Management of Undescended Testes: European Association of Urology
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Clinical, Hormonal and Genetic Characteristics of Androgen Insensitivity Syndrome in 39 Chinese Patients Qingxu Liu, Xiaoqin Yin and Pin Li*
Liu et al. Reproductive Biology and Endocrinology (2020) 18:34 https://doi.org/10.1186/s12958-020-00593-0 RESEARCH Open Access Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients Qingxu Liu, Xiaoqin Yin and Pin Li* Abstract Background: Abnormal androgen receptor (AR) genes can cause androgen insensitivity syndrome (AIS), and AIS can be classified into complete androgen insensitivity syndrome (CAIS), partial androgen insensitivity syndrome (PAIS) and mild AIS. We investigated the characteristics of clinical manifestations, serum sex hormone levels and AR gene mutations of 39 AIS patients, which provided deeper insight into this disease. Methods: We prospectively evaluated 39 patients with 46, XY disorders of sex development (46, XY DSD) who were diagnosed with AIS at the Department of Endocrinology of Shanghai Children’s Hospital from 2014 to 2019. We analysed clinical data from the patients including hormone levels and AR gene sequences. Furthermore, we screened the AR gene sequences of the 39 AIS patients to identify probable mutations. Results: The 39 AIS patients came from 37 different families; 19 of the patients presented CAIS, and 20 of them presented PAIS. The CAIS patients exhibited a higher cryptorchidism rate than the PAIS (100 and 55%, P = 0.001). There were no significant difference between the CAIS and PAIS groups regarding the levels of inhibin B (INHB), sex hormone-binding globulin (SHBG), basal luteinizing hormone (LH), testosterone (T), or basal dihydrotestosterone (DHT), the T:DHT ratio, DHT levels after human chorionic gonadotropin (HCG) stimulation or T levels after HCG stimulation. However, the hormone levels of AMH (P = 0.010), peak LH (P = 0.033), basal FSH (P = 0.009) and peak FSH (P = 0.033) showed significant differences between the CAIS group and the PAIS group. -
Guidelines on Paediatric Urology S
Guidelines on Paediatric Urology S. Tekgül (Chair), H.S. Dogan, E. Erdem (Guidelines Associate), P. Hoebeke, R. Ko˘cvara, J.M. Nijman (Vice-chair), C. Radmayr, M.S. Silay (Guidelines Associate), R. Stein, S. Undre (Guidelines Associate) European Society for Paediatric Urology © European Association of Urology 2015 TABLE OF CONTENTS PAGE 1. INTRODUCTION 7 1.1 Aim 7 1.2 Publication history 7 2. METHODS 8 3. THE GUIDELINE 8 3A PHIMOSIS 8 3A.1 Epidemiology, aetiology and pathophysiology 8 3A.2 Classification systems 8 3A.3 Diagnostic evaluation 8 3A.4 Disease management 8 3A.5 Follow-up 9 3A.6 Conclusions and recommendations on phimosis 9 3B CRYPTORCHIDISM 9 3B.1 Epidemiology, aetiology and pathophysiology 9 3B.2 Classification systems 9 3B.3 Diagnostic evaluation 10 3B.4 Disease management 10 3B.4.1 Medical therapy 10 3B.4.2 Surgery 10 3B.5 Follow-up 11 3B.6 Recommendations for cryptorchidism 11 3C HYDROCELE 12 3C.1 Epidemiology, aetiology and pathophysiology 12 3C.2 Diagnostic evaluation 12 3C.3 Disease management 12 3C.4 Recommendations for the management of hydrocele 12 3D ACUTE SCROTUM IN CHILDREN 13 3D.1 Epidemiology, aetiology and pathophysiology 13 3D.2 Diagnostic evaluation 13 3D.3 Disease management 14 3D.3.1 Epididymitis 14 3D.3.2 Testicular torsion 14 3D.3.3 Surgical treatment 14 3D.4 Follow-up 14 3D.4.1 Fertility 14 3D.4.2 Subfertility 14 3D.4.3 Androgen levels 15 3D.4.4 Testicular cancer 15 3D.5 Recommendations for the treatment of acute scrotum in children 15 3E HYPOSPADIAS 15 3E.1 Epidemiology, aetiology and pathophysiology -
Single Scrotal Incision Orchiopexy - a Systematic Review ______Hugo Fabiano Fernandes Novaes, José Abraão Carneiro Neto, Antonio Macedo Jr, Ubirajara Barroso Júnior
