Dermatology EM SPR Handout

Total Page:16

File Type:pdf, Size:1020Kb

Dermatology EM SPR Handout 9/20/19 Objectives East of England – Emergency Medicine Dermatology • Understand common terminology • Common exanthems Dr D Vijayasankar HST Training Day • Tips 20th Sept 2019 For Exam Preparation Know the difference • Common terminologies in Dermatology • Erythema Multiforme, Marginatum, • Criteria's in diagnosing skin/systemic conditions presenting with dermatological Nodosum problem • Differential diagnosis of common and life • SSS/TEN/Necrotising Fascitis threatening conditions • Pemphigoid and Pemphigus • Aetiology • Causative organism • Common viral exanthems 1 9/20/19 Why is it Important? Anatomy Epidermis • Sebaceous Extra ordinary structure gland • Skin diseases are very common Capillary • Everyone will have suffered Dermis Erector pilae • 10-15% of GP work • Second commonest cause of loss of work. Subcutaneous Hair follicle tissue Nerve Sweat gland Question History and Why it is necessary • Primary skin disease or manifestation of systemic disease • Enlist four things you would elicit in Dermatology • Onset, duration, spread,phasic history? • Pruritis • Wet or dry • Why history is important in dermatology? • Exacerbating factors • Medication • PMH, FH, SH (occupation) 2 9/20/19 Examination Question • Distribution – Spread • List six categories in distribution examination? – Unilateral or bilateral – Symmetrical or asymmetrical – Flexor or extensor – Exposed or protected – Centripetal or centrifugal – Nail, hair, scalp, mucosae Examination Question • Morphology – Monomorphic or pleomorphic • What are the generic treatments in – Bizarre shapes, ring, linear dermatology? – Palpate – Common terms • Other exam as required, e.g hepatosplenomegaly, LN 3 9/20/19 Treatments Dermatology Atlas • Dressings • Emollients • Antibiotics http://dermatlas.med.jhmi.edu/derm/ • Antihistamines • Analgesia • Steroids • Other, PUVA, counselling Lesion Types • Macule • Purpura • Papule • Pustule • Plaque • Cyst • Wheal • Scale • Nodule • Erosion • Vesicle • Crust • Excoriations Zebra Principle 4 9/20/19 Erythematous Exanthems History Clue’s – Erythematous Exanthems • Starts on Face • Rash – Measles, Rubella, Infectiosum • Usually viral in origin • Starts on Trunk • Could be secondary to toxin produced by – Roseola, Scarlet organism • Papulo vesicular • Systemic symptoms – Chicken pox • Extremities – Headache, Malaise and fever – Hand, foot and mouth Measles Measles (Rubeola) • RNA paramyxovirus • Lasts 4 – 7 days • From prodrome till 4 days • 7 – 18 days incubation period after rash onset (Infectivity) • Preceded by fever, cough and red eyes (look unwell) • Rash lasts 4 - 7 days • Koplik’s Spots • Typically begins at the hairline and spreads caudally 5 9/20/19 Rubella Rubella (German Measles) • RNA virus • Rash from face to whole • Young children though body in 24hrs adolescents and adults • generalized, tender can get infected lymphadenopathy that • Seven days before and involves all nodes four days after (Infectivity) • Prodrome may not be present Fifth Disease (Erythema Infectiosum) • Classic slapped-cheek • Human parvovirus B19 • A benign self-limited appearance. • Primarily is a disease of disease • bright red erythema appears children aged 3-15 years • oral analgesics and abruptly over the cheeks • Not infectious once rash antihistamines or topical • erythematous macular-to- appears antipruritic lotions morbilliform eruption occurs • prognosis is excellent for primarily on the extremities typical childhood cases • lacy pattern 6 9/20/19 Roseola infantum ( 6th Disease) • Exanthum Subitum • Children less than 2 years of age • History of high fever followed by rapid fall in tempt and a characteristic maculopapular Scarlet Fever rash • HHV-6 • Has a complete recovery in few days ChickenPox • Streptococcus