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1 n remission, and one with toxoplasmosis plus lymphomatoid granulomatosis).
2 n of central nervous system involvement from lymphomatoid granulomatosis.
3 monary T- or NK-cell angiocentric lymphomas (lymphomatoid granulomatosis), 12/19 T-cell anaplastic la
4 ma closely mimics the full spectrum of human lymphomatoid granulomatosis, an EBV-associated malignanc
5 lfa-2b is efficacious for treating low-grade lymphomatoid granulomatosis and hence reducing progressi
6 crosis and vascular damage from EBV-positive lymphomatoid granulomatosis and nasal or nasal-type T/na
7 mally elevated in patients with EBV-positive lymphomatoid granulomatosis and nasal or nasal-type T/NK
8 er with untreated, or relapsed or refractory lymphomatoid granulomatosis at the National Cancer Insti
11 n this study, we hypothesised that low-grade lymphomatoid granulomatosis is immune-dependent and high
13 Epstein-Barr virus (EBV) infection, such as lymphomatoid granulomatosis (LG) or post-transplant lymp
17 de disease, whereas patients with high-grade lymphomatoid granulomatosis showed expected responses to
18 , and he had a biopsy-confirmed diagnosis of lymphomatoid granulomatosis that evolved into fatal B-ce
19 y-one patients with pathologically confirmed lymphomatoid granulomatosis were enrolled in a natural h