Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Lymphocytic Interstitial Pneumonia
- Radiologic Findings
- HRCT images shows (Figure 1-3) show diffuse reticulation, diffuse GGO, and traction bronchiectasis with both lower lobe dominancy. Chest radiograph (Figure 4) shows both lower lung dominant reticular opacity and diffuse ground-glass opacity (GGO). We can see a 5.5cm sized bulla in retrocardiac area of the left lower lobe.
- Brief Review
- The lymphocytic interstitial pneumonia (LIP) is a rare disease characterized by diffuse infiltration of lymphocytes and plasma cells within the lung parenchyma. It is usually associated with various conditions, including HIV or EBV infection, Sj�ren's syndrome, pernicious anemia, and autoimmune hemolytic anemia. Especially, 25% of all LIP cares are associated with Sj�ren's disease.
Reflecting diffuse infiltration of lymphocytes and plasma cells, HRCT usually reveals thickening of perilymphatic interstitium, ground-glass opacity, and poorly defined centrilobular nodules. Furthermore, multiple variable sized thin-walled cystic airspaces are common finding, and should be good differential point from other idiopathic interstitial pneumonias. Other findings include lymphnode enlargement (in about 50% of cases) and bronchiectasis.
Definite diagnosis can be made with lung biopsy. Although there is no standard treatment for LIP, steroid therapy is commonly used and other immunosuppressive drugs may be combined.
Prognosis is variable, and can be grave. Therefore, keen radiologic suspicion and early diagnosis is crucial.
- References
- 1. T Johkoh, N Muller, H Pickford, et al. Lymphocytic interstitial pneumonia: thin-section CT findings in 22 patients. Radiology 1999;212:567
- Keywords
- lung, lymphoproliferative disease, Interstitial lung disease, ILD,