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hematology clinical acromegaly common endocrinology gangrenosum hemeonc hemophagocytic hemophilia hlh hypogammaglobulinemia immunodeficiency immunology lymphohistiocytosis pathophysiology pg pyoderma rash rheumatology sjogrens
Secondary Syphilis Rash Secondary syphilis is the most contagious of all the stages of this disease, and
characterized by a systemic ... resembling rashes caused ... #Rash #Diagnosis ... #Clinical #Photo ... #Dermatology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
infection risk secondary ... hemolytic anemia) • Systemic ... and M panel Management ... DDX - Other causes ... #diagnosis #management
Hemophilia - Diagnosis and Management Diagnosis: • Consistent bleeding history (unless screening for disease in family members
normal in mild cases ... activity Mild: Local ... Avoid meds that ... #Management #treatment ... #hematology
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
paresthesias (carpal ... Mortality due to CVD ... Acromegaly occurs secondary ... or refractory cases ... #Treatment #Pathophysiology
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
lacrimal glands: • Focal ... other diseases • Secondary ... Hypocomplementemia • Can cause ... Adenocarcinoma Treatment ... #Management
Pyoderma Gangrenosum (PG) 50 M Crohn’s dz had a small pustule on the ankle 4 mo ago
Diagnosis? ... Management of PG ... treatment options ... #PG #clinical #photo ... #dermatology #ulcer
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
recognition and management ... hyperinflammatory syndrome caused ... of the immune system ... STX11, STXBP2 • Secondary ... #Management #Hematology
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