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ORIGINAL ARTICLE a Clinical and Histopathological Study of Lichenoid Eruption of Skin in Two Tertiary Care Hospitals of Dhaka
ORIGINAL ARTICLE A Clinical and Histopathological study of Lichenoid Eruption of Skin in Two Tertiary Care Hospitals of Dhaka. Khaled A1, Banu SG 2, Kamal M 3, Manzoor J 4, Nasir TA 5 Introduction studies from other countries. Skin diseases manifested by lichenoid eruption, With this background, this present study was is common in our country. Patients usually undertaken to know the clinical and attend the skin disease clinic in advanced stage histopathological pattern of lichenoid eruption, of disease because of improper treatment due to age and sex distribution of the diseases and to difficulties in differentiation of myriads of well assess the clinical diagnostic accuracy by established diseases which present as lichenoid histopathology. eruption. When we call a clinical eruption lichenoid, we Materials and Method usually mean it resembles lichen planus1, the A total of 134 cases were included in this study prototype of this group of disease. The term and these cases were collected from lichenoid used clinically to describe a flat Bangabandhu Sheikh Mujib Medical University topped, shiny papular eruption resembling 2 (Jan 2003 to Feb 2005) and Apollo Hospitals lichen planus. Histopathologically these Dhaka (Oct 2006 to May 2008), both of these are diseases show lichenoid tissue reaction. The large tertiary care hospitals in Dhaka. Biopsy lichenoid tissue reaction is characterized by specimen from patients of all age group having epidermal basal cell damage that is intimately lichenoid eruption was included in this study. associated with massive infiltration of T cells in 3 Detailed clinical history including age, sex, upper dermis. distribution of lesions, presence of itching, The spectrum of clinical diseases related to exacerbating factors, drug history, family history lichenoid tissue reaction is wider and usually and any systemic manifestation were noted. -
Urticaria - Primary Care Treatment Pathway
DORSET MEDICINES ADVISORY GROUP Urticaria - Primary Care Treatment Pathway Urticaria – also known as hives or nettle rash – is a raised, itchy rash that can occur on just one part of the body or be spread across large areas. The weals of urticaria last less than 24 hours although patients may develop new weals on a daily basis. If urticaria clears completely within six weeks, it is known as acute urticaria. Urticaria occurring for more than six weeks is referred to as chronic urticaria. Most cases of chronic disease occur without an obvious trigger (chronic spontaneous urticaria). Some urticaria has a physical trigger such as pressure (symptomatic dermographism or delayed pressure urticaria), cold or exercise (cholinergic urticaria), or may be drug induced (e.g. by NSAIDS, ACE inhibitors and opioids). All forms of urticaria can be treated with antihistamine although physical urticaria is less likely to respond to treatment than spontaneous urticaria. Most cases of urticaria settle spontaneously within two years but the condition can last for decades in some patients. Referral criteria Refer routinely to dermatology if patients are not responding to standard treatment (see primary care treatment below, up to step 4), they can then be considered for immunomodulation treatment such as ciclosporin (can be very useful for patients thought to have an autoimmune basis for their urticaria), methotrexate or omalizumab. The diagnosis of urticaria is primarily clinical therefore do not routinely refer for allergy testing. The British Association of Dermatologists (BAD) has produced a patient information leaflet which covers this in detail for patients. PRIOR TO SPECIALIST REFERRAL -conduct a full blood count (FBC), erythrocyte sedimentation rate (ESR), thyroid function tests (TFTs), liver function tests (LFTs), and Helicobacter pylori screening (if gastrointestinal symptoms are present). -
Clinical Study of Nail Changes in Papulosquamous Disorders
