Negative Emotions in Skin Disorders: a Systematic Review
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Guidelines of Care for the 10 Most Common Dermatologic Diseases
1 Guidelines of Care for the 10 most common dermatologic diseases: Copyright by the American Academy of Dermatology, Inc. Disclaimer Adherence to these guidelines will not ensure successful treatment in every situation. Further, these guidelines should not be deemed inclusive of all proper methods of care or exclusive of other methods of care reasonably directed to obtaining the same results. The ultimate judgment regarding the propriety of any specific procedure must be made by the physician in light of all the circumstances presented by the individual patient. For the benefit of members of the American Academy of Dermatology who practice in countries outside the jurisdiction of the United States, the listed treatments may include agents that not currently approved by the U.S. Food and Drug Administration. 1. Acne Vulgaris 2. Alopecia Areata 3. Atopic Dermatitis 4. Contact Dermatitis 5. Cutaneous Adverse Drug Reactions 6. Nail Disorders 7. Psoriasis 8. Superficial Mycotic Infections of the Skin: Mucocutaneous Candidiasis, Onychomycosis, Piedra, Pityriasis, Tinea Capitis , Tinea Barbae, Tinea Corporis, Tinea Cruris, Tinea Faciei, Tinea Manuum, and Tinea Pedis. 9. Vitiligo 10. Warts: Human Papillomavirus 1 2 1- Guidelines of Care for Acne Vulgaris* Reference: 1990 by the American Academy of Dermatology, Inc. I. Introduction The American Academy of Dermatology’s Committee on Guidelines of Care is developing guidelines of care for our profession. The development of guidelines will promote the continued delivery of quality care and assist those outside our profession in understanding the complexities and boundaries of care provided by dermatologists. II. Definition Acne vulgaris is a follicular disorder that affects susceptible pilosebaceous follicles, primarily of the face, neck, and upper trunk, and is characterized by both noninflammatory and inflammatory lesions. -
General Dermatology an Atlas of Diagnosis and Management 2007
An Atlas of Diagnosis and Management GENERAL DERMATOLOGY John SC English, FRCP Department of Dermatology Queen's Medical Centre Nottingham University Hospitals NHS Trust Nottingham, UK CLINICAL PUBLISHING OXFORD Clinical Publishing An imprint of Atlas Medical Publishing Ltd Oxford Centre for Innovation Mill Street, Oxford OX2 0JX, UK tel: +44 1865 811116 fax: +44 1865 251550 email: [email protected] web: www.clinicalpublishing.co.uk Distributed in USA and Canada by: Clinical Publishing 30 Amberwood Parkway Ashland OH 44805 USA tel: 800-247-6553 (toll free within US and Canada) fax: 419-281-6883 email: [email protected] Distributed in UK and Rest of World by: Marston Book Services Ltd PO Box 269 Abingdon Oxon OX14 4YN UK tel: +44 1235 465500 fax: +44 1235 465555 email: [email protected] © Atlas Medical Publishing Ltd 2007 First published 2007 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, without the prior permission in writing of Clinical Publishing or Atlas Medical Publishing Ltd. Although every effort has been made to ensure that all owners of copyright material have been acknowledged in this publication, we would be glad to acknowledge in subsequent reprints or editions any omissions brought to our attention. A catalogue record of this book is available from the British Library ISBN-13 978 1 904392 76 7 Electronic ISBN 978 1 84692 568 9 The publisher makes no representation, express or implied, that the dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up-to-date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. -
Alopecia Areata Part 1: Pathogenesis, Diagnosis, and Prognosis
