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Updated: May 11, 2025

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Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
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Bullous morphea: a blistering sclerotic disease
Ayema Haque1, Cindy Puga2, Allison C Billi3
1Internal Medicine, Western Michigan University Homer Stryker MD School of Medicine, Kalamazoo, Michigan, USA.
BMJ Case Reports
|April 18, 2025
Summary
Bullous morphea, a rare localized scleroderma variant, presents with skin thickening and blisters. This case report details a patient
Area of Science:
- Dermatology
- Rheumatology
- Pathology
Background:
- Bullous morphea is a rare variant of localized scleroderma.
- It is characterized by skin thickening and blister formation.
- Early recognition is crucial for effective management.
Purpose of the Study:
- To report a case of bullous morphea in a woman in her 60s.
- To describe the clinical presentation, diagnosis, and treatment of bullous morphea.
- To emphasize the distinct nature of bullous morphea.
Main Methods:
- Case report of a patient diagnosed with bullous morphea.
- Clinical examination including assessment of rash progression.
- Skin biopsy for histopathological analysis.
- Differential diagnosis consideration including generalized morphea and lichen sclerosis.
Main Results:
- The patient presented with a pruritic rash progressing to fluid-filled bullae.
- Histopathology revealed thickened collagen bundles and epidermal lifting.
- Treatment with methotrexate, UVA phototherapy, and physical therapy halted disease progression.
Conclusions:
- Bullous morphea is a distinct clinical entity within localized scleroderma.
- Accurate diagnosis requires integrating clinical and histopathological findings.
- Multimodal treatment can effectively manage bullous morphea progression.
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