Academic literature on the topic 'Carcinome cutané'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Carcinome cutané.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Carcinome cutané":
Ly, F., M. Diallo, K. Diop, L. Noufack, BA Diatta, A. Diop, MT Ndiaye Diop, et al. "C89: Carcinome épidermoïde (CSC) et dépigmentation cosmétique volontaire (DCV) de la peau en Afrique Subsaharienne." African Journal of Oncology 2, no. 1 Supplement (March 1, 2022): S37—S38. http://dx.doi.org/10.54266/ajo.2.1s.c89.hopw9969.
Kourda, Nadia, Ines Zaraa, Leila Abid, Karima Zitouni, Ali Adouani, Sarrah Baltagi-Ben Jilani, and Rachida Zermani. "Carcinome mucineux primitif cutané." Annales de Pathologie 26, no. 3 (June 2006): 211–14. http://dx.doi.org/10.1016/s0242-6498(06)70706-4.
Couillet, Didier, Anne Caille †, and Jean-Claude Guillaume. "Carcinome neuroendocrine cutané primitif." EMC - Dermatologie 1, no. 1 (January 2006): 1–8. http://dx.doi.org/10.1016/s0246-0319(06)73815-8.
Gouiaa, N., K. Abbes, A. Khabir, R. Kallel, I. Fakhfakh, I. Bahri, L. Ayadi, T. J. Meziou, S. Makni, and T. Boudawara-Sellami. "Carcinome mucineux primitif cutané." Annales de Dermatologie et de Vénéréologie 135, no. 11 (November 2008): 791–92. http://dx.doi.org/10.1016/j.annder.2008.04.014.
Abid, Najla, Héla Mnif, Slim Charfi, Hamida Turki, and Tahya Sallemi-Boudawara. "Carcinome épidermoïde pseudo-angiosarcomateux cutané." La Presse Médicale 42, no. 6 (June 2013): 1063–65. http://dx.doi.org/10.1016/j.lpm.2012.06.021.
Waroquier, D., J. Vadoud, P. Vereecken, J. Vangeertruyden, and M. Laporte. "Métastase neurotrope d’un carcinome épidermoïde cutané." Annales de Dermatologie et de Vénéréologie 131, no. 2 (February 2004): 187–89. http://dx.doi.org/10.1016/s0151-9638(04)93568-5.
Sans, V., T. Jouary, B. Vergier, A. Taieb, and M. Delaunay. "P148 - Carcinome basaloïde cutané primitif métastatique." Annales de Dermatologie et de Vénéréologie 132 (October 2005): 161. http://dx.doi.org/10.1016/s0151-9638(05)79877-x.
Kakiesse, Véronique Musumba, Mohesa Iteke, Richard Nzanza Matanda, Richard Mpileng Nkwembe, Jean Marie Ntumba Kayembe, Prosper Tshilobo Lukusa, Véronique Musumba Kakiesse, et al. "Déterminants du carcinome photo-induit chez les sujets de phototype albinos aux Cliniques Universitaires de Kinshasa." Annales Africaines de Medecine 16, no. 2 (May 22, 2023): e5072-e5078. http://dx.doi.org/10.4314/aamed.v16i2.6.
Auliard, A., X. Mirabel, MO Villain, V. Moncho, B. Castelain, and F. Piette. "P48 Le carcinome neuroendocrine primitif cutané: 21 cas." Cancer/Radiothérapie 2, no. 5 (September 1998): 629. http://dx.doi.org/10.1016/s1278-3218(98)80121-2.
Lebas, D., O. Carpentier, E. Martin de Lassalle, M. O. Vilain, and F. Piette. "Carcinome neuroendocrine cutané primitif géant de la jambe." Annales de Dermatologie et de Vénéréologie 131, no. 6-7 (June 2004): 579–82. http://dx.doi.org/10.1016/s0151-9638(04)93671-x.
