Erythema Annulare Centrifugum
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Inflammatory Or Infectious Hair Disease? a Case of Scalp Eschar and Neck Lymph Adenopathy After a Tick Bite
Case Report ISSN: 2574 -1241 DOI: 10.26717/BJSTR.2021.35.005688 Adherent Serous Crust of the Scalp: Inflammatory or Infectious Hair Disease? A Case of Scalp Eschar and Neck Lymph Adenopathy after a Tick Bite Starace M1, Vezzoni R*2, Alessandrini A1 and Piraccini BM1 1Dermatology - IRCCS, Policlinico Sant’Orsola, Department of Specialized, Experimental and Diagnostic Medicine, Alma Mater Studiorum, University of Bologna, Italy 2Dermatology Clinic, Maggiore Hospital, University of Trieste, Italy *Corresponding author: Roberta Vezzoni, Dermatology Clinic, Maggiore Hospital, University of Trieste, Italy ARTICLE INFO ABSTRACT Received: Published: April 17, 2021 The appearance of a crust initially suggests inflammatory scalp diseases, although infectious diseases such as impetigo or insect bites should also be considered among April 27, 2021 the differential diagnoses. We report a case of 40-year-old woman presentedB. Burgdorferi to our, Citation: Starace M, Vezzoni R, Hair Disease Outpatient Service with an adherent serous crust on the scalp and lymphadenopathy of the neck. Serological tests confirmed the aetiology of while rickettsia infection was excluded. Lyme borreliosis can mimic rickettsia infection Alessandrini A, Piraccini BM. Adherent and may present as scalp eschar and neck lymphadenopathy after a tick bite (SENLAT). Serous Crust of the Scalp: Inflammatory Appropriate tests should be included in the diagnostic workup of patients with necrotic or Infectious Hair Disease? A Case of Scalp scalpKeywords: eschar in order to promptly set -
Lepromatous Leprosy with Erythema Nodosum Leprosum Presenting As
Lepromatous Leprosy with Erythema Nodosum Leprosum Presenting as Chronic Ulcers with Vasculitis: A Case Report and Discussion Anny Xiao, DO,* Erin Lowe, DO,** Richard Miller, DO, FAOCD*** *Traditional Rotating Intern, PGY-1, Largo Medical Center, Largo, FL **Dermatology Resident, PGY-2, Largo Medical Center, Largo, FL ***Program Director, Dermatology Residency, Largo Medical Center, Largo, FL Disclosures: None Correspondence: Anny Xiao, DO; Largo Medical Center, Graduate Medical Education, 201 14th St. SW, Largo, FL 33770; 510-684-4190; [email protected] Abstract Leprosy is a rare, chronic, granulomatous infectious disease with cutaneous and neurologic sequelae. It can be a challenging differential diagnosis in dermatology practice due to several overlapping features with rheumatologic disorders. Patients with leprosy can develop reactive states as a result of immune complex-mediated inflammatory processes, leading to the appearance of additional cutaneous lesions that may further complicate the clinical picture. We describe a case of a woman presenting with a long history of a recurrent bullous rash with chronic ulcers, with an evolution of vasculitic diagnoses, who was later determined to have lepromatous leprosy with reactive erythema nodosum leprosum (ENL). Introduction accompanied by an intense bullous purpuric rash on management of sepsis secondary to bacteremia, Leprosy is a slowly progressive disease caused by bilateral arms and face. For these complaints she was with lower-extremity cellulitis as the suspected infection with Mycobacterium leprae (M. leprae). seen in a Complex Medical Dermatology Clinic and source. A skin biopsy was taken from the left thigh, Spread continues at a steady rate in several endemic clinically diagnosed with cutaneous polyarteritis and histopathology showed epidermal ulceration countries, with more than 200,000 new cases nodosa. -
Erythema Marginatum
