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Te2, Part Iii
TERMINOLOGIA EMBRYOLOGICA Second Edition International Embryological Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TE2, PART III Contents Caput V: Organogenesis Chapter 5: Organogenesis (continued) Systema respiratorium Respiratory system Systema urinarium Urinary system Systemata genitalia Genital systems Coeloma Coelom Glandulae endocrinae Endocrine glands Systema cardiovasculare Cardiovascular system Systema lymphoideum Lymphoid system Bibliographic Reference Citation: FIPAT. Terminologia Embryologica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, February 2017 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Embryologica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput V: ORGANOGENESIS Chapter 5: ORGANOGENESIS -
Genetic Syndromes and Genes Involved
ndrom Sy es tic & e G n e e n G e f Connell et al., J Genet Syndr Gene Ther 2013, 4:2 T o Journal of Genetic Syndromes h l e a r n a DOI: 10.4172/2157-7412.1000127 r p u y o J & Gene Therapy ISSN: 2157-7412 Review Article Open Access Genetic Syndromes and Genes Involved in the Development of the Female Reproductive Tract: A Possible Role for Gene Therapy Connell MT1, Owen CM2 and Segars JH3* 1Department of Obstetrics and Gynecology, Truman Medical Center, Kansas City, Missouri 2Department of Obstetrics and Gynecology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 3Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA Abstract Müllerian and vaginal anomalies are congenital malformations of the female reproductive tract resulting from alterations in the normal developmental pathway of the uterus, cervix, fallopian tubes, and vagina. The most common of the Müllerian anomalies affect the uterus and may adversely impact reproductive outcomes highlighting the importance of gaining understanding of the genetic mechanisms that govern normal and abnormal development of the female reproductive tract. Modern molecular genetics with study of knock out animal models as well as several genetic syndromes featuring abnormalities of the female reproductive tract have identified candidate genes significant to this developmental pathway. Further emphasizing the importance of understanding female reproductive tract development, recent evidence has demonstrated expression of embryologically significant genes in the endometrium of adult mice and humans. This recent work suggests that these genes not only play a role in the proper structural development of the female reproductive tract but also may persist in adults to regulate proper function of the endometrium of the uterus. -
World Journal of Pharmaceutical and Life Sciences
wjpls, 2017, Vol. 3, Issue 8, 66-68 Review Article ISSN 2454-2229 Farman . World Journal of Pharmaceutical World Journal and Lifeof Pharmaceutical Sciences and Life Sciences WJPLS www.wjpls.org SJIF Impact Factor: 4.223 ONE TOO MANY- POLYORCHIDISM A RARE CASE REPORT AND REVIEW OF LITERATURE Dr. Farman Ali* India. *Corresponding Author: Dr. Farman Ali India. Email ID: [email protected], Article Received on 12/08/2017 Article Revised on 03/09/2017 Article Accepted on 24/09/2017 ABSTRACT Polyorchidism is the incidence of more than two testicles in a male. It is a rare congenital anomaly involving the abnormal division of the genital ridge longitudinally or transversely, mainly occurring in the scrotum. Triorchidism(presence of 3 testes) is the most common occurrence of this condition. They mostly occur on the left side. There have been only 140-200 pathological cases that are published in world journal literature, out of which only a few cases have been reported in India. A rare case was reported of a 20 year old man with polyorchidism presenting with an inguinal hernia, describing the clinical features, it's surgical findings and a review of the literature. The most common sites are: Scrotal(66%), inguinal(25%), and abdominal(9%). This condition is mostly asymptomatic but may commonly present with features like maldescent(40%), hernia(30%), torsion(15%), hydrocoele(9%) and malignancy(6%). Spermatogenesis may be normal only in 50% of cases. If symptoms present, they may be scrotal pain, swelling and infertility. High accuracy of pre-operative ultrasound evaluation of scrotal mass differentiates this benign entity from ominous abnormalities and prevents unnecessary surgical exploration of sonographically normal, uncomplicated and orthotopic supernumerary testes. -
Vulvodynia: a Common and Underrecognized Pain Disorder in Women and Female Adolescents Integrating Current
