Hair Diseases: a Big Problem on a Small Surface
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Rapid Development of Perifolliculitis Following Mesotherapy
CASE LETTER Rapid Development of Perifolliculitis Following Mesotherapy Weihuang Vivian Ning, MD; Sameer Bashey, MD; Gene H. Kim, MD patient received mesotherapy with an unknown substance PRACTICE POINTS for cosmetic rejuvenation; the rash was localized only to the injection sites.copy She did not note any fever, chills, • Mesotherapy—the delivery of vitamins, chemicals, and plant extracts directly into the dermis via nausea, vomiting, diarrhea, headache, arthralgia, or upper injections—is a common procedure performed respiratory tract symptoms. She further denied starting in both medical and nonmedical settings for any new medications, herbal products, or topical therapies cosmetic rejuvenation. apart from the procedure she had received 2 weeks prior. • Complications can occur from mesotherapy treatment. Thenot patient was found to be in no acute distress and • Patients should be advised to seek medical care with vital signs were stable. Laboratory testing was remarkable US Food and Drug Administration–approved cosmetic for elevations in alanine aminotransferase (62 U/L [refer- techniques and substances only. ence range, 10–40 U/L]) and aspartate aminotransferase (72 U/L [reference range 10–30 U/L]). Moreover, she had Doan absolute neutrophil count of 0.5×103 cells/µL (refer- ence range 1.8–8.0×103 cells/µL). An electrolyte panel, To the Editor: creatinine level, and urinalysis were normal. Physical Mesotherapy, also known as intradermotherapy, is a examination revealed numerous 4- to 5-mm erythematous cosmetic procedure in which multiple -
Rapunzel Syndrome: a Case Report and Literature Review
Case Report Annals of Short Reports Published: 10 Jun, 2020 Rapunzel Syndrome: A Case Report and Literature Review Hemonta KD* Department of Pediatric Surgery, Assam Medical College, India Abstract Rapunzel syndrome is an extremely rare clinical condition in children. Usually affects girls of adolescent age group with history of hair ingestion (trichophagia) and trichotillomania (hair- pulling). Patients present with vague abdominal pain and bowel obstruction caused by a hairball in the stomach, with its tail extending into duodenum and beyond. We report a case of 13-year-old girl with poor general condition, who presented with recurrent abdominal pain, vomiting and a palpable mass in the abdomen. She gave history of trichophagia and trichotillomania for more than two years. On exploration, a large trichobezoar with a tail was noted in the stomach, duodenum and proximal jejunum. The bezoar was removed. The girl had uneventful recovery. She received psychiatric treatment and improved. Introduction Rapunzel syndrome is characterized by presence of hairballs or hair-like fibers in the stomach and intestine. These results from chewing and swallowing hair or any other indigestible materials (trichophagia) often associated with hair-pulling disorder (trichotillomania) in young girls [1-3]. The syndrome is named after the long-haired girl ‘Rapunzel’ in the fairy tale by the Brothers Grimm [4]. We present a case of Rapunzel syndrome in an adolescent girl, who needed surgical removal of the hairball and psychiatric treatment. Case Presentation A 13-year old girl with poor general condition presented with recurrent abdominal pain with distension, vomiting and constipation. She had a palpable mass in the epigastric region. -
Trichotillomania: an Impulsion Beyond Hair Pulling (A Case Report)
Iqbal MM, et al., J Clin Stud Med Case Rep 2019, 6: 70 DOI: 10.24966/CSMC-8801/100070 HSOA Journal of Clinical Studies and Medical Case Reports Case Report Trichotillomania: An Impulsion Introduction Trichotillomania evolves as an impulse control disorder in the lit- beyond Hair Pulling erature where hair puling ultimately leads to achievement of mental satisfaction and pleasure. Although rare, it has been reported in the (A Case Report) literature previously where adolescents and children between ages 9 -13 years have been frequently targeted by this psycho dermatologic morbidity [1]. Frequent misdiagnosis of trichotillomania with alope- Muhammad Mashood Iqbal*, Muhammad Ishaq Ghauri, Mohammad Shariq Mukarram, Mohammad Faisal Iftikhar and cia areata appears to be common according to studies and hence a Uzzam Ahmed Khawaja challenging task lies to clinically diagnose the former accurately [1- 3]. Trichotillomania repeatedly appears to be linked with depression, Department of Medicine, Jinnah Medical College Hospital, Karachi, Sindh, obsessive compulsive disorder, low self-esteem, poor social function- Pakistan ing and self-image [1,4]. Patients who clinically present with such psychiatric abnormalities should be evaluated for mental and behav- ioral disorders where they tend to carry out anomalous tasks in order Abstract to relieve anxiety. Introduction: Trichotillomania is a psycho dermatologic disorder Clinical interventions to precisely evaluate and further manage that has been identified as a common morbidity in children and ado- trichotillomanics require large scale studies with positive outcomes. lescents having a positive correlation with depression and Obsessive Most successful behavioral modifications and therapies such as habit Compulsive Disorder (OCD). Very few cases have been reported in reversal tend to outweigh the pharmacological approach where the the 20-30 age groups, therefore, we intend on reporting this case. -
