Table 2.
Differential table of IgG4-related coronary periarteritis.
| Differential | Clinical Presentation | CT Findings | PET Findings |
|---|---|---|---|
| IgG4-Related Coronary Periarteritis | Ranges from asymptomatic to symptoms of coronary ischemia or myocardial infarction. | Nodular or rind-like coronary arterial wall thickening. Stenosis, luminal ectasia, and aneurysm formation may be associated. | Variable FDG uptake. |
| Kawasaki Disease | Recent history of fever, conjunctival injection, mucositis, cervical lymphadenopathy, rash, and peripheral extremity edema or desquamation. | Coronary aneurysms, usually with calcifications and without pseudotumor formation. May stenose. | Unknown. |
| Polyarteritis Nodosa | Depends on organ involvement. Most common cardiac presentation is heart failure. | Coronary involvement may include stenosis, dilation, and dissection without pseudotumor formation. | Unknown. |
| Takayasu Arteritis | History of fever, fatigue, upper body pains, upper extremity pain and neuropathy. | Aortic and large vessel stenosis, dilation, and wall thickening. Coronary involvement rare but may include stenosis and aneurysms with possible calcifications. | Unknown. |
| Churg-Strauss Syndrome | History of allergic rhinitis, nasal polyposis, and bronchial asthma. Findings of myocarditis, heart failure, myocardial infarction, pericarditis, and pericardial effusion. | Coronary involvement rare but may include stenosis or giant aneurysms. | Unknown. |
| Lymphoma | “B symptoms” of fever, weight loss, night sweats, and generalized pruritis. Cardiac presentation includes pericardial effusion, heart failure, and AV block. | Enlarged or matted lymph nodes. May surround or encase coronary arteries. | Expected FDG uptake. |
| Castleman’s Disease | Associated with HIV and HHV-8. May present with symptoms related to a mass in unicentric disease and “B symptoms” in multicentric disease. | Largely indistinguishable from lymphoma. Case report of a coronary pseudotumor with calcifications. | Unknown. |
| Rosai-Dorfman Disease | Bilateral painless cervical lymphadenopathy. | Homogeneous soft tissue densities and local lymphadenopathy. Masses may surround vessels, including coronaries, and are usually without significant calcifications. | Unknown. |