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1 ure rates in patients with and those without mediastinal abnormalities at preoperative PET were compa
2 ung parenchymal, airway, pleural, hilar, and mediastinal abnormalities systematically reviewed initia
3  for enteral nutrition (n = 18), drainage of mediastinal abscess (n = 4), gastric decompression (n =
4 thickness oesophageal segment destroyed by a mediastinal abscess and leading to direct communication
5                                              Mediastinal activity appears to be constant over time an
6 t computed tomography images showed enlarged mediastinal adenopathy with increased [(18)F]fluorodeoxy
7 vealed a 5-cm right upper lobe mass, without mediastinal adenopathy, and a 6-cm cystic mass in the sp
8 ecoming standard of care for the sampling of mediastinal adenopathy.
9 h EBUS-TBNA requires a detailed knowledge of mediastinal anatomy.
10 n they involve either side of the neck, with mediastinal and distant metastases.
11 PV, and accuracy of hyperdense non-calcified mediastinal and hilar lymph nodes, known as "brilliant l
12 jective noise at the level of the trachea on mediastinal and lung parenchymal images (P < .001) and n
13 tion of the pleural cavity rapidly activates mediastinal and pericardial FALCs.
14  scored as lymphatic type 1 (little or no T2 mediastinal and supraclavicular signal) to type 4 (T2 si
15 solidation (63%), pulmonary nodules (31.4%), mediastinal and/or hilar lymphadenopathy (23%), mass-lik
16 encing of precursor, primary (testicular and mediastinal) and chemoresistant metastatic human GCTs, w
17 pectoral, supraclavicular, internal mammary, mediastinal, and abdominal nodes.
18 lysed based on parenchymal, airway, pleural, mediastinal, and vascular sequelae of PTB.
19       Classical Hodgkin lymphoma and primary mediastinal B cell lymphoma (PMBCL) are related lymphoma
20 es: diffuse large B-cell lymphoma or primary mediastinal B-cell lymphoma (DLBCL/PMBCL; n = 28), low-g
21 f Blood, Ceriani et al introduce, in primary mediastinal B-cell lymphoma (PMBCL), a new prognostic fa
22 clerosis Hodgkin lymphoma (NSHL) and primary mediastinal B-cell lymphoma (PMBL) are the common types,
23                                      Primary mediastinal B-cell lymphoma (PMBL) is a rare but aggress
24                                      Primary mediastinal B-cell lymphoma (PMBL) is a subtype of diffu
25  79), Burkitt lymphoma (BL; n = 36), primary mediastinal B-cell lymphoma (PMBL; n = 12), B-cell lines
26 btype showed biological overlap with primary mediastinal B-cell lymphoma and conferred excellent prog
27                                      Primary mediastinal B-cell lymphoma is a distinct subtype of dif
28 d histology (diffuse large B-cell lymphoma v mediastinal B-cell lymphoma v Burkitt lymphoma or Burkit
29 nsformed from any indolent lymphoma, primary mediastinal B-cell lymphoma, and follicular lymphoma gra
30 uding diffuse large B-cell lymphoma, primary mediastinal B-cell lymphoma, and transformed follicular
31  with diffuse large B-cell lymphoma, primary mediastinal B-cell lymphoma, or transformed follicular l
32 herapy in 51 patients with untreated primary mediastinal B-cell lymphoma.
33 ed for radiotherapy in patients with primary mediastinal B-cell lymphoma.
34 cases were molecularly classified as primary mediastinal B-cell lymphoma.
35 uding classical Hodgkin lymphoma and primary mediastinal B-cell lymphoma.
36 th diffuse large B-cell lymphoma and primary mediastinal B-cell lymphoma.
37 cell lymphoma, Hodgkin lymphoma, and primary mediastinal B-cell lymphoma.
38                                              Mediastinal B-cell lymphomas present in the mediastinum
39  of 6 with gray zone, 1 CR of 6 with primary mediastinal B-cell, and 1 CR of 3 with posttransplant ly
40                                              Mediastinal biopsy was the most frequent (26 subjects).
41                                              Mediastinal bleeding is common following pediatric cardi
42 ajor complications and postoperative 24-hour mediastinal blood loss.
