We studied the platelets of 8 patients with myelodysplasia aged 49-77
years, using both ultrastructural and functional techniques. Five of t
he 8 patients were classified as having refractory anaemia, and 3 as r
efractory anaemia with excess of blasts (RAEB). Electron microscopical
ly, the myelodysplastic patients had in addition to normal ones, plate
lets containing significantly less ct-granules. In part of these hypog
ranular platelets, the dense tubular system was abundant, but in contr
ast with normal platelets, it was not dispersed between the other orga
nelles, nor did it form a membrane complex with the open cannalicular
system. From a functional point of view, collagen-induced shape change
was the most frequently disturbed parameter: there was a total loss o
f collagen-induced shape change in 5 patients. In 2 patients, there wa
s a complete lack of response to collagen in platelet-rich plasma (bot
h shape change and aggregation); in one of them, there was also a tota
l loss of adenosine triphosphate secretion in response to all inducers
tested. After 4 years of follow-up, 5 patients had died, of whom 3 we
re RAEB patients. An initial complete absence of collagen-induced shap
e change was found in these 5 patients, while in the 3 patients who we
re still alive at the end of the follow-up period, collagen-induced sh
ape change was normal in 2 and slightly diminished in one.