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The number of patients having second reconstruction after mastectomy is increasing. The choice of the re-implantation site can be explained by the differences in local conditions and cosmetic factors. This article compares the advantages and disadvantages of both reconstruction types. After mastectomy, a scar with an acceptable width can be left in the breast without risk of contracting breast cancer. Re-implantation in the breast raises the risk of cancer but reduces the wound discharge. The best aesthetic result is achieved with implant placement in the opposite breast, but complications related to surgery and implant-related issues make this a less attractive option. Implant placement in the axilla is more difficult than in the breast, although the anterior axilla is chosen for re-implantation. While axillary re-implantation promotes better cosmesis, the risk of delayed or secondary lymph node metastasis is higher. On the other hand, the axilla provides good conditions for lymphadenectomy and does not limit the axillary lymph node dissection. The problems of scar and infection can be reduced with the use of acellular dermal matrix. Implant placement in the breast is the preferred option, because of both the shorter operation time and the lower risk of recurrent cancer. The choice of location is a compromise between the risks of recurrent breast cancer and the poor aesthetic result of implant placement in the axilla.I am 39 years old with an 8 year old son. I have been feeling the changes in my body, energy decrease, fatigue, sore throat and body pain. I went to my doc and after one visit, he wanted to give me a scope. I did not feel ready to have it done. A month later a different doctor suggested I have the scope. I did it and found a couple large polyps. I have been to the drs 2 times and they are fine. No more scopes or blood work. I can’t change my life around to fit it.

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The production of functionalized homopolymers was studied, using two N-vinylpyrrolidone (NVP) monomers and two N-vinylcaprolactam (NVC) monomers in the presence of functional groups. The NVP polymers were obtained through ring-opening polymerization, using a catalytic system based on LiTFSI in THF. The NVC polymers were produced by the copolymerization of the NVC and another vinyl monomer in the presence of a complex based on sodium benzenesulfonate or sodium citrate. In both cases, the NVP and NVC monomers present in the initial feed acted as chain-transfer agents, as confirmed by the analysis of molar mass distribution and the nature of the MALDI-TOF spectrum of the copolymer. The polymers were characterised by thermal analysis and the complete sets of proton chemical shift assignments for NMR spectroscopy were obtained for the NVP and NVC units in order to study the dynamics of the segmental motion during the polymerization process. The presence of functional groups is related to a decrease in conformational mobility and an increase in the glass transition temperature of the polymers. In addition, and as a consequence of the creation of reactive sites during the polymerization process, we also observed an effect on the reactivity of the polymers towards sol

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