Original Research Article Clinical study of Nail changes in papulosquamous disorders Vishal Wali1, Trivedi Rahul Prasad2* 1Associate Professor, 2Post Graduate, Department of Dermatology, Venereology and Leprology, Mahadevappa Rampure Medical College, Sedam Road, Kalaburagi (Gulbarga) 585105, Karnataka, INDIA. Email: [email protected] Abstract Background: Nail disorders comprise ~10% of all dermatologic conditions. Nail disorders include those abnormalities that effect any portion of the nail unit. The nail unit includes the plate, matrix, bed, proximal and lateral folds, hyponychium, and some definitions include the underlying distal phalanx. These structures may be effected by heredity, skin disorders, infections, systemic disease, and aging process, internal and external medications, physical and environmental agents, trauma, and tumours, both benign and malignant. The main contributors being papulosquamous disorder. Nail changes in papulosquamous disorder have been inadequately discussed and only limited studies are present. This study aims to throw some light about frequency of nail involvement in papulosquamous disorders and its various patterns. Methodology: This is the descriptive study. It was conducted in department of DVL of Mahadevappa Rampura Medical college and Basaveshwar teaching and general hospital, Kalaburagi from July 2019 to Feb 2021. General, systemic and dermatological examinations were done. Nails were examined in detail. Special investigations like skin biopsy and potassium hydroxide (KOH) mount was done in relevant cases. Results: There were 50 cases of papulosquamous disorder. The most common papulosquamous disorder was psoriasis, followed by lichen planus and PRP. Out of these the most common nail change was pitting (81%) and lest common was dorsal pterygium (%) Conclusion: Nail being an important appendage affecting various dermatosis and acts as window in diagnosis. -
Viral Rashes: New and Old Peggy Vernon, RN, MA, CPNP, DCNP, FAANP C5
Viral Rashes: New and Old Peggy Vernon, RN, MA, CPNP, DCNP, FAANP C5 Disclosures •There are no financial relationships with commercial interests to disclose Viral Rashes: New and Old •Any unlabeled/unapproved uses of drugs or products referenced will be disclosed Peggy Vernon, RN, MA, CPNP, DCNP, FAANP ©Pvernon2021 ©Pvernon2021 Restrictions Objectives • Permission granted to the 2021 National Nurse • Identify a potential sequelae from hand, foot and Practitioner Symposium and its attendees mouth disease • Describe the pattern of distribution and lesion • All rights reserved. No part of this presentation may description of varicella be reproduced, stored, or transmitted in any form or • Identify a precursor of Henoch Schonlein Purpura by any means without written permission of the author •Contact Peggy Vernon at [email protected] ©Pvernon2021 ©Pvernon2021 Viral Exanthems Morbilliform Exanthems •Morbilliform • Measles (rubeola) •Papular-nodular • Rubella •Vesiculobullous • Roseola •Petechial • Erythema Infectiosum •Purpuric • Pityriasis Rosea • Infectious Mono ©Pvernon2021 ©Pvernon2021 1 Viral Rashes: New and Old Peggy Vernon, RN, MA, CPNP, DCNP, FAANP C5 Measles (Rubeola) MEASLES (RUBEOLA) • Prodrome: fever, malaise, cough, DIFFERENTIAL DIAGNOSIS conjunctivitis. Patient appears quite ill •Other morbilliform eruptions: Rubella, • Koplik’s spots: bluish-white erythema infectiosum, pityriasis rosea, elevations on buccal mucosa infectious mono • Exanthem: erythematous •DRUG maculopapular eruption, from scalp to forehead, posterior -
Drug Treatments in Psoriasis
Drug Treatments in Psoriasis Authors: David Gravette, Pharm.D. Candidate, Harrison School of Pharmacy, Auburn University; Morgan Luger, Pharm.D. Candidate, Harrison School of Pharmacy, Auburn University; Jay Moulton, Pharm.D. Candidate, Harrison School of Pharmacy, Auburn University; Wesley T. Lindsey, Pharm.D., Associate Clinical Professor of Pharmacy Practice, Drug Information and Learning Resource Center, Harrison School of Pharmacy, Auburn University Universal Activity #: 0178-0000-13-108-H01-P | 1.5 contact hours (.15 CEUs) Initial Release Date: November 29, 2013 | Expires: April 1, 2016 Alabama Pharmacy Association | 334.271.4222 | www.aparx.org | [email protected] SPRING 2014: CONTINUING EDUCATION |WWW.APARX.Org 1 EducatiONAL OBJECTIVES After the completion of this activity pharmacists will be able to: • Outline how to diagnose psoriasis. • Describe the different types of psoriasis. • Outline nonpharmacologic and pharmacologic treatments for psoriasis. • Describe research on new biologic drugs to be used for the treatment of psoriasis as well as alternative FDA uses for approved drugs. INTRODUCTION depression, and even alcoholism which decreases their quality of Psoriasis is a common immune modulated inflammatory life. It is uncertain why these diseases coincide with one another, disease affecting nearly 17 million people in North America and but it is hypothesized that the chronic inflammatory nature of Europe, which is approximately 2% of the population. The highest psoriasis is the underlying problem. frequencies occur in Caucasians -
