Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Pyothorax-associated lymphoma
- Radiologic Findings
- Fig 1. Chest PA radiograph shows a large mass with rim calcification occupying the left hemithorax.
Fig 2-4. CT scans demonstrate a substantial mass within the left pneumonectomy cavity, featuring an enhancing soft tissue component and a protrusion into the anterior chest wall. A small lymph node is noted at the level of the left 8th/9th rib.
Fig 5. MRI reveals a strongly diffusion-restrictive lesion corresponding to the protruding mass in the anterior chest wall. The upper image represents the B1000 sequence, while the lower image shows the Apparent Diffusion Coefficient (ADC) map.
- Brief Review
- Pyothorax-associated lymphoma (PAL) is a rare type of non-Hodgkin's lymphoma strongly linked to long-standing chronic empyema, often resulting from artificial pneumothorax therapy for tuberculosis, which was common before 1970. The latency period between therapy and PAL onset typically exceeds 20 years, and in many cases, stretches beyond 40 years. This disease primarily affects men with a mean diagnosis age of 60–71 years. Symptoms include chest pain, palpable chest wall masses, respiratory issues, and systemic signs like fever and weight loss. Histologically, PAL is most commonly diffuse large B-cell lymphoma, frequently associated with Epstein-Barr virus (EBV) infection.
Imaging studies, including chest radiographs, CT scans, and gallium scans, are critical for diagnosing PAL. On chest radiographs, PAL typically appears as extrapulmonary soft-tissue masses associated with empyema cavities, often accompanied by pleural calcifications and chest wall abnormalities. On CT imaging, pyothorax-associated lymphoma (PAL) typically presents as a soft-tissue mass adjacent to an empyema cavity. These masses are commonly lenticular (60%) or crescent-shaped (20%) and are eccentrically located along the empyema margin. Internally, they are heterogeneous, with necrotic areas observed in 60% of cases—a distinctive feature of PAL. The masses are most often found on the lateral costal pleura (50%) or the costophrenic angle (30%). Chest wall invasion is common (75%), often involving osteolytic rib lesions (50%). Air-fluid levels or air bubbles within the empyema cavity frequently indicate fistula formation caused by tumor invasion, a finding that helps distinguish PAL from benign empyema complications. PAL masses usually exhibit external or symmetric growth, with rare internal expansion. They often invade adjacent structures such as the chest wall, ribs, lung parenchyma, and, in some cases, the abdominal cavity via the diaphragm. The relationship between the mass and the empyema cavity is a key diagnostic feature, with the masses always located at the empyema’s edge. This positional clue aids in guiding biopsies. CT is crucial for identifying PAL, differentiating it from benign empyema or other malignancies, and assessing disease extent for optimal management.
PAL has a poor prognosis, with a high mortality rate. Most patients succumb within two years of diagnosis despite treatments, which may include chemotherapy, radiation therapy, or combinations of both. Its malignant nature and rare occurrence emphasize the importance of early detection.
- References
- 1. Ueda T, Andreas C, Itami J, Miyakawa K, Fujimoto H, Ito H, Roos JE. Pyothorax-associated lymphoma: imaging findings. AJR Am J Roentgenol. 2010 Jan;194(1):76-84.
- Keywords