Medich giant platelet disorder: a unique α granule deficiency I. Structural abnormalities

Abstract

Human platelet granule deficiency disorders include the gray platelet syndrome (GPS), α δ storage pool deficiency, the Hermansky–Pudlak syndrome and the White platelet syndrome. The present study describes a patient with a lifelong history of easy bleeding, thrombocytopenia and giant platelets. Her cells were found to have normal numbers of dense bodies, but a markedly decreased number of α granules. Many platelets had no α granules and resembled the gray platelets of patients with GPS. However, the empty vacuoles without granule contents that fill the cytoplasm of GPS platelets were not present in significant numbers in her platelets. In addition to the decrease in α granules the patients platelets contained membranous inclusions resembling cigars or scrolls. Usually, only one scroll open at each end was present, but many platelets contained two and some as many as five. Freeze-fracture revealed an absence of intramembranous particles in many layers of the scrolls. They occur in no other human platelet disorder, but are common in platelets from the Wistar–Furth rat. Thus, the patient is a unique variant of human platelet granule deficiency disorders unlike any described previously.