Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Multicentric castleman disease (plasma cell type)
- Radiologic Findings
- Chest PA view shows bilateral hilar enlargement and multiple nodular opacities in both lung fields. CT scan shows multiple enlarged lymph nodes in the mediastinum, bilateral hila and axillae. There is poorly defined ground-glass opacities in centrilobular distribution and suspicious interstitial thickening in both lungs.
- Brief Review
- Castleman disease is a non-clonal lymphoproliferative disorder and one of the more common causes of nonneoplastic lymphadenopathy. There are two major histopathologic classification of Castleman disease: Hyaline vascular type & Plasma cell type.
Plasma cell type much more common multicentric form occurs in an older age group, with a median age in the 6th decade. Plasma cell type of Castleman disease is frequently associated with (a) systemic manifestations such as fever, night sweats, and malaise; (b) hematologic and immunologic abnormalities such as anemia, thrombocytopenia, and hyperglobulinemia;
and (c) splenomegaly (5)
Plasma cell type of Castleman disease typically demonstrates less avid enhancement after contrast material administration as compared to the hyaline vascular type. Calcification is uncommon. Plasma cell Castleman disease occurs more frequently as multicentric Castleman disease, with diffuse lymphadenopathy that involves multiple anatomic regions, including hilar and mediastinum, abdominal, pelvic, or cervical lymphadenopathy. Diffuse centrilobular pulmonary parenchymal nodular opacities in cases of plasma cell Castleman disease are often associated with lymphocytic interstitial pneumonitis.
- References
- 1. Bonekamp D, Horton KM, HrubanRH, et al. Castleman disease the greast mimic. Radiographics 2011 ;31 :1793-1807.
2. Ko SF, Hsieh MJ, Ng SH, et al. Imaging spectrum of Castleman’s disease. AJR 2004 ;182 :769-775.
- Keywords
- Lung, Lymph node,