Granulomatous disease: Difference between revisions
From IDWiki
No edit summary |
m (→) |
||
Line 16: | Line 16: | ||
*** [[Buruli ulcer]] ([[Mycobacterium ulcerans]]) |
*** [[Buruli ulcer]] ([[Mycobacterium ulcerans]]) |
||
*** BCG vaccination |
*** BCG vaccination |
||
** Fungi: [[histoplasmosis]], [[coccidiomycosis]], [[blastomycosis]], [[sporotrichosis]], aspergillosis |
** Fungi: [[histoplasmosis]], [[coccidiomycosis]], [[blastomycosis]], [[sporotrichosis]], [[aspergillosis]], [[cryptococcosis]] |
||
* , [[cryptococcosis]] |
|||
** Protozoa: [[toxoplasmosis]], [[schistosomiasis]] |
** Protozoa: [[toxoplasmosis]], [[schistosomiasis]] |
||
** Spirochetes |
** Spirochetes |
Latest revision as of 17:50, 19 May 2023
Background
- Granulomatous inflammation is chronic inflammation that involves macrophages and T lymphocytes to wall off an infectious organism
- T cells are activated and in turn activate macrophages, which undergo morphological changes to become more epithelioid
- Creates two main types of granulomas: foreign body granulomas, and immune ganulomas
- In immune granulomas, macrophages active T cells to produce IL-2
Differential Diagnosis
- See also Granulomatous lung disease
- Infections
- Mycobacteria
- Tuberculosis: caseating granulomas, with acid-fast bacilli
- Leprosy: non-caseating granulomas, with acid-fast bacilli in macrophages
- Non-tuberculous mycobacteria
- Buruli ulcer (Mycobacterium ulcerans)
- BCG vaccination
- Fungi: histoplasmosis, coccidiomycosis, blastomycosis, sporotrichosis, aspergillosis, cryptococcosis
- Protozoa: toxoplasmosis, schistosomiasis
- Spirochetes
- Syphilis: gummas, which contain a wall of histiocytes, plasma cell infiltrate, and necrotic central cells without loos of cellular outline
- Treponema carateum
- Treponema pertenue
- Bacteria
- Cat scratch disease: rounded or stellate granulomas with central granular debris and neutrophils; giant cells are uncommon
- Brucella, Yersinia, Whipple diseaes
- Mycobacteria
- Vasculitis: GPA, eGPA, lymphomatoid vasculitis, polyarteritis nodosa, bronchocentric vasculitis, giant cell arteritis, systemic lupus erythematosus
- Other inflammatory disorders:
- Sarcoidosis: non-caseating granulomas with abundant activated macrophages
- Crohn disease: occasional non-caseating granulomas in intestinal wall
- Primary biliary cirrhosis, hepatic granulomatous disease, Langerhan granulomatosis, Peyronie disease, Blau syndrome, hypogammaglobulinemia, Langerhan cell histiocytosis, immune complex disease
- Leukocyte oxidase defects: chronic granulomatous disease
- Hypersensitivity pneumonitis: farmer's lung, bird fancier's lung, mushroom worker's lung, suberosis (cork dust), bagassosis, maple bark stripper's lung, paprika splitter's lung, coffee bean lung, Spatlese lung
- Chemical exposures: beryllium, zirconium, silica, starch, talc
- Neoplasms: carcinoma, reticulosis, pinealoma, dysgerminoma, seinoma, reticulum cell sarcoma, malignant nasal granuloma
- Miscellaneous: lymphogranuloma, Kikuchi syndrome
Further Reading
- James DG. A clinicopathological classification of granulomatous disorders. Postgrad Medical J. 2000;76:457-465. doi: 10.1136/pmj.76.898.457