Meningococcal Meningitis and Sepsis
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Cryptococcal Meningoencephalitis with Fulminant Intracranial Hypertension: an Unexpected Cause of Brain Death
Case Report Singapore Med J 2010; 51(8) : e133 Cryptococcal meningoencephalitis with fulminant intracranial hypertension: an unexpected cause of brain death Teo Y K ABSTRACT and later developed fulminant cryptococcal The diagnosis of brain death requires the meningoencephalitis, leading to brain death. presence of unresponsiveness and a lack of receptivity, the absence of movement, CASE REPORT breathing and brain stem reflexes, as well as A 61-year-old Caucasian man presented with a two-week a state of coma in which the cause has been history of generalised malaise, loss of appetite, nausea, identified. We report a case of brain death that headache and unsteady gait with frequent falls. The was diagnosed based on clinical neurological patient was initially seen at a local hospital, where a non- examinations, and supported by the absence contrast computed tomography (CT) of the brain did not of cerebral blood flow on magnetic resonance reveal any abnormality. He was treated symptomatically angiography and electroencephalography with oral analgesics. The patient had end-stage renal demonstrating the characteristic absence failure secondary to hypertension and had undergone of electrical activity. Thorough clinical an autologous renal transplant from his wife one year examination and repeated imaging of the ago. The patient was on prednisolone 10 mg once a brain revealed no apparent clinical cause or day, tacrolimus 3 mg twice a day and mycophenolate mechanism of brain death. We proceeded (mofetil) 1 g twice a day for immunosuppression. He with organ donation of the deceased’s liver had persistent symptoms, as described above and was and corneas. However, postmortem revealed admitted to a tertiary hospital for further evaluation. -
In Diagnosis Must Be Based on Clinical Signs and Symptoms. in This Paper
242 POST-GRADUATE MEDICAL JOURNAL August, 1938 Postgrad Med J: first published as 10.1136/pgmj.14.154.242 on 1 August 1938. Downloaded from SOME REMARKS ON DIFFERENTIAL DIAGNOSIS OF BLOOD DISEASES. By A. PINEY, M.D., M.R.C.P. (Assistant Physician, St. Mary's Hospital for Women and Children.) Differential diagnosis of blood diseases has been discussed time and again, but, as a rule, blood-pictures, rather than clinical features, have been taken into account, so that the impression has become widespread that the whole problem is one for the laboratory, rather than for the bed-side. It is obvious, however, that the first steps in diagnosis must be based on clinical signs and symptoms. In this paper, there- fore, certain outstanding clinical features of blood diseases, and various rather puzzling syndromes will be described. The outstanding external sign that leads the practitioner to consider the possi- bility of a blood disease is pallor, which is not quite so simple a state as is often supposed. It is, of course, well known that cutaneous pallor is not an infallible sign of anaemia, but it is often presumed that well-coloured mucous membranes are fairly good evidence that anaemia is not present. This is not necessarily true. The conjunctive may be bright pink in spite of anaemia, because mild inflammationProtected by copyright. may be present, masking the pallor. This is quite frequently due to irritation by eyelash dyes. Similarly, the finger-nails, which used to serve as a reliable index of pallor, are now found disguised with coloured varnish. -
Analysis of Fourteen New Cases of Meningovascular Syphilis: Renewed Interest in an Old Problem
