Final Program

Total Page:16

File Type:pdf, Size:1020Kb

Final Program AMERICAN COLLEGE OF MOHS SURGERY Final Program http://www.mohscollege.org/annualmeeting Follow the Mohs College Annual Meeting on Twitter! Twitter.com/mohscollege 43 rd Annual Meeting ● April 28 – May 1, 2011 ● Caesars Palace Final Program ● Las Vegas, NV Las Vegas, © 2010-2011 American College of Mohs Surgery No part of this publication may be reproduced without the prior written permission of the ACMS . Photos courtesy of the Las Vegas News Bureau and Caesars Palace American College of Mohs Surgery Photography Policy 555 East Wells Street, Suite 1100 The ACMS has arranged for a photographer to be present throughout the 2011 Annual Meeting . ACMS Milwaukee, WI 53202 may use these photos on its World Wide Web site Phone: (414) 347-1103 • (800) 500-7224 or in other offi cial printed publications . Individuals Fax: (414) 276-2146 photographed will not receive compensation for Email: info@mohscollege .org the use and release of these photos and will be deemed to have consented to the use and release Website: www .mohscollege .org of photos in which they appear . Individuals also acknowledge ACMS’ right to crop or treat the photographs at its discretion . If you are opposed to being photographed, please immediately notify the photographer or an ACMS staff member if your 1 picture is taken . Thank you for your cooperation . Table of Contents ACMS Board of Directors . 3 ACMS Committees and Task Forces . 3 Welcome Messages . 4 Program-at-a-Glance . 6 Caesars Palace Tear-Out Floor Maps . 10 Las Vegas, NV Las Vegas, Caesars Palace Concierge & Transportation Info . 12 ● Fellowship Training Director Listing . 13 Guest Speaker Biographies . 14 Las Vegas Maps & Attractions . 17 Faculty and Guest Speaker Listing . 19 CME Information . 20 Learning Objectives . 21 Caesars Palace ● Faculty Disclosure Information . 22 Scientific Program Schedule Thursday, April 28 . 23 Friday, April 29 . 28 Saturday, April 30 . 31 Sunday, May 1 . 34 Abstract Presentations Thursday, April 28; Clinical Pearls . 35 Thursday, April 28; Tromovitch Award . 42 April 28 – May 1, 2011 Friday, April 29; Research . 47 ● Poster Presentation List . 52 Poster Presentation Summaries . 56 Exhibitor Floor Plan . 86 Exhibitor Listing . 87 ASMH Program-at-a-Glance . 91 Speaker Index . 93 Annual Meeting rd 43 2 2010-2011 Officers and Board of Directors Committees and Task Forces - 2011 43 Officers Bylaws Committee rd Leonard M. Dzubow, MD Vicki J. Levine, MD, Chair Annual Meeting President CME and Education Committee Brett M. Coldiron, MD, FACP Mary E. Maloney, MD, Chair Vice President Communications & PR Committee Marc D. Brown, MD Alysa R. Herman, MD, Chair Secretary Treasurer Diagnostic Quality Control & Teaching Library Committee Duane C. Whitaker, MD Sumaira Z. Aasi, MD, Chair ● Immediate Past-President Ethics Committee April 28 – May 1, 2011 Board of Directors Marta J. Van Beek, MD, Chair John G. Albertini, MD Frederick S. Fish, III, MD Finance and Investment Committee Glenn D. Goldman, MD Marc D. Brown, MD, Chair Andrew J. Kaufman, MD, FACP Frederic E. Mohs Award Committee Gary P. Lask, MD Ronald G. Wheeland, MD, Chair Ken K. Lee, MD Gregg M. Menaker, MD Membership Committee Marcy Neuburg, MD Brett M. Coldiron, MD, FACP, Chair Suzanne M. Olbricht, MD Newsletter Committee Scientific Program Committee Désirée Ratner, MD, Chair Tatyana R. Humphreys, MD, Chair ● Nominating Committee Caesars Palace Deborah F. MacFarlane, MD, Vice Chair C. William Hanke, MD, Chair Leonard M. Dzubow, MD Brett M. Coldiron, MD, FACP Scientific Program Committee Marc D. Brown, MD Tatyana R. Humphreys, MD, Chair Roberta