Manual of Diagnostic Ultrasound Volume1
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Congenital Diarrheal Disorders: an Updated Diagnostic Approach
4168 Int. J. Mol. Sci.2012, 13, 4168-4185; doi:10.3390/ijms13044168 OPEN ACCESS International Journal of Molecular Sciences ISSN 1422-0067 www.mdpi.com/journal/ijms Review Congenital Diarrheal Disorders: An Updated Diagnostic Approach Gianluca Terrin 1, Rossella Tomaiuolo 2,3,4, Annalisa Passariello 5, Ausilia Elce 2,3, Felice Amato 2,3, Margherita Di Costanzo 5, Giuseppe Castaldo 2,3 and Roberto Berni Canani 5,6,* 1 Department of Gynecology-Obstetrics and Perinatal Medicine, University of Rome “La Sapienza”, Viale del Policlinico 1, Rome 00161, Italy; E-Mail: [email protected] 2 CEINGE-Advanced Biotechnology, Via Comunale Margherita, Naples 80131, Italy; E-Mails: [email protected] (R.T.); [email protected] (A.E.); [email protected] (F.A.); [email protected] (G.C.) 3 Department of Biochemistry and Biotechnology, University of Naples “Federico II”, Via Pansini 5, Naples 80131, Italy 4 Biotechnology Science, University of Naples “Federico II”, Via De Amicis, Naples 80131, Italy 5 Department of Pediatrics, University of Naples “Federico II”, Via Pansini 5, Naples 80131, Italy; E-Mails: [email protected] (A.P.); [email protected] (M.D.C.) 6 European Laboratory for the Investigation of Food Induced Diseases, University of Naples “Federico II”, Via Pansini 5, Naples 80131, Italy * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel./Fax: +39-0817462680. Received: 18 February 2012; in revised form: 2 March 2012 / Accepted: 19 March 2012 / Published: 29 March 2012 Abstract: Congenital diarrheal disorders (CDDs) are a group of inherited enteropathies with a typical onset early in the life. -
Colonoscopic Review and Surgical Approach in the Management of Colorectal Carcinoma–A Retrospective Study of 50 Cases
Original Paper Colonoscopic Review and Surgical Approach in the Management of Colorectal Carcinoma–A Retrospective Study of 50 cases 1 2 3 Ershad-ul-Quadir M , Rahman MMM , Rahman MM Abstract Introduction: There is no exact statistics about the with abdominal pain 12 out of 22 cases (56%) and incidence of colorectal cancer in Bangladesh. weight loss 15 cases (68%). For left colon cancer According to National Cancer Institute, London, it is commonest symptom was weight loss and weakness the 2nd most common cancer affecting more than and altered bowel habit. Almost all cases with rectal 30,000 people in each year. As many patients with carcinoma presented with bleeding per rectum. colon cancer do not develop symptoms until it is advanced and detection in early stage can only be Conclusion: About 50% of lesions were found in achieved by screening of asymptomatic person. recto-sigmoid junction and male: female ratio was Maximum patients present lately with distance 1.9:1. All efforts and modern technology should be metastases when there is nothing to treat except applied for early detection and treatment. The palliative therapy. survival rate is usually very poor in rectal carcinoma. In this study most of the cases were subjected to Objectives: To identify the risk factors, early post operative Chemo and Radiotherapy, but more symptoms, signs, treatment modalities, operative were treated with neoadjuvant chemoradiation for outcome, morbidity and mortality rate. down staging. The need for early detection of Colorectal Carcinoma (CRC) should be stressed in Materials and Methods: This retrospective study the form of screening patient awareness and was carried out at CMH Dhaka during August 2002 understanding about symptomatology. -
Ultrasonography and Elastography Imaging
Jemds.com Case Report Post Traumatic Hematocele - Ultrasonography and Elastography Imaging Shivesh Pandey1, Suresh Vasant Phatak2, Gopidi Sai Nidhi Reddy3, Apoorvi Bharat Shah4 1, 2, 3, 4 Department of Radio diagnosis, Jawaharlal Nehru Medical College, Sawangi (Meghe), Wardha, Maharashtra India. INTRODUCTION Hematocele with blunt scrotal trauma is an uncommon cause of the testicular pain. Corresponding Author: Elastography is the new recent advance in the field of ultrasound. USG and Dr. Suresh Vasant Phatak, elastography findings of the acute hematocele is described in this aricle. Department of Radiodiagnosis, Jawaharlal Testicular trauma is the third most