prompt identification and treatment of the underlying malignancy are paramount for managing these disorders.
- Emphasizes the necessity of collaborative care between rheumatologists, oncologists, and primary care practitioners for optimal patient outcomes.
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