D. Sengelmann, MD, Ex-officio Tromovitch Award Committee Staff Michael Murphy, MD, Chair Kim Schardin, CAE, Executive Director Erin O’Krongly, Communications Manager Website Committee ● Clarence W. Brown, Jr., MD, Chair Michelle Ridolfi, Meetings Manager Las Vegas, NV Las Vegas, Susan Sadowski, Education Manager Josh de Beer, Membership & Meetings Coordinator Site Inspection & Slide Review Board, LLC (An ACMS subsidiary) Fellowship Training Committee Suzanne M. Olbricht, MD, Chair Slide Review Committee Glenn D. Goldstein, MD, Chair 3 WELCOME from the president Dear ACMS Members and Colleagues, On behalf of the ACMS Board of Directors, I welcome you to fabulous Las Vegas for the 43rd Annual Meeting of the American College of Mohs Surgery . I hope you have been looking forward to this week as much as I have; to join the nearly 900 fellowship-trained skin cancer and reconstructive surgeons to learn, Las Vegas, NV Las Vegas, collaborate, and share with one another for the benefit of our patients . My sincere ● hope is that you are able to take much away from this meeting, which will resonate long after in your own practice . I extend my sincere appreciation and gratitude to the Scientific Program Committee, headed by Chair, Dr . Tatyana R . Humphreys, who has put together an outstanding program that will highlight many relevant topics to enhance your practice skills in cutaneous oncology, Mohs micrographic surgery, and reconstruction . Special thanks Caesars Palace ● go to the members of the Scientific Program Committee: Drs . Marc Brown, Brett Coldiron, Deborah MacFarlane, and Roberta Sengelmann, for their dedication and contributions in planning this year’s events . In addition to an excellent program, the Exhibit Hall will provide information and extensive resources to benefit your practice . I strongly encourage you to take full advantage of the exhibitors’ presence and visit them during their time here (Thursday, 5 – 7 pm, Friday, 12 – 6 pm & Saturday, 8 am – 2 pm) . Aside from the opportunities available at our meeting for you to grow as a Mohs surgeon, take the time to explore Las Vegas . Since it is dubbed The Entertainment Capital of the World, I’m sure you will not be at a loss for places to visit and April 28 – May 1, 2011 experience . ● I hope you enjoy your time here in Las Vegas for what I believe will be another outstanding Annual Meeting of the American College of Mohs Surgery! Sincerely, Annual Meeting Leonard M . Dzubow, MD rd ACMS President 43 4 WELCOME from the scientific program chair 43 Dear Colleagues, rd Annual Meeting I am pleased to present the educational program for the 2011 ACMS Annual Meeting . The program has been created in direct response to your feedback following last year’s meeting to enhance your practice skills in Mohs surgery and cutaneous oncology . Member feedback from last year’s meeting allowed us to identify specific practice gaps and areas of interest such as dermatopathology and reconstruction . Since we are in Las Vegas, we made this year’s Annual Meeting a star-studded event with several outstanding guest speakers featured in the program . On Thursday, Frank ● April 28 – May 1, 2011 J . Lexa, MD, MBA, from the Wharton School, University of Pennsylvania, will speak on Health Care Reform . On Friday, back by popular demand, Clay J . Cockerell, MD, from UT Southwestern, will present Dermatopathology Challenges in Mohs Surgery and be a guest panelist on Mohs Frozen Section Challenges . Homer A . Macapinlac, MD, FACNM, from University of Texas MD Anderson Cancer Center, will speak on PET/CT & Cutaneous Tumors and be a panelist on Tumor Board on Friday afternoon . Last, but not