Infections, Infestations and Neoplasms of the Scalp Infections, Infestations and Neoplasms of the Scalp
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Dermatologists' Perceptions on the Utility and Limitations
RESEARCH/Original Article Journal of Telemedicine and Telecare 2021, Vol. 27(3) 166–173 Dermatologists’ perceptions on the ! The Author(s) 2019 utility and limitations of teledermatology Article reuse guidelines: sagepub.com/journals-permissions after examining 55,000 lesions DOI: 10.1177/1357633X19864829 journals.sagepub.com/home/jtt Mara Giavina Bianchi , Andre Santos and Eduardo Cordioli Abstract Introduction: Few studies have assessed the perception of teledermatologists about the utility and limitations of teledermatology, especially to diagnose a broad range of skin diseases. This study aimed to evaluate dermatologists’ confidence in teledermatology, its utility and limitations for dermatological conditions in primary care. Methods: An analytical study that used a survey for dermatologists who diagnosed 30,916 patients with 55,012 lesions through teledermatology during a 1-year project in S~ao Paulo, Brazil. Results: Dermatologists found teledermatology useful for triage and diagnosis, especially for xerotic eczema, pigmen- tary disorders and superficial infections. Their confidence in teledermatology was statistically higher by the end of the project (p ¼ 0.0012). Limitations included some technical issues and the impossibility to suggest how soon the patient should be assisted face-to-face by a dermatologist. The most treatable group of diseases by teledermatology was superficial infections (92%). The use of dermoscopy images would significantly increase the confidence to treat atypical naevi and malignant tumours (p < 0.0001 and p ¼ 0.0003 respectively). Follow-ups by teledermatology or feedback from primary-care physicians would be desirable, according to the dermatologists. Discussion: We found it interesting that dermatologists became increasingly confident in teledermatology after the project and how they classified teledermatology as useful for triage, diagnosis and even treatment of most types of skin conditions followed at primary care. -
Abstract Case Synopsis
Volume 20 Number 4 April 2014 Case presentation Solitary papule over scalp 1 1 1 2 Nidhi Singh , Laxmisha Chandrashekar , Devinder Mohan Thappa , Rakhee Kar Dermatology Online Journal 20 (4): 6 1Department of Dermatology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India 2Department of Pathology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India Correspondence: Laxmisha Chandrashekar Associate Professor, Department of Dermatology, Jawaharlal Institute of Postgraduate Medical Education and Research Puducherry, India [email protected] Abstract Folliculosebaceous cystic hamartoma (FSCH) is a rare cutaneous hamartoma characterized by follicular, sebaceous, and mesenchymal elements. Folliculosebaceous cystic hamartoma is probably not as rare as previously thought and its inclusion in the differential diagnosis of asymptomatic skin colored papules or nodules is warranted, especially if it is present in the head and neck region. Key words: folliculosebaceous cystic hamartoma, sebaceous tumor Case synopsis A 33-year-old woman presented with an asymptomatic papule that had persisted for the past 11 years. She noticed slow growth in the size of the lesion over the past 5 years. Repeated trauma to the papule while combing her hair resulted in discomfort. Physical examination revealed a single non-tender, skin colored, firm, hairless papule of 5 x 4 x 3 mm diameter over