Penegyres P K, Kakulas B A
Department of Neuropathology, Royal Perth Hospital, Western Australia.
Muscle Nerve. 1991 May;14(5):411-5. doi: 10.1002/mus.880140505.
To determine the natural history of minicore-multicore myopathy (MMM) we studied 5 patients who were found to have this disorder from 6 to 16 years ago. Four of these patients had improved muscle strength since their original assessment and one patient had deteriorated. There were no clinical electrophysiological or pathological features that distinguished this last patient from the others. We conclude, therefore, that most patients with MMM may be expected to improve as time passes but, for unknown reasons, a minority may deteriorate. This information should be helpful to clinicians in their prognostic advice to new patients.
为了确定微小核心-多核肌病(MMM)的自然病史,我们研究了5例在6至16年前被诊断患有这种疾病的患者。其中4例患者自最初评估以来肌肉力量有所改善,1例患者病情恶化。没有临床、电生理或病理特征能将最后这名患者与其他患者区分开来。因此,我们得出结论,大多数MMM患者可能会随着时间推移而改善,但出于未知原因,少数患者可能会恶化。这些信息应有助于临床医生为新患者提供预后建议。