Open Access Original Article DOI: 10.7759/cureus.16951 Analysis of Fourteen New Cases of Meningovascular Syphilis: Renewed Interest in an Old Problem Faiza Aziouaz 1 , Fatima Zahra Mabrouki 2 , Mohammed Chraa 3 , Nisrine Louhab 3 , Nawal Adali 3 , Imane Hajjaj 3 , Najib Kissani 3 , Yassine Mebrouk 1 1. Neurology, Faculty of Medicine and Pharmacy, Mohammed VI University Hospital, Oujda, MAR 2. Ophthalmology, Faculty of Medicine and Pharmacy, Mohammed VI University Hospital, Oujda, MAR 3. Neurology, Faculty of Medicine and Pharmacy, Mohammed VI University Hospital, Marrakech, MAR Corresponding author: Faiza Aziouaz, [email protected] Abstract Neurosyphilis (NS) remains a public health problem. Several recent reports suggest a worldwide increase in the incidence of this condition. Various syndromes can occur in NS, such as syphilitic meningitis, meningovascular syphilis, parenchymatous and gummatous neurosyphilis. Syphilis meningovascular will be the focus of this study. We report 14 new observations of meningovascular syphilis. A review of demographic and clinical features, neuroimaging findings, cerebrospinal fluid changes, treatment and outcome, pathophysiology mechanism of meningovascular syphilis are presented. Categories: Neurology, HIV/AIDS, Infectious Disease Keywords: neurosyphilis, stroke, vasculitis, csf, acquired immune deficiency syndrome (aids) Introduction The incidence of stroke is approximately 2.3/1000/year, based on community surveys [1]. Stroke can be a complication of a central nervous system infection [2]. Some infections are more often associated with cerebrovascular complications than others, and the pathogenesis of vascular lesions varies widely from one disease to another [2, 3]. Most of these conditions cause stroke through a mechanism of angitis [4]. This review focuses on meningovascular syphilis as an infectious cause of stroke. -
Myalgic Encephalomyelitis/Chronic Fatigue
2019 Science & Discovery Webinar Series ME/CFS in the Era of the Human Microbiome: Persistent Pathogens Drive Chronic Symptoms by Interfering With Host Metabolism, Gene Expression, and Immunity with Amy Proal, Ph.D. November 14, 2019 | 1:00 PM Eastern www.SolveME.org About Our Webinars • Welcome to the 2019 Webinar Series! • The audience is muted; use the question box to send us questions. Dr. Proal will address as many questions as time permits at the end of the webinar • Webinars are recorded and the recording is made available on our YouTube channel http://youtube.com/SolveCFS • The Solve ME/CFS Initiative does not provide medical advice www.SolveCFS.org 2019 Science & Discovery Webinar Series ME/CFS in the Era of the Human Microbiome: Persistent Pathogens Drive Chronic Symptoms by Interfering With Host Metabolism, Gene Expression, and Immunity with Amy Proal, Ph.D. November 14, 2019 | 1:00 PM Eastern www.SolveME.org Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in the Era of the Human Microbiome: Persistent Pathogens Drive Chronic Symptoms by Interfering With Host Metabolism, Gene Expression, and Immunity Amy Proal, Autoimmunity Research Foundation/PolyBio Millions of patients across the globe are suffering with myalgic encephalomyelitis (ME/CFS) Currently there is no one disease-specific biomarker and severely ill patients are often wheelchair dependent, bedridden and unable to perform basic tasks of work or daily living. #millionsmissing Myalgic Encephalomeylitis (ME) = swelling of the brain • Unrelenting fatigue that does -
Concurrent Beau Lines, Onychomadesis, and Retronychia Following Scurvy
CASE REPORT Concurrent Beau Lines, Onychomadesis, and Retronychia Following Scurvy Dayoung Ko, BS; Shari R. Lipner, MD, PhD the proximal nail plate from the distal nail plate leading to shedding of the nail. It occurs due to a complete growth PRACTICE POINTS arrest in the nail matrix and is thought to be on a con- • Beau lines, onychomadesis, and retronychia are nail tinuum with Beau lines. The etiologies of these 2 condi- conditions with distinct clinical findings. tions overlap and include trauma, inflammatory diseases, • Beau lines and onychomadesis may be seen 1-5 concurrently following trauma, inflammatory dis- systemic illnesses, hereditary conditions, and infections. eases, systemic illnesses, hereditary conditions, In almost all cases of both conditions, normal nail plate and infections. production ensues upon identification and removal of the 3,4,6 • Retronychia shares a common pathophysiology inciting agent or recuperation from the causal illness. with Beau lines and onychomadesis, and all reflect Beau lines will move distally as the nail grows out and slowing or cessation of nail plate production. can be clipped. In onychomadesis, the affected nails will be shed with time. Resolution of these nail defects can be estimated from average nail growth rates (1 mm/mo for fingernails and 2–3 mm/mo for toenails).7 Beau lines, onychomadesis, and retronychia are nail conditions with Retronychia is defined as a proximal ingrowing of their own characteristic clinical findings. It has been hypothesized the nail plate into the ventral surface of the proximal nail that these 3 disorders may share a common pathophysiologic fold.4,6 It is thought to occur via vertical progression of mechanism of slowing and/or halting nail plate production at the the nail plate into the proximal nail fold, repetitive nail nail matrix. -
