Lymphadenopathy & Cervical Lymphadenitis Guidelines
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Isolated Cervical Lymph Node Sarcoidosis Presenting in an Asymptomatic Neck Mass: a Case Report
http://dx.doi.org/10.4046/trd.2013.75.3.116 CASE REPORT ISSN: 1738-3536(Print)/2005-6184(Online) • Tuberc Respir Dis 2013;75:116-119 Isolated Cervical Lymph Node Sarcoidosis Presenting in an Asymptomatic Neck Mass: A Case Report Yong Shik Kwon, M.D.1, Hye In Jung, M.D.1, Hyun Jung Kim, M.D.1, Jin Wook Lee, M.D.1, Won-Il Choi, M.D., Ph.D.1, Jin Young Kim, M.D.2, Byung Hak Rho, M.D., Ph.D.2, Hye Won Lee, M.D.3 and Kun Young Kwon, M.D., Ph.D.3 Departments of 1Internal Medicine, 2Radiology, and 3Pathology, Keimyung University Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea Sarcoidosis, a systemic granulomatous disease of unknown etiology. The presentation of sarcoidal granuloma in neck nodes without typical manifestations of systemic sarcoidosis is difficult to diagnose. We describe the case of a 37-year-old woman with an increasing mass on the right side of neck. The excisional biopsy from the neck mass showed noncaseating epithelioid cell granuloma of the lymph nodes. No evidence of mycobacterial or fungal infection was noted. Thoracic evaluations did not show enlargement of mediastinal lymph nodes or parenchymal abnormalities. Immunohistochemistry showed abundant expression of tumor necrosis factor-α in the granuloma. However, transforming growth factor-β was not expressed, although interleukin-1β was focally expressed. These immunohistochemical findings supported characterization of the granuloma and the diagnosis of sarcoidosis. Sarcoidosis can present with cervical lymph node enlargement without mediastinal or lung abnormality. Immunohistochemistry may support the diagnosis of sarcoidosis and characterization of granuloma. -
The Male Reproductive System
Management of Men’s Reproductive 3 Health Problems Men’s Reproductive Health Curriculum Management of Men’s Reproductive 3 Health Problems © 2003 EngenderHealth. All rights reserved. 440 Ninth Avenue New York, NY 10001 U.S.A. Telephone: 212-561-8000 Fax: 212-561-8067 e-mail: [email protected] www.engenderhealth.org This publication was made possible, in part, through support provided by the Office of Population, U.S. Agency for International Development (USAID), under the terms of cooperative agreement HRN-A-00-98-00042-00. The opinions expressed herein are those of the publisher and do not necessarily reflect the views of USAID. Cover design: Virginia Taddoni ISBN 1-885063-45-8 Printed in the United States of America. Printed on recycled paper. Library of Congress Cataloging-in-Publication Data Men’s reproductive health curriculum : management of men’s reproductive health problems. p. ; cm. Companion v. to: Introduction to men’s reproductive health services, and: Counseling and communicating with men. Includes bibliographical references. ISBN 1-885063-45-8 1. Andrology. 2. Human reproduction. 3. Generative organs, Male--Diseases--Treatment. I. EngenderHealth (Firm) II. Counseling and communicating with men. III. Title: Introduction to men’s reproductive health services. [DNLM: 1. Genital Diseases, Male. 2. Physical Examination--methods. 3. Reproductive Health Services. WJ 700 M5483 2003] QP253.M465 2003 616.6’5--dc22 2003063056 Contents Acknowledgments v Introduction vii 1 Disorders of the Male Reproductive System 1.1 The Male -
Genital Ulcers and Swelling in an Adolescent Girl
PHOTO CHALLENGE Genital Ulcers and Swelling in an Adolescent Girl Meghan E. Ryan, DO; Pui-Ying Iroh Tam, MD A 14-year-old previously healthy, postmenarcheal adolescent girl with a family history of thyroid dis- ease and rheumatoid arthritis presented with vulvar pain and swelling. Vulvar pruritus was noted 6 days prior, which worsened and became associated with vulvar swelling, yellow vaginal discharge, dif- ficulty walking, and a fever (temperature, 39.3°C). Her condition did not improve after a course of cephalexin andcopy trimethoprim-sulfamethoxazole. She denied being sexually active or exposing for- eign objects or chemicals to the vaginal area. not WHAT’S THE DIAGNOSIS? a. Behçet disease Dob. candida c. chlamydia d. Epstein-Barr virus e. herpes simplex virus PLEASE TURN TO PAGE E5 FOR THE DIAGNOSIS CUTIS Dr. Ryan was from Des Moines University College of Osteopathic