common cause of acute scrotal pain,1 and Nehru Medical College, Sawangi (Meghe), high-frequency ultrasonography (USG) with a linear array transducer is the first Wardha, Maharashtra – 442001, India. E-mail: [email protected] preferred modality for testicular trauma evaluation. Extra testicular haematoceles or blood collections inside the tunica vaginalis are the most common findings in the DOI: 10.14260/jemds/2021/340 scrotum after blunt injury.2 On clinical assessment, haematocele appears as a hard mass like swelling and causes pain in the scrotum. In the majority of cases, How to Cite This Article: spontaneous resolution occurs with the support of conservative therapy,3 even if Pandey S, Phatak SV, Reddy GSN, et al. Post treated conservatively, may result in infection, discomfort, or atrophy in undiagnosed traumatic hematocele - usg and broad hematoceles and testicular hematomas over time.4 elastography imaging. J Evolution Med A testis with its coverings, epididymis, and spermatic cord are all contained in Dent Sci 2021;10(21):1636-1638, DOI: 10.14260/jemds/2021/340 each hemiscrotum. -
Urological Trauma
Guidelines on Urological Trauma D. Lynch, L. Martinez-Piñeiro, E. Plas, E. Serafetinidis, L. Turkeri, R. Santucci, M. Hohenfellner © European Association of Urology 2007 TABLE OF CONTENTS PAGE 1. RENAL TRAUMA 5 1.1 Background 5 1.2 Mode of injury 5 1.2.1 Injury classification 5 1.3 Diagnosis: initial emergency assessment 6 1.3.1 History and physical examination 6 1.3.1.1 Guidelines on history and physical examination 7 1.3.2 Laboratory evaluation 7 1.3.2.1 Guidelines on laboratory evaluation 7 1.3.3 Imaging: criteria for radiographic assessment in adults 7 1.3.3.1 Ultrasonography 7 1.3.3.2 Standard intravenous pyelography (IVP) 8 1.3.3.3 One shot intraoperative intravenous pyelography (IVP) 8 1.3.3.4 Computed tomography (CT) 8 1.3.3.5 Magnetic resonance imaging (MRI) 9 1.3.3.6 Angiography 9 1.3.3.7 Radionuclide scans 9 1.3.3.8 Guidelines on radiographic assessment 9 1.4 Treatment 10 1.4.1 Indications for renal exploration 10 1.4.2 Operative findings and reconstruction 10 1.4.3 Non-operative management of renal injuries 11 1.4.4 Guidelines on management of renal trauma 11 1.4.5 Post-operative care and follow-up 11 1.4.5.1 Guidelines on post-operative management and follow-up 12 1.4.6 Complications 12 1.4.6.1 Guidelines on management of complications 12 1.4.7 Paediatric renal trauma 12 1.4.7.1 Guidelines on management of paediatric trauma 13 1.4.8 Renal injury in the polytrauma patient 13 1.4.8.1 Guidelines on management of polytrauma with associated renal injury 14 1.5 Suggestions for future research studies 14 1.6 Algorithms 14 1.7 References 17 2. -
Late Complications of Duplex System Ureterocele; Acute Urinary Retention, Stone Formation and Renal Atrophy Sipal Timucin¹*, Akdere Hakan² and Bumin Ors¹
Timucin et al. Int Arch Urol Complic 2015, 1:2 ISSN: 2469-5742 International Archives of Urology and Complications Case Report: Open Access Late Complications of Duplex System Ureterocele; Acute Urinary Retention, Stone Formation and Renal Atrophy Sipal Timucin¹*, Akdere Hakan² and Bumin Ors¹ 1Department of Urology, Cerkezkoy State Hospital, Turkey 2Trakya University Health Center for Medical Research and Practic, Turkey *Corresponding author: Sipal Timucin, Department of Urology, Cerkezkoy State Hospital, Tekirdag, Turkey, Tel: +905548430218, E-mail: [email protected] Abstract A 49- year-old woman was admitted to emergency department with a complaint of acute urinary retention. The investigation of the patient revealed right duplex system anomaly, ureterocele containing multiple stones and atrophic right kidney. After reliefing her urinary retention, endoscopic ureterocele de-roofing, two dj stents insertion and stones extraction were performed. The symptoms of the patient were relieved after treatment. The patient was asymptomatic at six month follow-up visit. Keywords Duplex system ureter, Multiple calculi, Transurethral ureterocele incision, Ureterocele, Renal atrophy Introduction Ureterocele is cystic dilation of the terminal ureter and its incidence among newborns was reported 1/500 – 1/4000 [1]. It may be associated with tissue defect of bladder, bladder neck and posterior urethra. Eighty percent of ureteroceles are seen in the ureter draining the upper pole of a complete ureteral duplication. The cases whose diagnoses are omitted in early ages may suffer from recurrent urinary Figure 1: KUB graphy revealed multiple stones in right lower quadrant tract infection, stone formation, septicaemia and renal failure in later years. They generally break out in single system, orthotropic and intravesical in adults [2]. -
