Congenital Penile Malformations: Dartos and Androgens Ghent University Hospital Maintains Database of Children Undergoing Surgery for CPM
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Case Report Full Text Online At
Case Report Full text online at http://www.jiaps.com Penile agenesis A. K. Bangroo, Ramji Khetri, Sashi Tiwari St Stephen's Hospital, Tis Hazari, Delhi Correspondence: AK Bangroo, 103, Administrative block, St. Stephens Hospital, Tis Hazari, Delhi-110054, India. E-mail: [email protected] ABSTRACT Penile agenesis is an extremely rare disorder with profound urological and psychological consequences. The goal of treatment is an early female gender assignment and feminizing reconstruction of the perineum. KEY WORDS: Aphallia, Penile agenesis, Ambiguous genitalia Penile agenesis (PA) is an extremely rare developmental the scrotal folds which were preserved for subsequent anomaly with the reported incidence of 1 in 30 million genital reconstruction. births[1]. PA is believed to result from either the absence of the genital tubercle, or its failure to develop.[2] Several DISCUSSION investigators claim the absence of corpora cavernosa and corpora spongiosum as a prerequisite for the diagnosis of The earliest case report of aphallia was by Imminger in penile agenesis.[3] Except for the reported XX-XY mosaic, 1853[2] since then only 75 cases have been reported in the patients have 46 XY karyotypes.[4] More than half of these literature[6]. Skoog and Belman[5] suggested three variants, have associated anomalies, including developmental de based on urethral position in relationship to the anal fects of the caudal axis, genitourinary and gastrointestinal sphincter, as: Postsphincteric; Presphincteric tract anomalies.[5] The scrotum, testes and testicular func (Prostatorectal fistula) and Urethral atresia. More proxi tion are usually normal[2]. mal the bladder outlet, greater is the likelihood of other anomalies and death.[5] CASE REPORT A two-day-old 3.2 kg genotypic male (46XY) neonate was brought, by a social organization, to our hospital with the complaint of absence of penis, and passage of meco nium mixed with urine through rectum. -
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Number 1 | January 2019 Prevalence and incidence of rare diseases: Bibliographic data Prevalence, incidence or number of published cases listed by diseases (in alphabetical order) www.orpha.net www.orphadata.org If a range of national data is available, the average is Methodology calculated to estimate the worldwide or European prevalence or incidence. When a range of data sources is available, the most Orphanet carries out a systematic survey of literature in recent data source that meets a certain number of quality order to estimate the prevalence and incidence of rare criteria is favoured (registries, meta-analyses, diseases. This study aims to collect new data regarding population-based studies, large cohorts studies). point prevalence, birth prevalence and incidence, and to update already published data according to new For congenital diseases, the prevalence is estimated, so scientific studies or other available data. that: Prevalence = birth prevalence x (patient life This data is presented in the following reports published expectancy/general population life expectancy). biannually: When only incidence data is documented, the prevalence is estimated when possible, so that : • Prevalence, incidence or number of published cases listed by diseases (in alphabetical order); Prevalence = incidence x disease mean duration. • Diseases listed by decreasing prevalence, incidence When neither prevalence nor incidence data is available, or number of published cases; which is the case for very rare diseases, the number of cases or families documented in the medical literature is Data collection provided. A number of different sources are used : Limitations of the study • Registries (RARECARE, EUROCAT, etc) ; The prevalence and incidence data presented in this report are only estimations and cannot be considered to • National/international health institutes and agencies be absolutely correct. -