REVIEW Article Vol. 39 (3): 305-311, May - June, 2013 doi: 10.1590/S1677-5538.IBJU.2013.03.02 Single scrotal incision orchiopexy - a systematic review _______________________________________________ Hugo Fabiano Fernandes Novaes, José Abraão Carneiro Neto, Antonio Macedo Jr, Ubirajara Barroso Júnior Section of Pediatric Urology, Division of Urology Bahiana School of Medicine and Federal University of Bahia and Federal University of São Paulo ABSTRACT ARTICLE INFO _________________________________________________________ ___________________ Objective: To conduct a systematic review on single scrotal incision orchiopexy. Key words: Materials and Methods: A search was performed using Pubmed, through which 16 ar- Cryptorchidism; Orchiopexy; ticles were selected out of a total of 133. The following conditions were considered ex- Scrotum; Surgical Procedures, clusion criteria: other surgical methods such as an inguinal procedure or a laparoscopic Operative approach, retractile testes, or patients with previous testicular or inguinal surgery. Results: A total of 1558 orchiopexy surgeries initiated with a transcrotal incision were Int Braz J Urol. 2013; 39: 305-11 analyzed. Patients’ ages ranged between 5 months and 21 years. Thirteen studies used __________________ high scrotal incisions, and low scrotal incisions were performed in the remainder of the studies. In 55 cases (3.53%), there was a need for inguinal incision. Recurrence was ob- Submitted for publication: served in 9 cases, testicular atrophy in 3, testicular hypotrophy in 2, and surgical site in- December 18, 2012 fections in 13 cases. High efficacy rates were observed, varying between 88% and 100%. __________________ Conclusions: Single scrotal incision orchiopexy proved to be an effective technique and is associated with low rates of complications. -
The History of Microsurgery in Urological Practice
Chen-1 The History of Microsurgery in Urological Practice Mang L. Chen1, Gregory M. Buncke2 and Paul J. Turek3 1G.U. Recon, San Francisco, CA, 94114 2The Buncke Clinic, San Francisco, CA 94114 3The Turek Clinic, Beverly Hills, CA 90210 Correspondence to: Mang Chen, MD G.U. Recon 45 Castro St, Suite 111 San Francisco, CA 94114 Tel: 415-481-3980 Email: [email protected] Chen-2 Abstract Operative microscopy spans all surgical disciplines, allowing human dexterity to perform beyond direct visual limitations. Microsurgery started in otolaryngology, became popular in reconstructive microsurgery, and was then adopted in urology. Starting with reproductive tract reconstruction of the vas and epididymis, microsurgery in urology now extends to varicocele repair, sperm retrieval, penile transplantation and free flap phalloplasty. By examining the peer reviewed and lay literature this review discusses the history of microsurgery and its subsequent development as a subspecialty in urology. Keywords: urology, microsurgery, phalloplasty, vasovasostomy, varicocelectomy Chen-3 I. Introduction Microsurgery has been instrumental to surgical advances in many medical fields. Otolaryngology, ophthalmology, gynecology, hand and plastic surgery have all embraced the operating microscope to minimize surgical trauma and scar and to increase patency rates of vessels, nerves and tubes. Urologic adoption of microsurgery began with vasectomy reversals, testis transplants, varicocelectomies and sperm retrieval and has now progressed to free flap phalloplasties and penile transplantation. In this review, we describe the origins of microsurgery, highlight the careers of prominent microsurgeons, and discuss current use applications in urology. II. Birth of Microsurgery 1) Technology The birth of microsurgery followed from an interesting marriage of technology and clinical need. -
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). -
Multiple Congenital Genitourinary Anomalies in a Polled Goat
