Sudden Onset of Generalized Scaly Eruptions
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Clinical Study of Nail Changes in Papulosquamous Disorders
Original Research Article Clinical study of Nail changes in papulosquamous disorders Vishal Wali1, Trivedi Rahul Prasad2* 1Associate Professor, 2Post Graduate, Department of Dermatology, Venereology and Leprology, Mahadevappa Rampure Medical College, Sedam Road, Kalaburagi (Gulbarga) 585105, Karnataka, INDIA. Email: [email protected] Abstract Background: Nail disorders comprise ~10% of all dermatologic conditions. Nail disorders include those abnormalities that effect any portion of the nail unit. The nail unit includes the plate, matrix, bed, proximal and lateral folds, hyponychium, and some definitions include the underlying distal phalanx. These structures may be effected by heredity, skin disorders, infections, systemic disease, and aging process, internal and external medications, physical and environmental agents, trauma, and tumours, both benign and malignant. The main contributors being papulosquamous disorder. Nail changes in papulosquamous disorder have been inadequately discussed and only limited studies are present. This study aims to throw some light about frequency of nail involvement in papulosquamous disorders and its various patterns. Methodology: This is the descriptive study. It was conducted in department of DVL of Mahadevappa Rampura Medical college and Basaveshwar teaching and general hospital, Kalaburagi from July 2019 to Feb 2021. General, systemic and dermatological examinations were done. Nails were examined in detail. Special investigations like skin biopsy and potassium hydroxide (KOH) mount was done in relevant cases. Results: There were 50 cases of papulosquamous disorder. The most common papulosquamous disorder was psoriasis, followed by lichen planus and PRP. Out of these the most common nail change was pitting (81%) and lest common was dorsal pterygium (%) Conclusion: Nail being an important appendage affecting various dermatosis and acts as window in diagnosis. -
Pityriasis Rosea DANIEL L
CARING FOR COMMON SKIN CONDITIONS Pityriasis Rosea DANIEL L. STULBERG, M.D., Utah Valley Regional Medical Center, Provo, Utah JEFF WOLFREY, M.D., Good Samaritan Regional Medical Center, Phoenix, Arizona Pityriasis rosea is a common, acute exanthem of uncertain etiology. Viral and bacterial causes have been sought, but convincing answers have not yet been found. Pityriasis O A patient informa- rosea typically affects children and young adults. It is characterized by an initial herald tion handout on pityriasis rosea, written patch, followed by the development of a diffuse papulosquamous rash. The herald by the authors of this patch often is misdiagnosed as eczema. Pityriasis rosea is difficult to identify until the article, is provided on appearance of characteristic smaller secondary lesions that follow Langer’s lines (cleav- page 94. age lines). Several medications can cause a rash similar to pityriasis rosea, and several diseases, including secondary syphilis, are included in the differential diagnosis. One small controlled trial reported faster clearing of the exanthem with the use of ery- thromycin, but the mechanism of effect is unknown. Resolution of the rash may be has- tened by ultraviolet light therapy but not without the risk of hyperpigmentation. Top- ical or systemic steroids and antihistamines often are used to relieve itching. (Am Fam Physician 2004;69:87-92,94. Copyright© 2004 American Academy of Family Physicians.) This article is one in a ityriasis rosea is a common skin cytes, a decrease in T lymphocytes, and an ele- series coordinated by condition characterized by a her- vated sedimentation rate.6 Daniel L. Stulberg, M.D., director of der- ald patch and the later appear- Unfortunately, even though electron matology curriculum at ance of lesions arrayed along microscopy shows some viral changes and the Utah Valley Family Langer’s lines (cleavage lines). -
History of Psoriasis and Parapsoriasis