Review Cutaneous Patterns Are Often the Only Clue to a a R T I C L E Complex Underlying Vascular Pathology
pp11 - 46 ABstract Review Cutaneous patterns are often the only clue to a A R T I C L E complex underlying vascular pathology. Reticulate pattern is probably one of the most important DERMATOLOGICAL dermatological signs of venous or arterial pathology involving the cutaneous microvasculature and its MANIFESTATIONS OF VENOUS presence may be the only sign of an important underlying pathology. Vascular malformations such DISEASE. PART II: Reticulate as cutis marmorata congenita telangiectasia, benign forms of livedo reticularis, and sinister conditions eruptions such as Sneddon’s syndrome can all present with a reticulate eruption. The literature dealing with this KUROSH PARSI MBBS, MSc (Med), FACP, FACD subject is confusing and full of inaccuracies. Terms Departments of Dermatology, St. Vincent’s Hospital & such as livedo reticularis, livedo racemosa, cutis Sydney Children’s Hospital, Sydney, Australia marmorata and retiform purpura have all been used to describe the same or entirely different conditions. To our knowledge, there are no published systematic reviews of reticulate eruptions in the medical Introduction literature. he reticulate pattern is probably one of the most This article is the second in a series of papers important dermatological signs that signifies the describing the dermatological manifestations of involvement of the underlying vascular networks venous disease. Given the wide scope of phlebology T and its overlap with many other specialties, this review and the cutaneous vasculature. It is seen in benign forms was divided into multiple instalments. We dedicated of livedo reticularis and in more sinister conditions such this instalment to demystifying the reticulate as Sneddon’s syndrome. There is considerable confusion pattern. -
Medical Management of Biological Casualties Handbook
USAMRIID’s MEDICAL MANAGEMENT OF BIOLOGICAL CASUALTIES HANDBOOK Sixth Edition April 2005 U.S. ARMY MEDICAL RESEARCH INSTITUTE OF INFECTIOUS DISEASES FORT DETRICK FREDERICK, MARYLAND Emergency Response Numbers National Response Center: 1-800-424-8802 or (for chem/bio hazards & terrorist events) 1-202-267-2675 National Domestic Preparedness Office: 1-202-324-9025 (for civilian use) Domestic Preparedness Chem/Bio Helpline: 1-410-436-4484 or (Edgewood Ops Center – for military use) DSN 584-4484 USAMRIID’s Emergency Response Line: 1-888-872-7443 CDC'S Emergency Response Line: 1-770-488-7100 Handbook Download Site An Adobe Acrobat Reader (pdf file) version of this handbook can be downloaded from the internet at the following url: http://www.usamriid.army.mil USAMRIID’s MEDICAL MANAGEMENT OF BIOLOGICAL CASUALTIES HANDBOOK Sixth Edition April 2005 Lead Editor Lt Col Jon B. Woods, MC, USAF Contributing Editors CAPT Robert G. Darling, MC, USN LTC Zygmunt F. Dembek, MS, USAR Lt Col Bridget K. Carr, MSC, USAF COL Ted J. Cieslak, MC, USA LCDR James V. Lawler, MC, USN MAJ Anthony C. Littrell, MC, USA LTC Mark G. Kortepeter, MC, USA LTC Nelson W. Rebert, MS, USA LTC Scott A. Stanek, MC, USA COL James W. Martin, MC, USA Comments and suggestions are appreciated and should be addressed to: Operational Medicine Department Attn: MCMR-UIM-O U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) Fort Detrick, Maryland 21702-5011 PREFACE TO THE SIXTH EDITION The Medical Management of Biological Casualties Handbook, which has become affectionately known as the "Blue Book," has been enormously successful - far beyond our expectations. -
Anemia in Children with Palmar Pallor Aged 02 Months to 05 Years
