Treatment of Poikiloderma of Civatte with Ablative Fractional Laser Resurfacing: Prospective Study and Review of the Literature Emily P
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Melasma on the Nape of the Neck in a Man
Letters to the Editor 181 Melasma on the Nape of the Neck in a Man Ann A. Lonsdale-Eccles and J. A. A. Langtry Sunderland Royal Hospital, Kayll Road, Sunderland SR4 7TP, UK. E-mail: [email protected] Accepted July 19, 2004. Sir, sunlight and photosensitizing agents may be more We report a 47-year-old man with light brown macular relevant. pigmentation on the nape of his neck (Fig. 1). It was The differential diagnosis for pigmentation at this site asymptomatic and had developed gradually over 2 years. includes Riehl’s melanosis, Berloque dermatitis and He worked outdoors as a pipe fitter on an oilrig module; poikiloderma of Civatte. Riehl’s melanosis typically however, he denied exposure at this site because he involves the face with a brownish-grey pigmentation; always wore a shirt with a collar that covered the biopsy might be expected to show interface change and affected area. However, on further questioning it liquefaction basal cell degeneration with a moderate transpired that he spent most of the day with his head lymphohistiocytic infiltrate, melanophages and pigmen- bent forward. This reproducibly exposed the area of tary incontinence in the upper dermis. It is usually pigmentation with a sharp cut off inferiorly at the level associated with cosmetic use and may be considered of his collar. He used various shampoos, aftershaves and synonymous with pigmented allergic contact dermatitis shower gels, but none was applied directly to that area. of the face (6, 7). Berloque dermatitis is considered to be His skin was otherwise normal and there was no family caused by a photoirritant reaction to bergapentin; it history of abnormal pigmentation. -
Poikiloderma of Civatte, Slapped Neck Solar Melanosis, Basal Melanin Stores
American Journal of Dermatology and Venereology 2019, 8(1): 8-13 DOI: 10.5923/j.ajdv.20190801.03 Slapped Neck Solar Melanosis: Is It a New Entity or a Variant of Poikiloderma of Civatte?? (Clinical and Histopathological Study) Khalifa E. Sharquie1,*, Adil A. Noaimi2, Ansam B. Kaftan3 1Department of Dermatology, College of Medicine, University of Baghdad 2Iraqi and Arab Board for Dermatology and Venereology, Dermatology Center, Medical City, Baghdad, Iraq 3Dermatology Center, Medical City, Baghdad, Iraq Abstract Background: Poikiloderma of Civatte although is a common complaint among population, especially European, still it was not reported in dark skin people as in Iraqi population. Objectives: To study all the clinical and histopathological features of Poikiloderma of Civatte in Iraqi population. Patients and Methods: This study is descriptive, clinical and histopathological study. It was carried out at the Dermatology Center, Medical City, Baghdad, Iraq, from September 2017 to October 2018. Thirty-one patients with Poikiloderma of Civatte were included and evaluated by history, physical examination, Wood’s light examination. Lesional skin biopsies were obtained from 9 patients, with histological examination of the sections stained with Hematoxylin and Eosin (H&E) and Fontana-Masson stain. Results: Thirty-one patients were included in this study, with mean age +/- SD was 53.32+/-10 years, and all patients were males. Twenty-six patients (84%) were with skin phenotype III&IV, The pigmentation was either mainly erythematous (22.5%), mainly dark brown pigmentation (29%), and mixed type of pigmentation (48.5%). These lesions were distributed on the sides of the neck and the face and the V shaped area of the chest. -
Hereditary Hearing Impairment with Cutaneous Abnormalities