least, on Saturday, Frederick J . Menick, MD, world renowned expert on nasal reconstruction from Tucson, AZ, will be guest speaking in the session, Nasal Reconstruction: Art & Practice and a panelist in sessions, How Would You Reconstruct It? and, The Undesirable Result . ● Additionally, on Saturday afternoon, we are both pleased and honored to welcome Caesars Palace our keynote speaker, Fred Mohs Jr ., son of Dr . Frederic Mohs, to the 2011 Annual Meeting . Mr . Mohs will speak to the College membership in his keynote address, Remembering Dr. Frederic Mohs . During his address, he will be talking intimately of his father, sharing personal and professional anecdotes, both for the College members who knew him and the younger members who never had the pleasure . You won’t want to miss out on this historic occasion . ● I extend special thanks to the Scientific Program Committee members: Drs . Deborah Las Vegas, NV Las Vegas, MacFarlane, Roberta Sengelmann, Len Dzubow, Brett Coldiron and Marc Brown, who have been an incredible sounding board and shared their time and insights with me so generously to bring this quality program to you . I also thank the members of the CME committee for their guidance, Chair, Dr . Mary Maloney, and Drs . John Albertini and Jeremy Bordeaux . The Scientific Program Committee hopes that you are as excited as we are about what the 2011 ACMS Annual Meeting offers . Welcome to the fabulous Las Vegas! Sincerely, Tatyana R . Humphreys, MD Chair, ACMS 2011 Scientific Program Committee 5 PROGRAM-AT-A-GLANCE Wednesday, April 27 1:00 – 6:00 pm Registration Office 5 Registration Desk; Emperors Level (outside of Palace Ballroom) 1:00 – 6:00 pm Speaker Ready Room Genoa; Promenade Level 1:00 – 6:00 pm Slide Library & Diagnostic Quality Control Self-examination Tarranto; Emperors Level Thursday, April 28 Las Vegas, NV Las Vegas, ● 6:30 am – 5:00 pm Registration Office 5 Registration Desk;Emperors Level (outside of Palace Ballroom) 6:30 am – 5:00 pm Speaker Ready Room Genoa; Promenade Level 7:00 am – 9:00 pm Slide Library & Diagnostic Quality Control Self-examination Tarranto; Emperors Level 7:00 – 8:30 am Concurrent Morning Mini-sessions: 103.1 Regional Reconstruction Pompeian Ballroom 1; Promenade Level 103.2 Merkel Cell Carcinoma & Dermatofibrosarcoma
Recommended publications
  • Neonatal Dermatology Review
    NEONATAL Advanced Desert DERMATOLOGY Dermatology Jennifer Peterson Kevin Svancara Jonathan Bellew DISCLOSURES No relevant financial relationships to disclose Off-label use of acitretin in ichthyoses will be discussed PHYSIOLOGIC Vernix caseosa . Creamy biofilm . Present at birth . Opsonizing, antibacterial, antifungal, antiparasitic activity Cutis marmorata . Reticular, blanchable vascular mottling on extremities > trunk/face . Response to cold . Disappears on re-warming . Associations (if persistent) . Down syndrome . Trisomy 18 . Cornelia de Lange syndrome PHYSIOLOGIC Milia . Hard palate – Bohn’s nodules . Oral mucosa – Epstein pearls . Associations . Bazex-Dupre-Christol syndrome (XLD) . BCCs, follicular atrophoderma, hypohidrosis, hypotrichosis . Rombo syndrome . BCCs, vermiculate atrophoderma, trichoepitheliomas . Oro-facial-digital syndrome (type 1, XLD) . Basal cell nevus (Gorlin) syndrome . Brooke-Spiegler syndrome . Pachyonychia congenita type II (Jackson-Lawler) . Atrichia with papular lesions . Down syndrome . Secondary . Porphyria cutanea tarda . Epidermolysis bullosa TRANSIENT, NON-INFECTIOUS Transient neonatal pustular melanosis . Birth . Pustules hyperpigmented macules with collarette of scale . Resolve within 4 weeks . Neutrophils Erythema toxicum neonatorum . Full term . 24-48 hours . Erythematous macules, papules, pustules, wheals . Eosinophils Neonatal acne (neonatal cephalic pustulosis) . First 30 days . Malassezia globosa & sympoidalis overgrowth TRANSIENT, NON-INFECTIOUS Miliaria . First weeks . Eccrine
