17 results
hematology differential management oncology classification erythema reactions vasculitis aafp agep aids algorithm anemia aplastic clinical cryofibrinogenemia dermatologic exanthematous generalized gpa
Causes of Erythema Nodosum - Mnemonic NO cause found in 60% of cases Drugs (antibiotics e.g., sulfonamides, amoxicillin) Oral
Nodosum - Mnemonic ... Drugs (antibiotics ... HepB, HepC Bacterial ... #Differential #Diagnosis ... #Dermatology #SkinRash
Causes of Erythema Nodosum Common - Idiopathic (up to 55 percent) - Infections: streptococcal pharyngitis (28 to
Causes of Erythema ... Nodosum Common ... to 10 percent): antibiotics ... - Bacterial ... #Diagnosis #Clinical
Causes of Isolated Neutropenia - Differential Diagnosis Algorithm Congenital Medications • Anticonvulsants • Antibiotics • Antithyroid • Antihypertensive
Causes of Isolated ... - Differential Diagnosis ... Anticonvulsants • Antibiotics ... • Epstein-Barr Virus ... #Hematology
Blood Product Transfusions One Pager Summary Type and screen - determines blood type and detects in recipient
Blood Product Transfusions ... Blood products contain ... - Bacterial ... #diagnosis #management ... #hematology #reactions
Blood Transfusion Reactions Immune Mediated: • Febrile Non-Hemolytic Transfusion Reaction (FNHTR): Most common immune reaction to transfusion.
Blood products contain ... very rare), or bacterial ... • Bacterial contamination ... #diagnosis #management ... #hematology #reactions
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
of fibrin split products ... which can plug blood ... cryoglobulins • Negative causes ... #rheumatology # ... hematology
Dermatologic Manifestations of Granulomatosis with Polyangiitis (GPA) Skin involvement in granulomatosis with polyangiitis (GPA) is common and
GPA causes disease ... Polyarteritis nodosa ... vasculitis (inflamed blood ... #rash #diagnosis ... #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Phagocytosis of blood ... Infections+++: Virus ... CMV, HHV8,...), Bacteria ... Drugs, Unknown cause ... treatment #summary #rheumatology
TTP - Laboratory Evaluation for Thrombotic Thrombocytopenic Purpura Activity of von Willebrand factor-cleaving protease activity - A
activity is the diagnostic ... available for rapid diagnosis ... Fibrin degradation products ... of Peripheral blood ... #Workup #Hematology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
and petechiae Causes ... - β-lactam antibiotics ... result from low blood ... Anemia #oncology #hematology ... #diagnosis #management
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