Medicine, Iowa. Dr. Ryan currently is from and Dr. Iroh Tam is from the University of Minnesota Masonic Children’s Hospital, Minneapolis. Dr. Iroh Tam is from the Department of Pediatric Infectious Diseases and Immunology. The authors report no conflict of interest. Correspondence: Pui-Ying Iroh Tam, MD, 3-210 MTRF, 2001 6th St SE, Minneapolis, MN 55455 ([email protected]). E4 I CUTIS® WWW.CUTIS.COM Copyright Cutis 2017. No part of this publication may be reproduced, stored, or transmitted without the prior written permission of the Publisher. PHOTO CHALLENGE DISCUSSION THE DIAGNOSIS: Epstein-Barr Virus hysical examination revealed bilateral 1-cm ulcer- is the assumed etiology of genital ulcers, especially in ated lesions on the labia minora with vulvar edema sexually active patients, and misdiagnosis in the setting of P(Figure). -
| Tidsskrift for Den Norske Legeforening a Previously Healthy Man in His Late Forties Consulted His Doctor About a Lump in His Anus
A man in his forties with anal tumour and inguinal lymphadenopathy NOE Å LÆRE AV SVETLANA SHARAPOVA E-mail: [email protected] Department of Gastrointestinal and Paediatric Surgery Oslo University Hospital Svetlana Sharapova, specialty registrar in general surgery and gastrointestinal surgery, and acting consultant. The author has completed the ICMJE form and declares no conflicts of interest. USHA HARTGILL Olafia Clinic Department of Venereology Oslo University Hospital Usha Hartgill, specialist in dermatological and venereal diseases, head of department and senior consultant. The author has completed the ICMJE form and declares no conflicts of interest. PREMNAATH TORAYRAJU Olafia Clinic Department of Venereology Oslo University Hospital Premnaath Torayraju, specialty registrar in the Department of Medicine at Diakonhjemmet Hospital, specialising in dermatological and venereal diseases. The author has completed the ICMJE form and declares no conflicts of interest. BETTINA ANDREA HANEKAMP Department of Radiology Oslo University Hospital Bettina Andrea Hanekamp, specialist in radiology, and senior consultant in the Section for Oncological and Abdominal Imaging. The author has completed the ICMJE form and declares no conflicts of interest. SIGURD FOLKVORD Department of Gastrointestinal and Paediatric Surgery Oslo University Hospital Sigurd Folkvord, PhD, senior consultant and specialist in gastrointestinal surgery. The author has completed the ICMJE form and declares no conflicts of interest. A man in his late forties was examined for suspected cancer of the anal canal with spreading to inguinal lymph nodes. When biopsies failed to confirm malignant disease, other differential diagnoses had to be considered. A man in his forties with anal tumour and inguinal lymphadenopathy | Tidsskrift for Den norske legeforening A previously healthy man in his late forties consulted his doctor about a lump in his anus. -
Case 3.1 X-Linked Agammaglobulinaemia (Bruton’S Disease)
Case 3.1 X-linked agammaglobulinaemia (Bruton’s disease) Peter was born after an uneventful pregnancy, weighing 3.1 kg. At 3 months, he developed otitis media; at the ages of 5 months and 11 months, he was admitted to hospital with untypable Haemophilus influenzae pneumonia. These infections responded promptly to appropriate antibiotics on each occasion. He is the fourth child of unrelated parents: his three sisters showed no predisposition to infection. Examination at the age of 18 months showed a pale, thin child whose height and weight were below the third centile. There were no other abnormal features. He had been fully immunized as an infant (at 2, 3 and 4 months) with tetanus and diphtheria toxoids, acellular pertussis, Hib and Mening. C conjugate vaccines and polio (Salk). In addition, he had received measles, mumps and rubella vaccine at 15 months. All immunizations were uneventful. Immunological investigations (Table 3.4) into the cause of his recurrent infections showed severe reduction in all three classes of serum immunoglobulins and no specific antibody production. Although there was no family history of agammaglobulinaemia, the lack of mature B lymphocytes in his peripheral blood suggested a failure of B-cell differentiation and strongly supported a diagnosis of infantile X-linked agammaglobulinaemia (Bruton’s disease). This was confirmed by detection of a disease-causing mutation in the Btk gene. The antibody deficiency was treated by 2-weekly intravenous infusions of human normal IgG in a dose of 400 mg/kg body weight/month. Over the following 7 years, his health steadily improved, weight and height are now on the 30th centile, and he has had only one episode of otitis media in the last 4 years. -