43 or with residual [18F]FDG activity below the mediastinal blood pool (MBP) uptake.
44          (68)Ga-DOTATOC uptake was higher in mediastinal blood pool at the 1-h time point (P = 0.018)
45      Patients with stage IA to IIA HL and no mediastinal bulk underwent PET assessment after three cy
46 als involving patients without B symptoms or mediastinal bulk, a score of 5 rather than a positive PE
47 age I and II (<3 nodal sites, no B symptoms, mediastinal bulk, or extranodal extension) enrolled betw
48                                   Air in all mediastinal compartments was also associated with increa
49 er, CT findings of posterior PNM, air in all mediastinal compartments, and concurrent hemothorax are
50 ertrophy of the bronchial arteries along the mediastinal course, diffuse thickening of the walls of n
51 ratification of early-stage HL patients with mediastinal disease and thus contribute to risk-adapted,
52                      LDH level at diagnosis, mediastinal disease, and combined BM-positive/CNS-positi
53 thermore, among the patients with refractory mediastinal disease, our model distinguished those who w
54 ies, such as pulmonary fibrosis, pleural and mediastinal disease, solid lesions, bronchial disease, a
55 vs 21 [14%]), and respiratory, thoracic, and mediastinal disorders (13 [9%] vs 17 [12%]).
56 ssure on the neighboring lung parenchyma and mediastinal displacement.
57 s an overall difference in mean (SD) 24-hour mediastinal drain loss: cohort, 12.6 mL/kg (6.4); FC, 11
58 n, if so, management may be conservative but mediastinal drainage is important if significant extrava
59 D103(+) myeloid dendritic cells migrating to mediastinal draining lymph nodes and bearing migratory a
60                    After TAC, enlarged heart mediastinal draining lymph nodes showed a high density o
61 trophils and monocytes and then delivered to mediastinal draining lymph nodes.
62 lated with an increase in donor cells in the mediastinal draining lymph nodes; increased lymphatic ve
63 re complicated by extensive subcutaneous and mediastinal emphysema that occurred without any obvious
64 a previous chest X-ray that showed bilateral mediastinal enlargement; for this purpose, enhanced ches
65 etion was confirmed in arterioles from human mediastinal fat in patients with essential hypertension
66 rticularly helpful in patients with positive mediastinal findings at preoperative PET.
67 rising in this setting genetically resembled mediastinal GCTs rather than de novo myeloid neoplasms.
68                                 The anterior mediastinal germ cell tumors (GCTs) are the most common
69 ymphoma (PMBL) are the common types, whereas mediastinal gray-zone lymphoma (MGZL) is extremely rare
70 s intermediate between PMBL and NSHL, called mediastinal gray-zone lymphomas, have been described.
71        For patients with stage I or II bulky mediastinal HL, no substantial statistically significant
72 nalysis in patients with stage I or II bulky mediastinal Hodgkin lymphoma (HL).
73 objective noise at the level of the aorta on mediastinal images (P = .507); (b) significantly higher
74  1279 Hodgkin lymphoma patients treated with mediastinal irradiation and quantified the standard inci
75 vors of Hodgkin's lymphoma (HL) who received mediastinal irradiation have an increased risk of corona
76 he excess risk of cardiac interventions from mediastinal irradiation.
77 d survivors of HL who survived 5 years after mediastinal irradiation.
78                                    Blood and mediastinal isolates were characterized as CA-MRSA by pu
79         Classical Hodgkin lymphoma (cHL) and mediastinal large B-cell lymphoma (MLBCL) are lymphoid m
80                                              Mediastinal large B-cell lymphoma (MLBL) represents 2% o
81 ssification of children and adolescents with mediastinal large B-cell lymphoma (MLBL), and highlight
82                       Cure rates for primary mediastinal large B-cell lymphoma (PMBCL) have improved
83                                      Primary mediastinal large B-cell lymphoma (PMBCL) is a subtype o
84                  The pathogenesis of primary mediastinal large B-cell lymphoma (PMBCL) is incompletel
85                                      Primary mediastinal large B-cell lymphoma (PMBL) cells depend on
86                                      Primary mediastinal large B-cell lymphoma (PMBL) represents a cl
87 natures to those of diffuse LBCL and primary mediastinal large B-cell lymphoma (PMBL).