Figurative Erythemas Michelle Goedken, DO Affiliated Dermatology Scottsdale, AZ Figurative Erythemas • Erythema annulare centrifugum • Erythema marginatum • Erythema migrans • Erythema gyratum repens • Erythema multiforme Erythemas • Erythemas represent a change in the color of the skin that is due to the dilation of blood vessels, especially those in the papillary and reticular dermis • The color is blanchable and most last for days to months • Figurative erythemas have an annular, arciform or polycyclic appearance ERYTHEMA ANNULARE CENTRIFUGUM ERYTHEMA ANNULARE CENTRIFUGUM • Pathogenesis: EAC represents a reaction pattern or hypersensitivity to one of many antigens – IL-2 and TNF-alpha may have a role – Most patients do not have an underlying disease identified ERYTHEMA ANNULARE CENTRIFUGUM • Associated with: – Infection » Dermatophytes and other fungi (Candida and Penicillium in blue cheese) » Viruses: poxvirus, EBV, VZV, HIV » Parasites and ectoparasites – Drugs: diuretics, antimalarials, gold, NSAIDs, finasteride, amitriptyline, etizolam, Ustekinumab (2012) ERYTHEMA ANNULARE CENTRIFUGUM – Foods – Autoimmune endocrinopathies – Neoplasms (lymphomas and leukemias) – Pregnancy – Hypereosinophilic syndrome – Lupus (2014) ERYTHEMA ANNULARE CENTRIFUGUM http://www.dermaamin.com Rongioletti, F., Fausti, V., & Parodi, A ERYTHEMA ANNULARE CENTRIFUGUM • 2 major forms: – Superficial: classic trailing scale, may have associated pruritus – Deep: infiltrated borders, usually no scale, edges are elevated, usually not pruritic ERYTHEMA ANNULARE CENTRIFUGUM -
Belly Button…
KNOWLEDGE TO PRACTICE DES CONNAISSANCES À LA PRATIQUE Diagnostic Challenge A “ticklish” belly button… Tahira Daya*; Conor McKaigney, MD† CASE HISTORY A 42-year-old woman presented to the emergency department (ED) with acute onset periumbilical pain and erythema, which started that morning. She felt nauseated but denied vomiting. Her bowel movements were regular and non-bloody. She did not have a fever. She had no significant prior medical history, no recent trauma, and had no previous surgeries. In the ED, she appeared uncomfortable from pain but was not in acute distress. Vital signs upon initial presentation included a heart rate of 120 beats/min, a blood pressure of 145/111 mm Hg, respiratory rate of 16 breaths/min, temperature of 36.8°C (98.2°F), and an oxygen saturation of 99% on room air. Her vital signs two hours later after a fluid challenge and analgesics had improved to a heart rate of 74 beats/min and blood pressure of 132/83 mm Hg, and the remaining vitals were the same. Her abdomen demonstrated periumbilical erythema, with a central clearing; the area was tender to Figure 1. Periumbilical rash with central clearing. palpation, and warm to touch. Images of her periumbilical region are shown in Figure 1. The rest of the abdomen was soft and non-tender, with no masses or organomegaly. An ED ultrasound was performed to assess for possible b) Cellulitis subcutaneous abscess, which was not seen. Cardiovascular and respiratory exams were unremarkable. c) Lyme disease d) Subcutaneous abscess e) Erythema multiforme QUESTION For the answer to this challenge, see next page. -
Lyme Disease Diagnostic Support Tool
1 / 11 For further details, click on the DIAGNOSTIC SUPPORT TOOL underlined words. Localized and disseminated stages of Lyme disease This diagnostic support tool is intended mainly for primary care clinicians. It is provided for information purposes only and should not replace the judgement of the clinician who performs the activities reserved under a statute or regulation. The recommendations in this tool were developed using a systematic process and are supported by the scientific literature and the knowledge and experience of Québec health professionals, experts and patients. For further details, go to the “Publications” section of INESSS’s website inesss.qc.ca. This tool does not deal with other tick-borne infections or with the much-debated form of Lyme disease, which is sometimes referred to as the chronic form. WHAT IS LYME DISEASE ? WHAT ARE THE DIFFERENT STAGES OF THE DISEASE? GENERAL INFORMATION • Lyme disease is an infectious disease caused by bacterial Localized stage (sometimes called the early stage): Beginning Patient with a tick genospecies of Borrelia burgdorferi, which are transmitted of the infection before dissemination of the bacteria in the • If tick is attached, refer to the procedure for removing it. to humans by black-legged ticks that are carriers. bloodstream. • Refer to the tick surveillance procedure. • Main manifestation observed: • It is a notifiable disease (MADO) • Consult the decision support tool or the Québec’s national and is on the increase in Québec. Not always present or noticed. medical protocol on post-exposure prophylaxis. • It can affect several anatomical systems at the same time. If present, usually appears • Identifying the tick and obtaining proof that it carries of Lym 3 to 30 days after infection or e d B. -
