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Prostatitis Explained Prostatitis
Prostate information Prostatitis Explained Prostatitis Prostatitis (prost-a-ty-tus) is the most common prostate problem for men under 50, but it can affect men of all ages. In fact, almost 1 out of 2 men between 18 and 50 may have at least one bout of prostatitis in their lifetime. Prostatitis is often described as an infection of the prostate but it can also mean that the prostate is inflammed or irritated. If you have prostatitis, you may have a burning feeling when passing urine, pass urine more often, be in a lot of pain, have a fever and chills and feel very tired. Once your doctor has diagnosed your symptoms as prostatitis, then the outlook tends to be good. There are many treatments available and your doctor will work with you to find the treatment(s) most suitable for you depending on the type of prostatitis you have. So, it may take slightly longer for some men to see an improvement in their symptoms. However, even when you feel your symptoms are starting to improve you should still continue with your treatment or medication. It may be reassuring to know that prostatitis is neither connected with cancer nor does it mean there is an increased risk of developing prostate cancer in the future, but it can cause worrying symptoms. Table of contents Page Types of prostatitis 3 Acute bacterial prostatitis 5 Chronic bacterial prostatitis 8 Chronic pelvic pain syndrome 9 Treatment for CBP and CPPS 13 Coping with pain 14 Tips to relieve prostatitis 16 Prostatitis There are different types of prostatitis. -
Improved Postmortem Diagnosis of Taenia Saginata Cysticercosis
IMPROVED POSTMORTEM DIAGNOSIS OF TAENIA SAGINATA CYSTICERCOSIS A Thesis Submitted to the College of Graduate Studies and Research in Partial Fulfilment of the Requirements for the Degree of Masters of Science in the Department of Veterinary Microbiology University of Saskatchewan Saskatoon By WILLIAM BRADLEY SCANDRETT Keywords: Taenia saginata, bovine cysticercosis, immunohistochemistry, histology, validation © Copyright William Bradley Scandrett, July, 2007. All rights reserved. PERMISSION TO USE In presenting this thesis in partial fulfilment of the requirements for a postgraduate degree from the University of Saskatchewan, I agree that the libraries of this university may make it freely available for inspection. I further agree that permission for copying of this thesis in any manner, in whole or in part, may be granted by the professor or professors who supervised my thesis work or, in their absence, by the Head of the Department or the Dean of the College in which my thesis work was done. It is understood that any copying or publication or use of this thesis or parts thereof for financial gain shall not be allowed without my written permission. It is also understood that due recognition be given to me and to the University of Saskatchewan in any scholarly use which may be made of any material in my thesis. Requests for permission to copy or to make use of material in this thesis in whole or in part should be addressed to: Head of the Department of Veterinary Microbiology University of Saskatchewan Saskatoon, Saskatchewan, S7N 5B4 i ABSTRACT Bovine cysticercosis is a zoonotic disease for which cattle are the intermediate hosts of the human tapeworm Taenia saginata. -
The Fine Art of Prostate Massage
The Fine Art of Prostate Massage Part I: What exactly are we dealing with here? Or, Anatomy, 101 • What is the prostate gland? Very simply, it is the part of the male body that store and secretes an essential part of semen. More specifically, the prostate gland produces an alkaline fluid that makes up about 30% of the semen. The alkalinity, interestingly, helps offset female vaginal acidity. • Where is the prostate gland? The prostate is located in lower abdominal area, roughly between the bladder and the rectal wall (which makes it easy to feel and to play with). Notice that one part of the prostate (shown in green) runs along the wall near the rectal area. This is the part that we are interested in. The prostate is slightly larger than a walnut, which can make both exams and play a bit challenging. Anatomy is highly variable, which means we have to be patient. • Do biological females have a prostate gland? Not in the same way that a biological male does. There is a small gland, also called the Skene’s Gland or the paraurethural gland. While it is homologous to the male prostate, it serves a slightly different purpose. An authoritative medical group officially called the female prostate such in 2002, and it is thus “officially” known as a prostate. It does play an active role during the female orgasm. The female prostate is located in approximately the same place as the male prostate. The anatomy here, though, is also highly variable. It may play a significant part in female “ejaculation”. -