Pyogens • Flushed face with circumoral • 1 – 7 days pallor. • Scarlatiniform rash • Petechiae on the soft palate. • Sandpaper rash • Strawberry tongue • Rash fades, peeling affects • The body rash appears 12-24 the fingertips, toes and groin hours after onset of illness area • Infectivity 5 – 7 days • 2-8 years age group 7 9/20/19 Varicella -zoster A 17 year old male presents to the ED with a rash which appeared suddenly over his trunk & tops of his arms & legs • Typical vesicular rash • Most infectious period 3 days ago. He has developed more • <10 years of age more 1-2 days lesions and they are slightly itchy. He completed a brief course of penicillin V common • Until the lesions have for tonsillitis 2 weeks ago. He feels • Trunk and then crusted otherwise well. spreading to the face and scalp 1) What is the likely diagnosis? (1) 2) What organism is most likely to have • oval teardrop on an precipitated this rash? (1) erythematous base 3) What information will you provide him regarding the prognosis? (1) SJS Stevens-Johnson Syndrome • Less than 10% TBSA • 10-30% TBSA mixed TEN/SjS • >30% TEN 8 9/20/19 Erythema Multiforme Management: A 32 year old male with • Majority if cases – no Rx required; resolves over 2-3 ulcerative colitis presents with a weeks rash. His temperature is 37.8 but other observations are normal. • Rx cause à HSV – aciclovir PO; Mycoplasma – antibiotics (e.g. erythromycin) 1) What is the likely diagnosis? • Stop offending drug (1) 2) Except for inflammatory • Supportive Rx à PO antihistamines; topical corticosteroid; bowel disease give 2 other mouthwashes causes of this skin disorder? • Eye involvement requires specialist ophthalmologist (1) 3) Name one other symptom assessment that may be associated with • Erythema multiforme major – may require admission for this skin disorder (1) supportive Rx Erythema Nodosum SAQ 3: • Hot, tender, ill-defined nodular erythematous eruption – A 17 year old male presents to the ED with a rash. He describes having a cold sore 1 week typically pretibial area of lower legs, can also affect forearms/ ago followed by the abrupt onset of the rash. trunk The rash started peripherally & spread centrally. He is unwell, febrile, tachycardic and • Inflammation of subcutaneous fat (panniculitis) with complaining of a headache. He also has a sore mouth, gritty eyes & haematuria on involvement of adjacent vasculature dipstick testing. • Immunological reaction affecting all age groups 1) Describe the key features of this rash? • Can be associated with arthralgia & fever (1) 2) What is the likely diagnosis? (1) • Clinical diagnosis 3) What is the most likely infective agent • Lasts 3-8 weeks à tends to leave bruised appearance that has precipitated the rash? (1) • Management according to cause 9 9/20/19 A 14 year old boy attends the ED with a sore left nostril. He has recently had a coryzal illness & his nose became cracked & sore after wiping it so much. He presents to the ED with his mother, 6 year old sister & 2 month old brother. They are attending as the affected area seems to be spreading. 1) What is the likely diagnosis? (1) 2) Name the causative microbe? (1) 3) What important advice will you provide prior to discharge home? (1) Impetigo • Superficial infection of skin caused by Group A A 52 year old woman presents with a swollen & exquisitely tender left lower limb. She recalls Streptococci or Staphylococcus aureus. scratching her ankle a few days ago with her fingernail whilst putting her trousers on. She is a • Initially ulcerative erythematous area à exudes serous diet controlled type 2 diabetic. The leg is fluid à golden brown crust. erythematous, hot to touch & very tender. She is nauseous, lost her appetite and has a • Highly contagious, spreads rapidly – temperature of 38.4 degrees. advice re: prevention of spread • Bullous impetigo – caused