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Number 1 | January 2019 Prevalence and incidence of rare diseases: Bibliographic data Prevalence, incidence or number of published cases listed by diseases (in alphabetical order) www.orpha.net www.orphadata.org If a range of national data is available, the average is Methodology calculated to estimate the worldwide or European prevalence or incidence. When a range of data sources is available, the most Orphanet carries out a systematic survey of literature in recent data source that meets a certain number of quality order to estimate the prevalence and incidence of rare criteria is favoured (registries, meta-analyses, diseases. This study aims to collect new data regarding population-based studies, large cohorts studies). point prevalence, birth prevalence and incidence, and to update already published data according to new For congenital diseases, the prevalence is estimated, so scientific studies or other available data. that: Prevalence = birth prevalence x (patient life This data is presented in the following reports published expectancy/general population life expectancy). biannually: When only incidence data is documented, the prevalence is estimated when possible, so that : • Prevalence, incidence or number of published cases listed by diseases (in alphabetical order); Prevalence = incidence x disease mean duration. • Diseases listed by decreasing prevalence, incidence When neither prevalence nor incidence data is available, or number of published cases; which is the case for very rare diseases, the number of cases or families documented in the medical literature is Data collection provided. A number of different sources are used : Limitations of the study • Registries (RARECARE, EUROCAT, etc) ; The prevalence and incidence data presented in this report are only estimations and cannot be considered to • National/international health institutes and agencies be absolutely correct. -
Is the Loose Anagen Hair Syndrome a Keratin Disorder? a Clinical and Molecular Study
STUDY Is the Loose Anagen Hair Syndrome a Keratin Disorder? A Clinical and Molecular Study Vale´rie Chapalain, MD; Hermelita Winter, PhD; Lutz Langbein, PhD; Jean-Michel Le Roy, MD; Christine Labre`ze, MD; Milos Nikolic, MD; Ju¨rgen Schweizer, PhD; Alain Taı¨eb, MD Objectives: To report the clinical features of the loose seldom cut their hair, and 4 had unmanageable hair. One anagen hair syndrome and to test the hypothesis that the patient had hypodontia. Two patients had an additional typical gap between the hair and the inner root sheath clinical phenotype of diffuse partial woolly hair. The fam- may result from hereditary defects in the inner root sheath ily history was positive for loose anagen hair syndrome or the apposed companion layer. in 5 patients. Marked improvement was noted after treat- ment with 5% minoxidil lotion in 7 of the 11 patients Design: Case series. treated. Polymerase chain reaction analysis of the gene segments encoding the ␣-helical 1A and 2B subdomains Setting: A pediatric dermatology unit (referral center). of K6hf, the type II cytokeratin exclusively expressed in the companion layer, was performed in 9 families. In Patients: A consecutive sample of 17 children (13 girls). 3 of these 9 families, a heterozygous glutamic acid and For 9 of them and their first-degree relatives, molecular lysine mutation, E337K, was identified in the L2 linker analyses were performed in the K6HF gene with 50 ap- region of K6HF. propriate controls. Conclusions: Diffuse partial woolly hair can be associ- Intervention: Minoxidil therapy (5% lotion) in 11 pa- ated with loose anagen hair syndrome. -
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. -
11A. GI Manifestations of Psychologic Disorders