the vertex of the scalp (Figure 1). It was excised and sent for histopathological examination (Figure 2, 3 & 4). Histopathological examination revealed a dilated follicular cystic structure with numerous sebaceous lobules radiating out from it in the dermis (Figure 2). The cyst showed a predominantly infundibular keratinization (Figure 3). This folliculosebaceous structure was surrounded by increased collagen in the dermis (Figure 2) and clefts were visible between the folliculosebaceous structures and the surrounding stroma (Figure 4). -
Cutaneous Neoplasms
torr CALIFORNIA TUMOR TISSUE REGISTRY 1 03RD SEMI-ANNUAL CANCER SEMINAR ON CUTANEOUS NEOPLASMS CASE HISTORIES 00•MODERAT.0RS: . PHILIP E. LE~0FJ', M.Q. Dir;ector O:f Oermatopafholo.gy ;Ser:Vice Associate Professor of Clinical Pathology U.C.S.F.- Elermatopa~hology San Francisco, ·californla and TIMGTH1f' H. MCG~WMON'f,, M ~D. Assistant Clinical Professor U.C~S.F. - Dermatopathology San Francisco, California December 7, 1997 Sheraton Palace Hotel San Francisco, California PLATFORM CHAIR: CLAUDE 0. BURDICK, M.D. Director of laboratory ValleyCare Health System Pleasanton, California CASE RISTORJES 10.3"" Semi-Annual Seminar (Due to in$uffient material, Case 115 is • compo~ite to two ca!ICll with an identical diagnosis, Ace. #15523 and Ace #12395.) Ca.c 1#1 - As:c 1#28070: The patient was a 12-ycaro{)ld male who had a fairly long history ofa very small bump in the scalp of the temporal area, which had recently become greally enlarged. The submitting denna!ologist mentioned that this was a soliwy lesion, with no other lesions apparent (Contributed by Prescott Rasmussen, MD.) c-111- As:c #11543: The patient was a 60-year-old Caucasian female wbo presented with a S.O em right suprapalellar subcutaneous mass which was reported to be present and gradually increasing in size for a period of approximately rn·o years. There was no history of prior trauma, and the remainder ofthe clinical history and physical findings wcze uoremarialble. An cxeisional biopsy was performed. The specimeD consisted ofa 4.S x 1.1 em elliptical segment ofeentnllly dimpled skin which surmowlted a S.3 x 4.4 x 3.6 em delicately encapsulated. -
Trichoblastoma Arising from the Nevus Sebaceus of Jadassohn
Open Access Case Report DOI: 10.7759/cureus.15325 Trichoblastoma Arising From the Nevus Sebaceus of Jadassohn Fatimazahra Chahboun 1 , Madiha Eljazouly 1 , Mounia Elomari 2 , Faycal Abbad 3 , Soumiya Chiheb 1 1. Dermatology Unit, Cheikh Khalifa International University Hospital, Mohammed VI University of Health Sciences, Casablanca, MAR 2. Plastic and Reconstructive Surgery, Cheikh Khalifa International University Hospital, Mohammed VI University of Health Sciences, Casablanca, MAR 3. Pathology, Cheikh Khalifa International University Hospital, Mohammed VI University of Health Sciences, Casablanca, MAR Corresponding author: Fatimazahra Chahboun, [email protected] Abstract Trichoblastoma is a rare benign skin adnexal tumour, belonging to the category of trichogenic tumours. The clinical and histological findings may often be confused with basal cell carcinoma, a malignant epidermal skin tumour. We report here a case of a 70-year-old man presented with a dome-shaped, dark-pigmented nodule within a yellowish hairless plaque on the scalp. The plaque had existed since childhood. However, the central pigmented nodule began appearing three months ago and enlarging gradually. The patient had no medical history. Furthermore the physical examination revealed a translucent, verrucous, and yellowish plaque, with central and pigmented nodule measuring 0.7 × 0.5 cm. Also basal cell carcinoma and trichoblastoma’s diagnosis were discussed. The patient was subsequently referred to the plastic surgery department, where he underwent a total excision. The histological examination was in favour of trichoblastoma arising from the nevus sebaceus. After 24 months of checking, no recurrence was observed. Trichoblastoma is a benign adnexal tumour. Its progression to malignant trichoblastoma (or trichoblastic carcinoma) is possible, but remains exceptional. -