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International Journal of Research in Medical Sciences Lekha KS et al. Int J Res Med Sci. 2021 Feb;9(2):364-370 www.msjonline.org pISSN 2320-6071 | eISSN 2320-6012 DOI: https://dx.doi.org/10.18203/2320-6012.ijrms20210050 Original Research Article Genital ambiguity: a cytogenetic evaluation of gender K. S. Lekha1*, V. Bhagyam2, P. D. Varghese3, M. Manju2 1Department of Anatomy, Government Medical College Thrissur, Kerala, India 2Department of Anatomy, Government Medical College Kozhikode, Kerala, India 3Department of Anatomy, Government Medical College Alappuzha, Kerala, India Received: 15 December 2020 Accepted: 31 December 2020 *Correspondence: Dr. K. S. Lekha, E-mail: [email protected] Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Background: Genital ambiguity is a complex genetic disorder of sexual differentiation into male or female. The purpose of the present study is to correlate the sex of rearing with the genetic sex and to find out the prevalence of chromosomal anomalies in patients with ambiguous genitalia. The findings can help in proper diagnosis, genetic counselling, and the reassignment of sex, if necessary. Methods: In this cross-sectional study, 22 patients from north Kerala, ranging in age from 17 days to 17 years, were included. All cases were subjected to the following: a detailed history, physical examination, evaluation of clinical data, and cytogenetic analysis. Based on the standard protocol, peripheral blood lymphocyte culture was done. -
Perineal Lipoma Mimicking an Accessory Penis with Scrotum
International Surgery Journal Jabbal HS et al. Int Surg J. 2017 Apr;4(4):1463-1465 http://www.ijsurgery.com pISSN 2349-3305 | eISSN 2349-2902 DOI: http://dx.doi.org/10.18203/2349-2902.isj20171160 Case Report Perineal lipoma mimicking an accessory penis with scrotum Harmandeep S. Jabbal*, Dhirendra D. Wagh Department of Surgery, Jawaharlal Nehru Medical College, Sawangi (Meghe), Wardha, Maharashtra, India Received: 18 January 2017 Accepted: 16 February 2017 *Correspondence: Dr. Harmandeep S. Jabbal, E-mail: [email protected] Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT A case of accessory penis with scrotum in a 4 months old boy is reported because of its rarity. The infant presented with a tumour mimicking an accessory penis with scrotum between the normal sited scrotum and anus. Both testes had descended into the scrotum. After complete evaluation, there was no other urological anomaly. The tumour was excised and the histo-pathological findings of the tumor indicated a perineal lipoma. An overview of normal development of male external genitalia has been provided and the deranged mechanism resulting in this anomaly has been reviewed with hypothesis regarding etiology of accessory scrotum. Keywords: Accessory penis, Accessory scrotum, Congenital urogenital deformities, Perineal lipoma INTRODUCTION palpation in each hemi-scrotum. Another mass of size 3 cm x 1.5 cm was situated between the normally sited Accessory scrotum is considered the rarest of all scrotum and the anal orifice. -
EAU-Guidelines-On-Paediatric-Urology-2019.Pdf
EAU Guidelines on Paediatric Urology C. Radmayr (Chair), G. Bogaert, H.S. Dogan, R. Kocvara˘ , J.M. Nijman (Vice-chair), R. Stein, S. Tekgül Guidelines Associates: L.A. ‘t Hoen, J. Quaedackers, M.S. Silay, S. Undre European Society for Paediatric Urology © European Association of Urology 2019 TABLE OF CONTENTS PAGE 1. INTRODUCTION 8 1.1 Aim 8 1.2 Panel composition 8 1.3 Available publications 8 1.4 Publication history 8 1.5 Summary of changes 8 1.5.1 New and changed recommendations 9 2. METHODS 9 2.1 Introduction 9 2.2 Peer review 9 2.3 Future goals 9 3. THE GUIDELINE 10 3.1 Phimosis 10 3.1.1 Epidemiology, aetiology and pathophysiology 10 3.1.2 Classification systems 10 3.1.3 Diagnostic evaluation 10 3.1.4 Management 10 3.1.5 Follow-up 11 3.1.6 Summary of evidence and recommendations for the management of phimosis 11 3.2 Management of undescended testes 11 3.2.1 Background 11 3.2.2 Classification 11 3.2.2.1 Palpable testes 12 3.2.2.2 Non-palpable testes 12 3.2.3 Diagnostic evaluation 13 3.2.3.1 History 13 3.2.3.2 Physical examination 13 3.2.3.3 Imaging studies 13 3.2.4 Management 13 3.2.4.1 Medical therapy 13 3.2.4.1.1 Medical therapy for testicular descent 13 3.2.4.1.2 Medical therapy for fertility potential 14 3.2.4.2 Surgical therapy 14 3.2.4.2.1 Palpable testes 14 3.2.4.2.1.1 Inguinal orchidopexy 14 3.2.4.2.1.2 Scrotal orchidopexy 15 3.2.4.2.2 Non-palpable testes 15 3.2.4.2.3 Complications of surgical therapy 15 3.2.4.2.4 Surgical therapy for undescended testes after puberty 15 3.2.5 Undescended testes and fertility 16 3.2.6 Undescended -