    [Show full text]
  • Ichthyosis Focus Spring 2002
    ICHTHYOSIS FOCUS Vol. 21, No. 1 A Quarterly Journal for Friends of F.I.R.S.T. Spring 2002 Unlocking the Secrets of a Rare Ichthyosis abriele Richard, MD, Assistant Professor of A note from Dr. Richard: Our research group GDermatology and Genetics at the Thomas greatly acknowledges the support of F.I.R.S.T., Jefferson University in Philadelphia, received an along with the ASA, NAAF, and the National American Skin Association Categorical Disease Registry for Ichthyosis and Related Disorders, as Grant for Childhood Skin Disease Research. well as the participation of many families in our Specifically, she studied the genetics of Netherton studies. With the help of a F.I.R.S.T. research award Syndrome (NTS), a rare form of severe ichthyosis (awarded in 1999) we were able to perform genetic associated with other abnormalities. linkage studies to localize the Netherton Syndrome NTS is an inherited disorder that presents at gene and to initiate mutation analysis of SPINK5. birth with generalized redness, thickening and The financial support allowed us to amass a critical scaling of the skin, which may persist through life amount of data to successfully apply for NIH fund- or change into scaly, itchy plaques. The hairs may Gabriele Richard, MD ing of our research. As a result, we were able to be sparse, fragile, and short due to multiple swellings along screen more than 31 NTS families to date, identifying 24 dis- the hair shafts, at which the hair breaks easily. Also charac- tinct SPINK5 mutations in 23 families. In 8 families genetic teristic of NTS is a predisposition to allergies, infections, and testing revealed no mutations in SPINK5, suggesting that these sometimes, failure to thrive.
    [Show full text]
  • 10Th Anniversary of the Human Genome Project
    Grand Celebration: 10th Anniversary of the Human Genome Project Volume 3 Edited by John Burn, James R. Lupski, Karen E. Nelson and Pabulo H. Rampelotto Printed Edition of the Special Issue Published in Genes www.mdpi.com/journal/genes John Burn, James R. Lupski, Karen E. Nelson and Pabulo H. Rampelotto (Eds.) Grand Celebration: 10th Anniversary of the Human Genome Project Volume 3 This book is a reprint of the special issue that appeared in the online open access journal Genes (ISSN 2073-4425) in 2014 (available at: http://www.mdpi.com/journal/genes/special_issues/Human_Genome). Guest Editors John Burn University of Newcastle UK James R. Lupski Baylor College of Medicine USA Karen E. Nelson J. Craig Venter Institute (JCVI) USA Pabulo H. Rampelotto Federal University of Rio Grande do Sul Brazil Editorial Office Publisher Assistant Editor MDPI AG Shu-Kun Lin Rongrong Leng Klybeckstrasse 64 Basel, Switzerland 1. Edition 2016 MDPI • Basel • Beijing • Wuhan ISBN 978-3-03842-123-8 complete edition (Hbk) ISBN 978-3-03842-169-6 complete edition (PDF) ISBN 978-3-03842-124-5 Volume 1 (Hbk) ISBN 978-3-03842-170-2 Volume 1 (PDF) ISBN 978-3-03842-125-2 Volume 2 (Hbk) ISBN 978-3-03842-171-9 Volume 2 (PDF) ISBN 978-3-03842-126-9 Volume 3 (Hbk) ISBN 978-3-03842-172-6 Volume 3 (PDF) © 2016 by the authors; licensee MDPI, Basel, Switzerland. All articles in this volume are Open Access distributed under the Creative Commons License (CC-BY), which allows users to download, copy and build upon published articles even for commercial purposes, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications.