Mimickers of Urothelial Carcinoma and the Approach to Differential Diagnosis
Review Mimickers of Urothelial Carcinoma and the Approach to Differential Diagnosis Claudia Manini 1, Javier C. Angulo 2,3 and José I. López 4,* 1 Department of Pathology, San Giovanni Bosco Hospital, 10154 Turin, Italy; [email protected] 2 Clinical Department, Faculty of Medical Sciences, European University of Madrid, 28907 Getafe, Spain; [email protected] 3 Department of Urology, University Hospital of Getafe, 28905 Getafe, Spain 4 Department of Pathology, Cruces University Hospital, Biocruces-Bizkaia Health Research Institute, 48903 Barakaldo, Spain * Correspondence: [email protected]; Tel.: +34-94-600-6084 Received: 17 December 2020; Accepted: 18 February 2021; Published: 25 February 2021 Abstract: A broad spectrum of lesions, including hyperplastic, metaplastic, inflammatory, infectious, and reactive, may mimic cancer all along the urinary tract. This narrative collects most of them from a clinical and pathologic perspective, offering urologists and general pathologists their most salient definitory features. Together with classical, well-known, entities such as urothelial papillomas (conventional (UP) and inverted (IUP)), nephrogenic adenoma (NA), polypoid cystitis (PC), fibroepithelial polyp (FP), prostatic-type polyp (PP), verumontanum cyst (VC), xanthogranulomatous inflammation (XI), reactive changes secondary to BCG instillations (BCGitis), schistosomiasis (SC), keratinizing desquamative squamous metaplasia (KSM), post-radiation changes (PRC), vaginal-type metaplasia (VM), endocervicosis (EC)/endometriosis (EM) (müllerianosis), -
And Diaphragm (Chilaiditi's Syndrome) in Children by A
Arch Dis Child: first published as 10.1136/adc.32.162.151 on 1 April 1957. Downloaded from INTERPOSITION OF THE COLON BETWEEN LIVER AND DIAPHRAGM (CHILAIDITI'S SYNDROME) IN CHILDREN BY A. D. M. JACKSON and C. J. HODSON From the Institute of Child Health, University ofLondon, and the Queen Elizabeth Hospitalfor Children, London (RECEIVED FOR PUBLICATION SEPTEMBER 24, 1956) In 1910 Chilaiditi published a paper in which he positions. On one occasion during the fluoroscopy the described three adult patients with gaseous ab- ascent of the colon and the displacement of the liver were dominal distension and intermittent displacement actually observed as the patient was rotated from the supine to the left lateral position. Fluoroscopy after an of the liver by a distended loop of colon. Although opaque meal excluded any form of intestinal obstruction there had been some earlier brief reports, for example and the interposed loop of bowel was identified as the those of Gontermann (1890), Cohn (1907) and hepatic flexure. Weinberger (1908), this was the first really detailed PROGRESS. During the six months following his first account of the condition which has come to be visit to hospital the child had recurrent attacks of severe known as Chilaiditi's syndrome. abdominal pain with vomiting and his mother became During the last 45 aware of his swallowing air. He was admitted to hos- years many more cases have copyright. been reported but very few of these have been pital in June, 1951, and put to bed. The attacks promptly children. It will be of some interest, therefore, ceased, although the abdominal distension persisted and the position of the liver could still be altered with posture. -
Complications of Splenectomy 2020; 4(2): 218-222 Received: 08-02-2020 Dr
