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Nodular Subtype of Bullous Pemphigoid
Björn Dangel1, Lukas Kofler2, Gisela Metzler1
1Eberhard-Karls-University, Tuebingen, Germany.
Bullous pemphigoid can present as itchy nodules and papules, mimicking prurigo. This rare nodular subtype shares features with classic bullous pemphigoid but lacks blisters.
Area of Science:
- Dermatology
- Immunodermatology
Background:
- Itchy papules and nodules are common dermatological findings.
- The nodular subtype of bullous pemphigoid is a rare differential diagnosis.
- Distinguishing this subtype is crucial for appropriate management.
Observation:
- A case study of a female patient with intensely itchy papules and nodules on her trunk and extremities.
- Clinical presentation included erythematous, excoriated papules and nodules.
- Histopathology revealed prurigo-like lesions.
Findings:
- Immunofluorescence assays were positive for BP180 and BP230 antibodies.
- Diagnosis confirmed as nodular bullous pemphigoid based on clinical, histological, and immunofluorescence data.
- The patient's lesions healed with combination therapy.
Implications:
- Pemphigoid nodularis is a prurigo variant of bullous pemphigoid.
- Histological and immunopathological features are consistent with common bullous pemphigoid.
- This subtype typically lacks the characteristic blistering seen in classic bullous pemphigoid, highlighting the importance of immunofluorescence in diagnosis.
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