88 ment options for relapsed/refractory primary mediastinal large B-cell lymphoma (rrPMBCL) are limited,
89 Patients with relapsed or refractory primary mediastinal large B-cell lymphoma (rrPMBCL) have a poor
90                                      Primary mediastinal large B-cell lymphomas (PMBLs) are aggressiv
91 ling molecules are down-regulated in primary mediastinal large B-cell lymphomas and Hodgkin's lymphom
92 ydatid presents as a fluid-density posterior mediastinal lesion on chest radiograph with destruction
93 est radiograph was suggestive of a posterior mediastinal lesion with fluid density and destruction of
94 f an elderly male with incidental finding of mediastinal lesion, which was initially thought to be an
95         In a total of 208 patients, 215 lung/mediastinal lesions (seven patients were biopsied twice)
96         For example, resolution modeling for mediastinal lesions and iterative deconvolution for lung
97  intraperitoneal inoculation, 1 to 8% of the mediastinal LN cells were infected.
98 of CD69+/CD103+ CD8+ T cells to the draining mediastinal LN via the lymphatic vessels, which we term
99 ns, and COX-2 inhibition markedly suppressed mediastinal LNM.
100  to have prognostic implications despite the mediastinal LNs being histologically negative.
101 ctive value for detecting lymph nodes in any mediastinal location and for patients without lymph node
102 sport of live bacteria from the lungs to the mediastinal lymph node (MDLN).
103 cell transfer, the T cells isolated from the mediastinal lymph node (med-LN) of aged animals exhibite
104                                              Mediastinal lymph node (MLN) enlargement on chest comput
105 atic proliferation were largely found in the mediastinal lymph node (mLN), rather than the airways; h
106 l recruitment mainly occurs in the posterior mediastinal lymph node (pMLN).
107 ium tuberculosis occurs in the lung-draining mediastinal lymph node and requires transport of M. tube
108                         After stimulation of mediastinal lymph node and spleen cells with UV-inactiva
109                                              Mediastinal lymph node and spleen epitope-specific CD8(+
110  significantly enhanced in the lung-draining mediastinal lymph node and spleen, and there is an incre
111  aortic surgery, the patient had undergone a mediastinal lymph node biopsy.
112 d the majority of prion-bearing cells in the mediastinal lymph node by six hours, indicating intranod
113                                              Mediastinal lymph node cells from Flt3L-treated mice sec
114           The in vitro cytokine secretion of mediastinal lymph node cells was determined using ELISA.
115 igh-affinity ligand CD155 was upregulated in mediastinal lymph node dendritic cells from allergic mic
116 m mass in the right upper lobe with multiple mediastinal lymph node disease ( Fig 1 ).
117 ned in a 1:1 ratio to SABR or lobectomy with mediastinal lymph node dissection or sampling.
118 l-cell lung cancer (NSCLC) is lobectomy with mediastinal lymph node dissection or sampling.
119  He then undergoes right upper lobectomy and mediastinal lymph node dissection, which demonstrate no
120                                Analysis of a mediastinal lymph node from one patient highlighted the
121 omography (FDG-PET/CT) imaging for detecting mediastinal lymph node involvement in patients with pote
122 l outcomes, including pathologic evidence of mediastinal lymph node involvement, distant metastasis,
123                    Sensitivity for detecting mediastinal lymph node metastases, using pathologic conf
124  with suspected lung cancer, the presence of mediastinal lymph node metastasis is a critical determin
125                                          The mediastinal lymph node NK cells were activated, expressi
126 h alloantigen-induced expression of IL-10 in mediastinal lymph node or splenic T cells, intragraft ex
127                                      Lastly, mediastinal lymph node re-stimulation experiments showed
128 mputed tomography screening with and without mediastinal lymph node resection (MLNR) under an Institu
129  as early as 2 days post-IN inoculation; the mediastinal lymph node was an early site of replication
130          Negative regulation of cells in the mediastinal lymph node was minimal compared with that pr
131  airways (bronchoalveolar lavage), lung, and mediastinal lymph node were examined 10 d postinfection
132 t ILC2s accumulated equally in the recipient mediastinal lymph node.
