التفاصيل البيبلوغرافية
| العنوان: |
Severe pemphigoid nodularis successfully treated with dupilumab. |
| المؤلفون: |
Jendoubi, Fatma1 (AUTHOR), Bost, Chloe2 (AUTHOR), Tournier, Emilie3 (AUTHOR), Paul, Carle1 (AUTHOR), Konstantinou, Maria Polina1 (AUTHOR) mariepaulinek@gmail.com |
| المصدر: |
Dermatologic Therapy. Sep2022, Vol. 35 Issue 9, p1-3. 3p. |
| مصطلحات موضوعية: |
*BULLOUS pemphigoid, *DUPILUMAB, *ITCHING, *TREATMENT effectiveness, *MUCOSA-associated lymphoid tissue lymphoma, *IMMUNOGLOBULIN E |
| مستخلص: |
Indirect immunofluorescence (IIF) on salt-split skin showed linear deposition of IgG on the blister roof (Figure 1E). Pemphigoid nodularis (PN) is a variant of bullous pemphigoid (BP) associating clinical features of prurigo and an immunological profile of BP.1 We present a case of PN successfully treated with dupilumab. (E) Indirect immunofluorescence on salt-split skin showing linear deposition of IgG antibodies localized on the blister roof. gl PN affects predominantly elderly, female patients. [Extracted from the article] |
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