by S.aureus 1) What is the likely diagnosis? (1) • Local infection à topical fusidic acid. 2) Name the causative microbe? (1) • Extensive à oral or IV antibiotics 3) Detail 2 components of your management plan? (1) 10 9/20/19 Erysipelas Cellulitis • Superficial form of cellulitis • Bacterial skin infection (usually streptococcal, occasionally • Area of intense redness, heat & clearly defined margins staph). • Very tender • Can occur in association with wounds or in the absence of • Typically caused by group A Strep (streptococcal infection) skin breach. • Usually associated with systemic upset • Area warm, erythematous, tender, poorly defined margins ± lymphadenopathy. • Treated with antibiotics – e.g. phenoxymethylpenicillin • Treatment depends on severity • Analgesia • Local infection – oral antibiotics (Pen V/ fluclox/ co-amox or erythro) • Systemically unwell – Admit + IV antibiotics. • Cellulitis of the face – risk of IC complication (CST) Cellulitis Necrotising Fasciitis • Rare but severe bacterial infection of soft tissues • Can occur with/ without trauma • May follow illicit IM heroin injection (“muscle popping”) • Typically Strep pyogenes, sometimes with Staph aureus or other bacteria • Often both aerobic & anaerobic organisms. • Infection involves fascia & subcutaneous tissues with gas formation & development of gangrene. • Infection may spread to adjacent muscles causing myonecrosis or pyogenic myositis. 11 9/20/19 Necrotising Fasciitis Necrotising Fasciitis • Rare but severe bacterial infection of soft tissues • Fournier’s gangrene – affects abdomen & groin. • Can occur with/ without trauma • Initial symptoms vague: severe pain but little to find on • May follow illicit IM heroin injection (“muscle popping”) examination. • Typically Strep pyogenes, sometimes with Staph aureus • Tenderness, swelling, erythema, crepitus, pyrexia. or other bacteria • Rapid spread of infection – marked swelling, • Often both aerobic & anaerobic
Recommended publications
  • Dermatology DDX Deck, 2Nd Edition 65
    63. Herpes simplex (cold sores, fever blisters) PREMALIGNANT AND MALIGNANT NON- 64. Varicella (chicken pox) MELANOMA SKIN TUMORS Dermatology DDX Deck, 2nd Edition 65. Herpes zoster (shingles) 126. Basal cell carcinoma 66. Hand, foot, and mouth disease 127. Actinic keratosis TOPICAL THERAPY 128. Squamous cell carcinoma 1. Basic principles of treatment FUNGAL INFECTIONS 129. Bowen disease 2. Topical corticosteroids 67. Candidiasis (moniliasis) 130. Leukoplakia 68. Candidal balanitis 131. Cutaneous T-cell lymphoma ECZEMA 69. Candidiasis (diaper dermatitis) 132. Paget disease of the breast 3. Acute eczematous inflammation 70. Candidiasis of large skin folds (candidal 133. Extramammary Paget disease 4. Rhus dermatitis (poison ivy, poison oak, intertrigo) 134. Cutaneous metastasis poison sumac) 71. Tinea versicolor 5. Subacute eczematous inflammation 72. Tinea of the nails NEVI AND MALIGNANT MELANOMA 6. Chronic eczematous inflammation 73. Angular cheilitis 135. Nevi, melanocytic nevi, moles 7. Lichen simplex chronicus 74. Cutaneous fungal infections (tinea) 136. Atypical mole syndrome (dysplastic nevus 8. Hand eczema 75. Tinea of the foot syndrome) 9. Asteatotic eczema 76. Tinea of the groin 137. Malignant melanoma, lentigo maligna 10. Chapped, fissured feet 77. Tinea of the body 138. Melanoma mimics 11. Allergic contact dermatitis 78. Tinea of the hand 139. Congenital melanocytic nevi 12. Irritant contact dermatitis 79. Tinea incognito 13. Fingertip eczema 80. Tinea of the scalp VASCULAR TUMORS AND MALFORMATIONS 14. Keratolysis exfoliativa 81. Tinea of the beard 140. Hemangiomas of infancy 15. Nummular eczema 141. Vascular malformations 16. Pompholyx EXANTHEMS AND DRUG REACTIONS 142. Cherry angioma 17. Prurigo nodularis 82. Non-specific viral rash 143. Angiokeratoma 18. Stasis dermatitis 83.
    [Show full text]
  • Skin Manifestation of SARS-Cov-2: the Italian Experience
    Journal of Clinical Medicine Article Skin Manifestation of SARS-CoV-2: The Italian Experience Gerardo Cazzato 1 , Caterina Foti 2, Anna Colagrande 1, Antonietta Cimmino 1, Sara Scarcella 1, Gerolamo Cicco 1, Sara Sablone 3, Francesca Arezzo 4, Paolo Romita 2, Teresa Lettini 1 , Leonardo Resta 1 and Giuseppe Ingravallo 1,* 1 Section of Pathology, University of Bari ‘Aldo Moro’, 70121 Bari, Italy; [email protected] (G.C.); [email protected] (A.C.); [email protected] (A.C.); [email protected] (S.S.); [email protected] (G.C.); [email protected] (T.L.); [email protected] (L.R.) 2 Section of Dermatology and Venereology, University of Bari ‘Aldo Moro’, 70121 Bari, Italy; [email protected] (C.F.); [email protected] (P.R.) 3 Section of Forensic Medicine, University of Bari ‘Aldo Moro’, 70121 Bari, Italy; [email protected] 4 Section of Gynecologic and Obstetrics Clinic, University of Bari ‘Aldo Moro’, 70121 Bari, Italy; [email protected] * Correspondence: [email protected] Abstract: At the end of December 2019, a new coronavirus denominated Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) was identified in Wuhan, Hubei province, China. Less than three months later, the World Health Organization (WHO) declared coronavirus disease-19 (COVID-19) to be a global pandemic. Growing numbers of clinical, histopathological, and molecular findings were subsequently reported, among which a particular interest in skin manifestations during the course of the disease was evinced. Today, about one year after the development of the first major infectious foci in Italy, various large case series of patients with COVID-19-related skin Citation: Cazzato, G.; Foti, C.; manifestations have focused on skin specimens.
    [Show full text]
  • HIV and the SKIN • Sudden Acute Exacerbations • Treatment Failure DR
    2018/08/13 KEY FEATURES • Atypical presentation of common disorders • Severe or exaggerated presentations HIV AND THE SKIN • Sudden acute exacerbations • Treatment failure DR. FREDAH MALEKA DERMATOLOGY UNIVERSITY OF PRETORIA:KALAFONG VIRAL INFECTIONS EXANTHEM OF PRIMARY HIV INFECTION • Exanthem of primary HIV infection • Acute retroviral syndrome • Herpes simplex virus (HSV) • Morbilliform rash (exanthem) : 2-4 weeks after HIV exposure • Varicella Zoster virus (VZV) • Typically generalised • Molluscum contagiosum (Poxvirus) • Pronounced on face and trunk, sparing distal extremities • Human papillomavirus (HPV) • Associated : fever, lymphadenopathy, pharyngitis • Epstein Barr virus (EBV) • DDX: drug reaction • Cytomegalovirus (CMV) • other viral infections – EBV, Enteroviruses, Hepatitis B virus 1 2018/08/13 HERPES SIMPLEX VIRUS(HSV) • Vesicular eruption due to HSV 1&2 • Primary lesion: painful, grouped vesicles on an erythematous base • HIV: attacks are more frequent and severe • : chronic, non-healing, deep ulcers, with scarring and tissue destruction • CLUE: severe pain and recurrences • DDX: syphilis, chancroid, lymphogranuloma venereum • Tzanck smear, Histology, Viral culture HSV • Treatment: Acyclovir 400mg tds 7-10 days • Alternatives: Valacyclovir and Famciclovir • In setting of treatment failure, viral isolates tested for resistance against acyclovir • Alternative drugs: Foscarnet, Cidofovir • Chronic suppressive therapy ( >8 attacks per year) 2 2018/08/13 VARICELLA • Chickenpox • Presents with erythematous papules and umbilicated
    [Show full text]
  • Experience with Molluscum Contagiosum and Associated Inflammatory Reactions in a Pediatric Dermatology Practice the Bump That Rashes