Etiology, Classification, and Treatment of Urticaria
CONTINUING MEDICAL EDUCATION Etiology, Classification, and Treatment of Urticaria Kjetil Kristoffer Guldbakke, MD; Amor Khachemoune, MD, CWS GOAL To understand urticaria to better manage patients with the condition OBJECTIVES Upon completion of this activity, dermatologists and general practitioners should be able to: 1. Discuss the clinical classification of urticaria. 2. Recognize how to diagnose urticaria. 3. Identify treatment options. CME Test on page 50. This article has been peer reviewed and approved Einstein College of Medicine is accredited by by Michael Fisher, MD, Professor of Medicine, the ACCME to provide continuing medical edu- Albert Einstein College of Medicine. Review date: cation for physicians. December 2006. Albert Einstein College of Medicine designates This activity has been planned and imple- this educational activity for a maximum of 1 AMA mented in accordance with the Essential Areas PRA Category 1 CreditTM. Physicians should only and Policies of the Accreditation Council for claim credit commensurate with the extent of their Continuing Medical Education through the participation in the activity. joint sponsorship of Albert Einstein College of This activity has been planned and produced in Medicine and Quadrant HealthCom, Inc. Albert accordance with ACCME Essentials. Drs. Guldbakke and Khachemoune report no conflict of interest. The authors discuss off-label use of colchi- cine, cyclophosphamide, cyclosporine, dapsone, intravenous immunoglobulin, methotrexate, montelukast sodium, nifedipine, plasmapheresis, rofecoxib, sulfasalazine, tacrolimus, thyroxine, and zafirlukast. Dr. Fisher reports no conflict of interest. Urticaria is among the most common skin dis- autoimmune mechanisms are now recognized as a eases. It can be acute, chronic, mediated by a cause of chronic urticaria. A search of the PubMed physical stimulus, or related to contact with an database (US National Library of Medicine) for urticant. -
Atypical Variants of Mycosis Fungoides
Altınışık et al. Atypical Variants of Mycosis Fungoides REVIEW DOI: 10.4274/jtad.galenos.2021.09719 J Turk Acad Dermatol 2021;15(2):30-33 Atypical Variants of Mycosis Fungoides Dursun Dorukhan Altınışık, Özge Aşkın, Tuğba Kevser Uzunçakmak, Burhan Engin Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Dermatology, Istanbul, Turkey ABSTRACT Mycosis fungoides (MF) is the most common type of cutaneous T-cell lymphoma (CTCL) and it is characterised by specific histological features. MF is in a spectrum of disorders which includes Sezary syndrome and other CTCL subtypes. Clinically and histopathologically it can imitate other T-cell mediated dermatosis hence making its diagnosis difficult. Due to different prognosis and difference in treatment strategies other subtypes of CTCL must be differentiated from MF. MF is a clinically indolent low-grade lymphoma which is seen in people aged between 55- 60 and it’s seen more commonly in men (2:1 ratio). Meanwhile other subtypes of MF like folliculotropic variant may show relatively a more aggressive course and our treatment strategy may differ. Keywords: Mycosis fungoides, Cutaneous T-cell lymphoma, Phototherapy, PUVA Introduction follicles frequently causing alopecia and in the paediatric population Mycosis fungoides (MF) is the most common type of cutaneous T-cell it tends to accompany hypopigmented patches and plaques. FMF lymphoma (CTCL) and it is characterised by specific histological preferentially involves the head and neck region however it can features [1]. MF is in a spectrum of disorders which includes Sezary sometimes involve the trunk or the extremities [6]. Patients with syndrome and other CTCL subtypes. Clinically and histopathologically FMF have significant pruritus which may be overlapped by S. -
The Management of Psoriasis in Adults