G C A T T A C G G C A T genes Review Hereditary Hearing Impairment with Cutaneous Abnormalities Tung-Lin Lee 1 , Pei-Hsuan Lin 2,3, Pei-Lung Chen 3,4,5,6 , Jin-Bon Hong 4,7,* and Chen-Chi Wu 2,3,5,8,* 1 Department of Medical Education, National Taiwan University Hospital, Taipei City 100, Taiwan; [email protected] 2 Department of Otolaryngology, National Taiwan University Hospital, Taipei 11556, Taiwan; [email protected] 3 Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei City 100, Taiwan; [email protected] 4 Graduate Institute of Medical Genomics and Proteomics, National Taiwan University College of Medicine, Taipei City 100, Taiwan 5 Department of Medical Genetics, National Taiwan University Hospital, Taipei 10041, Taiwan 6 Department of Internal Medicine, National Taiwan University Hospital, Taipei 10041, Taiwan 7 Department of Dermatology, National Taiwan University Hospital, Taipei City 100, Taiwan 8 Department of Medical Research, National Taiwan University Biomedical Park Hospital, Hsinchu City 300, Taiwan * Correspondence: [email protected] (J.-B.H.); [email protected] (C.-C.W.) Abstract: Syndromic hereditary hearing impairment (HHI) is a clinically and etiologically diverse condition that has a profound influence on affected individuals and their families. As cutaneous findings are more apparent than hearing-related symptoms to clinicians and, more importantly, to caregivers of affected infants and young individuals, establishing a correlation map of skin manifestations and their underlying genetic causes is key to early identification and diagnosis of syndromic HHI. In this article, we performed a comprehensive PubMed database search on syndromic HHI with cutaneous abnormalities, and reviewed a total of 260 relevant publications. -
Actinic Cheilitis
ACTINIC CHEILITIS http://www.aocd.org Actinic cheilitis, also known as solar cheilosis, farmer’s lip, or sailor’s lip, is a reaction to long-term sun exposure on the lips, primarily the lower lip. The lip is especially susceptible to UV radiation because it has a thinner epithelium and less pigment. Some believe actinic cheilitis represents a type of actinic keratosis and is therefore premalignant. Others believe it is a form of in-situ squamous cell carcinoma. Regardless, the literature is in agreement that its presence indicates an increased risk for invasive squamous cell carcinoma. Risk factors for actinic cheilitis include fair complexion, everted lips, male sex, advanced age, living at high altitudes, living close to the equator, outdoor working, history of non-melanoma skin cancer, and any condition that increases photosensitivity. Clinically, patients commonly have other signs of sun damage such as poikiloderma of Civatte, solar lentigines, actinic keratoses, Favre-Racouchot Syndrome, cutis rhomboidalis nuchae, and solar elastosis. Patients often complain of persistent chapped lips or lip tightness. Early changes include atrophy and blurring of the vermilion border. The lips become scaly and rough; erosions or fissures may occasionally present. When palpated, it can have a sandpaper-like texture. Differential diagnosis can include chronic lip licking, granulomatous cheilitis, drug-induced cheilitis, contact dermatitis, cheilitis glandularis, lupus erythematosus, and lichen planus. An appropriate history can help elicit the proper diagnosis, such as inquiring about new medications or lip balms, lip-licking habits, and cumulative sun exposure. When actinic cheilitis is suspected, one must determine whether a biopsy is appropriate. -
Xeroderma Pigmentosum: an Insight Into DNA Repair Processes