    STUDY ONLINE FIRST Experience With Molluscum Contagiosum and Associated Inflammatory Reactions in a Pediatric Dermatology Practice The Bump That Rashes Emily M. Berger, MD; Seth J. Orlow, MD, PhD; Rishi R. Patel, MD; Julie V. Schaffer, MD Objective: To investigate the frequency, epidemiol- (50.6% vs 31.8%; PϽ.001). In patients with molluscum ogy, clinical features, and prognostic significance of in- dermatitis, numbers of MC lesions increased during the flamed molluscum contagiosum (MC) lesions, mollus- next 3 months in 23.4% of those treated with a topical cum dermatitis, reactive papular eruptions resembling corticosteroid and 33.3% of those not treated with a topi- Gianotti-Crosti syndrome, and atopic dermatitis in pa- cal corticosteroid, compared with 16.8% of patients with- tients with MC. out dermatitis. Patients with inflamed MC lesions were less likely to have an increased number of MC lesions Design: Retrospective medical chart review. over the next 3 months than patients without inflamed MC lesions or dermatitis (5.2% vs 18.4%; PϽ.03). The Setting: University-based pediatric dermatology practice. GCLRs were associated with inflamed MC lesion (PϽ.001), favored the elbows and knees, tended to be Patients: A total of 696 patients (mean age, 5.5 years) pruritic, and often heralded resolution of MC. Two pa- with molluscum. tients developed unilateral laterothoracic exanthem– like eruptions. Main Outcome Measures: Frequencies, characteris- tics, and associated features of inflammatory reactions Conclusions: Inflammatory reactions to MC, including to MC in patients with and without atopic dermatitis. the previously underrecognized GCLR, are common. Treat- ment of molluscum dermatitis can reduce spread of MC Results: Molluscum dermatitis, inflamed MC lesions, and via autoinoculation from scratching, whereas inflamed MC Gianotti-Crosti syndrome–like reactions (GCLRs) oc- lesions and GCLRs reflect cell-mediated immune re- curred in 270 (38.8%), 155 (22.3%), and 34 (4.9%) of sponses that may lead to viral clearance.
    [Show full text]
  • 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.
    [Show full text]
  • Erythema Nodosum (En)
    Buffalo Medical Group, P.C. Robert E. Kalb, M.D. Phone: (716) 630-1102 Fax: (716) 633-6507 Department of Dermatology 325 Essjay Road Williamsville, New York 14221 ERYTHEMA NODOSUM (EN) Erythema Nodosum (EN) is a relatively uncommon reaction in the skin consisting of red shiny tender nodular lesions most commonly found on the legs. The erythema refers to the red color that is seen at the surface of the skin. The nodosum refers to the fact that these lesions feel like bumps or nodules underneath the skin surface. Erythema nodosum is a reaction pattern occurring in the subcutaneous tissue and fat. It may be preceded by a low grade fever, fatigue, and joint pains. In about half of the cases, there is an internal condition occurring in the body which contributes to its formation. These include the use of certain medications, certain infections, and a number of other less likely causes. In order to identify cause for the erythema nodosum, it may be necessary to perform blood and laboratory tests. At times, however, the cause cannot be determined and erythema nodosum is considered to be idiopathic in nature. Erythema nodosum often runs an acute course lasting for a brief period from weeks to months. In a small percentage of cases, it can be a more chronic condition. The red nodules are usually confined to the lower legs, but can develop anywhere there is fat under the skin including the thighs, arms, and trunk. Initially, the lesions are more red and inflamed in appearance, but with time become more bruise like.
