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1.
Gynecol Obstet Fertil Senol ; 45(2): 112-118, 2017 Feb.
Article in French | MEDLINE | ID: mdl-28368791

ABSTRACT

The fertility sparing management of endometrial cancer and atypical hyperplasia concern women in childbearing age with stage 1, grade 1, endometrioid adenocarcinoma confined to endometrium or atypical hyperplasia (simple or complex). These pathologies affecting more frequently postmenopausal women, the number of people involved is relatively low. The main risk factor is hyperestrogenism and these patients often present a history of infertility with a desire for pregnancy. The recommendations for this conservative management are scarce and unclear. The national observatory in the gynecology and obstetrics department of Bichat hospital gives expert advice to help doctors and patients concerned. We present a type of conservative management based on the expertise of the national observatory. Rigorous pre-therapeutic assessment must first be made to avoid missing a more advanced lesion. Hormone therapy is then started to obtain complete remission. In case of remission, fast achieving pregnancy is advised, and the use of assisted reproductive therapy is possible if necessary. Monitoring by hysteroscopy and histological examination is essential during the treatment. Hysterectomy is the last time the conservative management. It is motivated by the risk of recurrence and progression. The probability of remission after conservative treatment is estimated at 78.0 % at 12 months, the probability of recurrence at 29.2 % at 24 months, and the risk of progression at 15 % (stage 1A with myometrial invasion or more on the hysterectomy specimen). In terms of fertility, 32 % of women get at least one pregnancy.


Subject(s)
Carcinoma, Endometrioid/therapy , Endometrial Hyperplasia/therapy , Endometrial Neoplasms/therapy , Fertility Preservation/methods , Antineoplastic Agents, Hormonal/therapeutic use , Carcinoma, Endometrioid/pathology , Endometrial Hyperplasia/pathology , Endometrial Neoplasms/pathology , Female , Humans , Hysterectomy , Neoplasm Invasiveness/pathology , Neoplasm Recurrence, Local/prevention & control , Pregnancy , Remission Induction/methods
2.
Gynecol Obstet Fertil ; 43(3): 205-12, 2015 Mar.
Article in French | MEDLINE | ID: mdl-25708845

ABSTRACT

OBJECTIVES: The occurrence of a postoperative seroma is the main complication of mastectomy. In 2011, Ouldamer et al. adapted a quilting technique used in reconstructive surgery in mastectomy closure. The aim of this study is to evaluate the impact of quilting in the prevention of postoperative seroma. PATIENTS AND METHODS: This is an observational prospective study to the Centre Hospital-University of Tours. Hundred and forty-four patients who underwent a mastectomy between January 1st, 2011 and October 1st, 2012 were included. Patients were divided into 2 groups, one with a classic wound closure with drainage and the second with quilting suture of skin flaps to the underlying musculature after mastectomy without drainage. RESULTS: Quilting suture significantly reduces the postoperative seroma appearance (OR=0.15; CI95% [0.06-0.39]; P<0.001). Operative time is increased by 20minutes in the quilted group (P<0.001). Postoperative pain is not changed by quilting. The duration of hospitalization is significantly shorter (5.09±1.46 days versus 6.49±2.77 days; P<0.001). Quality of the healing and appearance of the scar, rated by patients, are identical in both groups. CONCLUSION: Quilting is an effective method not only for prevention of seroma, but also for reducing of hospitalization duration, without increasing of postoperative pain and complications.


Subject(s)
Breast Neoplasms/surgery , Mastectomy/adverse effects , Mastectomy/methods , Postoperative Complications/prevention & control , Seroma/prevention & control , Suture Techniques , Drainage , Female , Humans , Pain, Postoperative/epidemiology , Prospective Studies , Seroma/etiology , Surgical Flaps
5.
Cytogenet Genome Res ; 113(1-4): 325-35, 2006.
Article in English | MEDLINE | ID: mdl-16575197

ABSTRACT

X chromosome inactivation ensures the dosage compensation of X-linked genes in XX females compared to their XY male counterpart. It is characterised by the specific recruitment of an inhibitory ribonucleoprotein complex involving the non-coding Xist RNA to the presumptive inactive X chromosome and associated chromatin modifications, which result in the transcriptional silencing of the X chromosome. As an approach to the identification of some of the potential molecular players in this process we have performed comparative transcriptional profiling of mouse 6.5-dpc (days post-coitum) female and male embryos using a modified SAGE (Serial analysis of gene expression) technique which allows the analysis of small quantities of biological material. At 6.5 dpc, a moment when random X inactivation of embryonic tissues has just been achieved, some two hundred transcripts that were significantly enriched in the female gastrula compared to its male counterpart could be identified. The validation of an association with the X inactivation process of a subset of these transcripts has been studied, ex vivo, in differentiating female and male ES cells and in female ES cells in which the establishment of X inactivation is interrupted through the post-transcriptional inhibition of Xist synthesis.


Subject(s)
Embryonic Development/genetics , Gene Silencing , Transcriptional Activation , X Chromosome , Animals , Female , Gene Dosage , Male , Mammals , Mice , Polymerase Chain Reaction , RNA, Long Noncoding , RNA, Untranslated/genetics , Stem Cells/physiology
6.
EMBO J ; 17(12): 3495-502, 1998 Jun 15.
Article in English | MEDLINE | ID: mdl-9628885

ABSTRACT

Unstable minisatellites display high frequencies of spontaneous gain and loss of repeats in the human germline. Most length changes arise through complex recombination events including intra-allelic duplications/deletions and inter-allelic transfers of repeats. Definition of the factors modulating instability requires both measurement of mutation rate and detailed analysis of mutant structures at the level of individual alleles. We have measured mutation rates in sperm for a wide range of alleles of the highly unstable human minisatellite CEB1. Instability varies by three orders of magnitude between alleles and increases steadily with the size of the tandem array. Structural analysis of mutant molecules derived from six alleles revealed that it is the rate of intra-allelic rearrangements which increases with array size and that intra-allelic duplication events tend to cluster within homogeneous segments of alleles; both phenomena resemble features of trinucleotide repeat instability. In contrast, inter-allelic transfers occur at a fairly constant rate, irrespective of array length, and show a mild polarity towards one end of the minisatellite, suggesting the possible influence of flanking DNA on these conversion-like events.


Subject(s)
Minisatellite Repeats/genetics , Alleles , Humans , Male , Mutation/genetics , Repetitive Sequences, Nucleic Acid/genetics , Spermatozoa/metabolism
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