21/4/2017 www.medscape.org/viewarticle/877370_print www.medscape.org This article is a CME / CE certified activity. To earn credit for this activity visit: http://www.medscape.org/viewarticle/877370 Vulvodynia: A Common and UnderRecognized Pain Disorder in Women and Female Adolescents Integrating Current Knowledge Into Clinical Practice CME / CE Jacob Bornstein, MD; Andrew Goldstein, MD; Ruby Nguyen, PhD; Colleen Stockdale, MD; Pamela Morrison Wiles, DPT Posted: 4/18/2017 This activity was developed through a comprehensive review of the literature and best practices by vulvodynia experts to provide continuing education for healthcare providers. Introduction Slide 1. http://www.medscape.org/viewarticle/877370_print 1/69 21/4/2017 www.medscape.org/viewarticle/877370_print Slide 2. Historical Perspective Slide 3. http://www.medscape.org/viewarticle/877370_print 2/69 21/4/2017 www.medscape.org/viewarticle/877370_print Slide 4. What we now refer to as "vulvodynia" was first documented in medical texts in 1880, although some believe that the condition may have been described as far back as the 1st century (McElhiney 2006). Vulvodynia was described as "supersensitiveness of the vulva" and "a fruitful source of dyspareunia" before mention of the condition disappeared from medical texts for 5 decades. Slide 5. http://www.medscape.org/viewarticle/877370_print 3/69 21/4/2017 www.medscape.org/viewarticle/877370_print Slide 6. Slide 7. http://www.medscape.org/viewarticle/877370_print 4/69 21/4/2017 www.medscape.org/viewarticle/877370_print Slide 8. Slide 9. Magnitude of the Problem http://www.medscape.org/viewarticle/877370_print 5/69 21/4/2017 www.medscape.org/viewarticle/877370_print Slide 10. -
Massachusetts Birth Defects 2002-2003
Massachusetts Birth Defects 2002-2003 Massachusetts Birth Defects Monitoring Program Bureau of Family Health and Nutrition Massachusetts Department of Public Health January 2008 Massachusetts Birth Defects 2002-2003 Deval L. Patrick, Governor Timothy P. Murray, Lieutenant Governor JudyAnn Bigby, MD, Secretary, Executive Office of Health and Human Services John Auerbach, Commissioner, Massachusetts Department of Public Health Sally Fogerty, Director, Bureau of Family Health and Nutrition Marlene Anderka, Director, Massachusetts Center for Birth Defects Research and Prevention Linda Casey, Administrative Director, Massachusetts Center for Birth Defects Research and Prevention Cathleen Higgins, Birth Defects Surveillance Coordinator Massachusetts Department of Public Health 617-624-5510 January 2008 Acknowledgements This report was prepared by the staff of the Massachusetts Center for Birth Defects Research and Prevention (MCBDRP) including: Marlene Anderka, Linda Baptiste, Elizabeth Bingay, Joe Burgio, Linda Casey, Xiangmei Gu, Cathleen Higgins, Angela Lin, Rebecca Lovering, and Na Wang. Data in this report have been collected through the efforts of the field staff of the MCBDRP including: Roberta Aucoin, Dorothy Cichonski, Daniel Sexton, Marie-Noel Westgate and Susan Winship. We would like to acknowledge the following individuals for their time and commitment to supporting our efforts in improving the MCBDRP. Lewis Holmes, MD, Massachusetts General Hospital Carol Louik, ScD, Slone Epidemiology Center, Boston University Allen Mitchell, -
A Rare Case of Polyorchidism in a Cat with Four Intra&
Reprod Dom Anim doi: 10.1111/rda.12461 ISSN 0936–6768 Short Communication A Rare Case of Polyorchidism in a Cat with Four Intra-abdominal Testes J Roca-Ferrer, E Rodrıguez, GA Ramırez, C Moragas and M Sala Centre Veterinari Bonavista, Cornella de Llobregat, Catalonia, Spain Contents Polyorchidism, the presence of more than two testes, Polyorchidism is a rare congenital anomaly defined as the is an uncommon congenital anomaly both in human presence of more than two histologically proven testes. We and veterinary medicine. The first reports of polyorchi- report a case of a 9-month-old European cat with four intra- dism in veterinary medicine were concerned with the abdominal testes. The diagnosis was performed by means of finding of supernumerary testes in horses as incidental ultrasonography, intra-operative examination and histological events during castration (Earnshaw 1959) while in confirmation. The case reported here presents an extremely humans the first case was reported during a routine rare anomaly, as no previous studies in veterinary medicine have reported the presence of four testes. This case suggests autopsy in 1670 (Bergholz and Wenke 2009). The that supernumerary testes should be included as differential number of cases reported in the literature is very low. diagnoses for intra-abdominal masses. In veterinary medicine, five cases have been published up to now, as illustrated in Table 1. In human medicine, 140 cases have been reported (Bergholz and Wenke Introduction 2009). In both veterinary and human medicine, the most Cryptorchidism, the failure of one or both testes to common case of polyorchidism is the presence of a descend into scrotum, is a common congenital abnor- single supernumerary testis (triorchidism). -
Vulval Tuberculosis: the Histomorphological Spectrum In