ACCME/Disclosures The USCAP requires that anyone in a position to influence or control the content of CME disclose any relevant financial relationship WITH COMMERCIAL INTERESTS which they or their spouse/partner have, or have had, within the past 12 months, which relates to the content of this educational activity and creates a conflict of interest. Dr. Jennifer O. Black declares she has no conflict(s) of interest to disclose. Xeroderma Pigmentosum: An Insight into DNA Repair Processes Jennifer O. Black, MD Assistant Professor Division of Pediatric Pathology and Laboratory Medicine Children’s Hospital Colorado University of Colorado Anschutz Medical Campus Aurora, Colorado Introduction: Xeroderma Pigmentosum Xeroderma Pigmentosum (XP): • Initially described 1874 • Rare autosomal recessive disorder • Prevalence: 1-45/million, variable ethnic frequency • UV radiation sensitivity disorder characterized by: • Severe skin burning following minimal sun exposure • Early freckling (before 2 years of age) • Skin cancer at an early age Kraemer KH, DiGiovann JJ. Photochemistry and Photobiology 91:452-459, 2015 Introduction: Xeroderma Pigmentosum XP Clinical Spectrum: • Skin Changes: o Early freckling and subsequent checkered pigmentation o Thin, dry, contracted skin o Telangiectasias o Skin cancers: o Squamous cell carcinoma o Basal cell carcinoma o Melanoma Courtesy Dr. Bahig M. Shehata, Children’s Healthcare of Atlanta Introduction: Xeroderma Pigmentosum Squamous Cell Carcinoma Robbins and Cotran Pathologic Basis of Disease. Lazar, Alexander J.F.; -
Journal of Pigmentary Disorders Yayli, Pigmentary Disorders 2015, 2:1 DOI: 10.4172/2376-0427.1000158
igmentar f P y D l o i a so n r r d u e r o J s Journal of Pigmentary Disorders Yayli, Pigmentary Disorders 2015, 2:1 DOI: 10.4172/2376-0427.1000158 ISSN: 2376-0427 Review Open Access Treatment of Hyperpigmentation in Darker Skins Savas Yayli* Department of Dermatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey *Corresponding author: Savas Yayli, Department of Dermatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey, Tel: 90 462 377 53 88; E- mail: [email protected] Rec date: Dec 14, 2014; Acc date: Dec 28, 2014; Pub date: Jan 02, 2015 Copyright: © 2015 Yayli S, This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Introduction many newer agents are in the market [6]. Beside those newers, fixed TC including hydroquinone 4%, tretinoine 0.05%, flucinolon Darker skin or skin of colour means higher Fitzpatrick skin types in acetonide 0.01% is shown as the therapy with highest evidence – still a wide range of racial and ethnic groups referring to persons from little controlled studies - in Latin guide of melasma or recent reviews. African, Asian, Native American, Middle Eastern and Hispanic If there is an irritation or allergy to one of compounds of this TC, one backgrounds. Darker skin types are characterized by higher content of may use it as dual combinations. In Latin guide for treatment of melanin, higher eumelanin to pheomelanin ratio. This is an advantage melasma, second line therapies are TC plus peels or for protection against ultraviolet (UV) radiation, however it also microdermabrasion, and lastly lasers and light sources [4,7]. -
Reticulate Dermatoses
[Downloaded free from http://www.e-ijd.org on Tuesday, April 08, 2014, IP: 111.93.251.154] || Click here to download free Android application for this journal CME Article Reticulate Dermatoses Keshavmurthy A Adya, Arun C Inamadar, Aparna Palit From the Department of Dermatology, Venereology and Leprosy, SBMP Medical College, Hospital and Research Center, BLDE University, Bijapur, Karnataka, India Abstract The term “reticulate” is used for clinical description of skin lesions that are configured in a net-like pattern. Many primary and secondary dermatoses present in such patterns involving specific body sites. Certain cutaneous manifestations of systemic diseases or genodermatoses also present in such manner. This review classifies and describes such conditions with reticulate lesions and briefly, their associated features. Key Words: Mottling, net-like, reticulate, retiform What was known? 