The Best Diagnosis Is: H&E, Original Magnification 2
Dermatopathology Diagnosis The best diagnosis is: H&E, original magnification 2. a. adenoid cysticcopy carcinoma arising within a spiradenoma b. cylindroma and spiradenoma collision tumor c. microcysticnot change within a spiradenoma d. mucinous carcinoma arising within a spiradenoma Doe. trichoepithelioma and spiradenoma collision tumor CUTIS H&E, original magnification 100. PLEASE TURN TO PAGE 211 FOR DERMATOPATHOLOGY DIAGNOSIS DISCUSSION Amanda F. Marsch, MD; Jeffrey B. Shackelton, MD; Dirk M. Elston, MD Dr. Marsch is from the Department of Dermatology, University of Illinois at Chicago. Drs. Shackelton and Elston are from the Ackerman Academy of Dermatopathology, New York, New York. The authors report no conflict of interest. Correspondence: Amanda F. Marsch, MD, University of Illinois at Chicago, 808 S Wood St, Chicago, IL 60612 ([email protected]). 192 CUTIS® WWW.CUTIS.COM Copyright Cutis 2015. No part of this publication may be reproduced, stored, or transmitted without the prior written permission of the Publisher. Dermatopathology Diagnosis Discussion Trichoepithelioma and Spiradenoma Collision Tumor he coexistence of more than one cutaneous adnexal neoplasm in a single biopsy specimen Tis unusual and is most frequently recognized in the context of a nevus sebaceous or Brooke-Spiegler syndrome, an autosomal-dominant inherited disease characterized by cutaneous adnexal neoplasms, most commonly cylindromas and trichoepitheliomas.1-3 Brooke-Spiegler syndrome is caused by germline muta- tions in the cylindromatosis gene, CYLD, located on band 16q12; it functions as a tumor suppressor gene and has regulatory roles in development, immunity, and inflammation.1 Weyers et al3 first recognized the tendency for adnexal collision tumors to present in patients with Brooke-Spiegler syndrome; they reported a patient with Brooke-Spiegler syndrome with spirad- Figure 1. -
Hair Loss in Infancy
SCIENCE CITATIONINDEXINDEXED MEDICUS INDEX BY (MEDLINE) EXPANDED (ISI) OFFICIAL JOURNAL OF THE SOCIETÀ ITALIANA DI DERMATOLOGIA MEDICA, CHIRURGICA, ESTETICA E DELLE MALATTIE SESSUALMENTE TRASMESSE (SIDeMaST) VOLUME 149 - No. 1 - FEBRUARY 2014 Anno: 2014 Lavoro: 4731-MD Mese: Febraury titolo breve: Hair loss in infancy Volume: 149 primo autore: MORENO-ROMERO No: 1 pagine: 55-78 Rivista: GIORNALE ITALIANO DI DERMATOLOGIA E VENEREOLOGIA Cod Rivista: G ITAL DERMATOL VENEREOL G ITAL DERMATOL VENEREOL 2014;149:55-78 Hair loss in infancy J. A. MORENO-ROMERO 1, R. GRIMALT 2 Hair diseases represent a signifcant portion of cases seen 1Department of Dermatology by pediatric dermatologists although hair has always been Hospital General de Catalunya, Barcelona, Spain a secondary aspect in pediatricians and dermatologists 2Universitat de Barcelona training, on the erroneous basis that there is not much in- Universitat Internacional de Catalunya, Barcelona, Spain formation extractable from it. Dermatologists are in the enviable situation of being able to study many disorders with simple diagnostic techniques. The hair is easily ac- cessible to