Citations

Showing 10 of 108073 citations.

Vascularized appendicular lymph node transfer for treatment of extremity lymphedema: A case report
Ciudad, Pedro , Manrique, Oscar J. , Date, Shivprasad , Chang, Wei‐Ling , Nicoli, Fabio , Sapountzis, Stamatis , Cheng, Hsu‐Tang , Agko, Mouchammed , Chen, Hung‐Chi , Roberts, Lewis R. , Chen, Hung‐Chi , Roberts, Lewis R , Cheng, Hsu-Tang , Mouchammed, Agko

Mayo Clinic

Microsurgery | December 2, 2016 | Volume: 38 | Issue: 5 | Pages: 553-557

10.1002/micr.30134 | PMID 27911477 Get It

AbstractVascularized lymph node transfer has demonstrated promising results for the treatment of extremity lymphedema. In an attempt to find the ideal donor site, several vascularized lymph nodes have been described. Each has a common goal of decreasing morbidity and avoiding iatrogenic lymphedema while obtaining good clinical results. Herein, we present the preliminary clinical outcomes of an intra‐abdominal lymph node flap option based on the appendicular artery and vein used for the treatment of extremity lymphedema. A 62 year‐old woman with moderate lower extremity lymphedema, on chronic antibiotics because of recurrent infections and unsatisfactory outcomes after conservative treatment underwent a vascularized appendicular lymph node (VALN) transfer. At a follow‐up of 6 months, the reduction rate of the limb circumference was 17.4%, 15.1%, 12.0% and 9% above the knee, below the knee, above the ankle and foot respectively. In addition, no further episodes of infection or other complications were reported after VALN transfer. Postoperative lymphoscintigraphy demonstrated that the VALN flap was able to improve the lymphatic drainage of the affected limb. According to our findings, the use of VALN transfer minimizes donor‐site morbidity, avoids iatrogenic lymphedema and may provide a strong clearance of infection because of the strong immunologic properties of the appendiceal lymphatic tissue in selected patients. Despite these promising results, further research with larger number of patients and longer follow‐ up is needed.
Chapter 5 Ethical Considerations in the Use of Deep Brain Stimulation
Fiksdal, Alexander , Abulseoud, Osama A. , Sharp, Richard R.

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 85-98

10.1201/9781315364759-6 Get It

Chapter 2 Biophysical Fundamentals of Neural Excitation
Löffler, Susanne , Luján, J. Luis

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 25-50

10.1201/9781315364759-3 Get It

Chapter 21 Closed-Loop Control Systems for Deep Brain Stimulation Therapy
Trevathan, James K. , Luján, J. Luis , Trevathan, James K

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 389-414

10.1201/9781315364759-22 Get It

Chapter 18 The Role of Astrocytes in Deep Brain Stimulation
Chang, Su-Youne , Lee, Kendall H.

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 339-356

10.1201/9781315364759-19 Get It

Chapter 16 Functional Electrical Stimulation for the Treatment of Spinal Cord Injury
Grahn, Peter J. , Ruiz, Aldo A. Mendez, Ruiz, Aldo A. Mendez, Hachmann, Jan T. , Luján, J. Luis

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 283-310

10.1201/9781315364759-17 Get It

Chapter 14 Deep Brain Stimulation for Memory Dysfunction
Ross, Erika K., Ross, Erika K., Bieniek, Kevin F. , Min, Hoon-Ki Paul

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 257-274

10.1201/9781315364759-15 Get It

Chapter 11 Deep Brain Stimulation for Treatment-Resistant Depression
Kim, Yesul , Wininger, Katheryn M. , Tye, Susannah J.

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 197-214

10.1201/9781315364759-12 Get It

Chapter 9 Deep Brain Stimulation for Obsessive-Compulsive Disorder
Gaba, Prakriti , Blaha, Charles D.

Mayo Clinic

Deep Brain Stimulation | December 2, 2016 | Volume: No volume available | Issue: No issue available | Pages: 163-180

10.1201/9781315364759-10 Get It

Light/Dark Shifting Promotes Alcohol-Induced Colon Carcinogenesis: Possible Role of Intestinal Inflammatory Milieu and Microbiota
Khazaie, Khashayarsha , Engen, Phillip A. , Voigt, Robin M. , Shetuni, Brandon, Forsyth, Christopher B. , Shaikh, Maliha, Vitaterna, Martha Hotz , Turek, Fred W. , Saadalla, Abdulrahman , Bishehsari, Faraz , Keshavarzian, Ali

Mayo Clinic

International Journal of Molecular Sciences | December 2, 2016 | Volume: 17 | Issue: 12 | Pages: 2017

10.3390/ijms17122017 | PMID 27918452 Get It

Background: Colorectal cancer (CRC) is associated with the modern lifestyle. Chronic alcohol consumption—a frequent habit of majority of modern societies—increases the risk of CRC. Our group showed that chronic alcohol consumption increases polyposis in a mouse mode of CRC. Here we assess the effect of circadian disruption—another modern life style habit—in promoting alcohol-associated CRC. Method: TS4Cre × adenomatous polyposis coli (APC)lox468 mice underwent (a) an alcohol-containing diet while maintained on a normal 12 h light:12 h dark cycle; or (b) an alcohol-containing diet in conjunction with circadian disruption by once-weekly 12 h phase reversals of the light:dark (LD) cycle. Mice were sacrificed after eight weeks of full alcohol and/or LD shift to collect intestine samples. Tumor number, size, and histologic grades were compared between animal groups. Mast cell protease 2 (MCP2) and 6 (MCP6) histology score were analyzed and compared. Stool collected at baseline and after four weeks of experimental manipulations was used for microbiota analysis. Results: The combination of alcohol and LD shifting accelerated intestinal polyposis, with a significant increase in polyp size, and caused advanced neoplasia. Consistent with a pathogenic role of stromal tryptase-positive mast cells in colon carcinogenesis, the ratio of mMCP6 (stromal)/mMCP2 (intraepithelial) mast cells increased upon LD shifting. Baseline microbiota was similar between groups, and experimental manipulations resulted in a significant difference in the microbiota composition between groups. Conclusions: Circadian disruption by Light:dark shifting exacerbates alcohol-induced polyposis and CRC. Effect of circadian disruption could, at least partly, be mediated by promoting a pro-tumorigenic inflammatory milieu via changes in microbiota.