eCommons@AKU Department of Paediatrics and Child Health Division of Woman and Child Health 2-28-2017 Anemia in children with palmar pallor aged 02 months to 05 years Saroop Chand Farzana Shaikh Chetan Das Yasmeen Memon Mohammad Akbar Nizamani See next page for additional authors Follow this and additional works at: https://ecommons.aku.edu/ pakistan_fhs_mc_women_childhealth_paediatr Part of the Pediatrics Commons Authors Saroop Chand, Farzana Shaikh, Chetan Das, Yasmeen Memon, Mohammad Akbar Nizamani, and Zulfiqar Ali Qutrio Baloch IAJPS 2017, 4 (02), 290-295 Zulfiqar Ali Qutrio Baloch et al ISSN 2349-7750 CODEN (USA): IAJPBB ISSN: 2349-7750 INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES http://doi.org/10.5281/zenodo.345648 Available online at: http://www.iajps.com Research Article ANEMIA IN CHILDREN WITH PALMAR PALLOR AGED 02 MONTHS TO 05 YEARS Dr. Saroop Chand1, Dr. Farzana Shaikh1, Dr. Chetan Das1, Dr. Yasmeen Memon1, Dr. Mohammad Akbar Nizamani1 and *Dr. Zulfiqar Ali Qutrio Baloch2 1Department of pediatrics Liaquat University of Medical and Health Sciences (LUMHS). 2Brandon Regional Hospital, Brandon, Florida. Received: 10 February 2016 Accepted: 25 February 2017 Published: 28 February 2017 Absract: Objective: To determine the frequency of anemia in children with palmar pallor aged 02 months to 05 years Patients and Methods: This cross sectional descriptive study of six months (01-12-2012 to 31-05-2013) was conducted in the department of paediatrics at Liaquat University Hospital Hyderabad. All the children, from 02 months to 05 years, of either gender had palmar pallor on examination were recruited and evaluated for anemia by assessing the level of haemoglobin and categorized anemia as mild, moderate and severe. -
African Meningitis Belt
WHO/EMC/BAC/98.3 Control of epidemic meningococcal disease. WHO practical guidelines. 2nd edition World Health Organization Emerging and other Communicable Diseases, Surveillance and Control This document has been downloaded from the WHO/EMC Web site. The original cover pages and lists of participants are not included. See http://www.who.int/emc for more information. © World Health Organization This document is not a formal publication of the World Health Organization (WHO), and all rights are reserved by the Organization. The document may, however, be freely reviewed, abstracted, reproduced and translated, in part or in whole, but not for sale nor for use in conjunction with commercial purposes. The views expressed in documents by named authors are solely the responsibility of those authors. The mention of specific companies or specific manufacturers' products does no imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. CONTENTS CONTENTS ................................................................................... i PREFACE ..................................................................................... vii INTRODUCTION ......................................................................... 1 1. MAGNITUDE OF THE PROBLEM ........................................................3 1.1 REVIEW OF EPIDEMICS SINCE THE 1970S .......................................................................................... 3 Geographical distribution -
Truncal Rashes Stan L
Healthy Baby Practical advice for treating newborns and toddlers. Getting Truculent with Truncal Rashes Stan L. Block, MD, FAAP A B C All images courtesy of Stan L. Block, MD, FAAP. Figure 1. Afebrile 22-month-old white male presents to your office with this slowly spreading, somewhat generalized, and refractory truncal rash for the past 4 weeks. It initially started on the right side of his trunk (A) and later extended down his right upper thigh (B). The rash has now spread to the contralateral side on his back (C), and is most confluent and thickest over his right lateral ribs. n a daily basis, we pediatricians would not be readily able to identify this rash initially began on the right side of his encounter a multitude of rashes relatively newly described truncal rash trunk (see Figure 1A) and then extended O of varied appearance in children shown in some of the following cases. distally down to his right upper thigh (see of all ages. Most of us gently-seasoned As is typical, certain clues are critical, Figure 1B). Although the rash is now dis- clinicians have seen nearly all versions including the child’s age, the duration tributed over most of his back (see Figure of these “typical” rashes. Yet, I venture and the distribution of the rash. Several 1C), it is most confluent and most dense to guess that many practitioners, who of these rashes notably mimic more com- over his right lateral ribs. would be in good company with some of mon etiologies, as discussed in some of From Figure 1, you could speculate my quite erudite partners (whom I asked), the following cases. -
