Perforating Granuloma Annulare Mimicking Papulonecrotic Tuberculid
Myeong Heon Chae1, Jee Yon Shin1, Ji Yeoun Lee1
1Department of Dermatology, Medical Research Institute, Chungbuk National University School of Medicine, Cheongju, Korea.
Annals of Dermatology
|April 29, 2021
Summary
This case report details a rare variant of granuloma annulare, perforating granuloma annulare (PGA), which clinically mimicked papulonecrotic tuberculid (PNT). The patient
Area of Science:
- Dermatology
- Pathology
Background:
- Perforating granuloma annulare (PGA) is a rare variant of granuloma annulare.
- PGA presents clinically as an umbilicated papule with a central crust, often mistaken for papulonecrotic tuberculid (PNT).
- PNT is typically associated with tuberculosis infection and shows wedge-shaped dermal necrosis histologically.
Observation:
- A 43-year-old Korean woman presented with a year-long history of erythematous papules on her limbs.
- The patient had latent tuberculosis and was undergoing antituberculous medication, complicating the initial diagnosis.
- Despite treatment for tuberculosis, her skin lesions persisted, prompting further investigation.
Findings:
- Histopathological examination revealed wedge-shaped dermal necrosis, focal mucin deposition, and palisading granulomatous inflammation.
- These findings, along with clinical presentation, led to a diagnosis of PGA, distinct from PNT.
- The patient responded well to topical corticosteroid treatment.
Implications:
- This case highlights the importance of considering PGA in the differential diagnosis of PNT, especially when clinical and histological features overlap.
- Accurate diagnosis is crucial for appropriate treatment, as PGA and PNT require different management strategies.
- The successful treatment of PGA with topical corticosteroids suggests their efficacy in managing this rare condition.
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