Diagnosis, Classification, and Management of Erythema
Arch Dis Child 2000;83:347–352 347 Diagnosis, classification, and management of Arch Dis Child: first published as 10.1136/adc.83.4.347 on 1 October 2000. Downloaded from erythema multiforme and Stevens–Johnson syndrome C Léauté-Labrèze, T Lamireau, D Chawki, J Maleville, A Taïeb Abstract become widely accepted that EM and SJS, as Background—In adults, erythema multi- well as toxic epidermal necrolysis, are all part of forme (EM) is thought to be mainly a single “EM spectrum”. In both EM and SJS, related to herpes infection and Stevens– pathological changes in the earliest skin lesion Johnson syndrome (SJS) to drug reac- consist of the accumulation of mononuclear tions. cells around the superficial dermal blood Aims—To investigate this hypothesis in vessels; epidermal damage is more characteris- children, and to review our experience in tic of EM with keratinocyte necrosis leading to the management of these patients. multilocular intraepidermal blisters.5 In fact, Methods—A retrospective analysis of 77 there is little clinical resemblance between paediatric cases of EM or SJS admitted to typical EM and SJS, and recently some authors the Children’s Hospital in Bordeaux be- have proposed a reconsideration of the “spec- tween 1974 and 1998. trum” concept and a return to the original Results—Thirty five cases, inadequately description.15–17 According to these authors, the documented or misdiagnosed mostly as term EM should be restricted to acrally urticarias or non-EM drug reactions were distributed typical targets or raised oedema- excluded. Among the remaining 42 pa- tous papules. Depending on the presence or tients (14 girls and 28 boys), 22 had EM (11 absence of mucous membrane erosions the EM minor and 11 EM major), 17 had SJS, cases may be classified as EM major or EM 16 and three had isolated mucous membrane minor. -
Drug Eruptions
DRUG ERUPTIONS http://www.aocd.org A drug eruption is an adverse skin reaction to a drug. Many medications can cause reactions, especially antimicrobial agents, sulfa drugs, NSAIDs, chemotherapy agents, anticonvulsants, and psychotropic drugs. Drug eruptions can imitate a variety of other skin conditions and therefore should be considered in any patient taking medications or that has changed medications. The onset of drug eruptions is usually within 2 weeks of beginning a new drug or within days if it is due to re-exposure to a certain drug. Itching is the most common symptom. Drug eruptions occur in approximately 2-5% of hospitalized patients and in greater than 1% of the outpatient population. Adverse reactions to drugs are more prevalent in women, in the elderly, and in immunocompromised patients. Drug eruptions may be immunologically or non-immunologically mediated. There are 4 types of immunologically mediated reactions, with Type IV being the most common. Type I is immunoglobulin-E dependent and can result in anaphylaxis, angioedema, and urticaria. Type II is cytotoxic and can result in purpura. Type III reactions are immune complex reactions which can result in vasculitis and type IV is a delayed-type reaction which results in contact dermatitis and photoallergic reactions. This is important as different medications are associated with different types of reactions. For example, insulin is related with type I reactions whereas penicillin, cephalosporins, and sulfonamides cause type II reactions. Quinines and salicylates can cause type III reactions and topical medications such as neomycin can cause type IV reactions. The most common drugs that may potentially cause drug eruptions include amoxicillin, trimethoprim sulfamethoxazole, ampicillin, penicillin, cephalosporins, quinidine and gentamicin sulfate. -
Lyme Disease
