Hypereosinophilic Syndrome: eMedicine Hematology

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Hypereosinophilic Syndrome: eMedicine Hematology

emedicine.medscape.com

Overview: Hypereosinophilic syndrome (HES) is a myeloproliferative disorder (MPD) characterized by persistent eosinophilia that is associated with damage to multiple organs.1, 2, 3, 4 Peripheral eosinophilia with tissue damage has been noted for approximately 80 years, ...

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Most Recently Shared on April 14, 2010 at 2:22 am By:

SusanS_Health Susan Scroggins

Hypereosinophilic syndrome is a myeloproliferative disorder involving chronic eosinophilia w/ damage to multiple organs.http://bit.ly/aolyWB

2 years ago...

Factor XI Deficiency: eMedicine Hematology

emedicine.medscape.com — “Overview: Factor XI (FXI) deficiency is an autosomal disorder that may be associated with bleeding. Other terms for this disorder include plasma thromboplastin antecedent (PTA) deficiency, Rosenthal syndrome, and hemophilia C. Rosenthal first described this bleeding disorder ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 9:25 pm By:

Health_SS Susan S Health Advocate

Factor XI (FXI) deficiency is an autosomal disorder that may be associated with bleeding. Learn more about factor XI. http://bit.ly/bQKYGS

2 years ago...

Immune Thrombocytopenic Purpura: eMedicine Hematology

emedicine.medscape.com — “Overview: Immune thrombocytopenic purpura (ITP) is a clinical syndrome in which a decreased number of circulating platelets (thrombocytopenia) manifests as a bleeding tendency, easy bruising (purpura), or extravasation of blood from capillaries into skin and mucous membranes ...View full resource at emedicine.medscape.com

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Most Recently Shared on May 17, 2010 at 6:45 pm By:

MedscapeOphtha Medscape Ophtha Health Site

Now available - Immune Thrombocytopenic Purpura: eMedicine Hematology - http://bit.ly/blTC8W

2 years ago...

Wiskott-Aldrich Syndrome: eMedicine Dermatology

emedicine.medscape.com — “Overview: Wiskott-Aldrich syndrome (WAS) is an X-linked recessive disorder originally described as a clinical triad of thrombocytopenia, eczema (atopiclike dermatitis), and recurrent pyogenic infections. Only 27% of patients have the classic triad, 20% of patients have hematologic ...View full resource at emedicine.medscape.com

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Most Recently Shared on April 21, 2010 at 11:40 pm By:

J_Bohlen Julie Bohlen Health Executive and Active Health Library

Wiskott-Aldrich syndrome is a rare condition that affects blood cells and immune system cells. Learn more. http://bit.ly/dxaGuq

2 years ago...

Dermatologic Manifestations of Hematologic Disease: eMedicine Dermatology

emedicine.medscape.com — “Overview: Coagulation Disorders Antiphospholipid syndromeAntiphospholipid syndrome (APS) is an acquired, multisystemic disorder characterized by recurrent thromboses in the arterial system, venous system, or both. Antiphospholipid syndrome is classified into 2 groups: primary and secondary.Secondary antiphospholipid syndrome is often associated ...View full resource at emedicine.medscape.com

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Most Recently Shared on April 20, 2010 at 9:11 pm By:

SusanS_Health Susan Scroggins Active Health Library and Health Advocate

Diseases of the blood can result in skin changes. Learn the dermatologic manifestions of hematologic disease. http://bit.ly/9qdLp2

2 years ago...

Hypereosinophilic Syndrome: eMedicine Dermatology

emedicine.medscape.com — “Overview: Hypereosinophilic syndrome (HES) encompasses a wide range of clinical manifestations sharing 3 features defined by Chusid et al1: (1) a peripheral eosinophil count of greater than 1.5 X 109/L for longer than 6 months; (2) ...View full resource at emedicine.medscape.com

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Most Recently Shared on February 3, 2010 at 3:02 pm By:

MedscapeDerm Medscape Dermatology Health Site

Rare associations with hypereosinophilic syndrome reported in newly updated article: http://bit.ly/dxtPgc

2 years ago...

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