Treatment of Scleroedema Adultorum Buschke: A Systematic Review

Scleroedema adultorum Buschke is a rare skin disease, which can be divided into 3 subtypes: classic type, occurring after respiratory infections; a type lacking association with infections; and a type associated with diabetes. Scleroedema adultorum Buschke is characterized by thickening and tighteni...

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Main Authors: Diana Miguel, Sibylle Schliemann, Peter Elsner
Format: Article
Language:English
Published: Medical Journals Sweden 2017-12-01
Series:Acta Dermato-Venereologica
Subjects:
Online Access: https://www.medicaljournals.se/acta/content/html/10.2340/00015555-2846
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author Diana Miguel
Sibylle Schliemann
Peter Elsner
author_facet Diana Miguel
Sibylle Schliemann
Peter Elsner
author_sort Diana Miguel
collection DOAJ
description Scleroedema adultorum Buschke is a rare skin disease, which can be divided into 3 subtypes: classic type, occurring after respiratory infections; a type lacking association with infections; and a type associated with diabetes. Scleroedema adultorum Buschke is characterized by thickening and tightening of the skin, which typically starts at the neck. In half of patients, spontaneous remission may occur. The aim of this systematic review is to summarize all reported treatments for scleroedema adultorum Buschke, based on articles from PubMed database, using the query “scleroedema adultorum Buschke treatment”, English and German, published between 1970 and 2016 and documenting adequate treatments. The results are based mainly on individual case reports, small case series, and retrospective studies often reporting unsuccessful results. Treatment options include topical as well as systemic treatments, and physical modalities. There is a need for randomized controlled trials and studies on long-term outcomes after treatment.
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spelling doaj.art-28357a3e3e824720bad12cbe88aa1e542022-12-21T19:42:28ZengMedical Journals SwedenActa Dermato-Venereologica0001-55551651-20572017-12-0198330530910.2340/00015555-28465119Treatment of Scleroedema Adultorum Buschke: A Systematic ReviewDiana Miguel0Sibylle SchliemannPeter Elsner Department of Dermatology, Jena University Hospital Erfurter Straße 35, DE-07743 Jena, Germany. diana.miguel@med.uni-jena.de. Scleroedema adultorum Buschke is a rare skin disease, which can be divided into 3 subtypes: classic type, occurring after respiratory infections; a type lacking association with infections; and a type associated with diabetes. Scleroedema adultorum Buschke is characterized by thickening and tightening of the skin, which typically starts at the neck. In half of patients, spontaneous remission may occur. The aim of this systematic review is to summarize all reported treatments for scleroedema adultorum Buschke, based on articles from PubMed database, using the query “scleroedema adultorum Buschke treatment”, English and German, published between 1970 and 2016 and documenting adequate treatments. The results are based mainly on individual case reports, small case series, and retrospective studies often reporting unsuccessful results. Treatment options include topical as well as systemic treatments, and physical modalities. There is a need for randomized controlled trials and studies on long-term outcomes after treatment. https://www.medicaljournals.se/acta/content/html/10.2340/00015555-2846 scleroedemaadultorumBuschketreatment
spellingShingle Diana Miguel
Sibylle Schliemann
Peter Elsner
Treatment of Scleroedema Adultorum Buschke: A Systematic Review
Acta Dermato-Venereologica
scleroedemaadultorumBuschke
treatment
title Treatment of Scleroedema Adultorum Buschke: A Systematic Review
title_full Treatment of Scleroedema Adultorum Buschke: A Systematic Review
title_fullStr Treatment of Scleroedema Adultorum Buschke: A Systematic Review
title_full_unstemmed Treatment of Scleroedema Adultorum Buschke: A Systematic Review
title_short Treatment of Scleroedema Adultorum Buschke: A Systematic Review
title_sort treatment of scleroedema adultorum buschke a systematic review
topic scleroedemaadultorumBuschke
treatment
url https://www.medicaljournals.se/acta/content/html/10.2340/00015555-2846
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