2002 Asa Program.Pdf
schedule at a lance Wednesday, April 24, 2002 • Genetics and Biology of Adult Male Germ Cell 8:00 am Andrology Laboratory Workshop Tumors The Andrology Laboratory of the Future: Raju S.K. Chaganti, Memoria l Sloan-Kettering Impact of the Genomic and Proteomic • Modeling Human Disease Through Transgenesis Revolutions (concludes at 5:00 pm) Sarah Comerford, UTSWMS & HHI • How to Find Cellular Proteins that Sense the 5:30 pm Welcome and Opening Remarks Environment Da vid Garbers, HHM/ 5:45 pm Distinguished Andrologist Award 6:00 pm Serano Lecture 12:00 pm Laboratory Science Lunch • Of Genes and Genomes 1:30 pm Symposium Ill: Do Gene Defects Impact Da vid Botstein, Stanford University Male Reproduction: If So, How? •The Battle of the Sexes: Sry and the Control of Testis 7:15 pm Welcome Reception Organogenesis Blanche Capel, Duke Univ. Med. Ctr. Thursday, April 25, 2002 • Natural Potent Androgens: Lessons from Human Genetic Models 8:00 am Solvay/Unimed Lecture J. /mperato-McGinley, Cornell University •Androgen Therapy in the Older Man-Where • Genetic Defects in Male Reproduction Are We Now and Where Are We Going? Stephanie Seminara, Harvard University Lisa Te nover, Emory University 3:00 pm Refreshment Break and Exhibits 8:55 am Distinguished Service Award 3:15 pm Plenary Lecture 9:05 am Biopore Lecture • The Ins & Outs of PSMA, the Evolving and • Global Analysis of Germline Gene Expression Intriguing Tale of its Prostate Biology & Tumor Sam Wa rd, University of Arizona Targeting WO. Heston, Cleveland Clinic 10:00 am Coffee Break and Exhibits 4:05 pm Schering Lecture 10:30 am Concurrent Oral Sessions I, II, Ill • Bioethics and Stem Cell Research • Basic and Clinical Aspects of Male Sexual Laurie Zoloff, San Fra ncisco State Univ. -
Andrological Sciences Official Journal of the Italian Society of Andrology
Vol. 17 • No. 2 • June 2010 Journal of ANDROLOGICAL SCIENCES Official Journal of the Italian Society of Andrology Cited in Past Editors Editorial Board Fabrizio Menchini Fabris (Pisa) Antonio Aversa (Roma) SCOPUS Elsevier Database 1994-2004 Ciro Basile Fasolo (Pisa) Carlo Bettocchi (Bari) Edoardo Pescatori (Modena) Guglielmo Bonanni (Padova) Paolo Turchi (Pisa) Massimo Capone (Gorizia) 2005-2008 Tommasi Cai (Firenze) Luca Carmignani (Milano) Antonio Casarico (Genova) Editors-in-Chief Carlo Ceruti (Torino) Vincenzo Ficarra (Padova) Fulvio Colombo (Milano) Andrea Salonia (Milano) Luigi Cormio (Foggia) Federico Dehò (Milano) Giorgio Franco (Roma) Editor Assistant Andrea Galosi (Ancona) Ferdinando Fusco (Napoli) Giulio Garaffa (London) Andrea Garolla (Padova) Paolo Gontero (Torino) Managing Editor Vincenzo Gulino (Roma) Vincenzo Gentile (Roma) Massimo Iafrate (Padova) Copyright Sandro La Vignera (Catamia) SIAS S.r.l. • via Luigi Bellotti Bon, 10 Francesco Lanzafame (Catania) 00197 Roma Delegate of Executive Committee Giovanni Liguori (Trieste) of SIA Mario Mancini (Milano) Editorial Office Giuseppe La Pera (Roma) Alessandro Mofferdin (Modena) Lucia Castelli (Editorial Assistant) Nicola Mondaini (Firenze) Tel. 050 3130224 • Fax 050 3130300 Giacomo Novara (Padova) [email protected] Section Editor – Psychology Enzo Palminteri (Arezzo) Pacini Editore S.p.A. • Via A. Gherardesca 1 Annamaria Abbona (Torino) Furio Pirozzi Farina (Sassari) 56121 Ospedaletto (Pisa), Italy Giorgio Pomara (Pisa) Marco Rossato (Padova) Publisher Statistical Consultant Paolo Rossi (Pisa) Pacini Editore S.p.A. Elena Ricci (Milano) Antonino Saccà (Milano) Via A. Gherardesca 1, Gianfranco Savoca (Palermo) 56121 Ospedaletto (Pisa), Italy Omidreza Sedigh (Torino) Tel. 050 313011 • Fax 050 3130300 Marcello Soli (Bologna) [email protected] Paolo Verze (Napoli) www.pacinimedicina.it Alessandro Zucchi (Perugia) www.andrologiaitaliana.it INDEX Journal of Andrological Sciences EDITORIAL PCA3 a promising urine biomarker for prostate cancer diagnosis V. -
