2018
DOI: 10.1007/s12016-017-8666-8
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Cutaneous Granulomatosis: a Comprehensive Review

Abstract: Cutaneous granulomatosis is a heterogeneous group of diseases, characterized by a skin inflammatory reaction triggered by a wide variety of stimuli, including infections, foreign bodies, malignancy, metabolites, and chemicals. From a pathogenic point of view, they are divided into non-infectious and infectious granulomas. Pathophysiological mechanisms are still poorly understood. Non-infectious granulomatous skin diseases include granuloma annulare, necrobiosis lipoidica, rheumatic nodules, foreign body granul… Show more

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Cited by 84 publications
(57 citation statements)
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“…Through use of Seq-Well S^3, we survey, at unprecedented resolution, the diversity of cell-types and states – e.g., among tissue resident T cells and myeloid cells – present across multiple types of skin inflammation. For example, GA and leprosy are two granulomatous diseases characterized by aggregates of lymphocytes and macrophages within the dermis, which are both thought to arise from a delayed-type hypersensitivity response to M. leprae infection (leprosy) and an unknown agent (GA) (Modlin et al, 1984; Terziroli Beretta-Piccoli et al, 2018). Here, we find that both are characterized by the presence of T cell sub-cluster 0 (Immature CD8 + CTL) and T cell sub-cluster 8 (mature CTL effectors containing CD8 + T-CTL, γδ and NK cells; Figure 3 ).…”
Section: Discussionmentioning
confidence: 99%
“…Through use of Seq-Well S^3, we survey, at unprecedented resolution, the diversity of cell-types and states – e.g., among tissue resident T cells and myeloid cells – present across multiple types of skin inflammation. For example, GA and leprosy are two granulomatous diseases characterized by aggregates of lymphocytes and macrophages within the dermis, which are both thought to arise from a delayed-type hypersensitivity response to M. leprae infection (leprosy) and an unknown agent (GA) (Modlin et al, 1984; Terziroli Beretta-Piccoli et al, 2018). Here, we find that both are characterized by the presence of T cell sub-cluster 0 (Immature CD8 + CTL) and T cell sub-cluster 8 (mature CTL effectors containing CD8 + T-CTL, γδ and NK cells; Figure 3 ).…”
Section: Discussionmentioning
confidence: 99%
“…One of the main strategies used by microorganisms to escape this macrophage activity involves altering the response profile of macrophages. 185,[235][236][237][238][239][240][241][242][243][244][245][246][247][248][249][250][251][252] The activation of a response profile mediated by M1 macrophages is commonly associated with a protective tissue environment and has been described for infections by pathogens such as Helicobacter pylori, M. tuberculosis, Mycobacterium leprae, Salmonella typhi, and Chlamydia. [253][254][255][256][257][258] M1 macrophages elicit an effective immune response against S. typhi and H. pylori, and in the response against H. pylori, the induction of iNOS associated with the M1 profile is closely related to the occurrence of gastric cancer.…”
Section: Autophagymentioning
confidence: 99%
“…Whereas in our patient, the localisation was not compatible with the literature. Cutaneous sarcoidosis is also known as one of the great imitators in dermatology, together with syphilis and malignant melanoma (1). Lupus vulgaris, foreign body reaction, pseudolymphoma, tuberculoid leprosy, granuloma annulare, atypical mycobacterial infection, deep fungal infections, syphilis, lupus miliaris facia, discoid lupus erythematosus and granulomatous rosacea should be considered in differential diagnosis (7).…”
Section: Discussionmentioning
confidence: 99%
“…It is a granulomatous inflammatory reaction to a wide variety of stimuli, including infections, systemic inflammations, neoplasia, metabolic disorders, and chemicals. This group includes cutaneus sarcoidosis (1). Sarcoidosis is a systemic disease characterized by non-caseating granulomas with an unknown etiology.…”
Section: Introductionmentioning
confidence: 99%