examination but, paradoxically, this approach is often disregarded by non-dermatologist. This paper has Embryology and normal hair development been written on the purpose of trying to serve in the diag- nostic process of daily practice, and trying to help, for ex- ample, to distinguish between certain acquired and some The full complement of hair follicles is present genetically determined hair diseases. We will focus on all at birth and no new hair follicles develop thereafter. the data that can be obtained from our patients’ hair and Each follicle is capable of producing three different try to help on using the messages given by hair for each types of hair: lanugo, vellus and terminal. -
Proliferating Trichilemmal Cyst of the Scalp: Nine Cases and Literature Review
Otorhinolaryngology-Head and Neck Surgery Research Article ISSN: 2398-4937 Proliferating trichilemmal cyst of the scalp: Nine cases and literature review ElBenaye J1,3*, Sinaa M2,3, Elkhachine Y1,3, Sakkah A1,3, Jakar A1 and Elhaouri M1 1Department of Dermatology, Moulay Ismail Military Hospital, Meknes, Morocco 2Department of Cytopathology, Moulay Ismail Military Hospital, Meknes, Morocco 3Department of Medicine and Pharmacy, Sidi Mohammed Ben Abdellah University (USMBA), Fes, Morocco Abstract Background: proliferating trichilemmal cyst (PTC) is a rare adnexal tumor, primarily sitting on the scalp of elderly women. Its evolution is generally benign despite the rare malignant cases described. We report a series of 9 cases of which one is malignant and metastatic. Material and methods: We retrospectively reviewed data of all patients with PTC seen at department of dermatology in the Meknes military hospital, between January 2013 and December 2017. Results: Nine cases of PTC were diagnosed, which 8 in elderly women, with 62 years mean age. Trauma was found in one third of cases correlated with rapid growth of the tumor. The latter was symptomatic in 2/3 of the cases. Ulceration involved only the malignant case. The size varied from 1,5 to 12 cm. Recurrence after surgery was noted in 2 cases (malignant tumor and multi-cystic tumor). Discussion: PTC appears to have a well-distinguished profile of the simple trichilemmal cyst. Some clinical and histological features may constitute prognostic factors of aggressiveness. Histological and immunohistochemical study is crucial in the management. A large excision remains the only guarantee of complete remission without recurrence or metastasis. -
2016 Essentials of Dermatopathology Slide Library Handout Book
2016 Essentials of Dermatopathology Slide Library Handout Book April 8-10, 2016 JW Marriott Houston Downtown Houston, TX USA CASE #01 -- SLIDE #01 Diagnosis: Nodular fasciitis Case Summary: 12 year old male with a rapidly growing temple mass. Present for 4 weeks. Nodular fasciitis is a self-limited pseudosarcomatous proliferation that may cause clinical alarm due to its rapid growth. It is most common in young adults but occurs across a wide age range. This lesion is typically 3-5 cm and composed of bland fibroblasts and myofibroblasts without significant cytologic atypia arranged in a loose storiform pattern with areas of extravasated red blood cells. Mitoses may be numerous, but atypical mitotic figures are absent. Nodular fasciitis is a benign process, and recurrence is very rare (1%). Recent work has shown that the MYH9-USP6 gene fusion is present in approximately 90% of cases, and molecular techniques to show USP6 gene rearrangement may be a helpful ancillary tool in difficult cases or on small biopsy samples. Weiss SW, Goldblum JR. Enzinger and Weiss’s Soft Tissue Tumors, 5th edition. Mosby Elsevier. 