ch 11 pt 6 Flashcards
phagocytic stem cell (macrophages, dendritic cells) that can form a benign or malignant neoplasm
-can be unisystem (bone marrow erosion) or multisystem
histiocyte (histiocytic neoplasm)
“tennis racket” organelles found with langerhans cell histiocytosis of the epidermis
birbeck granules
____ langerhans cell histiocytosis occurs in kids
multisystem
disseminated intravascular coagulation immune thrombocytopenia purpura von willebrand disease hemophilia a and b -- are all \_\_\_ disorders
bleeding
widspread thrombi/clots from sepsis, endothelial injury from sle/stroke, or severe tissue injury like MVA or occupational
disseminated intravascular coagulation
disseminated intravascular coagulation tx is either __ or ___, as it can either cause excessive clotting or excessive bleeding
anti coagulants
coagulants
general term with decreased cell number
thrombocytopenia
with thrombocytopenia, increased ____ bleeding shows around 20k-50k cells, while increased ____ bleeding shows
post-traumatic
spontaneous
bleeding d/o in which antibodies attack platelet membranes and cause red/purple skin discoloration
ITP (immune thrombocytopenic purpura)
___ ITP is in children 2* to viral infx and is self limiting while ___ ITP is in F 20-40, insidious and from ADRs, lymphoma, or idiopathic
acute
chronic
MC inherited bleeding d/o that affects 1% of US, presents with bleeding gums, easy bruising
von willebrand disease
von willebrand disease occurs due to decreased or lacking _____ which causes dysfunctional platelet adherence to vessel wall
vWF (von willebrand factor)
hemophilia A and B are both x linked recessive mc in males, but A is due to mutated coagulation factor ___ while less common B is due to mutated coagulation factor ___
VIII
IX
hemophilia A and B tx involves ___ of their respective coagulation factors (VIII and IX respectively)
infusion
___ ___ occurs in pt with myasthenia gravis, SLE, RA, and is due to reactive b cells within the THYMUS
thymic hyperplasia