Transanal full thickness rectal mobilization with an ischiorectal fat pad to repair an H-Type rectovaginal fistula

CSurgeries ◽  
2017 ◽  
Author(s):  
Carlos Reck ◽  
Alejandra Vilanova ◽  
Richard Wood ◽  
Victoria Lane ◽  
Marc Levitt
Keyword(s):  
Rectovaginal Fistula ◽  
Full Thickness ◽  
Fat Pad ◽  
Rectal Mobilization

Martius labial fat pad graft (use in rectovaginal fistula repair)

2020 ◽  
Vol 31 (11) ◽  
pp. 2427-2429 ◽  
Author(s):  
D. Allan Leach ◽  
John B. Gebhart
Keyword(s):  
Rectovaginal Fistula ◽  
Fat Pad ◽  
Fistula Repair

No Rectopexy Versus Rectopexy Following Rectal Mobilization for Full-Thickness Rectal Prolapse: A Randomized Controlled Trial

2011 ◽  
Vol 54 (1) ◽  
pp. 29-34 ◽  
Author(s):  
Joshua R. Karas ◽  
Selman Uranues ◽  
Donato F. Altomare ◽  
Selman Sokmen ◽  
Zoran Krivokapic ◽  
...  
Keyword(s):  
Randomized Controlled Trial ◽  
Rectal Prolapse ◽  
Controlled Trial ◽  
Full Thickness ◽  
Randomized Controlled ◽  
Rectal Mobilization

Sites of Insulin Action Using Ferritin Labeling

1971 ◽  
Vol 29 ◽  
pp. 540-541
Author(s):  
Burton B. Silver ◽  
Ronald S. Nelson
Keyword(s):  
Electron Microscopy ◽  
Binding Sites ◽  
Anterior Pituitary ◽  
Insulin Action ◽  
Diabetic Rats ◽  
Insulin Antibody ◽  
Fat Pad ◽  
Target Organs ◽  
Uranium Salts ◽  
Sugar Levels

Some investigators feel that insulin does not enter cells but exerts its influence in some manner on the cell surface. Ferritin labeling of insulin and insulin antibody was used to determine if binding sites of insulin to specific target organs could be seen with electron microscopy.Alloxanized rats were considered diabetic if blood sugar levels were in excess of 300 mg %. Test reagents included ferritin, ferritin labeled insulin, and ferritin labeled insulin antibody. Target organs examined were were diaphragm, kidney, gastrocnemius, fat pad, liver and anterior pituitary. Reagents were administered through the left common carotid. Survival time was at least one hour in test animals. Tissue incubation studies were also done in normal as well as diabetic rats. Specimens were fixed in gluteraldehyde and osmium followed by staining with lead and uranium salts. Some tissues were not stained.

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