    [Show full text]
  • Bronchiolitis Obliterans • Mycoplasma Induced Asthma/Wheezing • Resistant Mycoplasma Infection
    CROSS CANADA ROUNDS - Long Case Mandeep Walia Clinical Fellow BC Children’s Hospital 21 June, 2018 Long Case History • 10 Y, Boy Feb 8th • Fever- low-moderate grade, rhinorrhea, cough (dry), mild sore throat • Nausea, non bilious vomiting Day 5- worsening cough -dry, sleep disturbance. • Walk in clinic- no wheeze. Prescribed ventolin. Minimal improvement Day 8- redness eyes, purulent discharge, blisters on lips, ulcers on tongue & buccal mucosa. Difficulty to swallow solids. History- cont • No headache, abnormal movements, visual or hearing loss • No chest pain/stridor/ • No diarrhoea. Vomiting stopped after D3 • No hematuria/dysuria. Feb 17 (D10)- BCCH ED : • concerns for extensive oral mucositis, new onset skin rash. Past Hx • Healthy pregnancy. No complications. • Born by SVD, no neonatal resuscitation/NICU stay. • Recurrent OM- evaluated by ENT-not required myringotomy tubes. • Mild eczema. Development - milestones normal Immunization- upto date Allergies- no known Treatment Hx- Tylenol/benadryl/Ventolin. No antibiotics/NSAIDS FHx- Caucasian descent. unremarkable. Social Hx- active in sports. No exposure to pets/smoke Physical exam • Weight- 37.9kg(77centile) Skin- • HR-96/min, RR-30/min , • pink papules, 2-3mm, central • SPO2 94% RA, T-39.2ᵒc, BP115/64 erosion, about 15-20 on trunk, • HEENT- upper & lower extremities. Sparing palms & soles. • B/L conjunctival injection, • purulent discharge MSK-no arthritis • • Lips, buccal mucosa , soft & hard Perianal skin, glans- normal palate-scattered vesicles & superficial erosions. No crusting (serous/hemorrhagic) • B/L ears-normal • No clubbing/lymphadenopathy Systemic Examination • Respiratory - tachyapnea. No retractions/indrawing. B/L air entry decreased. No wheeze/crackles. • CVS-S1 S2 normal. no murmur • PA- no HSM • Neurological - conscious.
    [Show full text]
  • MYELOPATHY ASSOCIATED with SYSTEMIC LUPUS ERYTHEMATOSUS (Erythema Nodosum)
    Paraplegia 16 (1978-79) 282-294 Original Articles MYELOPATHY ASSOCIATED WITH SYSTEMIC LUPUS ERYTHEMATOSUS (Erythema Nodosum) L. S. KEWALRAMANI, M.D., M.S.Orth., S. SALEEM, M.D. and D. BERTRAND, M.T. (ASCP) Texas Institute for Rehabilitation and Research and Department of Pathology, Baylor College of Medicine, Houston, Texas 77030, U.S.A. Abstract. Two patients with sudden onset of myelopathy associated with Systemic Lupus Erythematosus (Erythema Nodosum) are described. Pertinent literature is extensively reviewed and these two new patients are added to previously reported 26 patients. Key words: Myelopathy; Meningoencephalomyelopathy; Systemic lupus erythematosus. NEUROLOGICAL manifestations of systemic lupus erythematosus (SLE) have only recently been emphasised although they were mentioned by Kaposi in 1875, who observed stupor and coma as terminal manifestations of the disease. But focal neurological abnormalities were first reported by Osler (1903) and since then there have been several reports in the literature. Most commonly reported entities have been acute organic brain syndrome, seizures and cerebrovascular disorders. Chorea, Guillain Barre syndrome, subarachnoid haemorrhage, peripheral neuro­ pathy and cranial nerve palsies associated with SLE have also been reported on a few occasions. Myelopathy, however, has not received adequate emphasis as a complication of SLE. Fisher and Gilmour reported the first case of flaccid paraplegia in a female with SLE in 1939. Since then only 25 additional cases have been reported in the medical literature over the past 38 years. Twenty cases have been described in sufficient detail and six briefly, to permit a meaningful review of the spinal cord involvement in this disease. We feel that there are probably many more unreported cases of myelopathy associated with SLE.