History of Psoriasis and Parapsoriasis By Karl Holubar Summary Parapsoriasis is «oï a disease entity. Jt is an auxiliary term introduced in J 902 to group several dermatoses w>itk a/aint similarity to psoriasis. Tlie liistorical development leading to tlie creation o/ t/ie term parapsoriasis is outlined and t/te Itistory o/psoriasis is 6rie/ly reviewed. Semantic and terminological considerations Obviously, para-psoriasis as a term has been created in analogy to psoriasis. We should remember similar neologisms in medical language, e. g. protein and para-protein; typhoid and para-typhoid, thyroid and para-thyroid, phimosis and para-phimosis, eventually, pemphigus and para-pemphigus (the latter in 1955 this term was to be employed instead of pemphigoid but was not accepted by the dermatological world). Literally, para is a Greek preposition, (with the genitive, dative and accusative), meaning: by the side of, next to something, alongside something. In medicine, para is used often as a prefix to another term, which designates a condition somewhat similar to the one under consideration. The same holds for psoriasis and parapsoria- sis. In detail, though, it is a bit more complicated. Parapsoriasis has more than one "/at/ier", three in fact: ideiurick /Iu.spitz f 1835—1886,), Paul Gerson Luna (A850—1929j and Louis Procç fI856—I928J. Auspitz, in 1881, had published a new system of skin diseases the seventh class of which was called epidermidoses, subdivided into liypcrlcfiratose.s, parakeratoses, kerato/y- ses, the characteristics of which were excessive keratinization, abnormal keratinization and insufficent keratinization. When Unna, in 1890®, pub- lished his two reports on what he called parakeratosis variegata, he referred to Auspitz' system and term when coining his own. -
Errata to the 7/1/2016 Prioritized List
Errata to the 7/1/2016 Prioritized List 1) On 6/29/2017, the following corrections were made: a. Website addresses were corrected for the new Oregon Health Authority Web site in all guideline notes referencing a Coverage Guidance. In addition, a web address in the Multisector Interventions section on Tobacco Use was updated. b. M67.0 (Short Achilles tendon (acquired)) was moved to line 297 NEUROLOGICAL DYSFUNCTION IN POSTURE AND MOVEMENT CAUSED BY CHRONIC CONDITIONS from line 382 DYSFUNCTION RESULTING IN LOSS OF ABILITY TO MAXIMIZE LEVEL OF INDEPENDENCE IN SELF- DIRECTED CARE CAUSED BY CHRONIC CONDITIONS THAT CAUSE NEUROLOGICAL DYSFUNCTION c. Psoriasis corrections: i. Add psoriasis, parapsoriasis and similar ICD-10 codes to line 544 MILD PSORIASIS; DERMATOPHYTOSIS: SCALP, HAND, BODY, DEEP-SEATED 1. L40.0 Psoriasis vulgaris 2. L40.1 Generalized pustular psoriasis 3. L40.2 Acrodermatitis continua 4. L40.3 Pustulosis palmaris et plantaris 5. L40.4 Guttate psoriasis 6. L40.8 Other psoriasis 7. L40.9 Psoriasis, unspecified 8. L41.0 Pityriasis lichenoides et varioliformis acuta ii. Add psoriatic arthropathy ICD-10 codes to line 50 RHEUMATOID ARTHRITIS AND OTHER INFLAMMATORY POLYARTHROPATHIES) and remove from line SEVERE INFLAMMATORY SKIN DISEASE 1. L40.51 Distal interphalangeal psoriatic arthropathy 2. L40.52 Psoriatic arthritis mutilans 3. L40.53 Psoriatic spondylitis 4. L40.54 Psoriatic juvenile arthropathy 5. L40.59 Other psoriatic arthropathy d. Add line 544 to Guideline Note 21 SEVERE INFLAMMATORY SKIN DISEASE, and append “See Guideline Note 57 for the definition of mild psoriasis included on line 544.” e. Add line 430 to Guideline Note 57 MILD PSORIASIS and append “See Guideline Note 21 for the definition of moderate/severe psoriasis included on line 430.” f. -
The Prevalence of Paediatric Skin Conditions at a Dermatology Clinic
RESEARCH The prevalence of paediatric skin conditions at a dermatology clinic in KwaZulu-Natal Province over a 3-month period O S Katibi,1,2 MBBS, FMCPaed, MMedSci; N C Dlova,2 MB ChB, FCDerm, PhD; A V Chateau,2 BSc, MB ChB, DCH, FCDerm, MMedSci; A Mosam,2 MB ChB, FCDerm, MMed, PhD 1 Dermatology Unit, Department of Paediatrics and Child Health, University of Ilorin, Kwara State, Nigeria 2 Department of Dermatology, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa Corresponding author: O S Katibi ([email protected]) Background. Skin conditions are common in children, and studying their spectrum in a tertiary dermatology clinic will assist in quantifying skin diseases associated with greatest burden. Objective. To investigate the spectrum and characteristics of paediatric skin disorders referred to a tertiary dermatology