Specific Antigen Level and Serum Fasting Glucose, Total Cholesterol
Original Article DO I: 10.4274/uob.999 Bulletin of Urooncology 2018;17:59-62 Assessment of the Relationship Between Serum Prostate- Specific Antigen Level and Serum Fasting Glucose, Total Cholesterol and Neutrophil-Lymphocyte Ratio in Men Aged 50-70 Years with Prostate-Specific Antigen Level 0-10 ng/mL without Prostate Cancer Diagnosis Bora İrer MD İzmir Metropolitan Municipality Eşrefpaşa Hospital, Clinic of Urology, İzmir, Turkey Abstract Objective: To evaluate the relationship between serum prostate-specific antigen (PSA) level and total cholesterol, fasting blood glucose, and neutrophil- lymphocyte ratio (NLR) in men without prostate cancer. Materials and Methods: Between 2010 and 2017, 2631 male participants aged 50-70 years with a serum PSA level of 0-10 ng/mL were included from a population of 4643 healthy males who participated in a health screening program conducted by the İzmir Metropolitan Municipality Eşrefpaşa Hospital in the district villages of İzmir. Participants’ serum PSA, fasting blood glucose, total cholesterol levels, and NLR were retrospectively assessed. Participants were grouped as those with high and low serum PSA levels, high and low glucose levels, and high and low cholesterol levels. Differences between the groups in terms of serum PSA levels, serum total cholesterol, glucose, and NLR were analyzed. Results: The mean age of the participants was 60.2±5.4 years and the mean serum PSA level was 1.28±1.20 ng/mL. The mean PSA value was higher in the high cholesterol group (1.36±1.33 vs 1.19±1.02, p<0.001) compared to the low cholesterol group, and the mean PSA value in the high glucose group was lower than in the low glucose group (1.08±0.86 vs 1.32±1.25, p<0.001). -
Normal 3T MR Anatomy of the Prostate Gland and Surrounding Structures
Hindawi Advances in Medicine Volume 2019, Article ID 3040859, 9 pages https://doi.org/10.1155/2019/3040859 Review Article Normal 3T MR Anatomy of the Prostate Gland and Surrounding Structures K. Sklinda ,1 M. Fra˛czek,2 B. Mruk,1 and J. Walecki1 1MD PhD, Dpt. of Radiology, Medical Center of Postgraduate Education, CSK MSWiA, Woloska 137, 02-507 Warsaw, Poland 2MD, Dpt. of Radiology, Medical Center of Postgraduate Education, CSK MSWiA, Woloska 137, 02-507 Warsaw, Poland Correspondence should be addressed to K. Sklinda; [email protected] Received 24 September 2018; Accepted 17 December 2018; Published 28 May 2019 Academic Editor: Fakhrul Islam Copyright © 2019 K. Sklinda et al. +is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Development on new fast MRI scanners resulted in rising number of prostate examinations. High-spatial resolution of MRI examinations performed on 3T scanners allows recognition of very fine anatomical structures previously not demarcated on performed scans. We present current status of MR imaging in the context of recognition of most important anatomical structures. 1. Introduction also briefly present benign prostate hypertrophy (BPH) which is the most common condition of the prostate, oc- Aging of the society together with growing consciousness of curring in most patients over 50 years of age. the role of early detection of oncologic diseases leads to globally occurring rise in number of detected cases of 2. Imaging Protocol prostate cancer. Widely used transrectal sonography of the prostate gland despite additional support of contrast media According to PI-RADS v2, T1W and T2W sequences should and elastography does not provide sufficient sensitivity or be obtained for all prostate mpMR exams [1]. -
Narrative Review of Urinary Glycan Biomarkers in Prostate Cancer
1864 Review Article on Urinary Biomarkers of Urological Malignancies Narrative review of urinary glycan biomarkers in prostate cancer Shingo Hatakeyama1^, Tohru Yoneyama2^, Yuki Tobisawa3^, Hayato Yamamoto3, Chikara Ohyama1,2,3^ 1Department of Advanced Blood Purification Therapy, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; 2Department of Glycotechnology, Center for Advanced Medical Research, Hirosaki University Graduate School of Medicine, Hirosaki, Japan; 3Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan Contributions: (I) Conception and design: S Hatakeyama; (II) Administrative support: None; (III) Provision of study materials or patients: None; (IV) Collection and assembly of data: All authors; (V) Data analysis and