Differential Diagnosis for a 69-year-old Male with GPA and Rapidly Expanding Lymphadenopathy
Single Most Likely Diagnosis
- Relapse of Granulomatosis with Polyangiitis (GPA): Given the patient's history of GPA with polyangitis, ANCA vasculitis, and a biopsy showing necrotizing granulomatosis consistent with GPA, a relapse of the disease is the most likely explanation for the rapidly expanding lymphadenopathy. GPA can affect various organs, including the lymph nodes, and its relapse can manifest with a wide range of symptoms.
Other Likely Diagnoses
- Lymphoma: Patients with chronic inflammatory diseases, including GPA, have an increased risk of developing lymphoma. The rapidly expanding lymphadenopathy could be a sign of lymphoma, which would require immediate attention and a different treatment approach.
- Infections: Given the patient's immunocompromised state due to GPA and potential immunosuppressive treatment, infections such as tuberculosis or fungal infections could cause lymphadenopathy. These infections can mimic a relapse of GPA or other conditions and need to be ruled out.
- Drug-induced Lymphadenopathy: Certain medications, including those used to treat GPA, can cause lymphadenopathy as a side effect. This is an important consideration in a patient with a history of GPA and polyangitis.
Do Not Miss Diagnoses
- Malignancy (e.g., Metastatic Cancer): Although less likely, metastatic cancer to the lymph nodes could present with rapidly expanding lymphadenopathy. Given the potential for serious outcomes, it's crucial not to miss this diagnosis.
- Invasive Fungal Infections: In immunocompromised patients, invasive fungal infections can be life-threatening and may present with lymphadenopathy among other symptoms.
- Tuberculosis: Reactivation of latent tuberculosis or new infection can occur in immunocompromised individuals and may manifest as lymphadenopathy.
Rare Diagnoses
- Kikuchi-Fujimoto Disease: A rare form of lymphadenitis that can mimic lymphoma or other conditions, including GPA relapse. It's more common in younger females but can occur in any demographic.
- Castleman Disease: A rare disorder that involves an overgrowth of cells in the body's lymph nodes. It can present with lymphadenopathy and systemic symptoms, potentially mimicking a relapse of GPA or lymphoma.
- IgG4-related Disease: A condition characterized by an elevated level of IgG4, a type of antibody, which can cause inflammation in various organs, including the lymph nodes, and mimic other conditions such as GPA or lymphoma.