clinic in Durban, KwaZulu-Natal (KZN) Province, South Africa. Methods. A cross-sectional study of children attending the dermatology clinic at King Edward VIII Hospital, KZN, was carried out over 3 months. Relevant demographic information and clinical history pertaining to the skin conditions were recorded and diagnoses were made by specialist dermatologists. Data were analysed with EPI Info 2007 (USA). Results. There were 419 children included in the study; 222 (53%) were males and 197 (47%) were females. A total of 64 diagnosed skin conditions were classified into 16 categories. The most prevalent conditions by category were dermatitis (67.8%), infections (16.7%) and pigmentary disorders (5.5%). For the specific skin diseases, 60.1% were atopic dermatitis (AD), 7.2% were viral warts, 6% seborrhoeic dermatitis and 4.1% vitiligo. -
A Deep Learning System for Differential Diagnosis of Skin Diseases
A deep learning system for differential diagnosis of skin diseases 1 1 1 1 1 1,2 † Yuan Liu , Ayush Jain , Clara Eng , David H. Way , Kang Lee , Peggy Bui , Kimberly Kanada , ‡ 1 1 1 Guilherme de Oliveira Marinho , Jessica Gallegos , Sara Gabriele , Vishakha Gupta , Nalini 1,3,§ 1 4 1 1 Singh , Vivek Natarajan , Rainer Hofmann-Wellenhof , Greg S. Corrado , Lily H. Peng , Dale 1 1 † 1, 1, 1, R. Webster , Dennis Ai , Susan Huang , Yun Liu * , R. Carter Dunn * *, David Coz * * Affiliations: 1 G oogle Health, Palo Alto, CA, USA 2 U niversity of California, San Francisco, CA, USA 3 M assachusetts Institute of Technology, Cambridge, MA, USA 4 M edical University of Graz, Graz, Austria † W ork done at Google Health via Advanced Clinical. ‡ W ork done at Google Health via Adecco Staffing. § W ork done at Google Health. *Corresponding author: [email protected] **These authors contributed equally to this work. Abstract Skin and subcutaneous conditions affect an estimated 1.9 billion people at any given time and remain the fourth leading cause of non-fatal disease burden worldwide. Access to dermatology care is limited due to a shortage of dermatologists, causing long wait times and leading patients to seek dermatologic care from general practitioners. However, the diagnostic accuracy of general practitioners has been reported to be only 0.24-0.70 (compared to 0.77-0.96 for dermatologists), resulting in over- and under-referrals, delays in care, and errors in diagnosis and treatment. In this paper, we developed a deep learning system (DLS) to provide a differential diagnosis of skin conditions for clinical cases (skin photographs and associated medical histories). -
PWO for Home Phototherapy
Physician’s Written Order For Office Use Only : Daavlin PO Box 626 Bryan, OH 43506 For Home Phototherapy Fax To: 419-636-7916 Other__________________________ Rx Prescriber Instructions: This form is a Prescription and Statement of Medical Necessity for Billing Entity ___________________________________ Daavlin home phototherapy products. (For Levia orders, please use the Levia version of ___________________________________ this form.) All fields are required for insurance approval. Call 800-322-8546 for assistance. First Name _______________________ Last Name _________________________ Middle Initial ____ DOB ____/____/____ Address _________________________________________ City_________________________ State_______ Zip___________ Patient: Gender: M F Phone #________________________________ Alt Phone #_________________________________ Physician Name _________________________________ ICD-10 : Description ICD-10 Code L40 . _____ Psoriasis Must Be Practice ________________________________________ Indicated L80 Vitiligo NPI# ____________________________________________ ______ . ____ Other: ____________________ (See back for ICD -10 Code Quick Referrence Guide) Address _______________________________________ Estimated Duration of Need: ___ Months ( 99 = Lifetime ) City ____________________ State ____ Zip _________ Body Area Affected (Check all that apply) Prescribing Physician: Prescribing Phone (____)_____________*Fax (____)_____________ 3 % - 10 % (Moderate) Hands (2 %) * IMPORTANT: We will use this fax number to fax the Prescriber’s Dosing -
Pediatric Psoriasis
