Histology Flashcards
normal epidermis but thickened dermis with broad bands of collagen that appear separated on histology due to mucin between the bundles
Scleredema
normal epidermis, perivascular mononuclear cell infiltrate, mucin deposition in papillary dermis, fibroblast proliferation and fibrosis
Scleromyxedema
typically has inflammation and fibrosis in all layers (except epidermis which is normal), they are most intense in subcutis and fascia. Inflammatory infiltrate consists of abundant lymphocytes, plasma cells, histiocytes. Eosinophilic infiltration can be seen
Eosinophilic Fasciitis
Increased number of dermal fibroblasts, increased dermal collagen, increased mucin deposition, no inflammatory cells, increased CD34+ fibrocytes and CD68+ monocytes
Nephrogenic Systemic Fibrosis
CD8+ T cells invading healthy muscle fibers, increased MHCI on muslces, red-ragged fibers, red-rimmed autophagocytic vacuoles, amyloid deposits
Inclusion Body Myositis
mixed inflammatory infiltrate in walls of medium arteries with areas of fibrinoid necrosis
PAN
Focal and segmental transmural necrotizing vasculitis of medium and small arteries
Hyerkeratosis, epidermal atrophy, vacuolar interface dermatitis (liquefactive degeneration of basal layer of epidermis), superficial/perivascular and perifollicular mononuclear cell inflammatory infiltrate, BM thickening
Cutaneous lupus
Hyperkeratosis and follicular plugging, BM thickened
Discoid lupus
Lupus Tumidus
absent interface changes at dermal-epidermal junction
caclification, fibrointimal hyperplasia and thrombosis in microvessels in the subcutaneous adipose tissue and dermis
Calciphylaxis
Pt will have ESRD, hyperphos, hyperPTH and painful skin lesions (ulcerative/nodular/necrotic) of lower extremities and trunk
Calcifications can be intravascular or extra
aggregates of multinucleated giant cells and histiocytes that have a granular ground glass appearance
MRH
histiocytes also called tissue macrophages
Nodule biopsy: spindle shaped myofibroblasts
Fibroblastic rheumatism
Palmar thickening is a hallmark, inability to extend fingers. Symmetric polyarthritis similar to MRH.
marked lymphocyte and plasma cell infiltrate, storiform or swirling fibrosis, obliterative phlebitis. Plasma cells
IgG4
Can present: AI pancreatitis/cholangitis, oribital disease, salivary glands, kidney disese
Can see: elevated serum IgG4, polyclonal gammopathy
Plasma cells: >40% IgG4+, >10/hpf