Clinical Review Alopecia areata Part 1: pathogenesis, diagnosis, and prognosis Frank Spano MD CCFP Jeff C. Donovan MD PhD FRCPC Abstract Objective To provide family physicians with a background understanding of the epidemiology, pathogenesis, histology, and clinical approach to the diagnosis of alopecia areata (AA). Sources of information PubMed was searched for relevant articles regarding the pathogenesis, diagnosis, and prognosis of AA. Main message Alopecia areata is a form of autoimmune hair loss with a lifetime prevalence of approximately 2%. A personal or family history of concomitant autoimmune disorders, such as vitiligo or thyroid disease, might be noted in a small subset of patients. Diagnosis can often be made clinically, based on the characteristic nonscarring, circular areas of hair loss, with small “exclamation mark” hairs at the periphery in those with early stages of the condition. The diagnosis of more complex cases or unusual presentations can be facilitated by biopsy and histologic examination. The prognosis varies widely, and poor outcomes are associated with an early age of onset, extensive loss, the ophiasis variant, nail changes, a family history, or comorbid autoimmune disorders. Conclusion Alopecia areata is an autoimmune form of hair loss seen regularly in primary care. Family physicians are well placed to identify AA, characterize the severity of disease, and form an appropriate differential diagnosis. Further, they are able educate their patients about the clinical course of AA, as well as the overall prognosis, depending on the patient subtype. Case A 25-year-old man was getting his regular haircut when his EDITor’s KEY POINTS • Alopecia areata is an autoimmune form of barber pointed out several areas of hair loss. -
Topographical Dermatology Picture Cause Basic Lesion
page: 332 Chapter 12: alphabetical Topographical dermatology picture cause basic lesion search contents print last screen viewed back next Topographical dermatology Alopecia page: 333 12.1 Alopecia alphabetical Alopecia areata Alopecia areata of the scalp is characterized by the appearance of round or oval, smooth, shiny picture patches of alopecia which gradually increase in size. The patches are usually homogeneously glabrous and are bordered by a peripheral scatter of short broken- cause off hairs known as exclamation- mark hairs. basic lesion Basic Lesions: None specific Causes: None specific search contents print last screen viewed back next Topographical dermatology Alopecia page: 334 alphabetical Alopecia areata continued Alopecia areata of the occipital region, known as ophiasis, is more resistant to regrowth. Other hair picture regions can also be affected: eyebrows, eyelashes, beard, and the axillary and pubic regions. In some cases the alopecia can be generalized: this is known as cause alopecia totalis (scalp) and alopecia universalis (whole body). basic lesion Basic Lesions: Causes: None specific search contents print last screen viewed back next Topographical dermatology Alopecia page: 335 alphabetical Pseudopelade Pseudopelade consists of circumscribed alopecia which varies in shape and in size, with picture more or less distinct limits. The skin is atrophic and adheres to the underlying tissue layers. This unusual cicatricial clinical appearance can be symptomatic of cause various other conditions: lupus erythematosus, lichen planus, folliculitis decalvans. Some cases are idiopathic and these are known as pseudopelade. basic lesion Basic Lesions: Atrophy; Scars Causes: None specific search contents print last screen viewed back next Topographical dermatology Alopecia page: 336 alphabetical Trichotillomania Plucking of the hair on a large scale. -
Alopecia Areata: Evidence-Based Treatments
Alopecia Areata: Evidence-Based Treatments Seema Garg and Andrew G. Messenger Alopecia areata is a common condition causing nonscarring hair loss. It may be patchy, involve the entire scalp (alopecia totalis) or whole body (alopecia universalis). Patients may recover spontaneously but the disorder can follow a course of recurrent relapses or result in persistent hair loss. Alopecia areata can cause great psychological distress, and the most important aspect of management is counseling the patient about the unpredictable nature and course of the condition as well as the available effective treatments, with details of their side effects. Although many treatments have been shown to stimulate hair growth in alopecia areata, there are limited data on their long-term efficacy and impact on quality of life. We review the evidence for