3. Poikilodermatous Reticulate configuration of lesions is seen in many primary dermatoses and a. Inherited also as cutaneous reaction patterns consequent to internal pathology. • Rothmund–Thomson syndrome • Dyskeratosis congenita Reticulate Dermatoses • Xeroderma pigmentosum • Cockayne syndrome The term “reticulate” is commonly used for clinical • Fanconi anemia description of “net-like”, “sieve-like,” or “chicken wire” • Mendes da Costa syndrome configuration of the skin lesions. Various congenital • Kindler syndrome and acquired dermatoses present with this pattern of • Degos–Touraine syndrome skin lesions. Many systemic diseases also present with • Hereditary sclerosing poikiloderma of Weary such cutaneous manifestations providing useful clues to • Hereditary acrokeratotic poikiloderma of Weary diagnosis. • Werner’s syndrome (adult progeria) Classification • Chanarin–Dorfman syndrome • Diffuse and macular atrophic dermatosis 1. Vascular b. Acquired a. Cutis marmorata • Poikiloderma of Civatte b. -
Reversal of Laser-Induced Hypopigmentation with a Narrow-Band UV-B Light Source in a Patient with Skin Type VI
Reversal of Laser-Induced Hypopigmentation with a Narrow-Band UV-B Light Source in a Patient with Skin Type VI Ã y yz ANETTA RESZKO, MD, PHD, SEAN A. SUKAL, MD, PHD, AND ROY G. GERONEMUS,MD Dr. Geronemus is on the Lumenis Medical Advisory Board. evus of Ota (nevus fuscoceruleus ophthalmo- tion after clearance of a nevus of Ota with a QSRL Nmaxillaris) is a benign dermal melanocytic in an African American Skin Type VI male with a hematoma clinically appearing as a bluish-brown narrow-band ultraviolet B (NB UV-B) source. discoloration in the ophthalmic and/or maxillary branches of the trigeminal nerve. The condition first Case described by Ota and Tanino occurs predominantly in Asians with estimated frequency of 0.014% to A 36-year-old African American male, Fitzpatrick 0.034%, but can be found in other ethnicities.1 Skin Type VI, with no significant medical history, Historical therapies for nevus of Ota include surgery, presented for treatment of a 10 Â 16-cm Tanino dermabrasion, electrodesiccation, skin grafting, and Stage III (V1 and V2 distribution) nevus of Ota cryotherapy and are all associated with a significant (Figure 1). The patient was treated with a QSRL, at a risk of dyschromia and scarring.2–5 fluence of 3 to 5 J, spot size 6.5 mm with no greater than 10% overlap between pulses. After 20 treat- The introduction of the theory of selective ment sessions, of which several were partial treat- photothermolysis and subsequent development of ments of the same area of the nevus of Ota over a Q-switched lasers revolutionized the treatment period of 6 years, the lesion was completely cleared. -
Table I. Genodermatoses with Known Gene Defects 92 Pulkkinen
92 Pulkkinen, Ringpfeil, and Uitto JAM ACAD DERMATOL JULY 2002 Table I. Genodermatoses with known gene defects Reference Disease Mutated gene* Affected protein/function No.† Epidermal fragility disorders DEB COL7A1 Type VII collagen 6 Junctional EB LAMA3, LAMB3, ␣3, 3, and ␥2 chains of laminin 5, 6 LAMC2, COL17A1 type XVII collagen EB with pyloric atresia ITGA6, ITGB4 ␣64 Integrin 6 EB with muscular dystrophy PLEC1 Plectin 6 EB simplex KRT5, KRT14 Keratins 5 and 14 46 Ectodermal dysplasia with skin fragility PKP1 Plakophilin 1 47 Hailey-Hailey disease ATP2C1 ATP-dependent calcium transporter 13 Keratinization disorders Epidermolytic hyperkeratosis KRT1, KRT10 Keratins 1 and 10 46 Ichthyosis hystrix KRT1 Keratin 1 48 Epidermolytic PPK KRT9 Keratin 9 46 Nonepidermolytic PPK KRT1, KRT16 Keratins 1 and 16 46 Ichthyosis bullosa of Siemens KRT2e Keratin 2e 46 Pachyonychia congenita, types 1 and 2 KRT6a, KRT6b, KRT16, Keratins 6a, 6b, 16, and 17 46 KRT17 White sponge naevus KRT4, KRT13 Keratins 4 and 13 46 X-linked recessive ichthyosis STS Steroid sulfatase 49 Lamellar ichthyosis TGM1 Transglutaminase 1 50 Mutilating keratoderma with ichthyosis LOR Loricrin 10 Vohwinkel’s syndrome GJB2 Connexin 26 12 PPK with deafness GJB2 Connexin 26 12 Erythrokeratodermia variabilis GJB3, GJB4 Connexins 31 and 30.3 12 Darier disease ATP2A2 ATP-dependent calcium 14 transporter Striate PPK DSP, DSG1 Desmoplakin, desmoglein 1 51, 52 Conradi-Hu¨nermann-Happle syndrome EBP Delta 8-delta 7 sterol isomerase 53 (emopamil binding protein) Mal de Meleda ARS SLURP-1 -
