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Eosinophil Count
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Eosinophil Count
, Eosinophil, Eosinophilia
See Also
Complete Blood Count
Hypereosinophilic Syndrome
Eosinophilia-Myalgia Syndrome
Physiology
Maturation
Forms in
Bone Marrow
from
Myeloblast
s as with other
Granulocyte
s (
Basophil
s,
Neutrophil
s,
Monocyte
s)
Matures in
Bone Marrow
over 8 days
Moves to peripheral blood where it spends 8-12 hours
Moves to target tissue where it spends 1-2 weeks
Function: Response to Allergy and
Parasitic Infection
Responds to
Mast Cell
,
Basophil
chemotactic factors
Type 1 Hypersensitivity
Response - Late Phase (hours after exposure)
Phagocyte
(engulfs extracellular pathogens)
Parasite
(e.g.
Helminth
) response
Antigen Presenting Cell
Eosinophil granule contents (
Protein
s)
Antiparasitic Agent
s with tissue toxicity effect
Major Basic
Protein
(MBP)
Eosinophil Cationic
Protein
(ECP)
Eosinophil Peroxidase (EPO)
Neurotoxin
s
Eosinophil-Derived
Neurotoxin
(EDN)
Eosinophil Peroxidase (EPO) - also listed above
Markers of Eosinophil activity in
Asthma
Major Basic
Protein
(MBP) - also listed above
Eosinophil Cationic
Protein
(ECP) - also listed above
Other
Protein
s
Charcot-Leyden Crystals
Lysophosphatase
Cytokine
s
Surf
ace Receptors
IgE Receptors
IgE-
Antigen
complex binding results in Eosinophil activation and degranulation
IgG Receptors
Complement Receptors
Labs
Morphology on Blood Smear
Granulocyte
stains brightly with Eosin Stain (due to Major Basic
Protein
or MBP)
Bilobed nucleus
Diameter: 12-17 microns
Interpretation
Normal
Range: 1-4% of peripheral blood cells
Types
Eosinophilia
Familial Eosinophilia (Familial
Hypereosinophilic Syndrome
)
Rare autosomal condition (most
Hypereosinophilic Syndrome
s are not inherited)
Acquired
Primary Eosinophilia
Idiopathic
Hypereosinophilic Syndrome
(>1500 Eosinophils/uL x6 months without known cause)
Clonal Eosinophilia
Acute Myeloid Leukemia
and other malignancies (see below)
Secondary Eosinophilia
See below
Causes
Increased (Eosinophilia)
See
Hypereosinophilic Syndrome
Allergy
Allergic Rhinitis
Atopy
Asthma
Dermatologic Disorders
Pemphigus
Pemphigoid
Polyarteritis Nodosa
Parasitic or Tropical infection (esp. worm infestation)
Trichinosis
Aspergillosis
Hydatidosis
Angiostrongylus
Ascaris
lumbricoides
Capillariasis
Cysticercosis
Echinococcus
Fascioliasis
Filariasis
Gnat
hostomiasis
Paragonimiasis
Schistosomiasis
Strongyloidiasis
Toxocara
Trichuris trichiura
Bacterial Infection
Scarlet Fever
Leprosy
Viral Infection
Human Immunodeficiency Virus
(HIV)
West Nile Virus
Fungal Infection
Allergic Bronchopulmonary Aspergillosis
(
ABPA
)
Myeloproliferative disorders and other Malignancies (primary clonal Eosinophilia)
Chronic Myelogenous Leukemia
Hodgkin's Lymphoma
Non-Hodgkin's Lymphoma
Polycythemia Vera
Myelofibrosis
Collagen
-vascular diseases
Rheumatoid Arthritis
Periarteritis
Systemic Lupus Erythematosus
Eosinophilia-Myalgia Syndrome
Linked to L-
Tryptophan
and 5-Hydroxytryptophan (
5-HT
P) usage in 1989 (suspected contaminant)
Medications
Antibiotic
s
Ampicillin
Penicillin
Minocycline
Nitrofurantoin
Erythromycin
Sulfonamide
s
NSAID
S and antiinflammatory agents
Acetylsalicylic Acid
(
Aspirin
)
Ibuprofen
Naproxen
Methotrexate
Psychiatric Agents
Imipramine
Trazodone
Fluoxetine
(
Prozac
)
Miscellaneous
Chlorpropamide
(hypoglycemic agent)
Procarbazine
(
Chemotherapy
)
Miscellaneous
Radiation Therapy
Eosinophilic
Gastroenteritis
Sarcoidosis
Addison's Disease
Loffler's Syndrome
Evaluation
Eosinophilia (Eosinophils >500/mm3)
See
Leukocytosis
History and potential causes
Travel history
New medications
Diagnostics (consider)
Dermatitis biopsy (if present)
Consider allergy and immunology
Consultation
or testing
Consider
Parasite
testing (e.g. stool
Ova and Parasite
s)
References
Mahmoudi (2014)
Immunology
Made Ridiculously Simple, MedMaster, Miami, FL
Saiki in Friedman (1991) Medical Diagnosis, p. 227
Abramson (2000) Am Fam Physician 62(9):2053-60 [PubMed]
Riley (2015) Am Fam Physician 92(11):1004-11 [PubMed]
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