Lymphadenopathy Flashcards
Follicles are round or irregular and may be confluent
Follicular Hyperplasia
Describe flow of lymph from the afferent to efferent lymphatics.
Afferent –> lymph node –> subcapsular sinus –> radial sinuses –> efferent lymphatics
common B cell reaction which can cause enlarged lymph nodes and is predominantly characterized by (1) hyperplasia and multiple (2) cells within the (3)
- germinal center 2. plasma 3. medullary cords REFERS TO Follicular hyperplasia
common in lymph nodes draining (1) but are also seen, albeit less frequently, in lymph nodes draining inflammatory and infectious lesions.
- cancers refers to Sinus histiocytosis
Within the lymph node the stellate shaped (1) with long cytoplasmic processes present antigens to B cells and transfer antiapoptotic signals to B lymphocytes with higher affinity binding antibodies.
- follicular dendritic cells (FDCs)
reactive hyperplasias
mostly B cell reactions (follicular), but also T cell (interfollicular) and macrophage (sinus histiocytosis)
follicular hyperplasia with plump pink macrophages in the interfollicular areas.
Toxoplasmosis
Circulating lymphocytes enter lymph nodes through the (1) of the (2) in the (3) of the lymph nodes.
- tall endothelial cells 2. postcapillary venules 3. paracortex
(1) lymphadenopathy tends to be rapid and painful
- benign
This is a mechanism for lymphocytes to produce tighter binding antibodies.
FDCs transfer antiapoptotic signals to B lymphocytes with higher affinity binding antibodies
Cat scratch disease has (1) hyperplasia and suppurative granulomas with (2).
- follicular 2. neutrophils and macrophages
The B cells develop in the (1) of humans
- bone marrow
lymph nodes associated with venereal and leg infections
inguinal lymph nodes
After activation and clonal expansion in germinal centers, B lymphocytes migrate to the B cell-dependent (1) of the lymph nodes to become (2) or to exit lymph nodes as (3)
- medullary cords
- Ig-secreting plasma cells
- memory B lymphocytes
CD8+ cells are activated by association with (1) HLA
suppressor/cytotoxic cells. Limit expansion of activated
B cells and stop their immune response
- class I
Lymph nodes that drain acute bacterial infections can have (1)
- suppurative (neutrophilic) or necrotizing lymphadenitis.
regional sites for the immune system to respond to microbes or other stimuli.
Lymph nodes
When activated by antigen and stimulated by an appropriate (1) cell, B cells develop into plasma cells that synthesize and export (2). At this stage, they no longer display (3) on the surface membrane
- T helper cell
- immunoglobulins
- heavy or light Ig chains
germinal center hyperplasia and multiple plasma cells within the medullary cords.
Follicular hyperplasia
plasma cells migrate to?
medullary cords
(1) lymphadenopathy tends to be slower and painless
- malignant
(1) look like plasma cells and are also seen in reactive disorders.
- Plasmacytoid lymphs
increased macrophages in the subcapsular and trabecular sinuses.
Sinus Histiocytosis
B lymphocytes travel to the (1) and T lymphs then travel predominantly to the deeper (2).
- germinal centers 2. paracortex
interfollicular or diffuse hyperplasias
T cell reactions
A well-defined mantle of (1) surrounds the follicles, sharply separating them from the interfollicular regions
- normal small B lymphocytes
macrophages containing erythrocytes and hemosiderin pigment in sinus histiocytosis
autoimmune hemolytic anemia
The T cells differentiate and mature in the (1) where self-reacting lymphocytes (2) or (3) by other mechanisms.
- thymus 2. apoptose 3. develop tolerance
numerous (1) line the subcapsular sinus
- macrophages
Where is metastatic cancer first seen and why?
subcapsular sinus of lymph because that’s where the lymph enters and the cancer cells are trapped there
Hyperplasia of secondary follicles (germinal centers) and plasmacytosis of medullary cords
Follicular hyperplasia
(1) patients can have interfollicular hyperplasia producing lymphadenopathy and can show focal or generalized (2) within the lymph nodes along with prominent (3)
- SLE 2. necrosis 3. immunoblasts.
The B cell precursors in the bone marrow have not undergone immunoglobulin heavy chain rearrangement but express precursor markers including (2), and express (3) in their nuclei.
- CD19, CD10 (also called CALLA-common ALL antigen 3. Terminal transferase (TdT)