    [Show full text]
  • Discovery in Genetic Skin Disease: the Impact of High Throughput Genetic Technologies
    Genes 2014, 5, 615-634; doi:10.3390/genes5030615 OPEN ACCESS genes ISSN 2073-4425 www.mdpi.com/journal/genes Review Discovery in Genetic Skin Disease: The Impact of High Throughput Genetic Technologies Thiviyani Maruthappu †, Claire A. Scott † and David P. Kelsell * Centre for Cutaneous Research, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, 4 Newark Street, London E1 2AT, UK; E-Mails: [email protected] (T.M.); [email protected] (C.A.S.) † These authors contributed equally to this work and should be considered joint first authors. * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel: +44-20-7882-7167; Fax: +44-20-7882-7172. Received: 4 April 2014; in revised form: 7 July 2014 / Accepted: 14 July 2014 / Published: 4 August 2014 Abstract: The last decade has seen considerable advances in our understanding of the genetic basis of skin disease, as a consequence of high throughput sequencing technologies including next generation sequencing and whole exome sequencing. We have now determined the genes underlying several monogenic diseases, such as harlequin ichthyosis, Olmsted syndrome, and exfoliative ichthyosis, which have provided unique insights into the structure and function of the skin. In addition, through genome wide association studies we now have an understanding of how low penetrance variants contribute to inflammatory skin diseases such as psoriasis vulgaris and atopic dermatitis, and how they contribute to underlying pathophysiological disease processes. In this review we discuss strategies used to unravel the genes underlying both monogenic and complex trait skin diseases in the last 10 years and the implications on mechanistic studies, diagnostics, and therapeutics.
    [Show full text]
  • Hereditary Ichthyosis
    !" #$%&'# $(%&) #'# %*+&,*'#'* -#.*&%* --#.# // Dissertation for Degree of Doctor of Philosophy (Faculty of Medicine) in Dermatology and Venereology presented at Uppsala University in 2002 ABSTRACT Gånemo, A. 2002. Hereditary ichthyosis. Causes, Skin Manifestations, Treatments and Quality of Life. Acta Universitatis Upsaliensis. Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine 1125. 68 pp Uppsala ISBN 91-554-5246-9 Hereditary ichthyosis is a collective name for many dry and scaly skin disorders ranging in frequency from common to very rare. The main groups are autosomal recessive lamellar ichthyosis, autosomal dominant epidermolytic hyperkeratosis and ichthyosis vulgaris, and x-linked recessive ichthyosis. Anhidrosis, ectropion and keratodermia are common symptoms, especially in lamellar ichthyosis, which is often caused by mutations in the transglutaminase 1 (TGM1) gene. The aim of this work was to study patients with different types of ichthyosis regarding (i) the patho-aetiology (TGM1 and electron microscopy [EM] analysis), (ii) skin signs and symptoms (clinical score and subjective measure of disease activity), (iii) quality of life (questionnaires DLQI, SF-36 and NHP and face-to-face interviews) and (iv) a search for new ways of topical treatment. Patients from Sweden and Estonia with autosomal recessive congenital ichthyosis (n=83) had a broader clinical spectrum than anticipated, but a majority carried TGM1 mutations. Based on DNA analysis and clinical examinations the patients were classified into three groups, which could be further subdivided after EM analysis. Our studies indicate that patients with ichthyosis have reduced quality of life as reflected by DLQI and by some domains of SF- 36, by NHP and the interviews. All the interviewees reported that their skin disease had affected them negatively to varying degrees during their entire lives and that the most problematic period was childhood.
    [Show full text]
  • Differential Diagnosis of Neonatal and Infantile Erythroderma
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE Acta Dermatovenerol Croat 2007;15(3):178-190 REVIEW Differential Diagnosis of Neonatal and Infantile Erythroderma Lena Kotrulja1, Slobodna Murat-Sušić2, Karmela Husar2 1University Department of Dermatology and Venereology, Sestre milosrdnice University Hospital; 2University Department of Dermatology and Venereology, Zagreb University Hospital Center and School of Medicine, Zagreb, Croatia Corresponding author: SUMMARY Neonatal and infantile erythroderma is a diagnostic and Lena Kotrulja, MD, MS therapeutic challenge. Numerous underlying causes have been reported. Etiologic diagnosis of erythroderma is frequently difficult to University Department of Dermatology establish, and is usually delayed, due to the poor specificity of clinical and Venereology and histopathologic signs. Differential diagnosis of erythroderma is Sestre milosrdnice University Hospital a multi-step procedure that involves clinical assessment, knowledge of any relevant family history and certain laboratory investigations. Vinogradska 29 Immunodeficiency must be inspected in cases of severe erythroderma HR-10000 Zagreb with alopecia, failure to thrive, infectious complications, or evocative Croatia histologic findings. The prognosis is poor with a high mortality rate [email protected] in immunodeficiency disorders and severe chronic diseases such as Netherton’s syndrome. Received: June 14, 2007 KEY WORDS: erythroderma, neonatal, infantile, generalized Accepted: July 11, 2007 exfoliative dermatitis INTRODUCTION Erythroderma is defined as an inflammatory Neonatal and infantile erythroderma is a diag- skin disorder affecting total or near total body sur- nostic and therapeutic challenge. Erythrodermic face with erythema and/or moderate to extensive neonates and infants are frequently misdiagnosed scaling (1). It is a reaction pattern of the skin that with eczema and inappropriate topical steroid can complicate many underlying skin conditions at treatment can lead to Cushing syndrome.
