Literature DB >> 29869129

[Skin biopsy of inflammatory skin diseases in childhood-when is it reasonable?]

A Böer-Auer1,2, R Fölster-Holst3.   

Abstract

Compared with adulthood, inflammatory skin diseases are relatively rarely biopsied in children. Apart from the invasiveness of the procedure, the required local anesthesia, and the risks of infection and scarring, the psychological trauma of the operation has a higher impact in childhood. If a biopsy is performed, expectations towards the dermatopathology report are high. However, the evaluation of biopsies taken from children is challenging for the dermatopathologist: on the one hand, because the biopsies are often tiny or just superficial shaves and, on the other hand, because criteria for evaluation have mostly been developed from findings in adult biopsy specimens. In children, the immune system is still in the process of maturation and, therefore, infiltrates in the skin may look different from those seen in adults; however, knowledge about that is very limited to date. Moreover, numerous rare genodermatoses may manifest themselves first in childhood and need to be considered in the differential diagnosis while experience with them is often limited. Starting from the clinical presentation, this article presents histopathological features of possible differential diagnoses in order to demonstrate the value or necessity of a skin biopsy in a pediatric patient. In addition, communication with parents and child, methods of local anesthesia and biopsy techniques will be considered.

Entities:  

Keywords:  Erythema; Exanthema; Histopathology; Local anesthesia; Pediatric dermatology

Mesh:

Year:  2018        PMID: 29869129     DOI: 10.1007/s00105-018-4205-7

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  44 in total

Review 1.  [Blaschkitis in adults].

Authors:  E Grosshans; L Marot
Journal:  Ann Dermatol Venereol       Date:  1990       Impact factor: 0.777

2.  Histomorphology and Immunophenotype of Eczematous Skin Lesions Revisited-Skin Biopsies Are Not Reliable in Differentiating Allergic Contact Dermatitis, Irritant Contact Dermatitis, and Atopic Dermatitis.

Authors:  Verena G Frings; Almut Böer-Auer; Kristine Breuer
Journal:  Am J Dermatopathol       Date:  2018-01       Impact factor: 1.533

3.  Extensive subcutaneous fat necrosis of the newborn associated with therapeutic hypothermia.

Authors:  Marcia Hogeling; Katharine Meddles; David R Berk; Anna L Bruckner; Thomas K Shimotake; Ronald S Cohen; Ilona J Frieden
Journal:  Pediatr Dermatol       Date:  2011-09-09       Impact factor: 1.588

4.  Nickel allergy: localized, id, and systemic manifestations in children.

Authors:  Jessica W Hsu; Catalina Matiz; Sharon E Jacob
Journal:  Pediatr Dermatol       Date:  2010-11-18       Impact factor: 1.588

5.  Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.

Authors:  Gabriele Richard; Nkecha Brown; Fatima Rouan; Jan-Gerrit Van der Schroeff; Emilia Bijlsma; Lawrence F Eichenfield; Virginia P Sybert; Kenneth E Greer; Peter Hogan; Carmen Campanelli; John G Compton; Sherri J Bale; John J DiGiovanna; Jouni Uitto
Journal:  J Invest Dermatol       Date:  2003-04       Impact factor: 8.551

6.  Fast, sensitive and specific diagnosis of infections with Leishmania spp. in formalin-fixed, paraffin-embedded skin biopsies by cytochrome b polymerase chain reaction.

Authors:  M Gebhardt; B Ertas; T M Falk; N Blödorn-Schlicht; D Metze; A Böer-Auer
Journal:  Br J Dermatol       Date:  2015-10-23       Impact factor: 9.302

7.  Immunohistochemical differentiation between inflammatory linear verrucous epidermal nevus (ILVEN) and psoriasis.

Authors:  W H P M Vissers; L Muys; P E J Van Erp; E M G J de Jong; P C M van de Kerkhof
Journal:  Eur J Dermatol       Date:  2004 Jul-Aug       Impact factor: 3.328

8.  Genotyping of Borrelia from formalin-fixed paraffin-embedded skin biopsies of cutaneous borreliosis and tick bite reactions by assays targeting the intergenic spacer region, ospA and ospC genes.

Authors:  F C Brandt; B Ertas; T M Falk; D Metze; A Böer-Auer
Journal:  Br J Dermatol       Date:  2014-08-27       Impact factor: 9.302

Review 9.  Neurological findings in incontinentia pigmenti; a review.

Authors:  Marije E C Meuwissen; Grazia M S Mancini
Journal:  Eur J Med Genet       Date:  2012-05-04       Impact factor: 2.708

10.  Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.

Authors:  A Smahi; G Courtois; P Vabres; S Yamaoka; S Heuertz; A Munnich; A Israël; N S Heiss; S M Klauck; P Kioschis; S Wiemann; A Poustka; T Esposito; T Bardaro; F Gianfrancesco; A Ciccodicola; M D'Urso; H Woffendin; T Jakins; D Donnai; H Stewart; S J Kenwrick; S Aradhya; T Yamagata; M Levy; R A Lewis; D L Nelson
Journal:  Nature       Date:  2000-05-25       Impact factor: 49.962

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