Dissertations / Theses on the topic "Carcinome cutané":
Amouroux, Marine. "Caractérisation de la transformation néoplasique de la peau par spectroscopies optiques sur fantôme de mélanome et carcinome épidermoïde murin photo-induit." Phd thesis, Université Henri Poincaré - Nancy I, 2008. http://tel.archives-ouvertes.fr/tel-00339385.
Colas, Victor. "Modeling and estimation of human skin optical properties using spatially resolved autofluorescence and diffuse reflectance spectroscopy." Electronic Thesis or Diss., Université de Lorraine, 2022. http://www.theses.fr/2022LORR0129.
In the context of cutaneous carcinoma, optical biopsy offers a in-vivo non-destructive alternative to conventional biopsy to inform the dermatologist of the state of health of the deep tissue during cancer resection. The latter is indeed at the origin of morphological and physiological modifications of the skin, which explains why the optical measurements resulting from the light/tissue interactions are sensitive to it. The work presented in this manuscript exploits the data obtained with the optical biopsy device extit{SpectroLive} on about a hundred patients just before cancer resection by the clinician. In contact with the skin, this spectroscopic device acquires diffuse reflectance (white broadband excitation) and autofluorescence (monochromatic emission to excite endogenous fluorophores in the skin) spatially resolved signals, extit{i.e.}, for several separation distances between the light emitting fiber and the collecting fibers at the periphery. This spatial resolution is of particular interest for the skin, since the different distances introduced allow the collection of photons traveling through the different layers in depth (epidermis, dermis and hypodermis) of the organ. The main part of the work presented here concerns the estimation of the optical properties of the skin by solving the inverse problem from these clinical acquisitions. This consists first in establishing a photon transport simulation faithful to the characteristics (geometrical and spectral) of the real device before building a multilayer model of the skin in which the optical parameters (e.g. absorption and scattering coefficients, the anisotropy factor) and geometrical parameters e.g. layer thickness) can be estimated by an optimization process aiming at minimizing the differences between the spectra generated by the simulation and the ``target'' spectra obtained in clinic. The main contributions developed in this manuscript are first the development and the full exploitation of the simulation, with in particular a study whose purpose is to characterize the penetration of the photons detected at the various source/detector separations, and this for various skin models in order to represent the inter- and intra-individual differences. The knowledge acquired with this study of probed depths is then used in the second major contribution, aiming at adapting the process of estimating optical properties from clinical spectra (inverse problem) to the skin. Finally, the last contribution, more metrological, is the development of an optical bench with double integrating spheres allowing to obtain these same optical properties for a sample ex-vivo, and thus to allow the comparison of the estimates resulting from the two modalities
MORAND, TOURAINE PASCALE. "Carcinome neuroendocrine cutane : a propos de sept observations." Limoges, 1989. http://www.theses.fr/1989LIMO0164.
Bourdely, Pierre. "Caractérisation ontogénique, phénotypique et fonctionnelle des cellules dendritiques et des macrophages dans les carcinomes épidermoïdes cutanés." Thesis, Université Côte d'Azur (ComUE), 2017. http://www.theses.fr/2017AZUR4139.
Skin Squamous cell carcinoma (sSCC) are invasive keratinocyte tumor that develop after immune system subversion. The reprogrammation of anti-tumoral immunity using local stimulation of dendritic cells (DC) and macrophages could be useful. In this line, the aim of my thesis was to understand ontogenic, phenotypic and functional heterogeneity of these cell subsets along skin carcinogenesis to develop new immunotherapies. First, we characterized skin macrophage subsets in mouse and those infiltrating sSCC in human. Using spectral flow cytometry, we identified matured autofluorescent tissue-resident macrophages. These macrophages are anti-inflammatory polarized. In human sSCC, autofluorescent macrophages seem to have same properties that their mouse counterparts. In second study, we identified tumor-infiltrating DC with altered functions. We used a local immunotherapy composed by a TLR9 agonist and blocking antibody against α-chain of IL-10 receptor. This combination induced tumor regression through DC reprogrammation and IFNγ+, TNFα+ IL17A+ T CD8+ lymphocyte generation. These results highlight functional myeloid heterogeneity in skin and sSCC. Their reprogrammation could promote the development of immunotherapies against sSCC in human
Brugière, Charlotte. "L'invasion péri-nerveuse des carcinomes épidermoïdes cutanés humains." Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCC193.
