1859 results
Skin Hypopigmentation - Differential Diagnosis Algorithm

Diffuse Congenital - Generalized hypopigmentation of hair, eyes, skin
 • Phenylketonuria
Differential Diagnosis Algorithm ... versicolor (can also be hyperpigmented ... Differential #Diagnosis #Algorithm
Causes of Anemia with elevated Mean Corpuscular Volume (MCV) - Differential Diagnosis Algorithm
Normal Blood Smear
 •
Differential Diagnosis Algorithm ... Oval Macrocytes, Hypersegmented ... Differential #Diagnosis #Algorithm
Adrenal Insufficiency Diagnosis Algorithm
Clinical features: 
 - Weight loss, anorexia, Weakness, fatigue, GI distress
 - Hypotension,
Insufficiency Diagnosis Algorithm ... orthostasis - Hyperpigmented ... findings (see algorithm ... Insufficiency #Diagnosis #Algorithm
Disorders of Pigmentations - Hypopigmentation and Hyperpigmentation - Differential Diagnosis Algorithm

HYPOPIGMENTATION
Diffuse Congenital - Generalized hypopigmentation of
Differential Diagnosis Algorithm ... versicolor (can also be hyperpigmented ... Differential #Diagnosis #Algorithm
Hypersegmented neutrophil in a case of acute myeloid leukemia.

Dysplastic neutrophils are typically hypolobated but can be
Hypersegmented neutrophil ... hypolobated but can be hypersegmented ... oncopathmmb #Hypersegmented
Megaloblastic Anemia vs Normal Peripheral Smear

#Megaloblastic #Anemia #Peripheral #Smear #Comparison #Clinical #Hypersegmented #Neutrophil
Comparison #Clinical #Hypersegmented
Signs of Graves disease: 
• Goiter 
• Periorbital edema 
• Non-pitting edema causing hyperpigmented plaques 
•
edema causing hyperpigmented
General Algorithms for Assessment of the Left Ventricular Assist Device (LVAD) (Algorithms 1, 2 and 3)

Algorithm
General Algorithms ... Device (LVAD) (Algorithms ... 1, 2 and 3) Algorithm ... LVAD) Patient Algorithm ... troubleshooting Algorithm
Combination of Skin Findings and Arthritis in Pediatrics Patient - Differential Diagnosis
Malar rash: 
 • A
erythematous or hyperpigmented ... Target sign with hyperpigmented
Peutz–Jeghers Syndrome
An autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the
gastrointestinal tract and hyperpigmented