19 results
Kawasaki Disease - Clinical Criteria #Diagnosis #Peds #Pediatrics #Kawasaki #Disease #Manifestations #Criteria #ALiEM
Kawasaki Disease ... - Clinical Criteria ... #Diagnosis #Peds ... #Pediatrics #Kawasaki ... #Criteria #ALiEM
Causes of Pediatric Constipation - Differential Diagnosis Algorithm
Dietary / Functional:
 • Insufficient Volume / Bulk
Neurologic:
 •
Causes of Pediatric ... Hirschsprung's Disease ... Withholding • Painful (e.g ... Algorithm #Causes #Peds ... #Pediatrics
Clinical diagnosis of Alcoholic Hepatitis (AH)
 • Onset of jaundice within prior 8 weeks
 • Ongoing
Clinical diagnosis ... Alcoholic Hepatitis (AH ... (Wilson disease ... Alcoholic #Hepatitis #AH ... #hepatology #criteria
Pediatric Constipation - Differential Diagnosis Algorithm
Dietary/Functional
 • lnsufficient Volume / Bulk
Neurologic
 • Hirschsprung's Disease
 • Imperforate
Pediatric Constipation ... Volume / Bulk Neurologic ... Hirschsprung's Disease ... Withholding • Painful (e.g ... Algorithm #Causes #Peds
THE LIMPING OR NON-WEIGHT BEARING CHILD PATHWAY

RED FLAGS - In all cases there are specific
markers which
suspicion of severe disease ... splenomegaly, abnormal neurology ... Rheumatology ... Pathway #Child #Peds ... #Pediatrics #Diagnosis
Behcet's Syndrome - Diagnosis
Diagnostic Criteria for Behget's Syndrome (International Study Group for Behget's Disease):
 • Recurrent,
Diagnosis Diagnostic Criteria ... the following 4 criteria ... test Most Common Clinical ... #Diagnosis #criteria ... #rheumatology
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... if they have no clinical ... #Diagnosis #Peds ... #Pediatrics #Kawasaki ... #Disease #Incomplete
Diagnosis of IgA Vasculitis (Henoch-Schönlein Purpura) - French Vasculitis Study Group 

1) Suggestive clinical manifestations
1) Suggestive clinical ... individuals - Clinical ... - Systemic disease ... HSP #Diagnosis #Rheumatology ... #Peds #Pediatrics
Macrophage Activation Syndrome (MAS)
Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH)

What?
A subset of
fever syndromes Clinical ... Fever is the main clinical ... • Infection (eg ... Histopathologic criteria ... #Rheumatology
IGG-4 RELATED DISEASE

WHAT?
 • A chronic, immune-mediated fibroinflammatory disease with tumefactive infiltration of IgG4+ plasma cells
specific) COMMON CLINICAL ... • Essential Criteria ... : Clinical/radiologic ... 2019 ACR/EULAR Criteria ... Diagnosis #Management #Rheumatology