Multiple Congenital Genitourinary Anomalies in a Polled Goat WILLIAM W. KING, DVM, PHD, DIPLOMATE, ACLAM,1,2* MELVIN E. YOUNG,1 AND M. EUGENE FOX, DVM3 A 1-day-old, Toggenburg/Nubian crossbred goat of polled parentage was referred for necropsy because of a large (diameter, 5 cm) bladder-like mass protruding from the perineal midline and difficult urination. Differential diagnoses included cutaneous cyst, ectopic urinary bladder, and urethral diverticulum/dilatation. Several genitourinary aberrations were noted. A second, smaller (diameter, 1 cm), more distal cystic structure was adjacent to an ambiguous prepuce. Testicles were discovered within a con- stricted, subcutaneous space near the inguinal canals. A rudimentary penis was located dorsal to the penile urethra with no appreciable urethral process. A tiny external urethral orifice was discerned only after liquid was injected into the lumen of the cystic structures, confirming their identity as urethral dilatations. The dilatations were separated by a constricting band of fibrous tissue. No other significant findings were detected. This case illustrates a combination of congenital anomalies including bilateral cryptorchidism with scrotal absence, segmental urethral hypoplasia, and urethral dilatation, most likely associated with the intersex condition seen in polled breeds. The continued production and use of small ruminants as animal models demands the prompt recognition of congenital anomalies. This case also exemplifies the precautions required when breeding goats with polled ancestry. The domestic goat (Capra hircus) has historically served and Nubian/Toggenburg sire. The owner reported that the doe had continues to play an important role in biomedical research (1). completed a normal gestation period on a diet of natural grass/ Many small breeds are available, facilitating common labora- alfalfa hay and water. -
Answer Key Chapter 1
Instructor's Guide AC210610: Basic CPT/HCPCS Exercises Page 1 of 101 Answer Key Chapter 1 Introduction to Clinical Coding 1.1: Self-Assessment Exercise 1. The patient is seen as an outpatient for a bilateral mammogram. CPT Code: 77055-50 Note that the description for code 77055 is for a unilateral (one side) mammogram. 77056 is the correct code for a bilateral mammogram. Use of modifier -50 for bilateral is not appropriate when CPT code descriptions differentiate between unilateral and bilateral. 2. Physician performs a closed manipulation of a medial malleolus fracture—left ankle. CPT Code: 27766-LT The code represents an open treatment of the fracture, but the physician performed a closed manipulation. Correct code: 27762-LT 3. Surgeon performs a cystourethroscopy with dilation of a urethral stricture. CPT Code: 52341 The documentation states that it was a urethral stricture, but the CPT code identifies treatment of ureteral stricture. Correct code: 52281 4. The operative report states that the physician performed Strabismus surgery, requiring resection of the medial rectus muscle. CPT Code: 67314 The CPT code selection is for resection of one vertical muscle, but the medial rectus muscle is horizontal. Correct code: 67311 5. The chiropractor documents that he performed osteopathic manipulation on the neck and back (lumbar/thoracic). CPT Code: 98925 Note in the paragraph before code 98925, the body regions are identified. The neck would be the cervical region; the thoracic and lumbar regions are identified separately. Therefore, three body regions are identified. Correct code: 98926 Instructor's Guide AC210610: Basic CPT/HCPCS Exercises Page 2 of 101 6. -
Transgender Identity and Cryptorchidism: a Case Study
ORIGINAL ARTICLE Volume 42, Issue 1, January-February 2019 doi: 10.17711/SM.0185-3325.2019.007 Transgender identity and cryptorchidism: A case study Tania Real Quintanar,1 Rebeca Robles García,1 María Elena Medina-Mora,1 Juan Carlos Jorge,2 Lucía Vázquez Pérez3 1 Centro de Investigación en Salud ABSTRACT Mental Global, Dirección de In- vestigaciones Epidemiológicas y There is a wide range of possible combinations in relation to sex at birth, gender identity, and Psicosociales, Instituto Nacional de Introduction. Psiquiatría Ramón de la Fuente Mu- sexual orientations. Specific medical and psychological treatment needs may also vary depending on these ñíz, Mexico City, Mexico. combinations. Objective. In order to promote interventions that focus on the perceived needs of those directly 2 Departamento