C S & lini ID ca A l f R o e l s Journal of Nhlonzi et al., J AIDS Clin Res 2017, 8:8 a e n a r r c u DOI: 10.4172/2155-6113.1000719 h o J ISSN: 2155-6113 AIDS & Clinical Research Research Article Open Access Vulval Tuberculosis: The Histomorphological Spectrum in Patients with HIV Co-Infection and AIDS Nhlonzi GB1, Ramdial PK1*, Nargan K2, Lumamba KD2, Pillay B3, Kuppusamy JB1, Naidoo T1 and Steyn AJC2,4,5 1Department of Anatomical Pathology, National Health Laboratory Service and University of KwaZulu-Natal, Durban, South Africa 2Africa Health Research Institute, Durban, KwaZulu-Natal, South Africa 3Department of Vascular/Endovascular Surgery, Nelson R Mandela School of Medicine, University of KwaZulu-Natal and Inkosi Albert Luthuli Central Hospital, Durban, KwaZulu-Natal, South Africa 4Department of Microbiology, School of Medicine, University of Alabama at Birmingham, Birmingham, USA 5UAB Centers for AIDS Research and Free Radical Biology, University of Alabama at Birmingham, Birmingham, USA Abstract Objective: Vulval tuberculosis (TB) is reported rarely. The histomorphological spectrum and diagnostic mimicry thereof in patients with concomitant HIV infection/ AIDS is unreported to date. This study aimed to appraise the histopathologic spectrum of vulval TB in HIV co-infected patients and to identify histopathological diagnostic challenges, mimicry and pitfalls. Methods: Ten year retrospective study that reappraised the histomorphological features of vulval TB in HIV-infected patients. Results: The clinical descriptions of the biopsied lesions from 19 patients that form the study cohort encompassed nodules (9), ulcers (5), hypertrophy/edema (3) and abscesses (2). The main microscopic features included necrotizing and non-necrotizing granulomatous inflammation, ulceration with a zoned inflammatory response and chronic suppurative inflammation. -
Ultrasound of the Scrotum
Ultrasound of scrotum 21.06.2011 12:42 1 EFSUMB – European Course Book Editor: Christoph F. Dietrich Ultrasound of the scrotum Paul S. Sidhu, Boris Brkljacic2, Lorenzo E. Derchi3 2Medical School, University of Zagreb, 3Department of Radiology, University of Genoa Corresponding author: Paul S. Sidhu BSc MBBS MRCP FRCR DTM&H Consultant Radiologist and Senior Lecturer King‟s College London Department of Radiology King‟s College Hospital Denmark Hill London SE5 9RS United Kingdom Tel: ++44 (0) 20 3299 3063 Fax: ++44 (0) 20 3299 3157 E-mail: [email protected] Ultrasound of scrotum 21.06.2011 12:42 2 Content Content ................................................................................................................................................. 2 Introduction .......................................................................................................................................... 3 Sonographic examination technique .................................................................................................... 3 Gross Anatomy..................................................................................................................................... 4 Embryology ...................................................................................................................................... 4 Scrotal sac and testicular anatomy ................................................................................................... 4 Vascular anatomy ............................................................................................................................ -
See Anorgasmia Absent Ejaculation: See Anejaculation Adaptive Filter, 6
Index A ultrasonography, 41 Absence of Orgasm: see Anorgasmia Beta-human chorionic gonadotropin, 193 Absent ejaculation: see Anejaculation Blue dot sign, 130 Adaptive filter, 6 Broadband transducer, 2 Addison disease, 328 selection, 5 Adenomatoid tumor, 160 handling, 5 MRI, 174 Broad-spectrum antibiotics, 95 ultrasonography, 174 Bulbourethral glands AdrenoCorticoTropic hormone (ACTH), 236, 285, 328 infection, 93 Adrenogenital syndrome, 328 parasitic, 113 Acute appendicitis, 122 non infection inflammation, 112 Androgen deficiency, 36, 303, 304 insensitivity syndrome, 286 C replacement factors, 210 Calcifications, 313 Androtest, 232 associated with cystic masses, 317 Anejaculation, 13, 36, 37 associated with solid masses, 317 Anorchidism, 34 MRI, 330 Anorgasmia, 37 ultrasonography, 330 Anosmia, 209 extra-testicular, 318 Antisperm antibodies, 211, 213 isolated and macroscopic, 318 Aromatase activity, 210 Carcinoma in situ (CIS), 314 Arteriography, 295 echopattern, 316 Arteriovenous fistula, 82 CEUS: see Contrast-enhanced ultrasonography Asthenospermia, 212 Chlamydia, 88, 211 Azoospermia, 208, 210, 241, 249, 292 Choriocarcinoma, 152, 168 factors regions (AZF), 234, 249 imaging, 168 non-obstructive (NOA), 234, 249–250, 255, 256 Coded transmission, 6 management, 249 Collection of the semen sample, 218 sperm retrival, 251 Colour Doppler Ultrasonography limits, 116 testis histology predominant patterns, 249 Complete Androgen Insensitivity Syndrome (CAIS) , 233 obstructive, 212 Computer Aided Sperm Analysis (CASA system), 219 clinical presentation, 242 Congenital adrenal hyperplasia, 285, 328 imaging, 275 Congenital testicular adrenal rest, 329 management, 242 MRI, 324 treatment options, 242 ultrasonography, 324 Coni vasculosi, 30 Contrast-enhanced ultrasonography: B see also Scrotal -enhanced ultrasonography Bag of worms: see also Varicocele, 144 complex cystic lesions, 348 Banking sperm, 152 contrast agents, 344 Behcet’s disease, 113 high degree testicular torsion, 345 Bell clapper deformity, 49 inflammation, 350 MRI, 163 low degree testicular torsion, 346 M. -
