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diagnosis management oncology rheumatology workup algorithm anemia aplastic complications damage exposure hemophagocytic hlh lymphohistiocytosis manifestations plasmacytoma pmr polymyalgia rheumatica sicklecell
Algorithm for the Evaluation and Management of Sickle Cell Crises Clinical Manifestations and Management #Diagnosis #Management #Hematology #SickleCell
Algorithm for the Evaluation ... Management of Sickle Cell ... Crises Clinical ... Diagnosis #Management #Hematology ... Workup #Algorithm #Ddxof
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
accumulation of clinical ... Assessment • Clinical ... Treatment: • ... inhibitors under evaluation ... #summary #rheumatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia Clinical ... and petechiae Causes ... Physical Agents: - Radiation ... aplastic anemia Treatment ... Anemia #oncology #hematology
A quick infographic on the importance of sun protection and the various results of sun damage
#wavelengths #causes ... #diagnosis #dermatology ... occupational disease evaluation ... Mechanisms and treatments ... damage in skin cells
Polymyalgia Rheumatica (PMR) Diagnosis and Management Summary WHAT? • Polymyalgia rheumatica (PMR) is a common systemic inflammatory
and Management Summary ... disease of unknown cause ... • An evaluation ... for giant cell ... TREATMENT: • The
Solitary Cell Plasmacytoma What? • Plasma cell neoplasms can present as a single lesion (solitary plasmacytoma) • In 3%
plasmacytoma) Clinical ... Diagnostic Evaluation ... Bone marrow Treatment ... (RT): Radiation ... Diagnosis #Workup #Hematology
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