Dermatochalasis

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Dermatochalasis
Classification according to ICD-10
Q82.8 Other specified congenital malformations of the skin - cutis laxa (hyperelastica)
H02.3 Blepharochalasis
L57.4 Cutis laxa senilis
ICD-10 online (WHO version 2019)

The dermatochalasis (from the Greek δέρμα derma "skin" and χαλασις chalasis "slackening". Synonym: Latin cutis laxa = "sagging skin") 'describes a group of mostly age-related connective tissue changes , often with familial accumulation. The term is often used in ophthalmology , but also in dermatology . A common characteristic is sagging, inelastic skin on different parts of the body that often sags in large folds, which makes the person concerned look older. Well-known manifestations can be found on the bags under the eyes , the eyelids or the skin on the back .

causes

Possible causes are:

diagnosis

The differentiation of the different forms is based on the age of onset, any previous changes such as urticaria , Quincke's edema , inflammatory skin changes or allergic reactions, for example to drugs. If a hereditary form is suspected, a detailed physical examination with a family history , possibly diagnostic imaging and, if necessary, further examinations must be carried out.

Differential diagnosis

The following are also to be distinguished:

therapy

Depending on the cause of the disease, there are different treatment approaches, such as conservative measures that tighten the skin (gymnastics, cold-warm showers, connective tissue massages, etc.) or surgical interventions (e.g. blepharoplasty). In the case of acquired forms, the focus is on the therapy of the underlying disease.

literature

Web links

Individual evidence

  1. Anselm Kampik, Franz Grehn: Ophthalmological differential diagnosis . Georg Thieme, 2008, ISBN 978-3-13-156782-6 .
  2. a b Peter Altmeyer, V. Paech: Therapy Glossary Dermatology and Allergy . Springer, 2005, ISBN 978-3-540-27648-7 .
  3. a b c Dermatochalasis. In: Orphanet (Rare Disease Database).
  4. ^ Institute for Medical Genetics and Human Genetics at Charité Berlin: Hereditary diseases of connective tissue
  5. O. Braun-Falco, M. Rupec, MJ Lindley: Congenital dermatochalasis as a key symptom of a symptom complex . In: Archives for Clinical and Experimental Dermatology . tape 220 , no. 2 , March 1964, p. 166-182 , doi : 10.1007 / BF00571834 .