Volume 91 No. 7 July 2008 Lyme Disease UNDER THE JOINT VOLUME 91 NO. 7 July 2008 EDITORIAL SPONSORSHIP OF: Medicine Health The Warren Alpert Medical School of Brown University HODE SLAND Edward J. Wing, MD, Dean of Medicine R I & Biological Science PUBLICATION OF THE RHODE ISLAND MEDICAL SOCIETY Rhode Island Department of Health David R. Gifford, MD, MPH, Director Quality Partners of Rhode Island Richard W. Besdine, MD, Chief Medical Officer COMMENTARIES Rhode Island Medical Society Nick Tsiongas, MD, MPH, President 206 When Is a Somatic Disorder Psychiatric? Joseph H. Friedman, MD EDITORIAL STAFF Joseph H. Friedman, MD 207 The Awkward Birth Pangs of Bolero Editor-in-Chief Stanley M. Aronson, MD Joan M. Retsinas, PhD Managing Editor CONTRIBUTIONS Stanley M. Aronson, MD, MPH SPECIAL ISSUE: Lyme Disease Editor Emeritus Guest Editors: Jerome Larkin, MD, and Jennifer Mitty, MD, MPH EDITORIAL BOARD 208 Introduction: Lyme Disease Stanley M. Aronson, MD, MPH Jerome Larkin, MD, and Jennifer Mitty, MD, MPH Jay S. Buechner, PhD John J. Cronan, MD 209 Ticks and Tick-Related Illness James P. Crowley, MD Jerome M. Larkin, MD Edward R. Feller, MD 212 Lyme Disease In Children and Pregnant Women John P. Fulton, PhD Peter A. Hollmann, MD Jerome M. Larkin, MD Sharon L. Marable, MD, MPH 213 Musculoskeletal Manifestations of Lyme Disease Anthony E. Mega, MD Imad Bitar, MD, and Edward V. Lally, MD Marguerite A. Neill, MD Frank J. Schaberg, Jr., MD 216 Neurological Complications of Lyme Disease Lawrence W. Vernaglia, JD, MPH Syed Rizvi, MD, and Amanda Diamond, MD Newell E. Warde, PhD 219 Updates and Controversy In the Treatment of Lyme Disease OFFICERS Jennifer Mitty, MD, MPH, and David Margolius Nick Tsiongas, MD, MPH President COLUMNS Diane R. -
Erythema Multiforme: Recognition and Management Kathryn P
Erythema Multiforme: Recognition and Management Kathryn P. Trayes, MD; Gillian Love, MD; and James S. Studdiford, MD Thomas Jefferson University Hospital, Philadelphia, Pennsylvania Erythema multiforme is an immune-mediated reaction that involves the skin and sometimes the mucosa. Classically described as target-like, the erythema multiforme lesions can be isolated, recur- rent, or persistent. Most commonly, the lesions of erythema multiforme present symmetrically on the extremities (especially on extensor surfaces) and spread centripetally. Infections, especially herpes simplex virus and Mycoplasma pneumoniae, and medications constitute most of the causes of erythema multiforme; immunizations and autoimmune diseases have also been linked to erythema multiforme. Erythema multiforme can be differentiated from urticaria by the duration of individual lesions. Ery- thema multiforme lesions are typically fixed for a minimum of seven days, whereas individual urticarial lesions often resolve within one day. Erythema multiforme can be confused with the more serious con- dition, Stevens-Johnson syndrome; however, Stevens-Johnson syndrome usually contains widespread erythematous or purpuric macules with blisters. The management of erythema multiforme involves symptomatic treatment with topical steroids or antihistamines and treating the underlying etiology, if known. Recurrent erythema multiforme associated with the herpes simplex virus should be treated with prophylactic antiviral therapy. Severe mucosal erythema multiforme can require hospitalization -
Paediatric Cookbook
® Paediatric Cookbook Paediatric bits and pieces for your own practice Anita Mang, MD, MRCPCH 2 Disclaimer The purpose of this publication is neutral information and training, it does not endorse or recommend any of the described diagnostic methods or treatments. All product and company names are trademarks or registered trademarks of their respective holders. Use of them does not imply any affiliation with or endorsement by them. The publication does not claim to be a complete by any means. While every precaution has been taken in the preparation of these contents, the publisher and authors assume no responsibility for errors or omissions, or for damages resulting from the use of the information contained herein. License This publication is licensed under Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0). To get a copy of this license visit https://creativecommons.org/licenses/by-nc- nd/4.0/legalcode.de or write to Creative Commons, postbox 1866, Mountain View, California, 94042, USA. Icons/Symbols by Font Aswome (www.fontawsome.com) licensed under Creative Commons BY 4.0 3 Acknowledgements I want to thank my supportive husband Clemens Schmuck, who is responsible for the layout in this project. Bibliographical data Author: Dr. Anita Mang, MRCPCH; General Practitioner, Paediatrician, Stadt 1, 8832 Oberwoelz, Austria; www.drmang.at Source This document is available at: www.drmang.at/bpp Change history Version change 2017-05-30 First Version Contents 4 1. Newborns / Infants < 3 mo 7 1.1 Bronchiolitis ........................................................................................................... 