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Granuloma annulare following initiation of interleukinâ17a antagonist
Clincal and Experimental Dermatology, 2021The introduction of biologics has rapidly expanded treatment options for patients suffering from severe plaque psoriasis. Currently, the mainstay of biologic therapy for psoriasis centers around three key classes: Anti-tumor necrosis factor (TNF), Anti ...
A. R. Gray +3 more
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Patch Type Granuloma Annulare: An institution-based study of 23 cases.
Journal of cutaneous pathology, 2020BACKGROUND Granuloma annulare (GA) is a skin disorder of uncertain etiology. Patch (type) GA is an uncommon variant of GA with a paucity of data characterizing it. We describe the features of 23 cases of patch GA.
Urmi Khanna, J. North
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Journal of the American Academy of Dermatology, 1980
Granuloma annular (GA) is a benign inflammatory skin disease usually localized to the distal extremities, although generalized, perforating, and subcutaneous variants have also been identified. A regular histopathologic feature is the presence of mononuclear cells, often in palisading array, around foci of altered collagen.
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Granuloma annular (GA) is a benign inflammatory skin disease usually localized to the distal extremities, although generalized, perforating, and subcutaneous variants have also been identified. A regular histopathologic feature is the presence of mononuclear cells, often in palisading array, around foci of altered collagen.
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Subcutaneous Granuloma Annulare
Archives of Dermatology, 1966Five cases are reported as examples of the subcutaneous form of granuloma annulare. Classical cutaneous lesions appeared at approximately the same time in cases 1 and 2; in other instances (cases 3 and 4) the subcutaneous lesions preceded the classical ones; a brother of this last patient (case 4) presented only subcutaneous nodular lesions (case 5 ...
Francis W. Lynch, Manly Rubin
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Subcutaneous granuloma annulare on the heel: A case report and review of the Japanese published work
Journal of dermatology (Print), 2020Subcutaneous granuloma annulare is a rare variant of granuloma annulare. It mostly presents as painless subcutaneous nodule(s) with or without annular lesions on the lower legs and scalp of children.
Y. Endo +3 more
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Journal of the European Academy of Dermatology and Venereology, 2020
Granuloma annulare (GA) and the related annular elastolytic giant cell granuloma (AEGCG) and interstitial granulomatous dermatitis (IGD) are idiopathic histiocytic inflammatory disorders, which are frequently recalcitrant to treatment.
Y.W. Yang +5 more
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Granuloma annulare (GA) and the related annular elastolytic giant cell granuloma (AEGCG) and interstitial granulomatous dermatitis (IGD) are idiopathic histiocytic inflammatory disorders, which are frequently recalcitrant to treatment.
Y.W. Yang +5 more
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Granuloma annulare and sarcoidosis
British Journal of Dermatology, 1977Granuloma annulare (GA) and sarcoidosis are two diseases of unknown cause which involve the skin and whose basic pathology is a mononuclear histiocytic cellular reaction. Biopsy plays the major role in the diagnosis of both diseases, and no other routine laboratory test for either disease is currently available.
Pablo Umbert, Richard K. Winkelmann
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Generalized Granuloma Annulare
Archives of Dermatology, 1969A clinical and histologic study of 26 patients with generalized granuloma annulare was made at the Mayo Clinic. The histologic features and sex ratio were found to be similar to the localized form of granuloma annulare. The generalized form, in addition to having a large number of lesions, differs from the localized form in that most patients involved ...
Richard K. Winkelmann +2 more
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Subcutaneous granuloma annulare mimicking dermatomyositis
Pediatric dermatology, 2020We present three children who presented with papules and plaques over the knuckles, mimicking Gottron's papules of juvenile dermatomyositis, as well as subcutaneous nodules over the joints of the extremities that were initially thought to represent ...
Karin Maoz +6 more
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Survey of Ophthalmology, 1987
A 2-year-old boy presented with a 3-month history of nontender masses involving the right superotemporal orbit and scalp. Over the three-week period before presentation he also developed nodules on his wrist, abdomen, and buttocks. The remainder of the ocular and general physical exam was unremarkable.
James W. Karesh, Andrew W. Lawton
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A 2-year-old boy presented with a 3-month history of nontender masses involving the right superotemporal orbit and scalp. Over the three-week period before presentation he also developed nodules on his wrist, abdomen, and buttocks. The remainder of the ocular and general physical exam was unremarkable.
James W. Karesh, Andrew W. Lawton
openaire +3 more sources