Early Vaginal Replacement in Cloacal Malformation
Pediatric Surgery International (2019) 35:263–269 https://doi.org/10.1007/s00383-018-4407-1 ORIGINAL ARTICLE Early vaginal replacement in cloacal malformation Shilpa Sharma1 · Devendra K. Gupta1 Accepted: 18 October 2018 / Published online: 30 October 2018 © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Purpose We assessed the surgical outcome of cloacal malformation (CM) with emphasis on need and timing of vaginal replacement. Methods An ambispective study of CM was carried out including prospective cases from April 2014 to December 2017 and retrospective cases that came for routine follow-up. Early vaginal replacement was defined as that done at time of bowel pull through. Surgical procedures and associated complications were noted. The current state of urinary continence, faecal continence and renal functions was assessed. Results 18 patients with CM were studied with median age at presentation of 5 days (1 day–4 years). 18;3;2 babies underwent colostomy; vaginostomy; vesicostomy. All patients underwent posterior sagittal anorectovaginourethroplasty (PSARVUP)/ Pull through at a median age of 13 (4–46) months. Ten patients had long common channel length (> 3 cm). Six patients underwent early vaginal replacement at a median age of 14 (7–25) months with ileum; sigmoid colon; vaginal switch; hemirectum in 2;2;1;1. Three with long common channel who underwent only PSARVUP had inadequate introitus at puberty. Complications included anal mucosal prolapse, urethrovaginal fistula, perineal wound dehiscence, pyometrocolpos, blad- der injury and pelvic abscess. Persistent vesicoureteric reflux remained in 8. 5;2 patients had urinary; faecal incontinence. 2 patients of uterus didelphys are having menorrhagia. -
Syndromic Aspects of Testicular Carcinoma
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by University of Groningen University of Groningen Syndromic aspects of testicular carcinoma Lutke-Holzik, MF; Sijmons, RH; Sleijfer, DT; Sonneveld, DJA; Hoekstra-Weebers, JEHM; van Echten-Arends, J; Hoekstra, HJ Published in: Cancer DOI: 10.1002/cncr.11155 IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below. Document Version Publisher's PDF, also known as Version of record Publication date: 2003 Link to publication in University of Groningen/UMCG research database Citation for published version (APA): Lutke-Holzik, MF., Sijmons, RH., Sleijfer, DT., Sonneveld, DJA., Hoekstra-Weebers, JEHM., van Echten- Arends, J., & Hoekstra, HJ. (2003). Syndromic aspects of testicular carcinoma. Cancer, 97(4), 984-992. https://doi.org/10.1002/cncr.11155 Copyright Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons). Take-down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum. Download date: 12-11-2019 984 Syndromic Aspects of Testicular Carcinoma 1 Martijn F. -
Is Vulval Vestibulitis Syndrome a Hormonal Condition?
VULVAL VESTIBULITIS SYNDROME A Thesis submitted for the Degree of Doctor of Medicine University of London Lois Eva 1 UMI Number: U591707 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. Dissertation Publishing UMI U591707 Published by ProQuest LLC 2013. Copyright in the Dissertation held by the Author. Microform Edition © ProQuest LLC. All rights reserved. This work is protected against unauthorized copying under Title 17, United States Code. ProQuest LLC 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106-1346 ABSTRACT Objective This project investigates ways of assessing Vulval Vestibulitis Syndrome (VVS), possible aetiological factors, and response to a range of treatments. Materials and Methods 1. Data were collected and analysed to identify possible epidemiological characteristics and compared to existing evidence. 2. Technology (an algesiometer) was used to reliably assess patients, and quantify response to treatment. 3. Immunohistochemistry was used to determine whether VVS is an inflammatory condition. 4. Immunohistochemistry was also used to investigate the expression of oestrogen and progesterone receptors in the vulval tissue of women with VVS and biochemical techniques were used to investigate any relationship with serum oestradiol. Results The cohort of women fulfilling the criteria for VVS were aged 22 to 53 (mean age 34.6) and for some there appeared to be an association with use of the combined oral contraceptive pill (cOCP).