Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Lymphomatoid granulomatosis
- Radiologic Findings
- Fig 1. Chest PA shows multifocal consolidation with nodules and interstitial thickening in both lungs showing middle to lower lung zone predominance.
Fig 2-4. CT scans reveals multiple variable sized nodules and peribronchovascular consolidation with surrounding peripheral GGOs in both lungs showing middle to lower lung zone predominance.
Fig 5-7. Follow-up CT scans after 5 weeks showed increased extent of conglomerated nodules and consolidation with some lesions showing internal low attenuation.
- Brief Review
- Lymphomatoid granulomatosis (LG) is a rare, aggressive extranodal Epstein-Barr virus (EBV)-positive B-cell lymphoproliferative disease with reactive T-cells. While histopathologic features in patients with grade I LG are compatible with benign lymphocytic angiitis and granulomatosis, grade II LG follows an aggressive course, and grade III LG lesions should be considered diffuse large B-cell malignant lymphomas. LG usually manifests in the 5th or 6th decade of life, is more common among immunocompromised patients, and affects male subjects twice as often as it affects female subjects. The lungs are the most commonly involved site in patients with LG, with less frequent involvement of the skin, kidney, liver, and central nervous system. Although LG is a lymphoproliferative disorder, it is found less commonly in lymph nodes, the spleen, and bone marrow. Symptoms range from nonspecific systemic manifestations
- References
- 1. Chung JH, Wu CC, Gilman MD, et al. Lymphomatoid Granulomatosis: CT and FDG-PET Findings. KJR 2011;12(6):672-678.
2. Rezai P, Hart EM, Patel SK. Case 169: Lymphomatoid Granulomatosis. Radiology. 2011 May;259(2):604-9.
3. Sheehy N, Bird B, OBriain DS, Daly P, Wilson G. Synchronous regression and progression of pulmonary nodules on chest CT in untreated lymphomatoid granulomatosis. Clin Radiol 2004;59(5):451
- Keywords
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lung, lymphoproliferative disease, Epstein Barr virus, lymphomatoid granulomatosis,