International Journal of Surgery Science 2020; 4(2): 218-222 E-ISSN: 2616-3470 P-ISSN: 2616-3462 © Surgery Science Complications of splenectomy www.surgeryscience.com 2020; 4(2): 218-222 Received: 08-02-2020 Dr. Ketan Vagholkar Accepted: 10-03-2020 Dr. Ketan Vagholkar DOI: https://doi.org/10.33545/surgery.2020.v4.i2d.420 Professor, Department of Surgery. DY Patil University School of Abstract Medicine Navi Mumbai, Spleen is an important organ of the reticuloendothelial system. It plays a crucial role in the immunological Maharashtra, India system of the body. Understanding the consequences and diagnosis of hyposlenic and asplenic states is essential. Splenectomy is performed for a variety of indications ranging from haematological conditions to trauma. Complications of splenectomy include surgical as well as immunological. Overwhelming post splenectomy infection is one of the most dreaded complication with high mortality. The physiological basis of immunological function of the spleen, hyposplenism and complications of splenectomy are presented in this paper. Keywords: Post splenectomy, complications, hyposplenia, OPSI Introduction Spleen is a very important constituent organ of the reticuloendothelial system. The organ is crucial in regulating immune homeostasis through its ability to link innate and adoptive immunity in the process of protecting against infection. Hyposplenism is impairment of splenic function. It is usually acquired and caused by severe haematological and immunological disorders. Asplenia refers to the absence of the spleen which is rarely congenital but predominantly post-surgical (splenectomy). The most important complication of asplenic state is infectious complications [1]. These infections have high mortality. In addition to infectious complications, splenectomy can lead to a series of other complications. -
(NCCN Guidelines®) Hepatobiliary Cancers
NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Hepatobiliary Cancers Version 2.2015 NCCN.org Continue Version 2.2015, 02/06/15 © National Comprehensive Cancer Network, Inc. 2015, All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®. Printed by Alexandre Ferreira on 10/25/2015 6:11:23 AM. For personal use only. Not approved for distribution. Copyright © 2015 National Comprehensive Cancer Network, Inc., All Rights Reserved. NCCN Guidelines Index NCCN Guidelines Version 2.2015 Panel Members Hepatobiliary Cancers Table of Contents Hepatobiliary Cancers Discussion *Al B. Benson, III, MD/Chair † Renuka Iyer, MD Þ † Elin R. Sigurdson, MD, PhD ¶ Robert H. Lurie Comprehensive Cancer Roswell Park Cancer Institute Fox Chase Cancer Center Center of Northwestern University R. Kate Kelley, MD † ‡ Stacey Stein, MD, PhD *Michael I. D’Angelica, MD/Vice-Chair ¶ UCSF Helen Diller Family Yale Cancer Center/Smilow Cancer Hospital Memorial Sloan Kettering Cancer Center Comprehensive Cancer Center G. Gary Tian, MD, PhD † Thomas A. Abrams, MD † Mokenge P. Malafa, MD ¶ St. Jude Children’s Dana-Farber/Brigham and Women’s Moffitt Cancer Center Research Hospital/ Cancer Center The University of Tennessee James O. Park, MD ¶ Health Science Center Fred Hutchinson Cancer Research Center/ Steven R. Alberts, MD, MPH Seattle Cancer Care Alliance Mayo Clinic Cancer Center Jean-Nicolas Vauthey, MD ¶ Timothy Pawlik, MD, MPH, PhD ¶ The University of Texas Chandrakanth Are, MD ¶ The Sidney Kimmel Comprehensive MD Anderson Cancer Center Fred & Pamela Buffett Cancer Center at Cancer Center at Johns Hopkins The Nebraska Medical Center Alan P. -
New Jersey Chapter American College of Physicians
NEW JERSEY CHAPTER AMERICAN COLLEGE OF PHYSICIANS ASSOCIATES ABSTRACT COMPETITION 2015 SUBMISSIONS 2015 Resident/Fellow Abstracts 1 1. ID CATEGORY NAME ADDITIONAL PROGRAM ABSTRACT AUTHORS 2. 295 Clinical Abed, Kareem Viren Vankawala MD Atlanticare Intrapulmonary Arteriovenous Malformation causing Recurrent Cerebral Emboli Vignette FACC; Qi Sun MD Regional Medical Ischemic strokes are mainly due to cardioembolic occlusion of small vessels, as well as large vessel thromboemboli. We describe a Center case of intrapulmonary A-V shunt as the etiology of an acute ischemic event. A 63 year old male with a past history of (Dominik supraventricular tachycardia and recurrent deep vein thrombosis; who has been non-compliant on Rivaroxaban, presents with Zampino) pleuritic chest pain and was found to have a right lower lobe pulmonary embolus. The deep vein thrombosis and pulmonary embolus were not significant enough to warrant ultrasound-enhanced thrombolysis by Ekosonic EndoWave Infusion Catheter System, and the patient was subsequently restarted on Rivaroxaban and discharged. The patient presented five days later with left arm tightness and was found to have multiple areas of punctuate infarction of both cerebellar hemispheres, more confluent within the right frontal lobe. Of note he was compliant at this time with Rivaroxaban. The patient was started on unfractionated heparin drip and subsequently admitted. On admission, his vital signs showed a blood pressure of 138/93, heart rate 65 bpm, and respiratory rate 16. Cardiopulmonary examination revealed regular rate and rhythm, without murmurs, rubs or gallops and his lungs were clear to auscultation. Neurologic examination revealed intact cranial nerves, preserved strength in all extremities, mild dysmetria in the left upper extremity and an NIH score of 1. -