    [Show full text]
  • Mallory Prelims 27/1/05 1:16 Pm Page I
    Mallory Prelims 27/1/05 1:16 pm Page i Illustrated Manual of Pediatric Dermatology Mallory Prelims 27/1/05 1:16 pm Page ii Mallory Prelims 27/1/05 1:16 pm Page iii Illustrated Manual of Pediatric Dermatology Diagnosis and Management Susan Bayliss Mallory MD Professor of Internal Medicine/Division of Dermatology and Department of Pediatrics Washington University School of Medicine Director, Pediatric Dermatology St. Louis Children’s Hospital St. Louis, Missouri, USA Alanna Bree MD St. Louis University Director, Pediatric Dermatology Cardinal Glennon Children’s Hospital St. Louis, Missouri, USA Peggy Chern MD Department of Internal Medicine/Division of Dermatology and Department of Pediatrics Washington University School of Medicine St. Louis, Missouri, USA Mallory Prelims 27/1/05 1:16 pm Page iv © 2005 Taylor & Francis, an imprint of the Taylor & Francis Group First published in the United Kingdom in 2005 by Taylor & Francis, an imprint of the Taylor & Francis Group, 2 Park Square, Milton Park Abingdon, Oxon OX14 4RN, UK Tel: +44 (0) 20 7017 6000 Fax: +44 (0) 20 7017 6699 Website: www.tandf.co.uk 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, electronic, mechanical, photocopying, recording, or otherwise, without the prior permission of the publisher or in accordance with the provisions of the Copyright, Designs and Patents Act 1988 or under the terms of any licence permitting limited copying issued by the Copyright Licensing Agency, 90 Tottenham Court Road, London W1P 0LP. 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.
    [Show full text]
  • University of Chicago, November 2005
    CHICAGO DERMATOLOGICAL SOCIETY CASE 1 PRESENTERS Amy Farmer, MD and Vesna Petronic-Rosic, MD HISTORY OF PRESENT ILLNESS A 66-year-old white male presented with a lesion on the neck of two months’ duration to an outside institution. The excised lesion was diagnosed as a malignant melanoma (nodular- type, Breslow thickness 4mm, ulcerated). The patient was referred to Oncology at the University of Chicago and was discussed at the multidisciplinary melanoma tumor board. After re-evaluating the original slides and performing additional immunostaining on the original specimen, a diagnosis of Langerhans’ cell histiocytosis was made. Over the course of 6 months, the patient has developed a total of four additional tender lesions on his cheek, abdomen, forearm and buttock. REVIEW OF SYSTEMS The patient denied dyspnea, polydipsia, polyuria, bone pain, fever, and weight loss. PAST MEDICAL HISTORY Parkinson’s disease Hodgkin’s disease, diagnosed in 1995 Hypertension Multiple non-melanoma skin cancers PAST SURGICAL HISTORY Wide excision of neck lesion for presumed melanoma MEDICATIONS Potassium Chloride, hydrochlorothiazide, lisinopril, cozaar, sinemet, tylenol, and vitamins. FAMILY HISTORY Mother with breast cancer, diagnosed age 63 Maternal aunt with breast cancer, diagnosed age 60 Sister with melanoma, diagnosed age 65 Brother with bladder carcinoma, diagnosed age 75 Niece with melanoma, diagnosed age 46 SOCIAL HISTORY Non-smoker, moderate drinker, married with four children PHYSICAL EXAMINATION On the abdomen, there was a 1.7 by 1.2 cm rubbery firm erythematous nodule with central hemorrhagic crust. Similar appearing lesions were subsequently seen on the cheek, forearm, and buttock over the ensuing 6 months. LABORATORY DATA Complete blood count, lactic dehydrogenase, comprehensive metabolic panel were all within normal limits.