7 1.2 Conjunctivitis, acute bacterial ................................................................................. 7 1.3 Diaper rash ............................................................................................................. 8 1.4 Erythema toxicum .................................................................................................. -
Research Article Bull's-Eye and Nontarget Skin Lesions of Lyme
Hindawi Publishing Corporation Dermatology Research and Practice Volume 2012, Article ID 451727, 6 pages doi:10.1155/2012/451727 Research Article Bull’s-Eye and Nontarget Skin Lesions of Lyme Disease: An Internet Survey of Identification of Erythema Migrans John N. Aucott,1 Lauren A. Crowder,2 Victoria Yedlin,2 and Kathleen B. Kortte3 1 Department of Medicine, Johns Hopkins University, 10755 Falls Road, Suite 200, Lutherville, MD 21093, USA 2 Division of Clinical Research, Lyme Disease Research Foundation, 10755 Falls Road, Suite 200, Lutherville, MD 21093, USA 3 Department of Physical Medicine and Rehabilitation, Johns Hopkins University School of Medicine, Phipps 174, 600 North Wolfe Street, Baltimore, MD 21287, USA Correspondence should be addressed to John N. Aucott, [email protected] Received 27 June 2012; Accepted 15 August 2012 Academic Editor: Jag Bhawan Copyright © 2012 John N. Aucott et al. This 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. Introduction. Lyme disease is an emerging worldwide infectious disease with major foci of endemicity in North America and regions of temperate Eurasia. The erythema migrans rash associated with early infection is found in approximately 80% of patients and can have a range of appearances including the classic target bull’s-eye lesion and nontarget appearing lesions. Methods.Asurvey was designed to assess the ability of the general public to distinguish various appearances of erythema migrans from non-Lyme rashes. Participants were solicited from individuals who visited an educational website about Lyme disease. -
Drug Eruption
Drug eruption March 25,2015 Outline • Clinical features • Pathogenesis • How to approach? • Management? Need to know • Urticaria • Exanthematous rash • DRESS • Stevens-Johnson syndrome/TEN • Fix drug eruptions • Acute generalized exanthematous pustulosis • Photoallergic/Phototoxic. • Chemotherapy induced.. Generalized erythematous and slightly edematous maculopapular rashes Erythema and edema of face and periorbital area Investigations 28/8/47 30/8/47 2/9//47 Total 1110 1690 2024 Eosinophil SGOT 42 98 69 SGPT 130 108 88 Your Dx is D R E S S ? Drug Rash with Eosinophilia and Systemic Symptoms DRESS • Aromatic antiepileptic agents (phenytoin, carbamazepine, phenobarbital) • Sulfonamides, allopurinol, gold salts, dapsone, and minocycline. 5 days after prednisolone 30mg/d 5 days after prednisolone 30mg/d Gout after 2 weeks of allopurinol Toxic Epidermal Necrolysis from allopurinol Approach to the Acute Generalized Blistering Patient History : Onset ,underlying disease, New Drug ,other symptoms? ( fever,sore throat ) Physical examination : target lesion nikolsky sign, epidermal necrolysis, mucosal involvement Investigation : baseline lab,skin biopsy + Direct Immonofluorescence Differential diagnosis of TEN • SSSS (Staphylococcal scalded skin syndrome ) • Autoimmune blistering disease ( pemphigus,linear IgA dermatosis.. ) • Erythema multiforme Generalized exanthem Blistering ,denudation Generalized Cutaneous tenderness Nikolsky sign + desquamation Apoptosis desmoglein-1 TEN SSSS Pemphigus vulgaris Bullous pemphigoid Erythema multiforme Take