Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Pyothorax associated lymphoma
- Radiologic Findings
- Fig.1. Chest radiograph shows calcified pleural thickening and increased extrapulmonary opacity in right lower hemithorax.
Fig. 2-4. Contrast-enhanced CT scan reveals lenticular empyema cavity with calcified wall and adjacent soft tissue mass in right lower hemithorax. The mass is extending into the chest wall and peritoneal cavity with a direct invasion of ribs and diaphragm.
Fig. 5. 18D-FDG-PET CT scan shows strong FDG uptake of soft tissue mass.

- Brief Review
- Malignant neoplasm is a rare complication of chronic empyema. Various malignant cell types can be associated with chronic empyema including malignant lymphoma, squamous cell carcinoma, malignant mesothelioma, and various sarcoma.
Among them, malignant lymphoma is the most common cell type (pyothorax associated lymphoma; PAL) and the most are non-Hodgkin’s lymphoma of exclusively B-cell phenotype.
PAL is usually secondary to iatrogenic pneumothorax for the treatment of tuberculosis. The development of PAL is triggered by a longstanding empyema lasting for more than 20 years after pneumothorax treatment. The current pathophysiologic understanding of the disease suggests that both chronic Epstein-Barr virus infection and immunocompromised conditions from long-standing inflammation due to chronic empyema may be the causative mechanism of the development of PAL.
PAL manifests as a lenticular or crescent-shaped soft tissue mass straddling the thickened pleura at the margin of a coexistent empyema cavity. It has a tendency to invade adjacent structures including the chest wall, rib, lung, and diaphragm. Heterogeneous attenuation due to necrosis, simulating empyema necessitates, is common in PAL (which is uncommon in the other types of non-Hodgkin’s lymphoma).
There are previous reports of distant involvement of PAL including cervical, mediastinal and abdominal lymph nodes; superficial lymph nodes; adrenal glands; liver; stomach, kidneys; central nervous system; spleen; small intestine, and pancreas.
Differential diagnoses of PAL are benign complications of chronic empyema including empyema necessitates and other rare empyema-associated malignant tumors such as mesothelioma, angiosarcoma, malignant fibrous histiocytoma, and squamous cell carcinoma.
The prognosis of PAL is poor.
- References
- Ueda T et al. AJR 2010;194:76-84
Bae JY et al. J Korean Scoc Radiol 202;81(5):1109-1120
Bligh MP et al. Radiographics 2017;37:439-461
- Please refer to
- Case 1241 Case 1052 Case 460
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- Keywords