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1 ary lesions in the lungs along with necrotic mediastinal lymphadenopathy.
2 ted Castleman disease manifests with diffuse mediastinal lymphadenopathy.
3 At CT, all lesions manifested with diffuse mediastinal lymphadenopathy.
4 ilar lymphadenopathy, mediastinal masses, or mediastinal lymphadenopathy.
5 One patient with a mediastinal mass also had mediastinal lymphadenopathy.
6 pital for examination of bilateral hilar and mediastinal lymphadenopathy.
8 FDG-PET also accurately characterized hilar/mediastinal lymphadenopathy in 12 patients with associat
11 and more interlobular septal thickening and mediastinal lymphadenopathy on computed tomography of th
12 enty-six patients with NSCLC with absence of mediastinal lymphadenopathy on CT were enrolled and foll
14 rdial delayed enhancement of the septum, and mediastinal lymphadenopathy should raise the suspicion f
15 osed in 5 of 77 patients (6.5%), while hilar/mediastinal lymphadenopathy was found in 25 of 76 patien
16 In 29 patients, endoscopic US-guided FNAB of mediastinal lymphadenopathy was performed as a component
17 rdial delayed enhancement of the septum, and mediastinal lymphadenopathy were more often see in those
19 o guide TBNA in 12 consecutive patients with mediastinal lymphadenopathy who had previously undergone
20 (PET) scan confirmed the lung lesion and the mediastinal lymphadenopathy without distant metastases.
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