interpretation: All authors; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors. Correspondence to: Shingo Hatakeyama, MD. Department of Urology, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki 036- 8562, Japan. Email: [email protected]. Abstract: Prostate cancer (PC) is the second most common cancer in men worldwide. The application of the prostate-specific antigen (PSA) test has improved the diagnosis and treatment of PC. However, the PSA test has become associated with overdiagnosis and overtreatment. Therefore, there is an unmet need for novel diagnostic, prognostic, and predictive biomarkers of PC. Urinary glycoproteins and exosomes are a potential source of PC glycan biomarkers. Urinary glycan profiling can provide noninvasive monitoring of tumor heterogeneity and aggressiveness throughout a treatment course. However, urinary glycan profiling is not popular due to technical disadvantages, such as complicated structural analysis that requires specialized expertise. The technological development of glycan analysis is a rapidly advancing field. A lectin-based microarray can detect aberrant glycoproteins in urine, including PSA glycoforms and exosomes. -
Controversies in Using Urine Samples for Prostate Cancer Detection: PSA and PCA3 Expression Analysis
Clinical Urology Prostate Cancer detection International Braz J Urol Vol. 37 (6): 719-726, November - December, 2011 Controversies in using urine samples for Prostate Cancer detection: PSA and PCA3 expression analysis S. Fontenete, J. Silva, A.L. Teixeira, R. Ribeiro, E. Bastos, F. Pina, R. Medeiros Molecular Oncology Group and Virology LB (SF, JS, ALT, RR, RM), Portuguese Institute of Oncol- ogy of Porto; ICBAS, Abel Salazar Institute for the Biomedical Sciences (SF, JS, ALT, RR, RM), University of Porto; Research Department - Portuguese League Against Cancer (NRN) (JS, ALT, RR, RM), Porto; Centre of Genetics and Biotechnology (EB), University of Trás-os-Montes and Alto Douro; Department of Urology (FP), S. João Hospital, University of Porto Medical School; CE- BIMED, Faculty of Health Sciences of Fernando Pessoa University (RM), Porto, Portugal ABSTRACT Purpose: Prostate cancer (PCa) is one of the most commonly diagnosed malignancies in the world. Although PSA utili- zation as a serum marker has improved prostate cancer detection it still presents some limitations, mainly regarding its specificity. The expression of this marker, along with the detection of PCA3 mRNA in urine samples, has been suggested as a new approach for PCa detection. The goal of this work was to evaluate the efficacy of the urinary detection of PCA3 mRNA and PSA mRNA without performing the somewhat embarrassing prostate massage. It was also intended to opti- mize and implement a methodological protocol for this kind of sampling. Materials and Methods: Urine samples from 57 patients with suspected prostate disease were collected, without under- going prostate massage. Increased serum PSA levels were confirmed by medical records review. -
Enophthalmos As the Initial Systemic Finding of Undiagnosed Metastatic Breast Carcinoma
International Medical Case Reports Journal Dovepress open access to scientific and medical research Open Access Full Text Article CASE SERIES Enophthalmos as the Initial Systemic Finding of Undiagnosed Metastatic Breast Carcinoma This article was published in the following Dove Press journal: International Medical Case Reports Journal Jessica El-Khazen Dupuis Purpose: To report on the importance of detecting and investigating non-traumatic Michael Marchand enophthalmos, which occurred as the first presenting sign of an undiagnosed metastatic Simon Javidi breast carcinoma in two patients with no prior history of neoplasia. Tuan Quynh Tram Nguyen Design: Case series. Observations: The first case consists of a 74-year-old woman with no significant past Department of Ophthalmology, Centre medical history, who presented with a non-traumatic enophthalmos and ptosis of her left eye, Hospitalier de l’Université de Montréal (CHUM), Montreal, QC H2X 3E4, and horizontal diplopia on right-gaze. Imaging revealed an intraconal lesion of her left orbit, Canada with orbital fat atrophy. Transcutaneous anterior orbitotomy was performed for tumor biopsy, and the histopathology study concluded on a diagnosis of orbital metastasis consistent with infiltrative breast carcinoma. Thorough breast imaging and multiple breast biopsies were not able to localize the primary tumor. The second case consists of a 76-year-old woman, with no prior relevant medical history, who presented for progressive enophthalmos and ptosis of her right eye. Imaging revealed an osteolytic lesion of her right frontal bone, and multiple infiltrative lesions implicating both orbits. A biopsy was performed through a transcutaneous anterior orbitotomy and histopathology study lead to a diagnosis of meta static lobular breast carcinoma. -
