Secondary Hemophagocytic Syndrome: The Importance of Clinical Suspicion
Hemophagocytic syndrome is a rare and potentially fatal disorder characterized by pathological immune activation associated with a primary familial disorder, genetic mutations, or occurring as a sporadic condition. The latter can be secondary to infections, malignancies, or autoimmune diseases. Clin...
Saved in:
Main Authors: | Cristina Oliveira, Sérgio Chacim, Isabel Ferreira, Nelson Domingues, José Mário Mariz |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2014-01-01
|
Series: | Case Reports in Hematology |
Online Access: | http://dx.doi.org/10.1155/2014/958425 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia
by: Nura El-Haj, et al.
Published: (2014-01-01) -
Perianal abscess with secondary hemophagocytic syndrome: Report of a rare case and literature review
by: Jiaxin Guo, et al.
Published: (2025-02-01) -
HAV Infection Associated with Hemophagocytic Syndrome
by: H. Aamri, et al.
Published: (2023-01-01) -
From Incidentaloma to Suspicion of Malignancy: The Diverse Clinical Presentation of Gonadal Schistosomiasis mansoni
by: Laiana do Carmo Almeida, et al.
Published: (2013-01-01) -
Hematological and biochemical variables in hospitalized patients with clinical suspicion of dengue
by: Rolando Rodríguez Puga, et al.
Published: (2025-01-01)