17 results
Hypereosinophilia and Hypereosinophilic Syndrome

 • Secondary Hypereosinophilic Syndrome
 • Clinically Relevant HES Variants
 • When to
Clinically ... Diagnosis and Treatment ... Algorithm Matthew ... #HES #Hematology ... diagnosis #management #algorithm
Black Hairy Tongue- ...A polymicrobial wound infection developed, and she received treatment with intravenous meropenem and
and she received treatment ... within 1 week after treatment ... and has no long-term ... returned to its normal ... #NEJM #photo #clinical
Giant Cell Arteritis (GCA) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines
 • Visual Symptoms/Loss or
Vasculitis Management Algorithm ... followed by daily oral ... Vasculitis #Management #Treatment ... ACR2021 #Guidelines #algorithm ... #rheumatology
Tinea Capitis in a Newborn- A 3-week-old male newborn was brought to the pediatrician with three
after 1 week of treatment ... was treated with oral ... #clinical #photo ... #NEJM #tinea #capitis ... #ringworm #derm
Behçet's Syndrome
Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy
Epidemiology:
 • Young
Behçet's Syndrome ... association • M > F Clinical ... (Clinical Dx). ... Arthritis, AS Treatment ... signs #symptoms #rheumatology
Aplastic Anemia - Overview

Who?
• M = F
• 3 peaks:	1) Childhood	2) 15-25 years	3) >60 years

What?
• Aplastic anemia
Aplastic Anemia Clinical ... (MDS) (normal or ... megakaryocytes and a normal ... aplastic anemia Treatment ... Anemia #oncology #hematology
Schistocytes - The arrows point to schistocytes which are fragmented red blood cells. Also called schizocytes,
are one of the abnormal ... a more generic term ... In the right photo ... hemolytic- uremic syndromes ... #Clinical #Path
Giant cell arteritis (GCA)

Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
Diagnosis = clinical ... 50 in GCA, but normal ... in literature (NEJM ... Treatment of GCA ... them, but urgent rheumatology
SAPHO Syndrome Summary

What?
SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... Diagnosis: • A clinical ... and lower jaw Treatment ... palmoplantar pustulosis: oral ... #Rheumatology #
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
& Dry) is the treatment ... transitioning to oral ... acute coronary syndrome ... & Dry” is the treatment ... #differential #algorithm