the following commonly used treatments: corticosteroids (topical, intralesional, and systemic), topical sensitizers (diphenylcyclopropenone), psor- alen and ultraviolet A phototherapy (PUVA), minoxidil and dithranol. Semin Cutan Med Surg 28:15-18 © 2009 Elsevier Inc. All rights reserved. lopecia areata (AA) is a chronic inflammatory condition caus- with AA having nail involvement. Recovery can occur spontaneously, Aing nonscarring hair loss. The lifetime risk of developing the although hair loss can recur and progress to alopecia totalis (total loss of condition has been estimated at 1.7% and it accounts for 1% to 2% scalp hair) or universalis (both body and scalp hair). Diagnosis is usu- of new patients seen in dermatology clinics in the United Kingdom ally made clinically, and investigations usually are unnecessary. Poor and United States.1 The onset may occur at any age; however, the prognosis is linked to the presence of other immune diseases, family majority (60%) commence before 20 years of age.2 There is equal history of AA, young age at onset, nail dystrophy, extensive hair loss, distribution of incidence across races and sexes. -
Case of Persistent Regrowth of Blond Hair in a Previously Brunette Alopecia Areata Totalis Patient
Case of Persistent Regrowth of Blond Hair in a Previously Brunette Alopecia Areata Totalis Patient Karla Snider, DO,* John Young, MD** *PGYIII, Silver Falls Dermatology/Western University, Salem, OR **Program Director, Dermatology Residency Program, Silver Falls Dermatology, Salem, OR Abstract We present a case of a brunette, 64-year-old female with no previous history of alopecia areata who presented to our clinic with diffuse hair loss over the scalp. She was treated with triamcinolone acetonide intralesional injections and experienced hair re-growth of initially white hair that then partially re-pigmented to blond at the vertex. Two years following initiation of therapy, she continued to have blond hair growth on her scalp with no dark hair re-growth and no recurrence of alopecia areata. Introduction (CBC), comprehensive metabolic panel (CMP), along the periphery of the occipital, parietal and Alopecia areata (AA) is a fairly common thyroid stimulating hormone (TSH) test and temporal scalp), sisaipho pattern (loss of hair in autoimmune disorder of non-scarring hair loss. antinuclear antibody (ANA) test. All values were the frontal parietotemporal scalp), patchy hair unremarkable, and the ANA was negative. The loss (reticular variant) and a diffuse thinning The disease commonly presents as hair loss from 2 any hair-bearing area of the body. Following patient declined a biopsy. variant. Often, “exclamation point hairs” can be hair loss, it is not rare to see initial growth of A clinical diagnosis of alopecia areata was seen in and around the margins of the hair loss. depigmented or hypopigmented hair in areas made. The patient was treated with 5.0 mg/mL The distal ends of these hairs are thicker than the proximal ends, and they are a marker of active of regrowth in the first anagen cycle. -
Safety and Efficacy of the JAK Inhibitor Tofacitinib Citrate in Patients with Alopecia Areata
Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata Milène Kennedy Crispin, … , Anthony E. Oro, Brett A. King JCI Insight. 2016;1(15):e89776. https://doi.org/10.1172/jci.insight.89776. Clinical Medicine Dermatology Inflammation BACKGROUND. Alopecia areata (AA) is an autoimmune disease characterized by hair loss mediated by CD8+ T cells. There are no reliably effective therapies for AA. Based on recent developments in the understanding of the pathomechanism of AA, JAK inhibitors appear to be a therapeutic option; however, their efficacy for the treatment of AA has not been systematically examined. METHODS. This was a 2-center, open-label, single-arm trial using the pan-JAK inhibitor, tofacitinib citrate, for AA with >50% scalp hair loss, alopecia totalis (AT), and alopecia universalis (AU). Tofacitinib (5 mg) was given twice daily for 3 months. Endpoints included regrowth of scalp hair, as assessed by the severity of alopecia tool (SALT), duration of hair growth after completion of therapy, and