133 lored DC subset present in the lung-draining mediastinal lymph node.
134  lung and enhanced the T(H)2 response in the mediastinal lymph node.
135 d with a decrease in the number of DC in the mediastinal lymph node.
136 sulted in an abolished T(H)2 response in the mediastinal lymph node.
137 berculosis Ag85B-specific CD4 T cells in the mediastinal lymph node.
138 ungs, it decreased trafficking of DCs to the mediastinal lymph node.
139                        Unlike examination of mediastinal lymph nodes (LNs), which depends on surgical
140 electively accumulated in the myocardium and mediastinal lymph nodes (med-LN) of infarcted mice, acqu
141 lymphocytes rapidly redistribute to regional mediastinal lymph nodes (MedLNs) during influenza infect
142 nd, to a lesser extent, in the lung-draining mediastinal lymph nodes (medLNs) of virus-infected mice.
143 ent activation and migration to the draining mediastinal lymph nodes (MLNs) during IV infection.
144 0) levels remained elevated in the lungs and mediastinal lymph nodes (mLNs) throughout the acute LCMV
145 ce, by residual antigen in the lung-draining mediastinal lymph nodes (MLNs).
146 g naive CD4 T cells appear to migrate to the mediastinal lymph nodes along a CD62L-independent, CCR7-
147 acterized the DC population in the heart and mediastinal lymph nodes and analyzed long-term cardiac i
148 uppressed the accumulation of T cells in the mediastinal lymph nodes and lung granulomatous regions w
149 regs rapidly accumulate in the lung-draining mediastinal lymph nodes and lungs.
150 tivation of DN1 T cells was initiated in the mediastinal lymph nodes and showed faster kinetics compa
151  arise in mesenteric, axillary/brachial, and mediastinal lymph nodes and spleen based on differential
152  influenza-specific CD8 T cells in lymphoid (mediastinal lymph nodes and spleen) and nonlymphoid tiss
153                               T cells in the mediastinal lymph nodes and the intramyocardial endothel
154 oreover, this drainage can occur directly to mediastinal lymph nodes and there is no interlobar lymph
155  failed to proliferate as extensively in the mediastinal lymph nodes as in mice infected only with BC
156 ere is a large right hilar mass and enlarged mediastinal lymph nodes but no pulmonary emboli.
157 ures yet contributed to TH2 expansion in the mediastinal lymph nodes but not in the lungs.
158  are retained in the peritoneum and draining mediastinal lymph nodes for a prolonged period following
159                               Granulomas and mediastinal lymph nodes from active-disease but not late
160                                              Mediastinal lymph nodes from airway-sensitized Abcg1(-/-
161 in vivo and likewise detect mKATE2(+) DCs in mediastinal lymph nodes from infected mice.
162 rformance of MR imaging in staging hilar and mediastinal lymph nodes in NSCLC on both a per-patient a
163 illus but greatly diminishes their egress to mediastinal lymph nodes independent of neutrophil microb
164 ession of interleukin (IL)-17 transcripts in mediastinal lymph nodes induced by effector cells alone.
165                                   Therefore, mediastinal lymph nodes may be false-positive on (18)F-F
166  was stratified according to the presence of mediastinal lymph nodes measuring 1 cm or more in the sh
167 xamined the T(H)2 cytokine production in the mediastinal lymph nodes of DEP-exposed CCR2 knockout and
168 -specific CD4(+) T-cell proliferation in the mediastinal lymph nodes of mice.
