| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 1995;26:1463-1466.)
© 1995 American Heart Association, Inc.
Articles |
From the Acute Stroke Unit, Service of Neurology (A.A., J.B.M., M.O.) and Unit of Hematology and Oncology 1973 (C.B., P.A., L.F., J.S.-S.), Hospitals de Barcelona de L'Aliança, Barcelona, Spain.
Background Ischemic stroke as a presenting sign of essential thrombocythemia has been infrequently reported. We describe six patients in whom cerebrovascular disease was the first manifestation of this myeloproliferative disease. A positive endogenous megakaryocyte and/or erythroid colony growth from blood was a diagnostic criterion of essential thrombocythemia in patients with platelets counts lower than 600x109/L.
Case Descriptions These six patients represented 0.54% of all patients with first stroke, 42.8% of all hematologic disorders associated with stroke, and 12.5% of all patients with essential thrombocythemia diagnosed from 1986 to 1992 at our institution. Eleven acute cerebrovascular accidents (6 transient ischemic attacks, 5 definitive cerebral infarcts) were registered. Mean time from ischemic stroke to diagnosis of essential thrombocythemia was 4.5 months (range, 1 to 12 months). The mean platelet count was 597x109/L (range, 414 to 760x109/L). Four patients had platelets counts lower than 600x109/L. All patients had circulating erythroid progenitors, megakaryocytic progenitors, or both.
Conclusions Ischemic stroke as a presenting manifestation of essential thrombocythemia is probably underrecognized. The diagnosis of thrombocythemia should not be excluded on the basis of platelet counts lower than 600x109/L. The availability of in vitro culture of hematopoietic progenitors from peripheral blood makes it possible to diagnose early and atypical cases.
Key Words: cerebral ischemia myeloproliferative disorders diagnosis thrombocythemia, hemorrhagic
This article has been cited by other articles:
![]() |
L. I. Kornblihtt, S. Cocorullo, C. Miranda, P. Lylyk, P. G. Heller, and F. C. Molinas Moyamoya Syndrome in an Adolescent With Essential Thrombocythemia: Successful Intracranial Carotid Stent Placement Stroke, August 1, 2005; 36(8): e71 - e73. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Spivak Polycythemia vera: myths, mechanisms, and management Blood, December 15, 2002; 100(13): 4272 - 4290. [Full Text] [PDF] |
||||
![]() |
F. Bernaudin, S. Verlhac, F. Freard, F. Roudot-Thoraval, M. Benkerrou, I. Thuret, R. Mardini, J.P. Vannier, E. Ploix, M. Romero, et al. Multicenter Prospective Study of Children With Sickle Cell Disease: Radiographic and Psychometric Correlation J Child Neurol, May 1, 2000; 15(5): 333 - 343. [Abstract] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1995 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |