Extramedullary hematopoiesis in a child with hereditary spherocytosis: an uncommon cause of an adrenal mass

2001 ◽  
Vol 31 (12) ◽  
pp. 879-881 ◽  
Author(s):  
S. K. Calhoun ◽  
R. C. Murphy ◽  
N. Shariati ◽  
N. Jacir ◽  
K. Bergman
2014 ◽  
Vol 6 (5) ◽  
Author(s):  
Hossein Karami ◽  
Mehrnoush Kosaryan ◽  
Mehrdad Taghipour ◽  
Rayka Sharifian ◽  
Aili Aliasgharian

2020 ◽  
Vol 30 ◽  
pp. 101120 ◽  
Author(s):  
N.H. Kolev ◽  
P.P. Genov ◽  
V.R. Dunev ◽  
B.A. Stoykov

2015 ◽  
Vol 3 (2) ◽  
Author(s):  
Shahryar Zeighami ◽  
Seyed Ali Eslahi ◽  
Mohammad Mehdi Hosseini ◽  
Ali Ariafar ◽  
Sara Pakbaz ◽  
...  

1990 ◽  
Vol 35 (4) ◽  
pp. 263-265 ◽  
Author(s):  
Yves Bastion ◽  
Bertrand Coiffier ◽  
Pascale Felman ◽  
David Assouline ◽  
Jean-Dominique Tigaud ◽  
...  

2020 ◽  
Vol 6 (1) ◽  
pp. 030-032
Author(s):  
Elorza-Echaniz Garazi ◽  
Borda-Aguirrezabalaga Nerea ◽  
Aguirre-Allende Ignacio ◽  
Andres-Imaz Ainhoa ◽  
Bollo-Arocena Elisabet ◽  
...  

2015 ◽  
Vol 34 (1-2) ◽  
pp. 39-44
Author(s):  
Andreea Jercan ◽  
Rusu Munteanu Gina ◽  
Camelia Dobrea ◽  
Daniel Coriu ◽  
Aurelia Tatic

Abstract Hereditary spherocytosis is an inherited hemolytic anemia due to red cell membrane defects, characterised by chronic hemolysis with different severity degrees, splenomegaly and microspherocytosis on the peripheral blood film. Among the possible complications in these patients are aplastic crisis and extramedullary hematopoiesis. In this article we present the case of a 42 years old man with hereditary spherocytosis diagnosed during childhood (average haemoglobin (Hb) value of 11-12 g/dl), which presented with worsening anemia, fever, chills, bone and muscle pain. The evolution was with accentuation of anemia (Hb 4.2 g/dl), decease of reticulocyte number (Ret 0,8%) and bilirubin (indirect bilirubin 2.7 g/dl). ParvovirusB19 DNA was 100.000.000 copies/ml. A computer tomography (CT)scan was performed and showed extramedullary hematopoiesis areas situated paravertebraly in the inferior thorax and hepatosplenomegaly. The infectious episode was self-limited and improved with substitution treatment.


2010 ◽  
Vol 2010 ◽  
pp. 1-4 ◽  
Author(s):  
Juliana França Carvalho ◽  
Edson Marchiori ◽  
Gláucia Zanetti ◽  
Claudia Mauro Mano ◽  
Branca Sarcinelli-Luz ◽  
...  

Extramedullary hematopoiesis is characterized by the presence of hematopoietic tissue outside of the bone marrow and is typically associated with chronic hemolytic anemias. Intrathoracic extramedullary hematopoiesis is a rare and usually asymptomatic condition. The authors report a case of a 57-year-old man with intrathoracic extramedullary hematopoiesis and hereditary spherocytosis. Clinical and laboratory evaluation, together with radiological findings, are described. The diagnosis of the disease was confirmed by tissue biopsy.


2013 ◽  
Vol 46 (2) ◽  
pp. 156-158 ◽  
Author(s):  
Sang Yoon Yeom ◽  
Jae Hong Lim ◽  
Kook Nam Han ◽  
Chang Hyun Kang ◽  
In Kyu Park ◽  
...  

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