169 ic analysis of CD11c(+) dendritic cells from mediastinal lymph nodes of the infected mice showed that
170 mic sites and morphologic characteristics of mediastinal lymph nodes on spiral computed tomography fo
171 MATERIAL/METHODS: Anatomical distribution of mediastinal lymph nodes on spiral CT was reviewed in 39
172                                 In contrast, mediastinal lymph nodes remained nonluminescent througho
173 cells and more IFN-gamma from PBMC, BAL, and mediastinal lymph nodes than monkeys with latent infecti
174 f) of naive CD4 T cells appears to enter the mediastinal lymph nodes through a blood-to-lung-to-lymph
175 lumen and did not need to spread through the mediastinal lymph nodes to cause a systemic infection.
176 es in murine hearts, pericardial AT, spleen, mediastinal lymph nodes, and bone marrow were quantified
177 of infection, is initially restricted to the mediastinal lymph nodes, and does not involve other lymp
178 nocyte-derived dendritic cell numbers in the mediastinal lymph nodes, and increased T-helper type 2 (
179 n early (36 h-4 d) expansion of Tregs in the mediastinal lymph nodes, and later (12-16 d) increases i
180 l distribution and morphological patterns of mediastinal lymph nodes, as demonstrated on spiral CT, c
181 ration (EBUS-TBNA) biopsies of the hilar and mediastinal lymph nodes, but the feasibility and usefuln
182 there was a marked expansion of cells within mediastinal lymph nodes, comprised mainly of innate lymp
183    Such granulomas occur in the lung and the mediastinal lymph nodes, in the heart, and in other vita
184    Using this novel approach to study DCs in mediastinal lymph nodes, we observed that most blood-der
185 h2, Th17 cells, and Tregs, in the spleen and mediastinal lymph nodes, with expansion of splenic antig
186 dritic cells (DCs) in lung and lung-draining mediastinal lymph nodes, with lung CD11b(+) DCs displayi
187 hemagglutinin were primarily observed in the mediastinal lymph nodes.
188 h greater regulatory T cell expansion in the mediastinal lymph nodes.
189 ease in the size of the right hilar mass and mediastinal lymph nodes.
190 ptoms unexpectedly showed high FDG uptake in mediastinal lymph nodes.
191 ased C. neoformans-specific Th2 cells in the mediastinal lymph nodes.
192 e number of DCs carrying OVA in the lung and mediastinal lymph nodes.
193 ung conventional dendritic cells to draining mediastinal lymph nodes.
194 res across the lung epithelium into draining mediastinal lymph nodes.
195 s in the cervical lymph nodes but not in the mediastinal lymph nodes.
196 ncreased numbers of NK cells in the lung and mediastinal lymph nodes.
197 uickly out of the lung and into the thoracic/mediastinal lymph nodes.
198  charge translocate rapidly from the lung to mediastinal lymph nodes.
199  production in blood but not in the affected mediastinal lymph nodes.
200 asized to other lobes of the lung and to the mediastinal lymph nodes.
201  the lungs and central memory T cells in the mediastinal lymph nodes.
202 ion of pulmonary dendritic cells (DC) to the mediastinal lymph nodes.
203 RNA expression and impaired DC homing to the mediastinal lymph nodes.
204 ll as several enlarged hilar and ipsilateral mediastinal lymph nodes.
205                           In most cases, the mediastinal lymphadenectomy included the low para-esopha
206 nic space-occupying lesions (35%); abdominal/mediastinal lymphadenopathy (20%), ocular disease (18%)
207 nic space-occupying lesions (35%), abdominal/mediastinal lymphadenopathy (20%), ocular disease (18%),
208                       Patients with isolated mediastinal lymphadenopathy (IML) are a common presentat
209 ings outside the parenchymal lung, including mediastinal lymphadenopathy and pericardial effusion, sh
210  and more interlobular septal thickening and mediastinal lymphadenopathy on computed tomography of th
211 rdial delayed enhancement of the septum, and mediastinal lymphadenopathy should raise the suspicion f
212 osed in 5 of 77 patients (6.5%), while hilar/mediastinal lymphadenopathy was found in 25 of 76 patien
213 rdial delayed enhancement of the septum, and mediastinal lymphadenopathy were more often see in those
214 (PET) scan confirmed the lung lesion and the mediastinal lymphadenopathy without distant metastases.