DORSET MEDICINES ADVISORY GROUP THE MANAGEMENT OF PSORIASIS IN ADULTS Psoriasis is a common, genetically determined, inflammatory and proliferative disorder of the skin, the most characteristic lesions consisting of chronic, sharply demarcated, dull-red, scaly plaques, particularly on the extensor prominences and in the scalp. Self-care advice Many people's psoriasis symptoms start or become worse because of a certain event, known as a trigger. Common triggers include: • an injury to skin such as a cut, scrape, insect bite or sunburn (this is known as the Koebner response) • drinking excessive amounts of alcohol • smoking • stress • hormonal changes, particularly in women (for example during puberty and the menopause) • certain medicines such as lithium, some antimalarial medicines, anti-inflammatory medicines including ibuprofen, ACE inhibitors (used to treat high blood pressure) and beta blockers (used to treat congestive heart failure) • throat infections - in some people, usually children and young adults, a form of psoriasis called guttate psoriasis (which causes smaller pink patches, often without a lot of scaling) develops after a streptococcal throat infection, although most people who have streptococcal throat infections do not develop psoriasis • other immune disorders, such as HIV, which cause psoriasis to flare up or to appear for the first time Advice for patients can be found here Management pathway For people with any type of psoriasis assess: • disease severity • the impact of disease on physical, psychological and social wellbeing • whether they have psoriatic arthritis • the presence of comorbidities. • Consider using the Dermatology quality of life assessment: www.pcds.org.uk/p/quality-of-life Assess the severity and impact of any type of psoriasis: • at first presentation • before referral for specialist advice and at each referral point in the treatment pathway • to evaluate the efficacy of interventions. -
10 Chronic Urticaria As an Autoimmune Disease
10 Chronic Urticaria as an Autoimmune Disease Michihiro Hide, Malcolm W. Greaves Introduction Urticaria is conventionally classified as acute, intermittent and chronic (Grea- ves 2000a). Acute urticaria which frequently involves an IgE-mediated im- munological mechanism, is common, its causes often recognised by the patient, and will not be considered further. Intermittent urticaria – frequent bouts of unexplained urticaria at intervals of weeks or months – will be dis- cussed here on the same basis as ‘ordinary’ chronic urticaria. The latter is conventionally defined as the occurrence of daily or almost daily whealing for at least six weeks. The etiology of chronic urticaria is usually obscure. The different clinical varieties of chronic urticaria will be briefly considered here, and attention will be devoted to a newly emerged entity – autoimmune chronic urticaria, since establishing this diagnosis has conceptual, prognostic and the- rapeutic implications. Contact urticaria and angioedema without urticaria will not be dealt with in this account. Classification of Chronic Urticaria The clinical subtypes of chronic urticaria are illustrated in the pie-chart of Fig. 1. The frequency of these subtypes is based upon the authors’ experience at the St John’s Institute of Dermatology in UK. Whilst there may well be mi- nor differences, it is likely that the frequency distribution of these subtypes will be essentially similar in most centres in Europe and North America (Grea- ves 1995, 2000b). However, our experience suggests that the incidence of angioedema, especially that complicated by ordinary chronic urticaria is sub- stantially lower in Japan and south Asian countries (unpublished observation). 310 Michihiro Hide and Malcolm W. -
Lichen Spinulosus: Case Report and Review of Literatures
Journal of Health Science 2015, 5(3A): 20-22 DOI: 10.5923/s.health.201501.07 Lichen Spinulosus: Case Report and Review of Literatures Khalid Al Hawsawi1,*, Kholood Almehmadi2, Bushra Alraddadi3, Ohood Aljuhani2 1Dermatology Consultant, Head of Dermatology Department, King Abdul Aziz Hospital, Makkah, Saudi Arabia 2Medical intern, King Abdul Aziz Hospital, Makkah, Saudi Arabia 3Dermatology Resident, King Abdul Aziz Hospital, Makkah, Saudi Arabia Abstract Lichen Spinulosus is a rare childhood disease. It is characterized by follicular hyperkeratotic papules that may coalesce into plaques. Individual lesion shows conical projection, hair like horny spine. The etiology is unknown but genetic predisposition has been suggested as a possible cause. It