A Rare Case of Aphallia- Moghtaderi M Et Al
A Rare case of Aphallia- Moghtaderi M et al Case Report J Ped. Nephrology 2016;4(2):74-77 http://journals.sbmu.ac.ir/jpn DOI: A Rare case of Aphallia How to Cite This Article: Moghtaderi M, Boroomand M, Kajbafzadeh A, Arshadi H, Ghohestani M, Mehdizadeh M. A Rare case of Aphallia, J Ped Nephrology2016;4(2):74-77. Mastaneh Moghtaderi,1* Maryam Boroomand,1 Aphallia (total absence of penis) is an extremely Abdolmohammad Kajbafzadeh,2 rare abnormality that can be part of the urorectal Hamid Arshadi, 2 septum malformation sequence. Mohammad Ghohestani,1 We are reporting a 40-day-old boy who was Mehrzad Mehdizadeh3 referred to our nephrology clinic due to the absence of the penis and urinating through the 1Department of Pediatric Nephrology, Chronic Kidney rectum. He was born to a 17-year-old mother and Disease Research Center. Children Medical Center a 24-year-old father, and was delivered term via Hospital, Tehran University of Medical Sciences, Tehran, normal vaginal delivery. Iran. The pregnancy was uncomplicated with no 2Pediatric Urology research Center, Children Medical maternal toxin or medication exposure. Both Center Hospital, Tehran University of Medical Sciences, parents were healthy and there was no family Tehran, Iran. history of congenital abnormality. The parents 3Department of Pediatric Radiology, Children Medical were also unrelated. Center Hospital, Tehran University of Medical Sciences, Physical examination revealed agenesis of the Tehran, Iran. penis, a normal scrotum, and bilateral normally positioned testises. Moreover, the heart, lungs, *Corresponding Author abdomen, head and neck, and spinal column were Mastaneh Moghtaderi, MD. all normal on examination. -
Research Opinions in Animal & Veterinary Sciences
www.roavs.com EISSN: 2223-0343 RESEARCH OPINIONS IN ANIMAL & VETERINARY SCIENCES Diphallia and double scrota in a donkey: A case report A.M. Abu-Seida* and F.M. Torad Department of Surgery, Anesthesiology & Radiology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt Abstract Diphallia and double scrota are rare congenital anomalies. This report records, for the first time, the gross pathological findings of a rare case of diphallia and double scrota in a two-year-old donkey. On physical examination of the donkey, double peni, double prepuces, double scrota and two testes were observed. The two peni were directed opposite to each other at the caudal ventral midline. The posterior penis was the functional one and appeared normal in structure. This penis had ventral deviation and was displaced caudally to the posterior scrotum and testes. The testes were atrophied, asymmetrical and located anterior to the posterior penis in a transverse plan. The anterior penis was not functional, rudimentary, replaced by a fibrous band, fixed to the prepuce and had normal cranial direction. The anterior prepuce was well developed with preputial orifice. The anterior scrotum was rudimentary, empty and located posterior to the anterior penis. Two rudimentary teats were also seen between anterior prepuce and scrotum. Keywords: Diphallia; double scrota; donkey To cite this article: Abu-Seida AM and FM Torad, 2014. Diphallia and double scrota in a donkey: A case report. Res. Opin. Anim. Vet. Sci., 4(3), 117-119. Introduction structure in the middle of the two scrota contained the urinary bladder and a loop of small intestine. -
Abnormalities of the External Genitalia and Groins Among Primary School Boys in Bida, Nigeria