215 pital for examination of bilateral hilar and mediastinal lymphadenopathy.
216 ary lesions in the lungs along with necrotic mediastinal lymphadenopathy.
217 ents were divided into four groups: anterior mediastinal lymphoma (group A, n=16), anterior mediastin
218  differences between prechemotherapy SUVt of mediastinal lymphoma and normal thymus and postchemother
219                                      De novo mediastinal lymphoma was correctly diagnosed by EBUS-TBN
220 n 100 cases of de novo or suspected relapsed mediastinal lymphoma was investigated by comparing EBUS-
221 nd accuracy of EBUS-TBNA in the diagnosis of mediastinal lymphoma were 89%, 97%, 98%, 83%, and 91%, r
222 diastinal lymphoma (group A, n=16), anterior mediastinal lymphoma with subsequent recurrence (group B
223 Vt of 3.4 or higher is a strong predictor of mediastinal lymphoma.
224 tion of normal thymus or thymic rebound from mediastinal lymphoma.
225 an be successful in the diagnosis of de novo mediastinal lymphomas and is ideally suited in distingui
226                           Emicro-Myc/DNMT3B7 mediastinal lymphomas have more chromosomal rearrangemen
227 NMT3B7 expression increases the frequency of mediastinal lymphomas in Emicro-Myc animals.
228                                    Recently, mediastinal lymphomas with features intermediate between
229 ibitor A20, in Hodgkin lymphomas and primary mediastinal lymphomas.
230  images demonstrated the presence of a large mediastinal mass (11x8 cm) located in the anterior media
231 or and transverse dimensions of the anterior mediastinal mass or thymus on axial CT images and measur
232 otic systems, involving the thoracic cavity (mediastinal mass resections, lobectomies, and esophagect
233 ximum standardized uptake values of anterior mediastinal mass, thymus (SUVt), and bone marrow at the
234 3 years (range, 14 to 59 years), and 46% had mediastinal masses >/=10 cm.
235 ssive tumors that typically present as large mediastinal masses in young women.
236 nts are usually young and present with large mediastinal masses.
237                               In response to mediastinal nerve stimulation, most IC neurons became ex
238 uisition and optimization, identification of mediastinal nodal and vascular structures, EBUS-TBNA sam
239 and colorectal cancers and of CT in lung and mediastinal nodal disease points to future tailored use
240  non-small-cell lung cancer with ipsilateral mediastinal nodal metastases (N2) have shown the feasibi
241 nths postoperatively and required a negative mediastinal node biopsy, no excessive vitamin intake, no
242 y significant decreases in FDG-avid lung and mediastinal node disease.
243 re biopsies of the lung mass and ipsilateral mediastinal nodes confirmed a poorly differentiated non-
244 F was seen in cases of mildly (18)F-FDG-avid mediastinal nodes in lung cancer and small liver metasta
245 , and cisplatin for relapse in the lungs and mediastinal nodes with a rising AFP level starting in Ja
246  (absence of (18)F-FDG-avid foci in nonhilar mediastinal nodes), symmetry (difference between left an
247  evidence of testicular, retroperitoneal, or mediastinal non-seminomatous germ cell tumours based on
248 e prognostic factors in both groups; primary mediastinal nonseminoma (group A) and elevations of alph
249 nd were particularly prevalent among primary mediastinal nonseminomas (72%).
250 avel the clonal relationship between primary mediastinal nonseminomas (PMNs) and hematologic somatic-
251                     Five (24%) of 21 primary mediastinal nonseminomatous GCTs are continuously diseas
252                                              Mediastinal nonseminomatous GCTs carry a poor prognosis
253        One in every 17 patients with primary mediastinal nonseminomatous GCTs develop an incurable he
254  metastatic disease, nor were there enlarged mediastinal or hilar lymph nodes.