Pediatric Papulosquamous and Eczematous Disorders St. John’s Episcopal Hospital Program Director- Dr. Suzanne Sirota-Rozenberg Dr. Brett Dolgin, DO Dr. Asma Ahmed, DO Dr. Anna Slobodskya, DO Dr. Stephanie Lasky, DO Dr. Louis Siegel, DO Dr. Evelyn Gordon, DO Dr. Vanita Chand, DO Pediatric Psoriasis Epidemiology • Psoriasis can first appear at any age, from infancy to the eighth decade of life • The prevalence of psoriasis in children ages 0 to 18 years old is 1% with an incidence of 40.8 per 100,000 ppl • ~ 75% have onset before 40 years of age What causes psoriasis? • Multifactorial • Genetics – HLA associations (Cw6, B13, B17, B57, B27, DR7) • Abnormal T cell activation – Th1, Th17 with increased cytokines IL 1, 2, 12, 17, 23, IFN-gamma, TNF-alpha • External triggers: – Injury (Koebner phenomenon) – medications (lithium, IFNs, β-blockers, antimalarials, rapid taper of systemic corticosteroids) – infections (particularly streptococcal tonsillitis). Pediatric Psoriasis Types: • Acute Guttate Psoriasis – Small erythematous plaques occurring after infection (MOST common in children) • 40% of patients with guttate psoriasis will progress to develop plaque type psoriasis • Chronic plaque Psoriasis – erythematous plaques with scaling • Flexural Psoriasis – Erythematous areas between skin folds • Scalp Psoriasis – Thick scale found on scalp • Nail Psoriasis – Nail dystrophy • Erythrodermic Psoriasis– Severe erythema covering all or most of the body • Pustular Psoriasis – Acutely arising pustules • Photosensitive Psoriasis – Seen in areas of sun -
Pityriasis Lichenoides Chronica Following Cesarean Delivery
Case Report DOI: 10.6003/jtad.1372c2 Pityriasis Lichenoides Chronica Following Cesarean Delivery İlknur Balta,1 MD, Özlem Ekiz,2 MD, Pınar Özuğuz,3 MD, Bilge Bülbül Şen,2 MD, Mehmet Doğan,4 MD Address: 1Department of Dermatology, Keçiören Training and Research Hospital, Ankara, Turkey; 2Department of Dermatology, Mustafa Kemal University, Tayfur Ata Sökmen Medical School, Hatay, Turkey, 3Department of Dermatology, Kocatepe University, School of Medicine, Afyon, Turkey, 4Department of Pathology, Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital, Ankara, Turkey E-mail: [email protected] * Corresponding Author: İlknur Balta MD, Ankara Keçiören Training and Research Hospital, 06380, Keçiören, Ankara, Turkey Published: J Turk Acad Dermatol 2013; 7 (2): 1372c2 This article is available from: http://www.jtad.org/2013/2/jtad1372c2.pdf Key Words: pityriasis lichenoides chronica, delivery Abstract Observations: Pityriasis lichenoides is a papulosquamous disorder with remissions and exacerbations. The aetiology of pityriasis lichenoides is unclear. There are isolated reports of the development of pityriasis lichenoides et varioliformis acuta during pregnancy. But pityriasis lichenoides chronica following cesarean delivery was never reported so far. We present a case of pityriasis lichenoides chronica that occurred within15 days after giving birth to her first child by cesarean section. Pregnancy is a condition with profound endocrine and metabolic alterations that are generally well tolerated by the body. However, it is known to generate a state of humoral and cellular immunosuppression. We have thought that is pityriasis lichenoides chronica following cesarean delivery may be associated with decreased immunosuppression after delivery. Introduction or infections and was otherwise healthy. She re- ported that pruritic papules appeared within 15 Pityriasis lichenoides (PL) is a papulosqua- days after giving birth to her first child by cesarean mous disorder with remissions and exacerba- section, six months ago. -
Histomorphology of Papulosquamous Skin Lesions with Special Stain Application-An Analysis”