Abnormalities of the external genitalia and groins among primary school boys in Bida, Nigeria. Adedeji O Adekanye1,2, Samuel A Adefemi1,3, Kayode A Onawola1,2, John A James1,2, Ibrahim T Adeleke1,4, Mark Francis1,2, Ezekiel U Sheshi1,3, Moses E Atakere1,5, Abdullahi D Jibril1,5 1. Centre for Health & Allied Researches (CHAR), Federal Medical Centre Bida, Nigeria 2. Department of Surgery, Federal Medical centre, Bida Nigeria 3. Department of Family Medicine, Federal Medical centre, Bida Nigeria 4. Department of Health Information management, Federal Medical centre, Bida Nigeria 5. Department of Obstetrics & Gynaecology, Federal Medical centre, Bida Nigeria Abstract Background: Abnormalities of the male external genitalia and groin, a set of lesions which may be congenital or acquired, are rather obscured to many kids and their parents and Nigerian health care system has no formal program to detect them. Objectives: To identify and determine the prevalence of abnormalities of external genitalia and groin among primary school boys in Bida, Nigeria. Methods: This was a cross-sectional study of primary school male pupils in Bida. A detailed clinical examination of the external genitalia and groin was performed on them. Results: Abnormalities were detected in 240 (36.20%) of the 663 boys, with 35 (5.28%) having more than one abnormality. The three most prevalent abnormalities were penile chordee (37, 5.58%), excessive removal of penile skin (37, 5.58%) and retractile testis (34, 5.13%). The prevalence of complications of circumcision was 15.40% and included excessive residual foreskin, exces- sive removal of skin, skin bridges and meatal stenosis. -
Meeting Report on the NIDDK/AUA Workshop on Congenital Anomalies of External Genitalia: Challenges and Opportunities for Translational Research
UCLA UCLA Previously Published Works Title Meeting report on the NIDDK/AUA Workshop on Congenital Anomalies of External Genitalia: challenges and opportunities for translational research. Permalink https://escholarship.org/uc/item/1vk2c98g Journal Journal of pediatric urology, 16(6) ISSN 1477-5131 Authors Stadler, H Scott Peters, Craig A Sturm, Renea M et al. Publication Date 2020-12-01 DOI 10.1016/j.jpurol.2020.09.012 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Journal of Pediatric Urology (2020) 16, 791e804 Review Article Meeting report on the NIDDK/AUA Workshop on Congenital Anomalies of External Genitalia: challenges and opportunities for translational research* aDepartment of Skeletal Biology, Shriners Hospital for Children, a, ,1 b,c, ,1 d,1 3101 SW Sam Jackson Park Road, H. Scott Stadler *** , Craig A. Peters ** , Renea M. Sturm , b e f,g Portland, OR, Oregon Health & Linda A. Baker , Carolyn J.M. Best , Victoria Y. Bird , Science University, Department of h i j Orthopaedics and Rehabilitation, Frank Geller , Deborah K. Hoshizaki , Thomas B. Knudsen , i k l, ,1 Portland, 97239, OR, USA Jenna M. Norton , Rodrigo L.P. Romao , Martin J. Cohn * b Department of Urology, Summary parents, and short interviews to determine familial University of Texas Southwestern, 5323 Harry Hines Blvd., Dallas, Congenital anomalies of the external genitalia penetrance (small pedigrees), would accelerate 75390-9110, TX, USA (CAEG) are a prevalent and serious public health research in this field. Such a centralized datahub concern with lifelong impacts on the urinary func- will advance efforts to develop detailed multi- cPediatric Urology, Children’s tion, sexual health, fertility, tumor development, dimensional phenotyping and will enable access to Health System Texas, University of and psychosocial wellbeing of affected individuals. -
UROLOGY Lecture Course for Students of Medical Universities
A.A. Zebentaev, P.V. Plotnikov UROLOGY Lecture course for students of medical Universities Vitebsk, 2017 Ministry of Health Care of the Republic of Belarus Higher Educational Establishment “Vitebsk State Medical University” A.A. Zebentaev, P.V. Plotnikov UROLOGY Lecture course for students of medical Universities Рекомендовано учебно-методическим объединением по высшему медицинскому, фармацевтическому образованию Республики Беларусь в качестве учебно-методического пособия для студентов учреждений высшего образования, обучающихся по специальности 1-79 01 01 “Лечебное дело” Vitebsk, 2017 УДК 616.6(042.3/.4)=111 ББК 56.9я73 Z 42 Reviewed by: N.A. Nechiporenko, MD, PhD Grodno State Medical University Urology Dpt., Belarusian State Medical University, Minsk Zebentaev A.A. Z42 Urology: Lecture course for students of medical universities/ А.