de Anatomía y Neu- involved, the aim of the present case study is to describe the clinical and life experiences of a 43-year old trans- robiología, Escuela de Medicina, gender woman with cryptorchidism and examine the interplay between this relative common testicular problem Universidad de Puerto Rico, San at birth, gender identity, and sexual orientation formation processes from her own perspective. An Juan, Puerto Rico. Method. in-depth interview was conducted at a specialized care centre in Mexico City, Mexico. The interview was audio 3 Departamento de Investigaciones Epidemiológicas y Psicosociales, recorded and transcribed for a content analysis. Results. The case under analysis was assigned to the male Dirección de Investigaciones Epi- sex and identified herself as a transgender woman and lesbian. Although it is not possible to conclude that demiológicas y Psicosociales, Insti- her gender identity or sexual orientation is related to her antecedent of cryptorchidism, as she reflected on her tuto Nacional de Psiquiatría Ramón related negative experiences, she concluded that her gender identity and sexual orientation trajectories, as well de la Fuente Muñíz, Mexico City, Mexico. -
Health and Wellbeing of People with Intersex Variations Information and Resource Paper
Health and wellbeing of people with intersex variations Information and resource paper The Victorian Government acknowledges Victorian Aboriginal people as the First Peoples and Traditional Owners and Custodians of the land and water on which we rely. We acknowledge and respect that Aboriginal communities are steeped in traditions and customs built on a disciplined social and cultural order that has sustained 60,000 years of existence. We acknowledge the significant disruptions to social and cultural order and the ongoing hurt caused by colonisation. We acknowledge the ongoing leadership role of Aboriginal communities in addressing and preventing family violence and will continue to work in collaboration with First Peoples to eliminate family violence from all communities. Family Violence Support If you have experienced violence or sexual assault and require immediate or ongoing assistance, contact 1800 RESPECT (1800 737 732) to talk to a counsellor from the National Sexual Assault and Domestic Violence hotline. For confidential support and information, contact Safe Steps’ 24/7 family violence response line on 1800 015 188. If you are concerned for your safety or that of someone else, please contact the police in your state or territory, or call 000 for emergency assistance. To receive this publication in an accessible format, email the Diversity unit <[email protected]> Authorised and published by the Victorian Government, 1 Treasury Place, Melbourne. © State of Victoria, Department of Health and Human Services, March 2019 Victorian Department of Health and Human Services (2018) Health and wellbeing of people with intersex variations: information and resource paper. Initially prepared by T. -
Individualized Treatment Guidelines for Postpubertal Cryptorchidism
pISSN: 2287-4208 / eISSN: 2287-4690 World J Mens Health 2015 December 33(3): 161-166 http://dx.doi.org/10.5534/wjmh.2015.33.3.161 Review Article Individualized Treatment Guidelines for Postpubertal Cryptorchidism Jae Min Chung1,2, Sang Don Lee1,2 1Department of Urology, Pusan National University School of Medicine, 2Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Korea Cryptorchidism is a well-known congenital anomaly in children. However, its diagnosis is often delayed for reasons including patient unawareness or denial of abnormal findings in the testis. Moreover, it has been difficult to establish an optimal treatment strategy for postpubertal cryptorchidism, given the small number of patients. Unlike cryptorchidism in children, postpubertal cryptorchidism is associated with an increased probability of neoplasms, which has led orchiectomy to be the recommended treatment. However, routine orchiectomy should be avoided in some cases due to quality-of-life issues and