Managing Tooth Pain in General Practice
Singapore Med J 2019; 60(5): 224-228 Practice Integration & Lifelong Learning https://doi.org/10.11622/smedj.2019044 CMEARTICLE Managing tooth pain in general practice Sky Wei Chee Koh1, MBChB, Chun Fai Li2, BDS, John Ser Pheng Loh2, MDS, MBBS, Mun Loke Wong2, BDS, MSc, Victor Weng Keong Loh1, MCFP, MHPE Mr Tan, a 48-year-old banker with no significant past medical history, visited your clinic with the complaint of severe right-sided tooth pain that radiated to the right temporal region of the head. The pain was excruciating and had affected his concentration at work. The over- the-counter paracetamol he had taken did not seem to relieve the pain and Mr Tan felt that it could not just be a simple toothache. He asked you to prescribe some antibiotics to treat what he believed was a dental infection. WHAT IS TOOTH PAIN? infection.(6) This bidirectional relationship underscores the pivotal Tooth pain, which is often known as toothache, refers to the role that primary care physicians play in the prompt diagnosis, symptom of pain arising from the tooth (or teeth). investigation and management of patients with oral conditions. HOW COMMON IS THIS IN MY WHAT CAN I DO IN MY PRACTICE? PRACTICE? Clinical history and examination Dental caries (Fig. 1) is a common dental condition. Globally, up Many oral conditions may mimic tooth pain and it is important to to 35% of people have untreated dental caries,(1) and an estimated delineate the different causes with history-taking and examination. 32.4% of the Singapore population will experience pain from We suggest the following: symptomatic dental caries in their lifetime.(2) Locally, oral disease • Identify the source of pain by taking a comprehensive pain is ranked 16th in terms of years lost to disability and has been history. -
Association of GUTB and Tubercular Inguinal Lymphadenopathy - a Rare Co-Occurrence
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) e-ISSN: 2279-0853, p-ISSN: 2279-0861.Volume 15, Issue 7 Ver. I (July 2016), PP 109-111 www.iosrjournals.org Association of GUTB and Tubercular inguinal lymphadenopathy - A rare co-occurrence. 1Hemant Kamal, 2Dr. Kirti Kshetrapal, 3Dr. Hans Raj Ranga 1Professor, Department of Urology & reconstructive surgery, PGIMS Rohtak-124001 (Haryana) Mobile- 9215650614 2Prof. Anaesthesia PGIMS Rohtak, 3Associate Prof. Surgery PGIMS Rohtak. Abstract : Here we present a rare combination of GUTB with B/L inguinal lymphadenopathy in a 55y old male patient presented with pain right flank , fever & significant weight loss for the last 3 months. Per abdomen examination revealed non-tender vague lump in right lumber region about 5x4cm dimensions , with B/L inguinal lymphadenopathy, firm, matted . Investigations revealed low haemoglobin count, high leucocytic & ESR count , urine for AFB was positive and ultrasound revealed small right renal & psoas abscess , which on subsequent start of ATT , got resolved and patient was symptomatically improved . I. Introduction Genitourinary tuberculosis (GUTB) is the second most common form of extrapulmonary tuberculosis after lymph node involvement [1]. Most studies in peripheral LNTB have described a female preponderance, while pulmonary TB is more common in adult males [2]. In approximately 28% of patients with GUTB, the involvement is solely genital [3]. However , the combination of GUTB and LNTB is rare condition. Most textbooks mention it only briefly. This report aims to present a case of GUTB with LNTB in a single patient. II. Case Report 55y male with no comorbidities , having pain right flank & fever X 3months. -
NCCN Guidelines for Penile Cancer from Version 1.2019 Include
NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Penile Cancer Version 2.2019 — May 13, 2019 NCCN.org Continue Version 2.2019, 05/13/19 © 2019 National Comprehensive Cancer Network® (NCCN®), All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN. NCCN Guidelines Index NCCN Guidelines Version 2.2019 Table of Contents Penile Cancer Discussion *Thomas W. Flaig, MD †/Chair Harry W. Herr, MD ϖ Sumanta K. Pal, MD † University of Colorado Cancer Center Memorial Sloan Kettering Cancer Center City of Hope National Medical Center *Philippe E. Spiess, MD, MS ϖ/Vice Chair Christopher Hoimes, MD † Anthony Patterson, MD ϖ Moffitt Cancer Center Case Comprehensive Cancer Center/ St. Jude Children’s Research Hospital/ University Hospitals Seidman Cancer Center The University of Tennessee Neeraj Agarwal, MD ‡ † and Cleveland Clinic Taussig Cancer Institute Health Science Center Huntsman Cancer Institute at the University of Utah Brant A. Inman, MD, MSc ϖ Elizabeth R. Plimack, MD, MS † Duke Cancer Institute Fox Chase Cancer Center Rick Bangs, MBA Patient Advocate Masahito Jimbo, MD, PhD, MPH Þ Kamal S. Pohar, MD ϖ University of Michigan Rogel Cancer Center The Ohio State University Comprehensive Stephen A. Boorjian, MD ϖ Cancer Center - James Cancer Hospital Mayo Clinic Cancer Center A. Karim Kader, MD, PhD ϖ and Solove Research Institute UC San Diego Moores Cancer Center Mark K. Buyyounouski, MD, MS § Michael P. Porter, MD, MS ϖ Stanford Cancer Institute Subodh M. Lele, MD ≠ Fred Hutchinson Cancer Research Center/ Fred & Pamela Buffett Cancer Center Sam Chang, MD ¶ Seattle Cancer Care Alliance Vanderbilt-Ingram Cancer Center Joshua J. -
Prostate Adenocarcinoma Presenting with Inguinal Lymphadenopathy
CASE REPORT PROSTATE ADENOCARCINOMA PRESENTING WITH INGUINAL LYMPHADENOPATHY EUGENE HUANG, BIN S. TEH, DINA R. MODY, L. STEVEN CARPENTER, AND E. BRIAN BUTLER ABSTRACT The lymphatic spread of prostate adenocarcinoma most often involves the iliac, obturator, and hypogastric nodes. Inguinal lymphadenopathy is very rare during the early stages of this disease, especially in the absence of pelvic lymphadenopathy or other metastases. We present a case of prostate adenocarcinoma with inguinal node involvement during the initial presentation, emphasizing the importance of a complete physical examination and the consideration of other concurrent diseases. UROLOGY 61: 463xxi–463xxii, 2003. © 2003, Elsevier Science Inc. 77-year-old man without significant past med- Aical or surgical history presented with an ele- vated prostate-specific antigen (PSA) level of 7.8 ng/mL on routine screening. At repeated testing 1 year later, his PSA level had increased to 17.0 ng/ mL. The patient remained asymptomatic without complaints. On physical examination, the patient had a painless, firm, right inguinal lymph node measuring 3 cm in diameter. Digital rectal exami- nation revealed an induration in the left lobe of the prostate. The physical examination was otherwise unremarkable, including examination of the scro- tum, penis, anus, and skin. Transrectal biopsy of the prostate demonstrated adenocarcinoma (Gleason score 4 ϩ 4 ϭ 8). Biopsy of the right inguinal lymph node also revealed a FIGURE 1. Biopsy of the right inguinal lymph node poorly differentiated adenocarcinoma with immu- showing a poorly differentiated adenocarcinoma with nohistochemical staining that was strongly posi- an immunohistochemical staining that is strongly posi- tive for PSA (Fig. -
An Approach to Cervical Lymphadenopathy in Children
Singapore Med J 2020; 61(11): 569-577 Practice Integration & Lifelong Learning https://doi.org/10.11622/smedj.2020151 CMEARTICLE An approach to cervical lymphadenopathy in children Serena Su Ying Chang1, MMed, MRCPCH, Mengfei Xiong2, MBBS, Choon How How3,4, MMed, FCFP, Dawn Meijuan Lee1, MBBS, MRCPCH Mrs Tan took her daughter Emma, a well-thrived three-year-old girl, to the family clinic for two days of fever, sore throat and rhinorrhoea. Apart from slight decreased appetite, Mrs Tan reported that Emma’s activity level and behaviour were not affected. During the examination, Emma was interactive, her nose was congested with clear rhinorrhoea, and there was pharyngeal injection without exudates. You discovered bilateral non-tender, mobile cervical lymph nodes that were up to 1.5 cm in size. Mrs Tan was uncertain if they were present prior to her current illness. There was no organomegaly or other lymphadenopathy. You treated Emma for viral respiratory tract illness and made plans to review her in two weeks for her cervical lymphadenopathy. WHAT IS LYMPHADENOPATHY? masses in children can be classified into congenital or acquired Lymphadenopathy is defined as the presence of one or more causes. Congenital lesions are usually painless and may be identified lymph nodes of more than 1 cm in diameter, with or without an at or shortly after birth. They may also present with chronic drainage abnormality in character.(1) In children, it represents the majority or recurrent episodes of swelling, which may only be obvious in later of causes of neck masses, which are abnormal palpable lumps life or after a secondary infection. -
