Results 201 to 210 of about 31,298 (246)
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Cytomegalovirus as a Cause of Pancytopenia
Leukemia and Lymphoma, 1996Human cytomegalovirus, HCMV, infects most of the population by adulthood; The primary infection is often accompanied by transient neutropenia and thrombocytopenia, and is followed by a period asymtomatic viral latency. In the setting of bone marrow transplantation, however, the immunosuppressed state of the recipient enables HCMV to re-activate or to ...
Graça Almeida-Porada
exaly +3 more sources
Levetiracetam-induced pancytopenia
Epilepsy & Behavior Case Reports, 2015 Pancytopenia is a rare side effect of levetiracetam (LEV) that is associated with severe morbidity that requires hospitalization. Here, we report a patient with a right temporoparietal tumor who underwent a temporal craniotomy with resection of the mass ...
Talal Alzahrani +2 more
exaly +3 more sources
British Journal of Haematology, 1979
Summary. Circulating T‐lymphocytes from a 13‐year‐old boy with autoimmune anaemia, severe neutropenia and thrombocytopenia inhibited autologous and normal homologous bone marrow myeloid colony formation in vitro. This inhibition was abolished when the patient's antithymocyte globulin and complement‐treated T‐lymphocytes were used.
G, Daneshbod-Skibba +3 more
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Summary. Circulating T‐lymphocytes from a 13‐year‐old boy with autoimmune anaemia, severe neutropenia and thrombocytopenia inhibited autologous and normal homologous bone marrow myeloid colony formation in vitro. This inhibition was abolished when the patient's antithymocyte globulin and complement‐treated T‐lymphocytes were used.
G, Daneshbod-Skibba +3 more
openaire +2 more sources
Journal of Psychopharmacology, 2006
Sodium valproate is a commonly used anticonvulsant, particularly in the management of childhood refractory epilepsy. There is a good literature base regarding its haematological effects in this group of patients including the potential for toxic effect on the bone marrow.
Keown P, McAllister-Williams H, Young A
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Sodium valproate is a commonly used anticonvulsant, particularly in the management of childhood refractory epilepsy. There is a good literature base regarding its haematological effects in this group of patients including the potential for toxic effect on the bone marrow.
Keown P, McAllister-Williams H, Young A
openaire +3 more sources
The American Journal of the Medical Sciences, 1999
There has been little systematic study of the clinical spectrum of pancytopenia, and the optimal diagnostic approach to pancytopenia remains undefined.The authors studied 134 hospitalized pancytopenic patients in Zimbabwe in both consecutive and nonconsecutive fashion.The most common cause of pancytopenia was megaloblastic anemia, followed by aplastic ...
D G, Savage +10 more
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There has been little systematic study of the clinical spectrum of pancytopenia, and the optimal diagnostic approach to pancytopenia remains undefined.The authors studied 134 hospitalized pancytopenic patients in Zimbabwe in both consecutive and nonconsecutive fashion.The most common cause of pancytopenia was megaloblastic anemia, followed by aplastic ...
D G, Savage +10 more
openaire +2 more sources
Annals of Internal Medicine, 1968
Abstract The unique occurrence of severe pancytopenia and splenomegaly in a young woman with brucellosis is reported.
E C, Lynch, J C, McKechnie, C P, Alfrey
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Abstract The unique occurrence of severe pancytopenia and splenomegaly in a young woman with brucellosis is reported.
E C, Lynch, J C, McKechnie, C P, Alfrey
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Posttransplantation and pancytopenia
Blood, 2012![Figure][1] A 33-year-old female with a history of a live related renal transplant on azathioprine and prednisolone and tacrolimus was asymptomatic until 3 years later when she developed low-grade fever, epigastric discomfort, and headache. She had hepatosplenomegaly but no lymphadenopathy.
Vikram, Narang, Updesh Singh, Sachdeva
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American Journal of Hematology, 1988
AbstractA case of thymoma associated with aplastic anemia is presented. Various therapeutic me dalities have been tried and a complete remission finally obtained by antithymocyte globulin.
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AbstractA case of thymoma associated with aplastic anemia is presented. Various therapeutic me dalities have been tried and a complete remission finally obtained by antithymocyte globulin.
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Dyskeratosis congenita with pancytopenia
Clinical and Experimental Dermatology, 1985Summary Dyskeratosis congenita is a rare inherited disorder characterized by skin pigmentation, nail dystrophy, leukoplakia and a variable number of additional features. This paper describes a patient who developed a serious manifestation, pancytopenia, as well as obliterated lacrimal puncta, gingivitis and loss of dermatoglyphics.
H J, Dodd, S, Devereux, I, Sarkany
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Journal of the American Veterinary Medical Association, 1970
SUMMARY Tropical canine pancytopenia (tcp) is a newly recognized disease of dogs in diverse tropical and subtropical areas. The disease has been responsible for the death of large numbers of military dogs in Southeast Asia. Unilateral or bilateral epistaxis is the most dramatic clinical sign of the disease.
D L, Huxsoll +3 more
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SUMMARY Tropical canine pancytopenia (tcp) is a newly recognized disease of dogs in diverse tropical and subtropical areas. The disease has been responsible for the death of large numbers of military dogs in Southeast Asia. Unilateral or bilateral epistaxis is the most dramatic clinical sign of the disease.
D L, Huxsoll +3 more
openaire +2 more sources