Kyriacou K, Michaelides Y, Senkus R, Simamonian K, Pavlides N, Antoniades L, Zambartas C
Department of Electron Microscopy and Molecular Pathology, Cyprus Institute of Neurology and Genetics (CING), Nicosia.
Ultrastruct Pathol. 2000 Mar-Apr;24(2):75-81. doi: 10.1080/01913120050118549.
Patients with beta-thalassaemia major frequently suffer from hypersiderosis which leads to hemochromatosis of major organs such as the heart and liver. Little information exists about the ultrastructural pathology of the human heart in beta-thalassaemia patients. Five Cypriot patients with elevated blood ferritin and intractable heart failure were investigated. Cardiac biopsies from these patients were studied by light and electron microscopy, as well as by X-ray microanalysis. Ultrastructural examination revealed the presence of disrupted myocytes showing loss of myofibers, dense nuclei, and a variable number of pleomorphic electron dense granules. These cytoplasmic granules or siderosomes consisted of iron-containing particles as confirmed by X-ray microanalysis. It is likely that the ultrastructural changes observed in myocytes of patients with beta-thalassaemia are largely due to iron deposition.
重型β地中海贫血患者常患有铁过载,进而导致心脏和肝脏等主要器官发生血色素沉着症。关于β地中海贫血患者心脏的超微结构病理学信息较少。对5名血铁蛋白升高且患有顽固性心力衰竭的塞浦路斯患者进行了研究。对这些患者的心脏活检组织进行了光镜、电镜检查以及X射线微分析。超微结构检查发现存在受损的心肌细胞,表现为肌纤维丧失、细胞核致密,以及数量不等的多形性电子致密颗粒。经X射线微分析证实,这些胞质颗粒或含铁小体由含铁颗粒组成。β地中海贫血患者心肌细胞中观察到的超微结构变化很可能主要是由于铁沉积所致。