11A. GI Manifestations of Psychologic Disorders Meredith Hitch, MD Robert Rothbaum, MD I. Psychogenic Associations Many psychological disorders have associated gastrointestinal manifestations. While evaluating a child for chronic abdominal pain, it is important to consider psychologic as well as organic etiologies for the symptoms II. Mood Disorder and Anxiety—Chronic Abdominal Pain A. There is a vicious cycle involving chronic pain, depression, and anxiety, each provoking the other B. Anxiety disorder is found in 80% of children with recurrent abdominal pain (RAP) in some studies C. Depressive symptoms found in 40% of children with RAP D. Possible explanations 1. Pain evokes mood and anxiety disorders 2. Affective disorders cause or exacerbate pain 3. A common biological predisposition underlies both problems 4. Common characteristics of both include somatization, social stress, and poor coping E. Life stressors provoke 1. Physiologic stress response with increased ccorticotropin-releasing factor (CRF) 2. CRF causes ↑ intestinal motility, hyperalgesia, psychoemotional inflammatory responses F. Typical life stresses 1. Maternal separation 2. Conflicting maternal relationships 3. Abusive environments – sexual or physical 4. Traumatic events – death, major illness, geographic dislocation 5. Marital discord 6. Peer pressure 7. Perfectionism III. Pathologic Aerophagia—Abdominal Distension A. Symptoms: eructation, abdominal cramping, flatulence, chronic diarrhea B. Tympanitic abdomen with very hyperactive bowel sounds C. Plain abdominal film showing uniform gassy distension from esophagus to rectum, without air fluid levels D. Hallmarks: 1. Increasing abdominal distension throughout the day 2. Increased flatus at night E. Visable air swallowing is often subtle and hard to detect F. Signs of abuse or stress IV. Mental Retardation/Anxiety/Obsessive Compulsive Disorder (OCD)— Solitary Rectal Ulcer Syndrome A. -
Rapunzel Syndrome—An Extremely Rare Cause of Digestive Symptoms in Children: a Case Report and a Review of the Literature
CASE REPORT published: 09 June 2021 doi: 10.3389/fped.2021.684379 Rapunzel Syndrome—An Extremely Rare Cause of Digestive Symptoms in Children: A Case Report and a Review of the Literature Cristina Oana Marginean 1, Lorena Elena Melit 1*, Maria Oana Sasaran 2, Razvan Marginean 3 and Zoltan Derzsi 4 1 Department of Pediatrics I, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Târgu Mures, ¸ Târgu Mure ¸s, Romania, 2 Department of Pediatrics III, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Târgu Mure ¸s, Târgu Mure ¸s, Romania, 3 Department of Pediatric Surgery, County Emergency Clinical Hospital of Târgu Mure ¸s, Târgu Mure ¸s, Romania, 4 Department of Pediatric Surgery, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Târgu Mure ¸s, Romania Rapunzel syndrome is an extremely rare condition seen in adolescents or young females with psychiatric disorders consisting of a gastric trichobezoar with an extension within Edited by: the small bowel. The delays in diagnosis are common since in its early stages, it is Matthew Wyatt Carroll, usually asymptomatic. We report the case of a 13-year-old girl admitted in our clinic for University of Alberta, Canada abdominal pain, anorexia, and weight loss. The clinical exam pointed out diffuse alopecia, Reviewed by: Yahya Wahba, a palpable mass in the epigastric area, and abdominal tenderness at palpation, the Mansoura University, Egypt patient weighing 32 kg. The laboratory tests showed anemia. The abdominal ultrasound Francesco Valitutti, Ospedali Riuniti San Giovanni di Dio e showed a gastric intraluminal mass with a superior hyperechoic arc. -
Trichotillomania
synvi ASSIUT UNIVERSITY DRUG INFORMATION BULLETIN Ass. Uni. D.I. Bull., Vol. 10 No. 2, June 2014 كليـــة الصيـدلــة Trichotillomania Trichotillomania is an impulse-control disorder (a psychological condition) is characterized by the persistent and excessive pulling of one’s own hair, Patients are unable to stop this behavior, even as their hair becomes thinner, resulting in noticeable hair loss. The scalp is the most common area, followed by the eyelashes and eyebrows. The alopecia that results from hair pulling can range from small undetectable areas of hair loss to total baldness. Trichotillomania is 7 times as prevalent in children as in adults, with the peak prevalence between the ages of 4 and 17 years. It can cause a child to experience distress and may result in moderate impairment in social or academic functioning. Additionally, trichotillomania may result in impairment in other important areas of functioning, such as family relationships. Etiology The etiology of trichotillomania is largely unknown, though both environmental and genetic causes have In This Issue been suspected. Explanations that have been proposed for the onset and maintenance of the hair- Trichotillomania…...……. 1 pulling behavior include the following: Terminology………………. 4 Coping mechanism for anxiety or stressful events FDA News…………….…… 5 A benign habit that developed from a sensory Test Your Knowledge....... 5 event (e.g., itchy eyelash) or another event and resulted in trichotillomania. Real Enquiries……..…….. 6 Co-occurring with another habitual behavior (i.e., Ask the Expert……………. 6 thumbsucking) in young children Serotonin deficiency - A link may exist between Complementary medicine 7 a deficiency of the neurotransmitter serotonin (5- Did You Know?.............. -
Trichotillomania: an Important Psychocutaneous Disorder