Other Relevant Data
4. Other Relevant Data 4.1 Transmission and absorption in biological tissues UVR may be transmitted, reflected, scattered or absorbed by chromophores in any layer of tissue, su ch as the skin and eye. Absorption is strongly related to wavelength, as it depends on the properties of the responsible chromophore(s). Accordingly, transmission is also wavelength-dependent. Transmission and other optical properties are affected by changes in the structure of the tissue and, especially in the case of the lens of the eye, by ageing. Absorption of radiation bya tissue chromophore is a prerequisite for any photochernical or photobiological effect; however, absorption does not necessarily have a biological con- sequence. 4.1.1 Epidermis Since UVR-induced skin cancer is an epidermal phenomenon, this section focuses on epidermis and excludes the dermis. The epidermis, a tissue with a high replication rate, can be divided functionally into two: an inner, living part (60-160-J-m thick in humans) of cells at various stages of differentiation and the outermost, non-living, terminally differentiated stratum corneum (8-15-J-m thick in humans). The dividing cell population is located in the innermost basal layer of the living epidermis. Optical properties have usually been studied using isolated strateum corneum or whole epidermis. Absorption and scattering of UVR by the stratum corneurn afford sorne protection to the living part of the epidermis from UVR exposure. Human and mouse epidermis have important structural differences. The living part and the stratum corneum of hum an epidermis have about 10 cell layers each. ln rnice, the living part has two to three celllayers and the stratum corne a one to two cell layers. -
Update on Lasers and Light Devices for the Treatment of Vascular Lesions Kenneth J
Update on Lasers and Light Devices for the Treatment of Vascular Lesions Kenneth J. Galeckas, MD Patients frequently present to dermatologists for the treatment of vascular lesions, includ- ing facial telangiectases, diffuse redness, port wine stains (PWS), hemangiomas, and leg veins. There are many laser and light devices that can be used with excellent results. This article summarizes the available platforms that are commonly used for the treatment of superficial vascular lesions. Newer devices and techniques are highlighted with respect to the unique characteristics of individual lesions. Semin Cutan Med Surg 27:276-284 Published by Elsevier Inc. he principle of selective photothermolysis, originally de- Lasers and Light Devices 1 Tscribed by Anderson and Parrish, defined how laser With Vascular Applications energy was absorbed by a particular chromophore within the skin leading to a specific biologic effect while sparing collat- KTP Laser eral structures. In this fashion, laser and light devices have The KTP laser is a Nd:YAG laser that is frequency-doubled become refined during the past several decades, leading to and emits green light at 532 nm. Superficial vessels can be our current ability to apply high fluences to tissues very spe- treated by taking advantage of the close proximity of the cifically resulting in selective destruction of unwanted lesions absorption peak of oxyhemoglobin at 542 nm.2 With com- while sparing the patient from nonspecific side effects such as monly available devices, spot sizes can range from 1 mm to crusting, bleeding, scabbing, or scarring. 10 mm, with variable pulse widths (1-100 ms). Contact cool- The range of superficial vascular lesions that can be treated ing is used with chilled sapphire windows with conduction with laser and light devices continues to expand. -
(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.