Laparoscopic Management of a Small Bowel Obstruction of Unknown Cause
View metadata, citation and similar papers at core.ac.uk brought to you by CORE CASE REPORT provided by PubMed Central Laparoscopic Management of a Small Bowel Obstruction of Unknown Cause E´lan Burton, MD, John McKeating, MD, Kurt Stahlfeld, MD ABSTRACT INTRODUCTION With the expanding indications for minimally invasive Adhesive small bowel obstruction (SBO) is a common and surgery, the management of small bowel obstruction is frequently encountered problem. If initial conservative evolving. The laparoscope shortens hospital stay, hastens management fails, operative exploration, and lysis of ad- recovery, and reduces morbidity, such as wound infection hesions is required. In patients with multiple previous and incisional hernia associated with open surgery. How- surgeries and significantly dilated small bowel, surgical ever, many surgeons are reluctant to attempt laparoscopy access to the peritoneal cavity can be quite difficult and is in patients with significantly distended small bowel and a associated with significant complications. Traditional dic- history of multiple previous abdominal operations. We tum would state that laparoscopy is contraindicated in present the management of a patient with a virgin abdo- such patients. men who presented with a small bowel obstruction most likely secondary to Fitz-Hugh-Curtis syndrome who was However, we are seeing an increased incidence of SBO in successfully managed with laparoscopic lysis of adhe- patients whose only previous abdominal surgery was via sions. the laparoscope. In these patients, and in those with virgin abdomens, the laparoscopic approach may be the pre- Key Words: Fitz-Hugh-Curtis syndrome, Chilaiditi syn- ferred way to diagnose and treat SBO. The following case drome, Small bowel obstruction. -
Well-Differentiated Angiosarcoma of Spleen: a Teaching Case Mimicking
Xu et al. World Journal of Surgical Oncology (2015) 13:300 DOI 10.1186/s12957-015-0716-1 WORLD JOURNAL OF SURGICAL ONCOLOGY CASE REPORT Open Access Well-differentiated angiosarcoma of spleen: a teaching case mimicking hemagioma and cytogenetic analysis with array comparative genomic hybridization Lichen Xu1†, Yimin Zhang1†, Hong Zhao1, Qingxiao Chen2, Weihang Ma1,3* and Lanjuan Li1 Abstract Primary splenic angiosarcoma is extremely rare but aggressive malignant vascular neoplasm. Here, we report a case of vascular tumor in spleen that was initially misinterpreted as hemangioma. Two years after splenectomy, the patient admitted again with aggravated abdomen pain and severe anemia. The magnetic resonance imaging (MRI) scan showed widely metastases. The ensuing biopsy for lesion both in liver and in bone marrow showed the similar pathological findings as that in spleen, which supported the final diagnosis of well-differentiated splenic angiosarcoma with extensive metastases. The patient was dead in 3 months after discharge without chemotherapy. The copy number changes for spleen lesion detected by array comparative genome hybridization showed copy number gain at 11q23.2, 11q24.3, 12q24.33, 13q34, copy number loss at 1q24.2-q31.3, 1q41-q42.2, 1 q42.3-q43, 2q36.3-q37.3, 2q37.7, 3q13.33-q26.2, 3q28 - q29, 9p11.2, 13q11, 15q11, homozygous copy loss at 8p11.22, 22q11.23. Less than 200 cases of splenic angiosarcoma have been published in literature of English. To the best of our knowledge, this is the first time analyzed cytogenetic alteration in a well-differentiated primary splenic angiosarcoma. Keywords: Angiosarcoma, Well-differentiation, Splenectomy, Array comparative genomic hybridization, Copy number change Background cytogenetic changes to this subgroup of angiosarcoma Primary splenic angiosarcoma (PSA) is a rare malignant has been published.