Transient pancytopenia induced by parvovirus B19 in a child with hereditary spherocytosis

2000 ◽  
Vol 76 (4) ◽  
pp. 323-619 ◽  
Author(s):  
Elvis T. Valera ◽  
Rosana Cipolotti ◽  
José E. Bernardes ◽  
Rodolfo C. Pacagnella ◽  
Danielle M. Lima ◽  
...  
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19

Hemolytic crisis due to parvovirus B19 in hereditary spherocytosis in two siblings

2015 ◽  
Author(s):  
Meltem Erol ◽  
Ozlem Bostan Gayret ◽  
Ozgul Yigit ◽  
Mahir Tiras ◽  
Sultan Bent
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Hemolytic Crisis

scholarly journals Acute parvovirus B19 infection in identical twins unmasking previously unidentified hereditary spherocytosis

2014 ◽  
Vol 2014 (jul29 1) ◽  
pp. bcr2013202957-bcr2013202957 ◽  
Author(s):  
D. G. Forde ◽  
A. Cope ◽  
B. Stone
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Identical Twins ◽  
Parvovirus B19 Infection

scholarly journals An Adult with Aplastic Crisis induced by Human Parvovirus B19 as an Initial Presentation of Hereditary Spherocytosis

2005 ◽  
Vol 20 (1) ◽  
pp. 96 ◽  
Author(s):  
Sook Eui Oh ◽  
Jung Han Kim ◽  
Chi Hun Choi ◽  
Kwang Hyuk Park ◽  
Joo Young Jung ◽  
...  
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Initial Presentation ◽  
Human Parvovirus B19 ◽  
Aplastic Crisis

scholarly journals Clinical Case of Aplastic Crisis Associated with Extramedullary Hematopoiesis in an Adult With Hereditary Spherocytosis and Parvovirus B19 Infection

2015 ◽  
Vol 34 (1-2) ◽  
pp. 39-44
Author(s):  
Andreea Jercan ◽  
Rusu Munteanu Gina ◽  
Camelia Dobrea ◽  
Daniel Coriu ◽  
Aurelia Tatic
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Extramedullary Hematopoiesis ◽  
Blood Film ◽  
Red Cell Membrane ◽  
Infectious Episode ◽  
Indirect Bilirubin ◽  
Aplastic Crisis ◽  
Chronic Hemolysis ◽  
Parvovirus B19 Infection

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.

scholarly journals Transient aplastic crisis triggered by parvovirus B19 in a family with hereditary spherocytosis

IDCases ◽  
2020 ◽  
Vol 21 ◽  
pp. e00802
Author(s):  
Nicolas Cilla ◽  
Léa Domitien ◽  
Neila Arrada ◽  
Delphine Chiffre ◽  
Perrine Mahe ◽  
...  
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Aplastic Crisis ◽  
Transient Aplastic Crisis

Human parvovirus B19-induced transient pancytopenia in a child with hereditary spherocytosis

1988 ◽  
Vol 70 (1) ◽  
pp. 113-115 ◽  
Author(s):  
Takashi Hanada ◽  
Kazutoshi Koike ◽  
Tosiki Takeya ◽  
Toshiro Nagasawa ◽  
Yasuko Matsunaga ◽  
...  
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Human Parvovirus B19

scholarly journals Role of Surgical Intervention in Hereditary Spherocytosis with Haemolytic Anaemia, Splenomegaly and Jaundice

2021 ◽  
pp. 222-226
Author(s):  
K. Senthil Kumar ◽  
K. Abinaya ◽  
R. Anantharamakrishnan ◽  
K. Pranay
Keyword(s):  
Haemolytic Anaemia ◽  
Surgical Intervention ◽  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Folic Acid Deficiency ◽  
Acid Deficiency ◽  
Parvovirus B19 Infection ◽  
Current Infection ◽  
One Year

haemolytic anaemia, splenomegaly and jaundice, admitted in Chettinad hospital and research institute during one year period from  January 2019 to January 2020. Surgical intervention is indicated for selected patients with hereditary spherocytosis with haemolytic anaemia and jaundice to abate the hemolytic process after correction of anaemia with blood transfusion. Pigmented gallstones are seen in more than 50% cases for which incidence increases with severity of hemolysis and with age. Complications include aplastic anemia (most common after parvovirus B19 infection), haemolytic crisis during inter-current infection, megaloblastic crisis – during folic acid deficiency, cardiomyopathy, hematological malignancies.

Viral-associated haemophagocytosis and elevated serum TNF-α with parvovirus-B19-related pancytopenia in patients with hereditary spherocytosis

2008 ◽  
Vol 16 (2) ◽  
pp. 179-182 ◽  
Author(s):  
M. WATANABE ◽  
Y. SHIMAMOTO ◽  
M. YAMAGUCHI ◽  
S. INADA ◽  
S. MIYAZAKI ◽  
...  
Keyword(s):  
Hereditary Spherocytosis ◽  
Parvovirus B19 ◽  
Elevated Serum ◽  
Tnf Α
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