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algorithm differential petechial hematology maculopapular management purpura activation anemia aplastic causes color dermatologic erythroderma fluidfilled general gpa granulomatosis macrophage mas
Generalized Algorithm for the Evaluation of Dermatologic Processes - Branches: Erythroderma Petechial Fluid-Filled Maculopapular #Diagnosis #Dermatology
Evaluation of Dermatologic ... : Erythroderma Petechial ... Maculopapular #Diagnosis ... #Dermatology #Rash ... Differential #General #Ddxof
Algorithm for Diagnosis of the Petechial / Purpuric Rash Febrile/Toxic, Palpable: - Meningococcaemia, Disseminated Gonococcal Infection,
Algorithm for Diagnosis ... / Purpuric Rash ... #Purpura #Rash ... #Algorithm #Diagnosis ... #Dermatology #Skin
Causes of Petechial Rash - Differential Diagnosis Algorithm Pinpoint areas (less than 2 mm) of hemorrhage, which
Diagnosis Algorithm ... • Fever • Toxic ... #Petechiae #Rash ... #Differential #Diagnosis ... Algorithm #Causes #dermatology
Petechiae/Purpura - Diagnostic Algorithm. Pathophysiology: 1) Represent the passage of erythrocytes from the intravascular to extravascular
Petechiae/Purpura ... - Diagnostic Algorithm ... #Dermatology #Rash ... #Petechiae #Purpura ... #Differential #Ddxof
Maculopapular - Diagnostic Algorithm Pathophysiology: - Catch-all term with a wide range of potential pathophysiologic mechanisms and causative
Maculopapular - Diagnostic ... erythroderma, petechiae ... New-onset fever with rash ... #Dermatology #Rash ... #Differential #Ddxof
Dermatologic Manifestations of Granulomatosis with Polyangiitis (GPA) Skin involvement in granulomatosis with polyangiitis (GPA) is common and
Skin Findings: • Petechiae ... Maculopapular rash ... Differential Diagnosis ... #rash #diagnosis ... #rheumatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Damage to Marrow (Toxic ... bleeding, and petechiae ... Anemia #oncology #hematology ... #diagnosis #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
mucosal bleeding (Petechial ... or purpuric rash ... Activation #Syndrome #Diagnosis ... #Management #Hematology ... #Rheumatology
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