2008. Erickson-Johnson MR, Chou MM, Evers BR, Roth CW, Seys AR, Jin L, Ye Y, Lau AW, Wang X, Oliveira AM. Nodular fasciitis: a novel model of transient neoplasia induced by MYH9-USP6 gene fusion. Lab Invest. 2011 Oct;91(10):1427-33. Amary MF, Ye H, Berisha F, Tirabosco R, Presneau N, Flanagan AM. Detection of USP6 gene rearrangement in nodular fasciitis: an important diagnostic tool. Virchows Arch. 2013 Jul;463(1):97-8. CONTRIBUTED BY KAREN FRITCHIE, MD 1 CASE #02 -- SLIDE #02 Diagnosis: Cellular fibrous histiocytoma Case Summary: 12 year old female with wrist mass. -
Histopathological Profile of Surgically Excised Scalp and Skull Lesions Asuman Kilitci¹ , Ziya Asan²
DOI: 10.5152/cjms.2018.442 Original Article Histopathological Profile of Surgically Excised Scalp and Skull Lesions Asuman Kilitci¹ , Ziya Asan² 1Department of Pathology, Ahi Evran University School of Medicine, Kırşehir, Turkey ²Department of Neurosurgery, Ahi Evran University School of Medicine, Kırşehir, Turkey ORCID ID of the author: A.K. 0000-0002-5489-2222; Z.A. 0000-0001-8468-9156 Cite this article as: Kilitci A, Asan Z. Histopathological Profile of Surgically Excised Scalp and Skull Lesions. Cyprus J Med Sci 2018; 3: 63-7. BACKGROUND/AIMS Although subcutaneous lesions of the scalp are more common than those of the skull, few studies in literature have assessed the frequency of scalp and skull diseases. The goal of this study was to establish the frequency and main histopathological findings of these lesions. Our study is one of the largest series and shows that the incidence of surgically excised scalp masses includes an array of diseases. MATERIAL and METHODS We reviewed 265 extracranial masses from 173 patients. The mean age of the patients, gender distribution, localization and characteristics of lesions, histopathological type and radiological features were analyzed. RESULTS One-hundred (57.8%) patients were males and 73 (42.2%) were females. The mean age was 42.98 (range, 5-87). In total, 261 were within the scalp, 1 involved the scalp and skull and 3 were within the limits of the skull. Six lesions exhibited malignant features. There were 101 trichilemmal cysts; 74 epidermal cysts; 38 intradermal nevus; 8 verruca vulgaris; -
Ntvdv Maart 2018, Nummer 3
COLOFON INHOUD Het Nederlands Tijdschrift voor Dermatologie en Venereologie is het officiële orgaan van de Nederlandse Vereniging voor Dermatologie en Venereologie en verschijnt 10x per jaar in een oplage van 1.200 exemplaren. Het NTvDV is vanaf 1 januari 2008 geïndexeerd in EMBase, de internationale wetenschappelijke database van Elsevier Science. NVDV NASCHOLING DERMATOLOGENDAGEN HOOFDREDACTIE Dr. W.P. Arnold, hoofdredacteur 3 Programma Ziekenhuis Gelderse Vallei, afdeling Dermatologie W. Brandtlaan 10 | 6716 RP Ede ARTIKELEN Telefoon 0318-435007 E-mail: [email protected] 5 Behandeling female pattern hair loss ARTIKELEN 8 Non-scarring alopecia Dr. R.C. Beljaards, dr. C.J.W. van Ginkel LEERZAME ZIEKTEGESCHIEDENISSEN 10 Cicatriciële alopecie Dr. R. van Doorn, dr. S. van Ruth, dr. J. Toonstra, dr. T.M. Le ALLERGEEN VAN DE MAAND 15 Trichoscopie Prof. dr. T. Rustemeyer DERMATOCHIRURGIE 19 Geriatrische dermato-oncologie Dr. R.I.F. van der Waal DERMATOLOGIE DIGITAAL 24 Ingenolmebutaat bij actinische keratosen DERMATOLOGIE IN BEELD 25 Beeldtechnologie ondersteunt de arts Dr. R.I.F. van der Waal, dr. A.J. Onderdijk DERMATOPATHOLOGIE 29 Dermatofyten in revisie P.K. Dikrama DERMATOSCOPIE 33 Diagnostiek in de dermatologie Dr. N.A. Kukutsch GESCHIEDENIS VAN DE DERMATOLOGIE 38 Infecties van de neonaat Dr. J. Toonstra, A. Glastra ONDERZOEK VAN EIGEN BODEM 40 Herpes zoster Dr. H.J. Bovenschen, J.C.J. Hellenbrand-Hendriks 42 Chemopreventie van huidkanker PRAKTIJKVOERING Dr. C. Vrijman 46 Mohschirurgie in Nederland: afspraken REFERATEN D.J.C. Komen, dr. M.B.A. van Doorn 48 Plaveiselcelcarcinoom in het hoofd-halsgebied RICHTLIJNEN Dr. J.J.E. van Everdingen 50 Systeemtherapie voor melanoom DERMATOLOGIE IN DE KUNST Dr. -
