Epidermolysis bullosa acquisita
Epidermolysis bullosa acquisita is a chronic subepidermal blistering disease associated with autoimmunity to type VII collagen[1] within anchoring fibril structures that are located at the dermoepidermal junction.[2]:609
See also
References
- ↑ Helen Chapel; Mansel Haeney; Siraj Misbah (2006). Essentials of clinical immunology. Wiley-Blackwell. pp. 207–. ISBN 978-1-4051-2761-5. Retrieved 25 June 2010.
- ↑ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 978-0-07-138076-8.
|
|---|
| Acantholysis
(epidermis) | |
|---|
| Pemphigoid
(dermis) | |
|---|
| | Other bullous | |
|---|
| In diseases
classified elsewhere | |
|---|
| |
|---|
| | Description |
- Anatomy
- Physiology
- Development
|
|---|
| | Disease |
- Infections
- Vesiculobullous
- Dermatitis and eczema
- Papulosquamous
- Urticaria and erythema
- Radiation-related
- Pigmentation
- Mucinoses
- Keratosis, ulcer, atrophy, and necrobiosis
- Vasculitis
- Fat
- Neutrophilic and eosinophilic
- Congenital
- Neoplasms and cancer
- nevi and melanomas
- epidermis
- dermis
- Symptoms and signs
- Terminology
|
|---|
| | Treatment |
- Procedures
- Drugs
- antibiotics
- disinfectants
- emollients and protectives
- itch
- psoriasis
- other
- Wound and ulcer
|
|---|
|
|