elastin and Granuloma-Annulare

elastin has been researched along with Granuloma-Annulare* in 2 studies

Other Studies

2 other study(ies) available for elastin and Granuloma-Annulare

ArticleYear
Keratoacanthomatous Changes: Unifying the Histologic Spectrum of Actinic Granuloma.
    The American Journal of dermatopathology, 2018, Volume: 40, Issue:10

    Actinic granuloma (AG) manifests as annular plaques on sun-damaged skin. There remains no universal consensus on the nosology, etiology, or clinicopathologic criteria of AG as a distinct entity. Broadly, AG is characterized by granulomatous inflammation, multinucleated giant cells, elastophagocytosis, and the absence of mucin and necrobiosis. It is not uncommon, however, to encounter overlapping histological features of other granulomas, such as granuloma annulare and necrobiosis lipoidica, confounding the diagnosis of this controversial entity. Herein, we describe 2 cases of AG with features of granuloma annulare and necrobiosis lipoidica, supporting the concept of AG as a histologic spectrum. These 2 cases displayed dilated follicular infundibula and pseudoepitheliomatous hyperplasia analogous to changes in keratoacanthomas. These unique epithelial changes, in tandem with characteristic elastin alterations and clinical findings, are helpful and unifying features that permit accurate diagnosis of this controversial entity.

    Topics: Biopsy; Diagnosis, Differential; Disease Progression; Elastic Tissue; Elastin; Epithelial Cells; Granuloma Annulare; Humans; Immunohistochemistry; Keratoacanthoma; Male; Middle Aged; Necrobiosis Lipoidica; Photosensitivity Disorders; Predictive Value of Tests; Skin

2018
Systemic elastolytic granulomatosis with cutaneous, ocular, lymph nodal, and intestinal involvement. Spectrum of annular elastolytic giant cell granuloma and sarcoidosis.
    Journal of the American Academy of Dermatology, 1992, Volume: 26, Issue:2 Pt 2

    A 15-year-old Japanese girl had widespread annular serpiginous erythematous plaques, bilateral granulomatous uveitis, bloody diarrhea, and seronegative arthralgia. She also had anemia and leukopenia. The histopathologic findings were compatible with those of annular elastolytic giant cell granuloma. Elastolytic granulomas were also found in the cervical lymph nodes, terminal ileum, parietal peritoneum, and mesentery. Bilateral hilar lymphadenopathy, hypercalcemia, and an increased level of angiotensin converting enzyme were not observed throughout the clinical course. To the best of our knowledge, systemic elastolytic granulomatosis has not been previously described in annular elastolytic giant cell granuloma or sarcoidosis. This case may represent a type of granulomatosis in the broad spectrum of annular elastolytic giant cell granuloma and sarcoidosis.

    Topics: Adolescent; Elastin; Erythema; Female; Granuloma Annulare; Granuloma, Giant Cell; Humans; Intestinal Diseases; Lymphatic Diseases; Neck; Sarcoidosis; Uveitis

1992