GAFFI Fact Sheet Cryptococcal Meningitis
OLD VERSION GLOBAL ACTION FUNDGAL FOR INFECTIONS FUN GAFFI Fact Sheet Cryptococcal meningitis Cryptococcal meningitis is caused by one of two closely related GLOBAL ACTION FUNDNGAL FOR INFECTIONS environmental fungi, Cryptococcus neoformans and C. gattii. C. FU neoformans has a world-wide distribution, while C. gattii is concentrated in tropical and sub-tropical zones (although C. gattii infections haDARKER AREASve recently AND SMALLER VERSION TEXT FIT WITHIN CIRCLE (ALSO TO BE USED AS MAIN emerged on Vancouver Island and the adjacent mainland in British Columbia, Canada). The LOGO IN THE FUTURE) frequency and circumstances of human exposure to these organisms are not precisely understood, but exposure is assumed to occur following inhalation for the environment from 3-4 years of age and to be nearly universal. Infection is usually controlled effectively by the immune system, but remains latent, so that, if immune function later wanes, due to HIV/AIDS, immunosuppressing medication, or another condition, disease develops, in particular a life-threatening meningitis or meningoencephalitis. C. neoformans causes most infections in HIV-infected patients; C. gattii, in particular, also causes disease in apparently immunocompetent persons. Person to person transmission does not occur. Incidence Cryptococcal meningitis remains a very common in patients with late stage HIV-infection. Despite expansion of antiretroviral programmes, cases have not decreased in most African countries. Furthermore, treatment is unsatisfactory: in Africa, mortality has ranged from 24% at 10 weeks to 95% at 12 weeks depending on the initial therapeutic regimen (see table, below). A recent CDC analysis estimated that in Africa, cryptococcosis-associated mortality at 3 months is ~70%1. -
Meningitis/Encephalitis Pathogen Panel
Meningitis/Encephalitis Pathogen Panel The list of pathogens which can potentially cause meningitis, encephalitis, and meningoencephalitis is broad. Early effective therapy for both bacterial and certain viral pathogens has been associated with improved outcomes. Patients whose history, exam, and/or imaging suggests one of these conditions should have a lumber puncture performed with appropriate diagnostic testing including a cell count with differential, protein, and glucose. Additional tests to consider include bacterial culture, cryptococcal antigen testing, fungal cultures, cultures for acid fast bacilli and/or the new Meningitis/Encephalitis Pathogen Panel. Nebraska Medicine has recently introduced a new FDA-approved test called the Meningitis/Encephalitis Pathogen Panel (MEPP). This test uses a nested multiplex PCR-approach to amplify DNA targets directly from cerebrospinal fluid (CSF) in patients with signs and symptoms of meningitis or encephalitis. It is able to detect a variety of common bacterial, viral, and fungal pathogens (Table 1). Table 1: Pathogens Detected by Meningitis/Encephalitis Pathogen Panel Bacteria Viruses Yeast Gram-negative Cytomegalovirus Cryptococcus Escherichia coli K1 Enterovirus neoformans/gattii Haemophilus influenzae Herpes simplex virus 1 Neisseria meningitidis Herpes simplex virus 2 Gram-positive Human herpesvirus 6 Listeria monocytogenes Human parechovirus Streptococcus agalactiae (Group B Strep) Varicella zoster virus (VZV) Streptococcus pneumoniae This test is sensitive and very specific (see Supplementary Table 1 for complete detail), and should only be performed in patients where CNS infection is being seriously considered. Previous studies have shown that using clinical and CSF criteria to determine when to perform PCR testing is unlikely to miss clinically significant results and is highly cost-effective.1-3 For example Wilen, et al.3 restricted herpes virus and enterovirus PCR testing to patients who were: age <2 years, immunosuppressed, or who had >10 WBCs/µl.