Mvdr. Natália Hvizdošová, Phd. Mudr. Zuzana Kováčová
MVDr. Natália Hvizdošová, PhD. MUDr. Zuzana Kováčová ABDOMEN Borders outer: xiphoid process, costal arch, Th12 iliac crest, anterior superior iliac spine (ASIS), inguinal lig., mons pubis internal: diaphragm (on the right side extends to the 4th intercostal space, on the left side extends to the 5th intercostal space) plane through terminal line Abdominal regions superior - epigastrium (regions: epigastric, hypochondriac left and right) middle - mesogastrium (regions: umbilical, lateral left and right) inferior - hypogastrium (regions: pubic, inguinal left and right) ABDOMINAL WALL Orientation lines xiphisternal line – Th8 subcostal line – L3 bispinal line (transtubercular) – L5 Clinically important lines transpyloric line – L1 (pylorus, duodenal bulb, fundus of gallbladder, superior mesenteric a., cisterna chyli, hilum of kidney, lower border of spinal cord) transumbilical line – L4 Bones Lumbar vertebrae (5): body vertebral arch – lamina of arch, pedicle of arch, superior and inferior vertebral notch – intervertebral foramen vertebral foramen spinous process superior articular process – mammillary process inferior articular process costal process – accessory process Sacrum base of sacrum – promontory, superior articular process lateral part – wing, auricular surface, sacral tuberosity pelvic surface – transverse lines (ridges), anterior sacral foramina dorsal surface – median, intermediate, lateral sacral crest, posterior sacral foramina, sacral horn, sacral canal, sacral hiatus apex of the sacrum Coccyx coccygeal horn Layers of the abdominal wall 1. SKIN 2. SUBCUTANEOUS TISSUE + SUPERFICIAL FASCIAS + SUPRAFASCIAL STRUCTURES Superficial fascias: Camper´s fascia (fatty layer) – downward becomes dartos m. Scarpa´s fascia (membranous layer) – downward becomes superficial perineal fascia of Colles´) dartos m. + Colles´ fascia = tunica dartos Suprafascial structures: Arteries and veins: cutaneous brr. of posterior intercostal a. and v., and musculophrenic a. -
Genitalia Blood Supply to Internal Female Course
U4-Reproductive BS+NS DEC 2016 FNF, approved by: DR.manoj Blood supply to internal female genitalia: artery origin distribution Anastamoses? Course Sup. large branch: Medially in base of broad Yes, cranially with Internal iliac uterus, inf. Small ligament to junction between ovarian, caudally uterine artery branch: cervix+ sup. cervix and uterus, run above with vaginal Vagina ureter, ascend to anastamose Middle +inferior part Yes, ant+post azygos Descand to vagina after Uterine of vagina along with arteries of vagina branching at junction between Vaginal artery pudendal artery with uterine artery uterus + cervix Yes, with uterine Descend along post. abdominal artery (collateral Ovarian Abdominal wall, at pelvic prim cross Ovary+ uterine tube circulation between artery aorta external iliac> enter suspensory abdominal +pelvic ligament source) vein Drainage Anastamoses? Course Vaginal venous plexus>vaginal vein> anastamose with uterine venous plexus Yes, vaginal plexus with Sides of vagina Vaginal >uterovaginal venous plexus>uterine uterine plexus vein>internal iliac vein uterine venous plexus >uterovaginal Yes, vaginal plexus with Uterine venous plexus>uterine vein>internal iliac Pass in broad ligament uterine plexus vein Pampiniform plexus of veins>ovarian vein Plexus in broad ligament Ovarian Rt:IVC - , ovarian vein in suspensory ligament Lt:LRV Note: -tubal veins drain in ovarian veins+ uterovaginal venous plexus -uterine vessels pass in cardinal ligament 1 | P a g e U4-Reproductive BS+NS DEC 2016 FNF, approved by: DR.manoj Blood supply to external female genitalia: artery origin distribution Course Perineum Leave pelvis through greater sciatic foramen hook Internal Internal iliac artery +external around ischial spine then enter through lesser pudendal genitalia sciatic foramen.