    [Show full text]
  • Boards' Fodder
    boards’ fodder Neonatal Ichthyosis by Alyx Rosen, MD and Kate Oberlin, MD Gene Additional Prognosis/ Disease Clinical Presentation Defect Manifestations Outcome Premature delivery; Survival rate Harlequin Thick membrane with deep cracks AR respiratory distress; ~50%; oral ichthyosis and fissures forming plate-like ABCA12 ear deformities; retinoids may help scales, ectropion, eclabium fluid imbalance prolong survival Congenital AR Generalized erythema and fine Heat intolerance; ichthyosiform TGM-1 No improvement scale; collodion membrane at birth; scarring alopecia; erythroderma (CIE) ALOX12B with age involves flexures; nail dystrophy rare ectropion ALOXE3 AR Thick, brown scale involving Lamellar ichthyosis Heat intolerance; No improvement TGM-1 flexural areas and trunk; eclabium, hypernatremia with age ABCA12 ectropion Evolves into Epidermolytic Widespread blistering and Failure to thrive; AD verrucous hyperkeratosis erythema at birth; involves flexures, hypernatremia; K1/K10 hyperkeratotic (EHK); Bullous CIE palmoplantar keratoderma recurrent infections plaques Ichthyosis vulgaris AD Generalized fine, adherent scale Atopic diathesis; Improves with age Filaggrin sparing flexures keratosis pilaris XLR Corneal opacities; Brown “dirty” X-linked ichthyosis Generalized fine scale and Steroid cryptorchidism; scales sparing desquamation at birth sulfatase prolonged labor flexures Trichorrhexis invaginata, ichthyosis Failure to thrive; Pruritus; Netherton AR linearis circumflexa, atopic infections; elevated IgE; eczematous syndrome SPINK5 dermatitis
    [Show full text]
  • Current Concepts in Dermatology
    CURRENT CONCEPTS IN DERMATOLOGY RICK LIN, D.O., FAOCD PROGRAM CHAIR Faculty Suzanne Sirota Rozenberg, DO, FAOCD Dr. Suzanne Sirota Rozenberg is currently the program director for the Dermatology Residency Training Program at St. John’s Episcopal Hospital in Far Rockaway, NY. She graduated from NYCOM in 1988, did an Internship and Family Practice residency at Peninsula Hospital Center and a residency in Dermatology at St. John’s Episcopal Hospital. She holds Board Certifications from ACOFP, ACOPM – Sclerotherapy and AOCD. Rick Lin, DO, FAOCD Dr. Rick Lin is a board-certified dermatologist practicing in McAllen, TX since 2006. He is the only board-certified Mohs Micrographic Surgeon in the Rio Grande Valley region. Dr. Rick Lin earned his Bachelor degree in Biology at the University of California at Berkeley and received his medical degree from University of North Texas Health Science Center at Fort Worth in 2001. He also graduated with the Master in Public Health Degree at the School of Public Health of the University of North Texas Health Science Center. He then completed a traditional rotating internship at Dallas Southwest Medical Center in 2002. In 2005 he completed his Dermatology residency training at the Northeast Regional Medical Center in Kirksville, Missouri in conjunction with the Dermatology Institute of North Texas. Dr. Rick Lin served as the Chief Resident of the residency training program for two years. He was also the Resident Liaison for the American Osteopathic College of Dermatology for two years prior to the completion of his residency. In addition to general dermatology and dermatopathology, Dr. Lin received specialized training in Mohs Micrographic surgery, advanced aesthetic surgery, and cosmetic dermatology.