has a tendency to disappear spontaneously at puberty. Herein we present a 12-year-old boy presented with 6- month- history of persistent asymptomatic skin lesions. Skin examinations revealed multiple grouped scaly, hypopigmented tiny follicular papules with horny spines on his back. Soles showed planter keratoderma. Skin biopsy showed dilated hair follicle filled with keratin plugging. Diagnosis of LS associated with planter keratoderma was made. The patient responded well to topical lactic acid (12%), urea (20-30%), and betamethasone valerate (0.1%) preparations. Keywords Lichen spinulosa, Lichen Spinulosus 1. Introduction appearance. LS usually involves extensor surfaces of arms, trochanteric regions, neck, abdomen, buttocks, thigh, Lichen spinulosus (LS) is a genetic disorder of popliteal fossae, and knees. The histopathology of the lesion is not specific showing dilated hair follicle with keratin keratinization of hair follicles. LS was first described by Adamson in 1908. [1] It is a member of the family of plugging. -
ALLCHRONIC URTICARIA About ANGIOEDEMA
ALLCHRONIC URTICARIA about& ANGIOEDEMA WHAT IS CHRONIC URTICARIA? may be a result of an immune system disorder. In very rare cases, The term chronic urticaria (CU) is another term for “chronic CU/angioedema can be identified as a reaction to a medication, hives.” Hives are an inflammation of the skin that results from cells food, insect or infection. Even when the cause cannot be identified, in your body releasing histamine and other allergic chemicals into there are common stimuli that may worsen or exacerbate the condi- the bloodstream. They appear as clusters of raised, red or white tion such as: welts that tend to be very itchy. Chronic hives are defined as hives • allergies (food, environmental) • medications that last more than six weeks, or may briefly go away, but often • temperatures (hot and cold) • illnesses recur frequently. About 40% of people with chronic urticaria often • pressure • sun exposure have another condition known as angioedema. There are several subtypes of CU, including cold urticaria, pressure urticaria, and HOW IS CU/ANGIOEDEMA DIAGNOSED? cholinergic urticaria. CU occurs in about 1% of the US population. The diagnosis of CU is based mostly on history of symptoms and physical exam that is done by either your pediatrician or an WHAT ARE THE SYMPTOMS OF CU? allergist. Although there are not specific laboratory tests that can be done to diagnose this condition, there are blood tests and allergy CU presents as hives - small or large patches that may be round, tests that can be done to identify triggers or rule out other condi- irregular shaped, rings, or may change shape throughout the day. -
Differentiating Keratosis Follicularis Spinulosa Decalvans from Monilithrix : Two Rare Causes of Scarring Alopecia in Young Male Siblings
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) e-ISSN: 2279-0853, p-ISSN: 2279-0861.Volume 18, Issue 5 Ser. 7 (May. 2019), PP 01-03 www.iosrjournals.org Differentiating Keratosis Follicularis Spinulosa Decalvans From Monilithrix : Two Rare Causes Of Scarring Alopecia In Young Male Siblings. 1 2 3 4 5 Heena Singdia , Rohit Garg , Sinni Jain , Vijay Paliwal , Puneet Bhargava , Deepak Mathur6 1,2,3,4,5,6(Department of dermatology, venereology and leprology, SMS Medical College, India) Corresponding Author: Heena Singdia Abstract: Keratosis follicularis spinulosa decalvans (KFSD) is a rare disorder affecting the hair follicles characterized by progressive cicatricial alopecia of the scalp and eyebrows, with usually X-linked recessive mode of transmission hence predominantly affecting Males.[1] Monilethrix is a rare structural Hair shaft disorder with autosomal dominant mode of transmission, characterized by short, fragile, brittle hair that breaks spontaneously resulting in patchy dystrophic alopecia.[2] Key words: Keratosis Follicularis Spinulosa Decalvans, Monilithrix, Hereditary Scarring Alopecias --------------------------------------------------------------------------------------------------------------------------------------- Date of Submission: 02-05-2019 Date of acceptance: 16-05-2019 --------------------------------------------------------------------------------------------------------------------------------------------------- I. Introduction KFSD is a rare type of primary scarring alopecia with lymphocytic predominance.