255 perforation or anastomotic leak with limited mediastinal or pleural contamination.
256 safe and effective when performed along with mediastinal or pleural drainage.
257 s; (c) similar visual perception of noise on mediastinal (P = .132) and lung (P = .366) images, mainl
258 scopy and surgery); 13 patients had positive mediastinal PET findings, and 77 had negative mediastina
259 ediastinal PET findings, and 77 had negative mediastinal PET findings.
260 gnosis (benign vs malignant) on the basis of mediastinal pleural thickening (sensitivity, 81%; specif
261 e interpretation, the diagnostic accuracy of mediastinal pleural thickening, shrinking lung (hemithor
262 ations, performing substantially better than mediastinal pleural thickness and shrinking lung, and mi
263 e finding of frequent TP53 alterations among mediastinal primary nonseminomas may explain the more fr
264                                              Mediastinal primary site and two or more lines of prior
265  later therapy, platinum-refractory disease, mediastinal primary tumor site, nonseminoma histology, i
266                                              Mediastinal primary, pulmonary metastases, age, or doses
267 llaborative Group (IGCCCG) prognostic group, mediastinal primary, pulmonary metastases, and smoking a
268 se (12 vs 19%) but a higher rate of previous mediastinal radiation (8.4 vs 1.8%) (P < 0.001).
269               Recently, the recognition that mediastinal radiation is associated with significant lon
270 ns for TI included porcelain aorta, previous mediastinal radiation, chest wall deformity, and potenti
271 lude a combination of immunochemotherapy and mediastinal radiation.
272  efficacy and challenge the need for routine mediastinal radiation.
273 flect treatment bias and history of previous mediastinal radiation.
274 D for patients receiving a MHD of 20 Gy from mediastinal radiotherapy, compared with patients not tre
275 e has resulted in routine consolidation with mediastinal radiotherapy, which has potentially serious
276 apy, compared with patients not treated with mediastinal radiotherapy.
277    Global innervation assessed with heart-to-mediastinal ratio and washout rates was preserved in all
278 ons including cardiopulmonary resuscitation, mediastinal reexploration, placement on extracorporeal m
279 t commonly found in sacrococcygeal, gonadal, mediastinal, retroperitoneal, cervicofacial and intracra
280                               Mean counts in mediastinal ROI were computed from a fixed volume in 3 d
281 method that incorporates various cardiac and mediastinal segmentation schemes in which upper and lowe
282                                              Mediastinal sequelae included lymph node calcification (
283 ed inflammatory and atelectatic changes with mediastinal shift to the right.
284             The ratio between myocardial and mediastinal signal at 15 and 125 min and extrapolated at
285                                          The mediastinal signal was measured and fitted to a linear m
286                              On MVA, primary mediastinal site (P < .001), two or more lines of prior
287                      Features extracted from mediastinal sites were highly predictive of primary refr
288 aphy-guided transbronchial needle aspiration mediastinal staging (EBUS group) in 62 patients (37.3%)
289 NA) is an established technique for invasive mediastinal staging of non-small cell lung cancer (NSCLC
290 nded as a first-line diagnostic modality for mediastinal staging.
291 th parameters allowing for identification of mediastinal structures and adrenal glands is still much
292  pneumonectomy, proximal to or involved with mediastinal structures, abutting the chest wall, or recu
293 nition of EBUS/computed tomography images of mediastinal structures.
294 pattern with increased (sometimes exclusive) mediastinal thoracic lymph node involvement, indicating
295 graphy (PET/CT) in the management of primary mediastinal (thymic) large B-cell lymphoma (PMBCL).
296                            It is within this mediastinal tissue that T cells develop and are extensiv
297 edge of benign conditions that might mimic a mediastinal vascular pathology is important for therapeu
298  PS if a solid portion was detectable in the mediastinal window setting (nonmeasurable, < 50%, or > 5
299 nclusion Detection of a solid portion in the mediastinal window setting allows subsolid nodules to be
300   When a solid portion was measurable in the mediastinal window, the specificity for adenocarcinoma i

 
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