Histopathology Squamous Cell Carcinoma
Squamous cell carcinoma - Mohs Ron Rapini MD No conflict of interest Josey Chair, Dept Dermatology • I am paid zero to speak at this Univ Texas Medical School at Houston MD Anderson Cancer Center course, other than travel • The tuition helps to run the ASMS programs Duplicate Actinic keratosis Actinic keratosis Rx • Whether you call it a “precancer” or • Treating orAKs is beyond this lecture “squamous cell carcinoma grade 1/2” or • Ill-defined dysplasias – usually a “field-effect” “SCC – AK type”, or “keratinocytic • Trying to eradicate totally is like playing intraepithelial neoplasia = KIN”, it still “whack a mole” so goal is to eradicate most doesn’t need Mohs surgery significant areas • Don’t over-read as invasive squamous cell ca • Cryo, curettage, laser, imiquimod, • AK and squamous cell carcinoma are often fluorouracil, diclofenac, etc multifocal with field effects in margins Keratinocytic intraepithelialDistribute Grading dysplasia in neoplasia = KIN 1, 2, 3 dysplastic nevi is analogous • Analogous to CIN, PIN, VIN 1,2,3 • Really in SKIN with most popular • NIH consensus conference 1992 system, we don’t have a “2”: recommended grading cytology despite Not lack of concordance AK = KIN-1 • I grade only cytology as mild, moderate, SCC in situ (Bowen’s) = KIN-3 Do severe 1 Lack of concordance on grading “dysplasia” in dysplastic nevi Other terms Piepkorn (J Cutan Pathol 6:542, 1992) • Bowenoid AK – “just call it found only 38% agreement SCCis?” Similar situation with KIN-2 (in between • Advanced AK – “beware” AK and SCC in situ) – -
Copyrighted Material
1 Index Note: Page numbers in italics refer to figures, those in bold refer to tables and boxes. References are to pages within chapters, thus 58.10 is page 10 of Chapter 58. A definition 87.2 congenital ichthyoses 65.38–9 differential diagnosis 90.62 A fibres 85.1, 85.2 dermatomyositis association 88.21 discoid lupus erythematosus occupational 90.56–9 α-adrenoceptor agonists 106.8 differential diagnosis 87.5 treatment 89.41 chemical origin 130.10–12 abacavir disease course 87.5 hand eczema treatment 39.18 clinical features 90.58 drug eruptions 31.18 drug-induced 87.4 hidradenitis suppurativa management definition 90.56 HLA allele association 12.5 endocrine disorder skin signs 149.10, 92.10 differential diagnosis 90.57 hypersensitivity 119.6 149.11 keratitis–ichthyosis–deafness syndrome epidemiology 90.58 pharmacological hypersensitivity 31.10– epidemiology 87.3 treatment 65.32 investigations 90.58–9 11 familial 87.4 keratoacanthoma treatment 142.36 management 90.59 ABCA12 gene mutations 65.7 familial partial lipodystrophy neutral lipid storage disease with papular elastorrhexis differential ABCC6 gene mutations 72.27, 72.30 association 74.2 ichthyosis treatment 65.33 diagnosis 96.30 ABCC11 gene mutations 94.16 generalized 87.4 pityriasis rubra pilaris treatment 36.5, penile 111.19 abdominal wall, lymphoedema 105.20–1 genital 111.27 36.6 photodynamic therapy 22.7 ABHD5 gene mutations 65.32 HIV infection 31.12 psoriasis pomade 90.17 abrasions, sports injuries 123.16 investigations 87.5 generalized pustular 35.37 prepubertal 90.59–64 Abrikossoff