    [Show full text]
  • A Clinical Study on Genodermatoses and Their Effect On
    A CLINICAL STUDY ON GENODERMATOSES AND THEIR EFFECT ON QUALITY OF LIFE – PROSPECTIVE OBSERVATIONAL STUDY IN A TERTIARY CARE HOSPITAL Dissertation Submitted to THE TAMILNADU DR.M.G.R. MEDICAL UNIVERSITY IN PARTIAL FULFILMENT FOR THE AWARD OF THE DEGREE OF DOCTOR OF MEDICINE IN DERMATOLOGY, VENEREOLOGY & LEPROSY Register No.: 201730253 BRANCH XX MAY 2020 DEPARTMENT OF DERMATOLOGY VENEREOLOGY & LEPROSY TIRUNELVELI MEDICAL COLLEGE TIRUNELVELI -11 BONAFIDE CERTIFICATE This is to certify that the dissertation titled as “A CLINICAL STUDY ON GENODERMATOSES AND THEIR EFFECT ON QUALITY OF LIFE – PROSPECTIVE OBSERVATIONAL STUDY IN A TERTIARY CARE HOSPITAL” submitted by Dr.P.KARTHIKRAJA to the Tamil Nadu Dr.M.G.R. Medical University, Chennai,in partial fulfilment of the requirement for the award of the Degree of DOCTOR OF MEDICINE in DERMATOLOGY, VENEREOLOGY AND LEPROSY during the academic period 2017 – 2020 is a bonafide research work carried out by him under direct supervision & guidance. Dr.P.Nirmaladevi MD., Dr.S.M.Kannan MS , MCh., Professor and HOD The Dean Department of Dermatology,Venereology &Leprosy Tirunelveli Medical College Tirunelveli Medical College Tirunelveli Tirunelveli CERTIFICATE This is to certify that the dissertation titled as “A CLINICAL STUDY ON GENODERMATOSES AND THEIR EFFECT ON QUALITY OF LIFE – PROSPECTIVE OBSERVATIONAL STUDY IN A TERTIARY CARE HOSPITAL” submitted by Dr.P.KARTHIKRAJA is a original work done by him in the Department of Dermatology,Venereology & Leprosy,Tirunelveli Medical College,Tirunelveli for the award
    [Show full text]
  • Proposed Classification for the Lip Lesions (Dr. Patil's Classification)
    Letter To Editor Proposed classification for the lip lesions (Dr. Patil’s classification) Sir, squamous cell carcinoma, basal cell carcinoma, leukoplakia, oral Lips are placed in a very prominent position and play an important submucous fibrosis, and actinic cheilitis are seen to be affecting role in the manipulation of food and phonetics, and are affected by the lips.[5] The problem of classification of lip diseases is extremely various disorders. These disorders may be simple without significant difficult and complex. When literature is analyzed, it can be seen functional morbidity or may be complex and alarming. Lips known to that no much attempts have been made to classify lip diseases. be more susceptible to damage from the elements, the environment, Consequently, we are proposing a simple classification for lip diseases trauma, and infection. Diagnosis and treatment of lip abnormalities which may be universally accepted [Table 1]. are important, not only to prevent disease morbidity and mortality, but also to restore social acceptance and self‑esteem. Most of the lip Financial support and sponsorship disorders may present with the common characteristics and may be Nil. indistinguishable clinically. Angular cheilitis, usually seen bilaterally at the corner of the mouth is a reactive process with variable etiological Conflicts of interest possibilities such as infections, mechanical, nutritional deficiency, There are no conflicts of interest. and dermatoses. Contact cheilitis may be seen because of a primary Santosh Patil irritant or a delayed hypersensitivity reactions. Exfoliative cheilitis is a reactive condition secondary to the factitious activity of the patient. Department of Oral Medicine and Radiology, College of Dentistry, AlJouf University, Skaka, Aljouf, Kingdom of Saudi Arabia Cheilitis glandularis is a chronic inflammatory disorder which affects the labial salivary glands and their ducts.
    [Show full text]