PEDIATRIC DERMATOLOGY Series Editor: Camila K. Janniger, MD Trichotillomania: An Important Psychocutaneous Disorder Alexander M. Witkowski; Robert A. Schwartz, MD, MPH; Camila K. Janniger, MD Trichotillomania (TTM) is a type of alopecia due Epidemiology to a psychocutaneous disorder, a self-induced An exact statistical representation of the number of illness classified as an impulse control disorder individuals with TTM in the general population is but with features of both obsessive-compulsive not available.8,9 A number of these patients avoid disorder (OCD) and addictive disorders. Although visiting their physicians and going into public places most common in children, this repetitive pulling where their disorder would be revealed.9-11 In addi- out of one’s own hair can occur at any age. The tion, adults may conceal their plucking habit with target usually is hair of the scalp, eyebrows, eye- wigs, hats, and makeup. The prevalence has been lashes, and pubic area using fingers, brushes, noted to be 0.6% to 3.4% of the total population, combs, and tweezers. Therapy for TTM can with a female to male ratio of 2 to 1.12-14 The inci- be challenging. CUTISdence of TTM appears to be higher in children than Cutis. 2010;86:12-16. in adolescents and adults.15 A small percentage of patients have first-degree family members with the same disorder as well as a history of OCD, depres- richotillomania (TTM) is an unusual type sion, and alcohol and drug abuse.16-20 of alopecia classified as an impulse control T disorder but with features of both obsessive- -
Expert-Level Diagnosis of Nonpigmented Skin Cancer by Combined Convolutional Neural Networks
Supplementary Online Content Tschandl P, Rosendahl C, Akay BN, et al. Expert-level diagnosis of nonpigmented skin cancer by combined convolutional neural networks. JAMA Dermatol. Published online November 28, 2018. doi:10.1001/jamadermatol.2018.4378 eFigure. Sensitivities (Blue) and Specificities (Orange) at Different Threshold Cutoffs (Green) of the Combined Classifier Evaluated on the Validation Set eAppendix. Neural Network Training eTable 1. Complete List of Diagnoses and Their Frequencies Within the Test-Set eTable 2. Education of Users According to Their Experience Group eTable 3. Percent of Correct Prediction of the Malignancy Status for Specific Diagnoses of a CNN Using Either Close-up or Dermatoscopic Images This supplementary material has been provided by the authors to give readers additional information about their work. © 2018 American Medical Association. All rights reserved. Downloaded From: https://jamanetwork.com/ on 09/25/2021 eFigure. Sensitivities (Blue) and Specificities (Orange) at Different Threshold Cutoffs (Green) of the Combined Classifier Evaluated on the Validation Set A threshold cut at 0.2 (black) is found for a minimum of 51.3% specificity. © 2018 American Medical Association. All rights reserved. Downloaded From: https://jamanetwork.com/ on 09/25/2021 eAppendix. Neural Network Training We compared multiple architecture and training hyperparameter combinations in a grid-search fashion, and used only the single best performing network for dermoscopic and close-up images, based on validation accuracy, for further analyses. We trained four different CNN architectures (InceptionResNetV2, InceptionV3, Xception, ResNet50) and used model definitions and ImageNet pretrained weights as available in the Tensorflow (version 1.3.0)/ Keras (version 2.0.8) frameworks. -
New Approach in Combined Therapy of Perifolliculitis Capitis Abscedens Et Suffodiens
726 Letters to the Editor New Approach in Combined Therapy of Perifolliculitis Capitis Abscedens et Suffodiens Felix Jacobs, Gisela Metzler, Jakub Kubiak, Martin Röcken and Martin Schaller Department of Dermatology, Eberhard Karls University, DE-72076 Tuebingen, Germany. E-mail: [email protected] Accepted March 14, 2011. Perifolliculitis capitis abscedens et suffodiens (PCAS) tract. In the upper dermis there was a suppurative inflam- is a rare scalp disease seen mostly in young males of mation with abscess material and hair shaft fragments being discharged via a draining sinus. Periodic acid-Schiff (PAS) Afro-American descent. The disease is characterized by staining for fungi, as well as immunohistochemical staining perifollicular pustules, suppurative nodules and fluctua- with anti-Mycobacterium bovis (BCG) and for T. pallidum was ting abscesses, as well as by intercommunicating sinus negative. Direct immunofluorescence of the perilesional scalp tracts on the scalp. We report here an elderly Caucasian skin was negative. woman who fulfilled the clinical and histological criteria Microbiological examinations failed to identify pathogenic organisms. for diagnosis of PCAS. Following the diagnosis of a PCAS, the patient was treated The patient was treated with initial prednisolone, with 10 mg acitretin and 30 mg prednisolone daily as an inpa- systemic acitretin, topical tacrolimus and oral zinc. tient. The prednisolone was reduced to 5 mg per day during the After 6 months, her condition was stable. course of treatment. Because of the decreased level of zinc, 100 mg zinc aspartate was given daily. In addition, topical gluco- corticoids and tacrolimus 0.1% were alternated. CASE REPOrt This regimen produced almost total healing within 11 days (Fig.