Cutaneous squamous cell carcinoma (SCC) is an important issue because of its frequency and potential severity.The aggressiveness of this cancer is related to perineural invasion (PNI), a mode of tumor dissemination recognized as a poor prognosis factor.The aim of this work is to study the mechanisms of PNI, comparing 2 matched- groups of human SCC with and without PNI.For this, we studied neurotrophins, epithelial-mesenchymal transition (EMT) markers, and the NCAM1 molecule, by immunohistochemistry analysis on surgical pieces of SCC and by molecular analysis with digital-droplet PCR on laser-microdissected tumor cells.Immunohistochemistry analysis found strong expression of BDNF, TrkB, p75NGFR, Snail 1 and NCMA1 in perineural tumor cells, contrasting with weak expression of these markers in tumor cells distant from the nerves. E-cadherin was decreased in perineural tumor cells.Molecular analysis in ddPCR showed decreased expression for E-cadherin and overexpression of BDNF, TrkB, p75NGFR, Snail1, Slug, Zeb2, Twist1 and NCAM1 in perineural tumor cells compared to tumor cells distant from the nerves.We have demonstrated in this work that PNI in human SCC is linked to neurotrophins and EMT, and involves NCAM1
Zaytsev, Sergey. "Combination of tissular multimodal spectro-imaging and optical clearing methods to improve detection depth in skin in vivo." Electronic Thesis or Diss., Université de Lorraine, 2022. http://www.theses.fr/2022LORR0067.
This thesis presents the results of research in the context of improved analysis of the skin optical properties using various optical techniques, such as multimodal tissular spectroscopy and optical coherence tomography (OCT) imaging. Since many years optical techniques of skin characterization are an effective alternative to traditional invasive diagnostic methods as they allow to get information about the structural and biochemical skin composition in vivo in real time, which led to their extensive implementation in the clinical practice of skin lesions analysis. In the last decades it was demonstrated that combined use of several optical techniques allows to increase the diagnostic accuracy by increasing the variety of data acquired in one measurement. Spatial resolution may also increase the diagnostic potential by providing depth discrimination (resolution) between assessed layers. Even though the main limitation for the use of the optical methods in skin diagnostics is the strong absorption and scattering of the latter, skin optical properties can be changed using the method of skin optical clearing (OC). The combination of optical clearing agents (OCA) with various chemical and physical enhancers of skin permeability may significantly improve the potential of multimodal optical approaches with spatial resolution. The aim of the first experimental study within this thesis framework was (i) to investigate the effect of the OC process applied to ex vivo human skin samples on spatially resolved (SR) diffuse reflectance (DR) and autofluorescence (AF) spectra using two combinations of OCA and chemical permeation enhancers (CPE), and (ii) to quantify the clearing- like effect of drying and of spectroscopic probe pressure on skin. A spatially resolved multimodal spectroscopic device was used on a two- layered “hybrid” model made of ex vivo skin and fluorescent gel. Time kinetics of fluorescence and diffuse reflectance spectra demonstrate d an increase in the gel fluorescence back reflected intensity after optical clearing. In addition, complementary experimental results showed increased light transmittance through the skin and confirmed that the improvement in the depth sensitivity of the multimodal spectroscopic approach was related not only to the dehydration and refractive indices matching due to optical clearing, but also to the mechanical compression of tissues caused by the application of the spectroscopic probe. Since when translating these methods into clinical use there is a need to comply with established regulations, including the use of chemicals on healthy and pathologically changed skin of patients, the concentrations of the OCA used may need to be reduced in order to pass the threshold of clinical utility and biocompatibility. Thus, the main goal of the consecutive experimental study was to experimentally evaluate, by using for the first time a Line-field Confocal OCT (LC-OCT) imaging technique, the e fficacy of OC of human skin in vivo with biocompatible OCA combined with chemical and physical permeability enhancers. To satisfy the biocompatible concentration requirements, the mixtures of OCA and CPE were developed according to the FDA inactive ingredients database. To enhance the clearing effect, physical permeation methods were also used. By analyzing simultaneously the average intensity and contrast of the images obtained by LC-OCT technique, we determined the in-depth effectiveness of skin in vivo biocompatible OC. The results showed that the best increase in image intensity and contrast after 10 minutes of ultrasound-assisted clearing was achieved using a mixture of PEG/OA/PG. The results of the experimental data fitting with the hypothesized biphasic exponential association model are in a good agreement with experimental results. Thus, the effectiveness of OC with biocompatible concentrations of OCA was demonstrated
DUCRON, HAAS ELISABETH. "Tumeur de merkel : revue de la litterature a partir d'une observation." Lille 2, 1994. http://www.theses.fr/1994LIL2M041.