“HISTOMORPHOLOGY OF PAPULOSQUAMOUS SKIN LESIONS WITH SPECIAL STAIN APPLICATION-AN ANALYSIS” Dissertation submitted in Partial fulfillment of the regulations required for the award of M.D. DEGREE In PATHOLOGY – BRANCH III THE TAMILNADU DR. M.G.R. MEDICAL UNIVERSITY CHENNAI MAY 2018 DECLARATION I hereby declare that the dissertation entitled “HISTOMORPHOLOGY OF PAPULOSQUAMOUS SKIN LESIONS WITH SPECIAL STAIN APPLICATION-AN ANALYSIS” is a bonafide research work done by me in the Department of Pathology, Coimbatore Medical College during the period from July 2016 to June 2017 under the guidance and supervision of Prof.Dr. C.Lalitha, M.D., Professor and Head of the Department, Department of Pathology, Coimbatore Medical College. This dissertation is submitted to The Tamilnadu Dr.MGR Medical University, Chennai towards the partial fulfilment of the requirement for the award of M.D., Degree (Branch III) in Pathology. I have not submitted this dissertation on any previous occasion to any University for the award of any Degree. Place: Coimbatore Date: Dr.V.Uma CERTIFICATE This is to certify that the dissertation entitled “Histomorphology of papulosquamous skin lesions with special stain application-an analysis” is a record of bonafide work done by Dr.V.Uma in the Department of Pathology, Coimbatore Medical College, Coimbatore under the guidance and supervision of Dr.G.S.Thiriveni Balajji M.D., Associate Professor, Department of Pathology, Coimbatore Medical College and submitted in partial fulfilment of the requirements for the award of M.D. Degree (Branch III) in Pathology by The Tamilnadu Dr. MGR Medical University, Chennai. Guide Head of the Department Dr.G.S.Thiriveni Balajji, M.D., Prof. -
Home Phototherapy Order Form
Physician’s Written Order for Home Phototherapy Fax to: 605-322-2475 or Email: [email protected] This form is a Prescription and Statement of Medical Necessity for Daavlin home phototherapy products Rx used for the treatment of skin conditions such as psoriasis. All fields required for insurance approval. First Name _______________________ Last Name _________________________ DOB ____/____/____ Gender: M F Address _____________________________________________ City_________________________ State_____ Zip__________ Patient Info: Patient Phone #________________________________ Alt Phone # or Email _______________________________________________ HCPCs: Product and Description: Physician Name ___________________________________ DermaPal: Hand-held treatment wand for scalp, Practice __________________________________________ E0691 spot treatment or travel. Includes comb attachment. NPI# ______________________________________________ E0691 1 Series: Small, light-weight panel for hands, face, Address _________________________________________ feet, elbows, or any other localized treatment area. City ______________________ State ____ Zip _________ 7 Series 8 Lamp: Six foot tall, multi-directional unit Info: Physician Prescribing Phone (____)______________*Fax (____)______________ Home Phototherapy Product: Home Phototherapy E0694 for large areas and/or full body treatment. * IMPORTANT: We will use this fax number to fax the Prescriber’s Dosing Guide ICD-10 Code: Description: ICD-10 Code Estimated Duration of Need: ___ Months ( -
The Conundrum of Parapsoriasis Versus Patch Stage of Mycosis Fungoides
View TThehe cconundrumonundrum ofof parapsoriasisparapsoriasis versusversus patchpatch stagestage Point ooff mmycosisycosis ffungoidesungoides KK.. NN.. SSarveswari,arveswari, PPatrickatrick YYesudianesudian Sundaram Medical Foundation, ABSTRACT Dr. Rangarajan Memorial Hospital, Chennai, Tamilnadu, Terminological confusion with benign dermatosis, such as parapsoriasis en plaques, makes India it difÞ cult to diagnose mycosis fungoides in the early patch stage. Early diagnosis of mycosis fungoides (MF) is important for deciding on type of therapy, prognosis and for further follow-up. Address for correspondence: Dr. K. N. Sarveswari, However, until recently, there has been no consensus on criteria that would help in diagnosing Sundaram Medical the disease early. Some believe that large plaque parapsoriasis (LPP) should be classiÞ ed Foundation, Dr. Rangarajan with early patch stage of MF and should be treated aggressively. However, there is no Þ rm Memorial Hospital, Shanthi clinical or laboratory criteria to predict which LPP will progress to MF and we can only discuss Colony - IV Avenue, Anna about statistical probability. Moreover, long-term outcome analysis of even patch stage of MF Nagar, Chennai - 600 040, Tamilnadu, India. is similar to that of control population. We therefore believe that LPP should be considered E-mail: sarveswari@ as a separate entity at least to prevent the patient from being given a frightening diagnosis. smfhospital.org We also feel that patients need not be treated with aggressive therapy for LPP and will need