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1 aphy-guided GFN blocks were performed in the retroperitoneum.
2 apancreatic sites are bile duct, kidney, and retroperitoneum.
3 rbor either viable cancer or teratoma in the retroperitoneum.
4  to 13 years), including two patients in the retroperitoneum.
5 operitoneum is critical to prevent LR in the retroperitoneum.
6 internal calcific densities was noted in the retroperitoneum.
7  and were found to have only teratoma in the retroperitoneum.
8 parates the perirenal space from the central retroperitoneum.
9 nvolving the perirenal spaces or the central retroperitoneum.
10 al layers separated mesocolon and underlying retroperitoneum.
11 ended caudally surrounding the ureter in the retroperitoneum.
12                             Where apposed to retroperitoneum, 2 mesothelial layers separated mesocolo
13 e located in the lower extremities (94%) and retroperitoneum (6%).
14 n of residual postchemotherapy masses in the retroperitoneum and chest, including three who also had
15 dle was fully visualized as it traversed the retroperitoneum and entered the SMV.
16 n = 2), axillary nodes (n = 1), and both the retroperitoneum and the mediastinum (n = 2).
17 drenal myelolipomas, found most often in the retroperitoneum); and (d) myelolipomatous foci within ot
18  the aneurysm wall, fibrosis of the adjacent retroperitoneum, and rigid adherence of the adjacent str
19 emonstrate that the contiguous mesocolon and retroperitoneum are separated by mesothelial and connect
20 valuation revealed an internal hernia in the retroperitoneum at the site of the nephrectomy.
21 llections in the mediastinum, chest wall, or retroperitoneum; (b) malignancies that were detected, st
22     One prominent cluster (n = 37; 36 testis retroperitoneum), consisting of 26 (70%) good-risk (GR),
23 e located in the liver, lung, adrenal gland, retroperitoneum, gluteal muscle, inguinal mass, and subc
24 were mainly observed at the following sites: retroperitoneum in 5/8 patients (62.5%), cardiovascular
25     Overall, 56 patients (75%) had LR in the retroperitoneum, including 25 (93%) of 27 patients initi
26                                          The retroperitoneum is a major site of vascular leak and the
27  data suggest that meticulous control of the retroperitoneum is critical to prevent LR in the retrope
28 mmon tumor sites were vagina (n = 7), pelvis/retroperitoneum (n = 6), and bladder (n = 4).
29 ion is the posterior paraspinal mediastinum, retroperitoneum, neck and adrenal gland.
30  patients (4%) experienced recurrence in the retroperitoneum, of whom two patients died of disease.
31 ease from the perirenal space to the central retroperitoneum or from the central retroperitoneum to t
32 ned as recurrence in the original tumor bed, retroperitoneum, or within the abdominal cavity or pelvi
33 an extremity in 34, the head/neck in 23, the retroperitoneum/pelvis in 21, and other sites in 11.
34 oscopic appearance of mesocolon, fascia, and retroperitoneum, prior to and after colonic mobilization
35 responsive to mechanical brushing within the retroperitoneum, the snare is likely to change serotoner
36  central retroperitoneum or from the central retroperitoneum to the perirenal space.
37 tiguous, the fascia remained in situ and the retroperitoneum undisturbed.
38   However, no leakage from the ureter to the retroperitoneum was observed, proving that the changes d
39 liac arteries, and spreads into the adjacent retroperitoneum, where it frequently causes ureteral obs

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