Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
Epidermolysis Bullosa Acquisita is a rare, chronic autoimmune blistering disorder characterized by vesicles and bullae on the skin and mucous membranes. This condition, presenting typically in adulthood, is caused by autoantibodies against type VII collagen. Conventional treatments, including system...
Saved in:
| Main Authors: | Fahad Alrashidi, Khalid Nabil Nagshabandi, Ruaa Alharithy |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-05-01
|
| Series: | Journal of the Egyptian Women’s Dermatologic Society |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/jewd.jewd_109_24 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
An Exceedingly Rare Case of Mechanobullous Epidermolysis Bullosa Acquisita in a Prepubertal Child: A Review of the Clinical and Laboratory Considerations
by: Aleksandra Wiktoria Bratborska, et al.
Published: (2025-04-01) -
Epidermolysis Bullosa Acquisita in Children: Case Series
by: Nikolay N. Murashkin, et al.
Published: (2019-04-01) -
Complexities of care in a pediatric patient with epidermolysis bullosa acquisita and duchenne muscular dystrophy: a case report
by: Khayry Al-Shami, et al.
Published: (2025-07-01) -
Pregnancy and childbirth in epidermolysis bullosa: A clinical case
by: M. A. Meretukova, et al.
Published: (2025-04-01) -
Epidermolysis bullosa of the esophagus: A case report
by: Radić Maja, et al.
Published: (2015-01-01)