593 results
diagnosis hematology differential algorithm management causes liver anemia treatment cirrhosis pathophysiology clinical workup oncology syndrome thrombocytopenia gastroenterology anticoagulation table pharmacology
Hepatomegaly - Differential Diagnosis Algorithm Malignant • Primary Carcinoma • Metastases • Lymphoma • Leukemia • Polycythemia
Hepatomegaly - Differential ... Cirrhosis #Hepatomegaly ... Algorithm #Causes #Hepatology
Hepatobiliary Manifestations of Sickle Cell Disease Acute sickle cell hepatic crisis: • Fever, acute onset RUQ pain,
jaundice and tender hepatomegaly ... onset RUQ pain, hepatomegaly ... Hepatobiliary #hepatology
Primary Biliary Cirrhosis - Diagnosis Algorithm Symptoms: Fatigue, Pruritus, Right upper quadrant discomfort Signs: Jaundice, Xanthelasmata, Hepatomegaly Associated history:
Xanthelasmata, Hepatomegaly ... Diagnosis #Algorithm #hepatology
Causes of Hepatomegaly and Splenomegaly in children #Hepatomegaly #Splenomegaly #Hepatosplenomegaly #HSM #Differential #Causes #Peds #Pediatrics
Causes of Hepatomegaly ... in children #Hepatomegaly
Approach to Leukocytosis - Differential Diagnosis Algorithm Features of hematologic malignancy: • Symptoms: B-symptoms, bruising/bleeding, fatigue/weakness, immunosuppression
splenomegaly, hepatomegaly ... Diagnosis #Algorithm #hematology
Right Sided Heart Failure Mnemonic: "AW HEAD" ANOREXIA & NAUSEA WEIGHT GAIN HEPATOMEGALY EDEMA (BIPEDAL) ASCITES DISTENDED
WEIGHT GAIN HEPATOMEGALY
Hemophagocytic Lymphohistiocytosis (HLH) Clinical Features: Fever, Splenomegaly, Hepatomegaly, Lymphadenopathy, Confusion Classic lab findings in HLH: ↑↑ ferritin, Anemia,
Splenomegaly, Hepatomegaly ... Lymphohistiocytosis #diagnosis #hematology
THE LIMPING OR NON-WEIGHT BEARING CHILD PATHWAY RED FLAGS - In all cases there are specific markers which
lymphadenopathy, hepatomegaly ... neurology, back pain Haematology
Clinical Features and Complications of β-thalassaemia Major - Pallor - Jaundice - Bossing of the skull
Splenomegaly and hepatomegaly
Gaucher Disease Pathophsiology • Lysosomal storage disorder • Deficiency of ß-glucocerebrosidase • Accumulation of glucosylceramide in macrophages Diagnosis
Splenomegaly > 90% • Hepatomegaly
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