Laboratory Diagnosis of Sexually Transmitted Infections, Including Human Immunodeficiency Virus
Laboratory diagnosis of sexually transmitted infections, including human immunodeficiency virus human immunodeficiency including Laboratory transmitted infections, diagnosis of sexually Laboratory diagnosis of sexually transmitted infections, including human immunodeficiency virus Editor-in-Chief Magnus Unemo Editors Ronald Ballard, Catherine Ison, David Lewis, Francis Ndowa, Rosanna Peeling For more information, please contact: Department of Reproductive Health and Research World Health Organization Avenue Appia 20, CH-1211 Geneva 27, Switzerland ISBN 978 92 4 150584 0 Fax: +41 22 791 4171 E-mail: [email protected] www.who.int/reproductivehealth 7892419 505840 WHO_STI-HIV_lab_manual_cover_final_spread_revised.indd 1 02/07/2013 14:45 Laboratory diagnosis of sexually transmitted infections, including human immunodeficiency virus Editor-in-Chief Magnus Unemo Editors Ronald Ballard Catherine Ison David Lewis Francis Ndowa Rosanna Peeling WHO Library Cataloguing-in-Publication Data Laboratory diagnosis of sexually transmitted infections, including human immunodeficiency virus / edited by Magnus Unemo … [et al]. 1.Sexually transmitted diseases – diagnosis. 2.HIV infections – diagnosis. 3.Diagnostic techniques and procedures. 4.Laboratories. I.Unemo, Magnus. II.Ballard, Ronald. III.Ison, Catherine. IV.Lewis, David. V.Ndowa, Francis. VI.Peeling, Rosanna. VII.World Health Organization. ISBN 978 92 4 150584 0 (NLM classification: WC 503.1) © World Health Organization 2013 All rights reserved. Publications of the World Health Organization are available on the WHO web site (www.who.int) or can be purchased from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for non-commercial distribution – should be addressed to WHO Press through the WHO web site (www.who.int/about/licensing/copyright_form/en/index.html). -
Infectious Mononucleosis Mimicking Lymphoma: Distinguishing Morphological and Immunophenotypic Features
Modern Pathology (2012) 25, 1149–1159 & 2012 USCAP, Inc. All rights reserved 0893-3952/12 $32.00 1149 Infectious mononucleosis mimicking lymphoma: distinguishing morphological and immunophenotypic features Abner Louissaint Jr, Judith A Ferry, Chad P Soupir, Robert P Hasserjian, Nancy L Harris and Lawrence R Zukerberg The James Homer Wright Pathology Laboratories, Massachusetts General Hospital, Boston, MA, USA The diagnosis of infectious mononucleosis (acute Epstein–Barr virus (EBV) infection) is usually made on the basis of clinical and laboratory findings. However, an atypical clinical presentation occasionally results in a lymph node or tonsillar biopsy. The morphological features of EBV-infected lymphoid tissue can easily mimic lymphoma. Furthermore, the immunophenotype of the immunoblasts has not been well characterized. To assess the morphological spectrum of acute EBV infection and the utility of immunohistochemistry in diagnosing difficult cases that resemble lymphoma, we reviewed 18 cases of acute EBV infection submitted in consultation to our institution with an initial diagnosis of/or suspicion for lymphoma. Patients included nine male and nine female individuals with a median age of 18 years (range 9–69). Biopsies were obtained from lymph nodes (3/18) or Waldeyer’s ring (15/18). Infectious mononucleosis was confirmed by monospot or serological assays in 72% of cases (13/18). All cases featured architectural distortion by a polymorphous infiltrate with an immunoblastic proliferation, sometimes forming sheets. Reed–Sternberg-like cells were present in 8/18 (44%) of the cases. Infiltrates were often accompanied by necrosis (10/18) and mucosal ulceration (6/15). The majority of immunoblasts in all cases were CD20 þ B cells with a post-germinal center immunophenotype (strongly positive for MUM1/IRF4 (18/18), CD10À (18/18 negative) and BCL-6À (16/18 negative; 2/18 faint BCL-6 expression in o10% of immunoblasts)).