Interstitial Granulomatous Dermatitis: A Clinicopathological Study. (August 2015)
- Record Type:
- Journal Article
- Title:
- Interstitial Granulomatous Dermatitis: A Clinicopathological Study. (August 2015)
- Main Title:
- Interstitial Granulomatous Dermatitis
- Authors:
- Coutinho, Inês
Pereira, Neide
Gouveia, Miguel
Cardoso, José Carlos
Tellechea, Oscar - Abstract:
- Abstract : Introduction: Interstitial granulomatous dermatitis (IGD) is an uncommon granulomatous dermatitis occurring in the setting of highly reactive immune states, with a polymorphic clinical presentation. Because there is overlap with other entities [namely palisading neutrophilic granulomatous dermatitis (PNGD)], controversy exists regarding its classification. Objective: To understand if there are features allowing clear-cut distinction between IGD and PNGD. Material and Methods: Retrospective analysis of 10 cases previously diagnosed as IGD or PNGD, from 2000 to 2013, with review of the histopathologic findings and clinical correlation. Results: Six females and 4 males presented mostly with erythematous papules/nodules (n = 7) but also with erythematous annular plaques (n = 3). In 2 patients, the lesions coexisted. They were mostly distributed symmetrically on the limbs. Associated disease was observed in 6 patients. Regarding histopathology, an inflammatory infiltrate occupying the superficial and mid dermis was present in 40% of cases, with an interstitial component in all biopsies and a palisaded arrangement in 60%. Neutrophils and mononuclear cells were present in all cases in varying proportions. Necrobiosis was found in 70%, and leukocytoclasia was observed in 80% of biopsies. Conclusions: Coexistence of the interstitial and palisaded inflammatory patterns occurred in 90% of cases, with no correlation between tissue neutrophilia and the predominant pattern ofAbstract : Introduction: Interstitial granulomatous dermatitis (IGD) is an uncommon granulomatous dermatitis occurring in the setting of highly reactive immune states, with a polymorphic clinical presentation. Because there is overlap with other entities [namely palisading neutrophilic granulomatous dermatitis (PNGD)], controversy exists regarding its classification. Objective: To understand if there are features allowing clear-cut distinction between IGD and PNGD. Material and Methods: Retrospective analysis of 10 cases previously diagnosed as IGD or PNGD, from 2000 to 2013, with review of the histopathologic findings and clinical correlation. Results: Six females and 4 males presented mostly with erythematous papules/nodules (n = 7) but also with erythematous annular plaques (n = 3). In 2 patients, the lesions coexisted. They were mostly distributed symmetrically on the limbs. Associated disease was observed in 6 patients. Regarding histopathology, an inflammatory infiltrate occupying the superficial and mid dermis was present in 40% of cases, with an interstitial component in all biopsies and a palisaded arrangement in 60%. Neutrophils and mononuclear cells were present in all cases in varying proportions. Necrobiosis was found in 70%, and leukocytoclasia was observed in 80% of biopsies. Conclusions: Coexistence of the interstitial and palisaded inflammatory patterns occurred in 90% of cases, with no correlation between tissue neutrophilia and the predominant pattern of the infiltrate. There was also no clear-cut correlation between the infiltrate pattern and semiologic aspect of the lesions. Therefore, the features described in our study suggest that IGD and PNGD belong to the same clinicopathological spectrum. … (more)
- Is Part Of:
- American journal of dermatopathology. Volume 37:Number 8(2015)
- Journal:
- American journal of dermatopathology
- Issue:
- Volume 37:Number 8(2015)
- Issue Display:
- Volume 37, Issue 8 (2015)
- Year:
- 2015
- Volume:
- 37
- Issue:
- 8
- Issue Sort Value:
- 2015-0037-0008-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-08
- Subjects:
- interstitial granulomatous dermatitis -- palisading neutrophilic granulomatous dermatitis -- Churg–Strauss granuloma -- Ackerman syndrome
Skin -- Diseases -- Periodicals
Histology, Pathological -- Periodicals
616.50705 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=00000372-000000000-00000 ↗
http://www.amjdermatopathology.com ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/DAD.0000000000000288 ↗
- Languages:
- English
- ISSNs:
- 0193-1091
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0824.240000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5014.xml