BORDAUX, ISABELLE. "A propos des merkélomes." Toulouse 3, 1990. http://www.theses.fr/1990TOU31118.
Schertenleib, Pierre. "Carcinome neuroendocrine cutané ou à cellules de Merkel /." [S.l.] : [s.n.], 1992. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.
Gastaldi, Cécile. "Études des microARNs dans le développement des carcinomes spinocellulaires cutanés." Thesis, Nice, 2013. http://www.theses.fr/2013NICE4120/document.
Cutaneous squamous cell carcinomas (cSCCs) are the second most common cancer and are responsible for up to 25% of all skin cancer deaths. It is therefore essential to characterize the mechanisms responsible for epidermis carcinogenesis to develop new treatments. In this context, miRNAs appear to be prime targets for the development of future anti-tumor therapies. However, their involvement in the pathophysiology of cSCCs is still poorly documented. In this study, I identified using Small RNA sequencing, 112 miRNAs whose expression is altered during tumor development in a mouse model of cutaneous two-stage chemical carcinogenesis. Then, I focused my attention on the miR-193b/365a cluster and on miR-708, that are down-regulated during tumorigenesis, suggesting tumor suppressor functions. Consistent with this hypothesis, the ectopic expression of these miRNAs inhibit the proliferation, survival and migration of tumor cells, while blocking their action with antisense oligonucleotides stimulates these cellular functions in normal keratinocytes. Combining in silico target-prediction approaches and transcriptome analyzes of cSCC cells over-expressing these miRNAs, I identified their potential target genes. I validated KRAS and MAX as direct targets of miR-193b and miR-365a, and I showed that repression of these genes using siRNAs mimics the effects of these miRNAs. These results suggest that targeting these genes might mediate, at least in part, the tumor suppressor action of miR-193b and miR-365a in cSCCs
Book chapters on the topic "Carcinome cutané":
Claudy, Alain. "Carcinome neuro-endocrini cutané." In Manifestations dermatologiques des maladies du système hématopoïétique et oncologie dermatologique, 167–74. Paris: Springer Paris, 2009. http://dx.doi.org/10.1007/978-2-287-72092-5_15.
Deraemaecker, R. "Les carcinomes cutanés." In Thérapeutique du cancer, 685–708. Paris: Springer Paris, 2011. http://dx.doi.org/10.1007/978-2-8178-0021-9_40.
"Carcinomes cutanés." In Méga Guide STAGES IFSI, 434–36. Elsevier, 2015. http://dx.doi.org/10.1016/b978-2-294-74529-4.00134-8.
Alexandre, J., A. Balian, L. Bensoussan, A. Chaïb, G. Gridel, K. Kinugawa, F. Lamazou, et al. "Carcinomes cutanés." In Le tout en un révisions IFSI, 393–95. Elsevier, 2009. http://dx.doi.org/10.1016/b978-2-294-70633-2.50133-5.
Conference papers on the topic "Carcinome cutané":
Landric, C., C. Alande, and M. Ndiaye. "Apport de la greffe gingivale épithélio conjonctive dans la reconstruction palpébrale." In 66ème Congrès de la SFCO. Les Ulis, France: EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206602014.