disease transcriptome. RESULTS. Of 66 subjects treated, 32% experienced 50% or greater improvement in SALT score. AA and ophiasis subtypes were more responsive than AT and AU subtypes. Shorter duration of disease and histological peribulbar inflammation on pretreatment scalp biopsies were associated with improvement in SALT score. Drug cessation resulted in disease relapse in 8.5 weeks. Adverse events were limited to grade I and II infections. An AA responsiveness to […] Find the latest version: https://jci.me/89776/pdf CLINICAL MEDICINE Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata Milène Kennedy Crispin,1 Justin M. -
Our Experience in 62 Patie
Comparison of the Efficacy and Safety of Topical 5% Minoxidil Solution Alone and in Combination with 0.05% Betamethasone Dipropionate Cream in the Treatment of Alopecia Areata Aman S.,1 Nadeem M.2 Address for Correspondence: Dr. Shahbaz Aman, Associate Professor, Department of Dermatology Unit-I, King Edward Medical University/ Mayo Hospital, Lahore 2-C, Hearn Road, Islampura, Lahore. Background: Alopecia Areata (AA) is a fairly common skin problem, accounting for approximately 2% of new derma- tological outpatients worldwide. There is a dire need for an innovative approach in the treatment of this disorder. Objective: Our objective was to assess the efficacy and safety of topical 5% minoxidil solution alone and in combination with 0.05% betamethasone dipropionate cream in the treatment of alopecia areata. Method: Fifty patients with alopecia areata, ages ranging from 18 to 55 years, were enrolled in the study. They were ran- domly divided into two groups, each having 25 patients. The patients in group A, were advised to apply 5% minoxidil solu- tion, twice daily for a period of three months. Whereas the patients of group B, were advised to apply 5% minoxidil solution followed by, 30-60 minutes later, the application of 0.05% betamethasone dipropionate cream. Patients of both groups applied the medicines for a period of three months after which they were followed up for the next three months. The efficacy of the drugs was assessed on the basis of percentage re-growth of hair as: Excellent (> 90%), Good (70 – 90%), Satisfactory (50-69%) and Poor (< 50%). The safety of treatment administered was assessed on the basis of local or systemic side effects of the drugs. -
(12) United States Patent (10) Patent No.: US 7,359,748 B1 Drugge (45) Date of Patent: Apr
USOO7359748B1 (12) United States Patent (10) Patent No.: US 7,359,748 B1 Drugge (45) Date of Patent: Apr. 15, 2008 (54) APPARATUS FOR TOTAL IMMERSION 6,339,216 B1* 1/2002 Wake ..................... 250,214. A PHOTOGRAPHY 6,397,091 B2 * 5/2002 Diab et al. .................. 600,323 6,556,858 B1 * 4/2003 Zeman ............. ... 600,473 (76) Inventor: Rhett Drugge, 50 Glenbrook Rd., Suite 6,597,941 B2. T/2003 Fontenot et al. ............ 600/473 1C, Stamford, NH (US) 06902-2914 7,092,014 B1 8/2006 Li et al. .................. 348.218.1 (*) Notice: Subject to any disclaimer, the term of this k cited. by examiner patent is extended or adjusted under 35 Primary Examiner Daniel Robinson U.S.C. 154(b) by 802 days. (74) Attorney, Agent, or Firm—McCarter & English, LLP (21) Appl. No.: 09/625,712 (57) ABSTRACT (22) Filed: Jul. 26, 2000 Total Immersion Photography (TIP) is disclosed, preferably for the use of screening for various medical and cosmetic (51) Int. Cl. conditions. TIP, in a preferred embodiment, comprises an A6 IB 6/00 (2006.01) enclosed structure that may be sized in accordance with an (52) U.S. Cl. ....................................... 600/476; 600/477 entire person, or individual body parts. Disposed therein are (58) Field of Classification Search ................ 600/476, a plurality of imaging means which may gather a variety of 600/162,407, 477, 478,479, 480; A61 B 6/00 information, e.g., chemical, light, temperature, etc. In a See application file for complete search history. preferred embodiment, a computer and plurality of USB (56) References Cited hubs are used to remotely operate and control digital cam eras. -
JAK Inhibition in the Treatment of Alopecia Areata – a Promising New Dawn?
