Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Pulmonary Intravascular Lymphomatosis
- Radiologic Findings
- Fig 1. Chest PA shows diffuse GGO in the both lungs.
Fig 2-5. CT scan shows diffuse GGO and centrilobular GGO nodules in both lungs with small amount of bilateral pleural effusion. It also shows splenomegaly on covered upper abdomen.
Fig 6. PET-CT shows diffuse FDG uptake in the both lungs.
- Brief Review
- Intravascular lymphomatosis, also known as malignant endotheliomatosis or angiotropic large-cell lymphoma, is a rare and distinct subtype of malignant lymphoma. It is characterized by the intravascular proliferation of neoplastic lymphoid cells, predominantly of B-cell lineage. Geographic variation has been observed in the clinical presentation. Reports indicate that patients diagnosed in Western countries exhibit a predilection for central nervous system and cutaneous involvement, whereas those diagnosed in Asian countries are more likely to present with hemophagocytic syndrome, bone marrow infiltration, fever, hepatosplenomegaly, and thrombocytopenia.
The main CT finding in pulmonary intravascular lymphomatosis is diffuse ground-glass opacity. Additional manifestations may include subpleural patchy areas of consolidation and reticulonodular lesions. These imaging features are nonspecific and can be seen in patients with diverse diseases, which may cause delayed diagnosis of this rapidly progressive and diffuse vascular tumorous condition.
- References
- 1. Cha MJ, Lee KS, Hwang HS, Kim TJ, Kim TS, Kim BT, Ko YH, Shim YM. Pulmonary Intravascular Lymphomatosis: Clinical, CT, and PET Findings, Correlation of CT and Pathologic Results, and Survival Outcome. Radiology. 2016 Aug;280(2):602-10. doi: 10.1148/radiol.2016151706.
- Keywords
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