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Published on: October 12, 2012
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Patch-type granuloma annulare: An institution-based study of 23 cases
Urmi Khanna1, Jeffrey P North1,2
1Department of Dermatology, University of California, San Francisco, California, USA.
Journal of Cutaneous Pathology
|April 13, 2020
Summary
Patch granuloma annulare (GA) is a rare skin condition primarily affecting women over 50. This variant presents as erythematous patches and can mimic other skin diseases, necessitating careful diagnosis.
Area of Science:
- Dermatology
- Pathology
- Immunology
Background:
- Granuloma annulare (GA) is a skin disorder with unknown causes.
- Patch GA is a rare subtype with limited available data.
- This study characterizes 23 patch GA cases.
Purpose of the Study:
- To describe the clinical and histopathologic features of patch GA.
- To differentiate patch GA from other dermatologic conditions.
- To improve the diagnosis and management of patch GA.
Main Methods:
- Retrospective review of dermatopathology archives for patch GA cases.
- Analysis of clinical history and morphology.
- Assessment of histopathologic features, including granulomatous inflammation patterns and cell types.
Main Results:
- Most patients were female (19/23) presenting with erythematous patches on the trunk and extremities.
- Common differential diagnoses included mycosis fungoides, morphea, and contact dermatitis.
- Histopathology revealed interstitial lymphocytes and histiocytes with dermal mucin; 1/3 of cases had eosinophils and plasma cells.
Conclusions:
- Patch GA is an uncommon variant with an interstitial granulomatous pattern, predominantly affecting women over 50.
- Clinically and histopathologically, it can resemble interstitial mycosis fungoides and early morphea.
- Recognizing patch GA aids in preventing misdiagnosis and inappropriate treatment.