Expert Review of Clinical Pharmacology ISSN: 1751-2433 (Print) 1751-2441 (Online) Journal homepage: https://www.tandfonline.com/loi/ierj20 JAK inhibition in the treatment of alopecia areata – a promising new dawn? Fathima Ferial Ismail & Rodney Sinclair To cite this article: Fathima Ferial Ismail & Rodney Sinclair (2019): JAK inhibition in the treatment of alopecia areata – a promising new dawn?, Expert Review of Clinical Pharmacology, DOI: 10.1080/17512433.2020.1702878 To link to this article: https://doi.org/10.1080/17512433.2020.1702878 Published online: 22 Dec 2019. Submit your article to this journal View related articles View Crossmark data Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=ierj20 EXPERT REVIEW OF CLINICAL PHARMACOLOGY https://doi.org/10.1080/17512433.2020.1702878 REVIEW JAK inhibition in the treatment of alopecia areata – a promising new dawn? Fathima Ferial Ismail a and Rodney Sinclaira,b aSinclair Dermatology, Melbourne, Australia; bDepartment of Medicine, University of Melbourne, Melbourne, Australia ABSTRACT ARTICLE HISTORY Introduction: Alopecia areata (AA) is a T-cell-mediated disease which produces circular patches of non- Received 9 November 2019 scarring hair loss and nail dystrophy. Current treatment options for AA are limited and often yield Accepted 6 December 2019 unsatisfactory results. Pharmacologic inhibition of the Janus kinase (JAK) enzyme family is regrowing KEYWORDS hair and reversing nail dystrophy in a number of patients with hitherto refractory AA. The six JAK Alopecia areata; Janus inhibitors which have been successful in treating AA are tofacitinib, ruxolitinib, baricitinib, CTP-543, PF- kinase inhibitors; tofacitinib; 06651600 and PF-06700841. -
Pediatric Dermatology Potpourri
Pediatric Dermatology Potpourri Jennifer Ruth, MD Assistant Professor of Pediatric & Adolescent Dermatology 9.7.19 Disclosures • I have no conflicts of interest or financial relationships to disclose Learning objectives • Discuss management of common pediatric dermatologic conditions. • Formulate a therapeutic plan for common pediatric dermatologic conditions. • Identify which patients benefit from a referral to pediatric dermatology. Case #1 • HPI: 7 y/o F presents with itchy, slightly scaly areas of hair loss peppered over the scalp for ~ 8 months. Previously tried griseofulvin microsize 10 mg/kg/day divided BID x 8 weeks with incomplete clearance. No current therapies. • PMH: negative • FH: androgenetic alopecia (FOC), no autoimmune disease Tinea capitis • Infection of hair caused by dermatophytic fungi • Usually due to Trichophyton tonsurans or Microsporum canis – Endothrix vs ectothrix • Many different presentations: – Broken off hair with scale (“black dot” tinea) – Diffuse scale (seborrheic dermatitis-like) – Pustular inflammation (folliculitis-like) – Kerion Tinea capitis - presentations Tinea capitis – a few pearls • Be suspicious of scaling of the scalp in prepubertal children – “An early school-age African American child with scaling of the scalp has tinea capitis until proven otherwise.” Tinea capitis – a few pearls • Diagnostic assistance – KOH – Fungal culture – Wood’s Lamp – Check for lymphadenopathy Photo credit: http://a1props.com/product/culture-swab-dual-head/ Tinea capitis – treatment • Tinea capitis ALWAYS requires systemic therapy • Griseofulvin remains the gold standard, but terbinafine use is rising • Laboratory monitoring is not needed in most children • Concomitant therapy with an antifungal shampoo 2-3x/week can help remove scales and viable spores • Consider a short course of oral corticosteroids (0.5-1 mg/kg/day x 2-4 wks) for kerions Tinea capitis – treatment Treatment Dose Duration Griseofulvin 20-25mg/kg/day div BID Min. -
Common Causes of Paediatric Alopecia
CLINICAL Common causes of paediatric alopecia William Cranwell, Rodney Sinclair HAIR LOSS IN CHILDREN aged 12 years to congenital or acquired conditions. and younger encompasses a number of The most common causes of paediatric common and rare conditions that may be alopecia seen in general practice are This article is the fourth in a series congenital or acquired. Differentiation of listed in Table 1. This article will discuss on paediatric health. Articles in this alopecia due to benign causes from that due the diagnosis and management of these series aim to provide information to serious illness is important for reducing conditions. Scarring alopecia and hair about diagnosis and management of presentations in infants, toddlers and patient and parent distress and offering shaft abnormalities are less common pre-schoolers in general practice. adequate and prompt diagnosis and and require further investigation by a treatment. Hair loss disorders are a large, dermatologist. Background heterogeneous group of conditions that Hair loss in children aged 12 years and have various clinical features, pathological younger is most often due to a benign Epidemiology findings and expected outcomes. or self-limiting condition. This article presents a review of the assessment of Alopecia in children can be Tinea capitis is a common condition to common causes of paediatric alopecia characterised as: which prepubertal children are predisposed and outlines the implications for • disorders of hair loss and aberrant (Figure 1A).3–5 The prevalence of positive