Non infectious granulomas Flashcards
Causes/risk factors of sarcoidosis
Name the clinical subtypes of sarcoidosis
Discuss NB points about sarcoidosis
Write a summary of the findings of cutaneous sarcoidosis
1) 20% skin lesions develop before systemic findings, 50% with systemic findings, 30% after systemic findings
2) lesions are astmptomatic (or mild itching)
3) Multiple, firm, elastic lesions - red, brown, purple, yellow
4) involve whole thickness of dermis
Clinical appearances: papular, plaques, annular, ulcerative, subcutaneous (Darier Roussy) - arms, skin may look normal, morpheiform, scars, icthyosiform, erythrodermic, alopecia, mucosal, hypopigmented
Name sarcoidosis syndromes
1) Lupus pernio
2) Lofgren’s sarcoidosis (acute sarcoidosis)
3) Heerfordt
4) Mikulicz syndrome
5) Unthoff phenomenon
Write short notes on lupus pernio
1) asymptomatic, red, brown papules on the nose, ears and cheeks - may ulcerate and leave telangiectatic scars. Nasal lesions may involve the septum and cause nosebleeding
2) increased association with chronic pulmonary fibrosis
3) Upper respiratory tract sarcoidosis (50%)
4) Granulomas/cysts bones (distal phalanges) -40%
5) clinically diascopy - apple jelly appearance
6) recalcitrant to rx - Topical and IL c/s, topical calcineurin inhibitors, systemic steroids if rapidly progressing skin lesions. other: Hydrochloroquine, minocycline
Write short notes on lofgren’s (acute) sarcoidosis
Acute sarcoidosis with triad: bilateral hilar LAD, erythema nodosum, acute arthritis (esp ankles)
Fever+malaise, female predominance, strong association with HLA-DRB1 allele
other: Respiratory symptoms: ( mild shortness of breath),
acute uveitis or iridocyclitis (inflammation of the eye), parotitis. Treatment : NSAIDs, colchicine, systemic c/s
Write short notes on Heerfordt syndrome
Subacute variant of sarcoidosis
(neurosarcoidosis)
Anterior uveitis, parotid/lacrimal gland enlargement, Cranial nerve palsy, low grade fever.
Heerfordt’s syndrome is classified into complete type, in which all four main symptoms are presented, and incomplete type, in which two out of the three symptoms of facial nerve palsy, parotid gland enlargement, and anterior uveitis are detected.
Write short notes on Mikulicz syndrome
Associations: IgG4-related diseases, Sjögren syndrome, gland involvement with sarcoidosis, gland involvement with lymphoma
Clinically - painless bilateral symmetric swelling of the lacrimal and salivary glands
-xerostomia
-xerophthalmia
Mikulicz syndrome is a non-specific inflammatory enlargement of at least two or more of the salivary and lacrimal glands with xerostomia.
Markers
IgG4 titres (80% sensitivity)
ANA
Write short notes on Unthoff phenomenon
Unthoff syndrome - transient, worsening of neurological function lasting less than 24 hours that usually occur in multiple sclerosis patients due to increases in core body temperature
Can also occur in atypical form of sarcoidosis
Name the systemic symptoms of sarcoidosis
Write notes on diagnosis/tests with re to sarcoidosis
Write notes on activity monitoring in sarcoidosis
Write short notes on the treatment of sarcoidosis
Write short notes on the outcome and prognosis of sarcoidosis
Write short notes on granuloma annulare with regards to granuloma annulare
Epidemiology
-children and young adults (2/3rds before 30)
- F>M
Pathogenesis
-unknown
-Th1 delayed type hypersensitivity reaction to a variety of triggers (trauma/isomorphic koenner repo se, insect bites, TBST, mycobacterial/viral infection or UV radiation)
Trigger-> Th1 reaction -> monocyte accumulation jn dermis -> release of lysosomal enzymes -> degredation of elastic fibres
Name the 2 main categories of granuloma annulare
1) localized
2) generalized
Name the associations which occur more commonly in generalized GA
1) hyperlipidemia
2) type I DM
3) HIV
4) Thyroid disease
5) Malignancy
Write key notes on Granuloma annulare
-clinical features
-variants
Write key notes on histopathology of Granuloma annulare
Write key notes on the treatment and prognosis of granuloma annulare
Write short notes on annular elastolytic giant cell granuloma
Write short note on interstisial granulomatous dermatititis and arthritis (IGDA) and Neutrophilic granulomatous dermatitis (PNGD)
Tabulate and compare IGDA and PNGD