the potential risk of perioperative mortality. Based on a literature review, this study proposes individualized treatment guidelines for postpubertal cryptorchidism. Key Words: Adolescent; Adult; Cryptorchidism INTRODUCTION egies for cryptorchidism in children are well-established. A surgical approach, most often orchiopexy, is recom- Cryptorchidism is a pathological condition in which the mended for testes that remain undescended after six testis fails to descend to the base of the scrotum. It is one months of age [3]. However, it has been difficult to estab- of the most common congenital anomalies encountered in lish a standard treatment for postpubertal cryptorchidism, pediatric urology. Despite extensive study, knowledge re- given the small number of patients with this condition. -
Icd-9-Cm (2010)
ICD-9-CM (2010) PROCEDURE CODE LONG DESCRIPTION SHORT DESCRIPTION 0001 Therapeutic ultrasound of vessels of head and neck Ther ult head & neck ves 0002 Therapeutic ultrasound of heart Ther ultrasound of heart 0003 Therapeutic ultrasound of peripheral vascular vessels Ther ult peripheral ves 0009 Other therapeutic ultrasound Other therapeutic ultsnd 0010 Implantation of chemotherapeutic agent Implant chemothera agent 0011 Infusion of drotrecogin alfa (activated) Infus drotrecogin alfa 0012 Administration of inhaled nitric oxide Adm inhal nitric oxide 0013 Injection or infusion of nesiritide Inject/infus nesiritide 0014 Injection or infusion of oxazolidinone class of antibiotics Injection oxazolidinone 0015 High-dose infusion interleukin-2 [IL-2] High-dose infusion IL-2 0016 Pressurized treatment of venous bypass graft [conduit] with pharmaceutical substance Pressurized treat graft 0017 Infusion of vasopressor agent Infusion of vasopressor 0018 Infusion of immunosuppressive antibody therapy Infus immunosup antibody 0019 Disruption of blood brain barrier via infusion [BBBD] BBBD via infusion 0021 Intravascular imaging of extracranial cerebral vessels IVUS extracran cereb ves 0022 Intravascular imaging of intrathoracic vessels IVUS intrathoracic ves 0023 Intravascular imaging of peripheral vessels IVUS peripheral vessels 0024 Intravascular imaging of coronary vessels IVUS coronary vessels 0025 Intravascular imaging of renal vessels IVUS renal vessels 0028 Intravascular imaging, other specified vessel(s) Intravascul imaging NEC 0029 Intravascular -
CRYPTORCHIDISM Patrick M. Mccue DVM, Phd, Diplomate American College of Theriogenologists
CRYPTORCHIDISM Patrick M. McCue DVM, PhD, Diplomate American College of Theriogenologists A horse is considered to be a cryptorchid to enter the scrotum in horses up to 2 to 3 (also known as a rig or ridgling) if one or years of age. both testes are not fully descended into the scrotum. Cryptorchid testes may be located Cryptorchid testes are incapable of under the skin outside of the inguinal canal, producing sperm due to the elevated within the inguinal canal or inside of the temperature of the retained testes. abdominal cavity. A horses with testes Consequently, a stallion would be sterile if located in the inguinal area outside of the both testes are cryptorchid. Stallions with body cavity is commonly known as a ‘high one retained testis and one scrotal testis are flanker’. usually fertile since an adequate number of motile sperm are produced by the descended Cryptorchidism in the horse can occur with testis to get mares pregnant. Libido and either the left or right testis or with both aggressive male behavior is present in testes. Failure of one or both testes to cryptorchid stallions since testosterone is descend into the scrotum may be due to still produced by the retained testes. As genetic predisposition, insufficient androgen shown in the photo below taken after (i.e. testosterone) stimulation, and other surgical removal of both testes, a factors. A genetic or heritable basis for the cryptorchid testis (right) is usually cryptorchid trait has been identified in the significantly smaller than the normal scrotal pedigrees of certain stallions. However, in testis.