А. Zebentaev, P.V. Plotnikov. – Vitebsk: VSMU. - 2017. - 188p. ISBN-978-985-466-862-8 The content of this lecture course “Urology” for students of medical Univer- sities corresponds with basic educational plan and program, approved by Minis- try of Health Care of the Republic of Belarus. This book corresponds to the typ- ical educational program on specialty Urology and suitable for foreign students. This edition accumulates in a chort form the data covering the most of essential areas and all basic topics of urology. УДК 616.6(042.3/.4)=111 ББК 56.9я73 Confirmed and recommended for edition by the Central educational - methodi- cal Council of Vitebsk State Medical University in 16 November 2016, the protocol № 10. ISBN-978-985-466-862-8 © Zebentaev A.A., Plotnikov P.V., 2017 © VSMU Press, 2017 • CONTENTS CONTENTS . 3 ABBREVIATIONS .LIST . -
The Approach to the Infant with Ambiguous Genitalia
334 Review Article Disorders/differences of sex development (DSDs) for primary care: the approach to the infant with ambiguous genitalia Justin A. Indyk Section of Endocrinology, Nationwide Children’s Hospital, the Ohio State University, Columbus, Ohio 43205, USA Correspondence to: Justin A. Indyk, MD, PhD. THRIVE Program, Section of Endocrinology, Nationwide Children’s Hospital, 700 Children’s Drive, Columbus, Ohio 43205, USA. Email: [email protected]. Abstract: The initial management of the neonate with ambiguous genitalia can be a very stressful and anxious time for families, as well as for the general practitioner or neonatologist. A timely approach must be sensitive and attend to the psychosocial needs of the family. In addition, it must also effectively address the diagnostic dilemma that is frequently seen in the care of patients with disorders of sex development (DSDs). One great challenge is assigning a sex of rearing, which must take into account a variety of factors including the clinical, biochemical and radiologic clues as to the etiology of the atypical genitalia (AG). However, other important aspects cannot be overlooked, and these include parental and cultural views, as well as the future outlook in terms of surgery and fertility potential. Achieving optimal outcomes requires open and transparent dialogue with the family and caregivers, and should harness the resources of a multidisciplinary team. The multiple facets of this approach are outlined in this review. Keywords: Sex; gender; genitalia; DSD; -
Intersex 101
INTERSEX 101 With Your Guide: Phoebe Hart Secretary, AISSGA (Androgen Insensitivity Syndrome Support Group, Australia) And all‐round awesome person! WHAT IS INTERSEX? • a range of biological traits or variations that lie between “male” and “female”. • chromosomes, genitals, and/or reproductive organs that are traditionally considered to be both “male” and “female,” neither, or atypical. • 1.7 – 2% occurrence in human births REFERENCE: Australians Born with Atypical Sex Characteristics: Statistics & stories from the first national Australian study of people with intersex variations 2015 (in press) ‐ Tiffany Jones, School of Education, University of New England (UNE), Morgan Carpenter, OII Australia, Bonnie Hart, Androgyn Insensitivity Syndrome Support Group Australia (AISSGA) & Gavi Ansara, National LGBTI Health Network XY CHROMOSOMES ..... Complete Androgen Insensitivity Syndrome (CAIS) ..... Partial Androgen Insensitivity Syndrome (PAIS) ..... 5‐alpha‐reductase Deficiency (5‐ARD) ..... Swyer Syndrome/ Mixed Gonadal Dysgenesis (MGD) ..... Leydig Cell Hypoplasia ..... Persistent Müllerian Duct Syndrome ..... Hypospadias, Epispadias, Aposthia, Micropenis, Buried Penis, Diphallia ..... Polyorchidism, Cryptorchidism XX CHROMOSOMES ..... de la Chapelle/XX Male Syndrome ..... MRKH/Vaginal (or Müllerian) agenesis ..... XX Gonadal Dysgenesis ..... Uterus Didelphys ..... Progestin Induced Virilization XX or XY CHROMOSOMES ...... Congenital Adrenal Hyperplasia (CAH) ..... Ovo‐testes (formerly called "true hermaphroditism") ....