    [Show full text]
  • 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
    [Show full text]
  • 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.
    [Show full text]
  • Fundamentals of Dermatology Describing Rashes and Lesions
    Dermatology for the Non-Dermatologist May 30 – June 3, 2018 - 1 - Fundamentals of Dermatology Describing Rashes and Lesions History remains ESSENTIAL to establish diagnosis – duration, treatments, prior history of skin conditions, drug use, systemic illness, etc., etc. Historical characteristics of lesions and rashes are also key elements of the description. Painful vs. painless? Pruritic? Burning sensation? Key descriptive elements – 1- definition and morphology of the lesion, 2- location and the extent of the disease. DEFINITIONS: Atrophy: Thinning of the epidermis and/or dermis causing a shiny appearance or fine wrinkling and/or depression of the skin (common causes: steroids, sudden weight gain, “stretch marks”) Bulla: Circumscribed superficial collection of fluid below or within the epidermis > 5mm (if <5mm vesicle), may be formed by the coalescence of vesicles (blister) Burrow: A linear, “threadlike” elevation of the skin, typically a few millimeters long. (scabies) Comedo: A plugged sebaceous follicle, such as closed (whitehead) & open comedones (blackhead) in acne Crust: Dried residue of serum, blood or pus (scab) Cyst: A circumscribed, usually slightly compressible, round, walled lesion, below the epidermis, may be filled with fluid or semi-solid material (sebaceous cyst, cystic acne) Dermatitis: nonspecific term for inflammation of the skin (many possible causes); may be a specific condition, e.g. atopic dermatitis Eczema: a generic term for acute or chronic inflammatory conditions of the skin. Typically appears erythematous,
    [Show full text]
  • Isotretinoin and the Risk of Erythema Multiforme Final SPC and PL
    Isotretinoin and the risk of erythema multiforme Final SPC and PL wording agreed by the PhVWP in June 2010 Doc. Ref.: CMDh/PhVWP/021/2010 Rev 1 July 2010 SUMMARY OF PRODUCT CHARACTERISTICS Section 4.4 There have been post-marketing reports of severe skin reactions (e.g. erythema multiforme (EM), Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN)) associated with isotretinoin use. As these events may be difficult to distinguish from other skin reactions that may occur (see section 4.8), patients should be advised of the signs and symptoms and monitored closely for severe skin reactions. If a severe skin reaction is suspected, isotretinoin treatment should be discontinued. Section 4.8 Skin and subcutaneous tissues Cheilitis, dermatitis, dry skin, localised exfoliation, pruritus, rash disorders: erythematous, skin fragility (risk of frictional trauma) Very common (≥ 1/10) Rare (≥ 1/10 000,< 1/1000) Alopecia Acne fulminans, acne aggravated (acne flare), erythema (facial), exanthema, hair disorders, hirsutism, nail dystrophy, paronychia, Very Rare (≤ 1/10 000) photosensitivity reaction, pyogenic granuloma, skin hyperpigmentation, sweating increased, ∗ Erythema multiforme, Stevens-Johnson Syndrome, toxic Unknown epidermal necrolysis. PACKAGE LEAFLET Possible side effects Skin and hair problems Unknown frequency Serious skin rashes (erythema multiforme, Stevens- Johnson syndrome, and toxic epidermal necrolysis), which are potentially life-threatening and require immediate medical attention. These appear initially as circular patches often with central blisters usually on arms and hands or legs and feet, more severe rashes may include blistering of the chest and back. Additional symptoms such as infection of the eye (conjunctivitis) or ulcers of the mouth, throat or nose may occur.
    [Show full text]