[Chronic trichinosis and neuromuscular diseases. Morphologic and pathogenetic aspects].

F Gullotta, W Fröscher
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引用次数: 0

Abstract

Muscle biopsies were carried out on five patients affected by a chronic neuromuscular disorder, mostly in the form of a spinal muscle atrophy. All patients had suffered from acute trichinellosis many years before, the interval between acute parasitic infection and the appearance of the slowly progressive neuromuscular syndrome being of 21, 13, 35, 26 and 16 years respectively. In biopsy specimens, morphological and enzyme-histochemical changes typical of a progressive neurogenic muscular atrophy were present; in addition, encapsulated but still living, enzyme-positive parasites and signs of focal myositis were detected. The possible pathogenetic correlations between the "chronic" trichinellosis and the "degenerative" neuromuscular disorder are discussed.

慢性旋毛虫病和神经肌肉疾病。形态学和发病方面]。
对5名慢性神经肌肉疾病患者进行了肌肉活组织检查,主要表现为脊髓肌萎缩。所有患者多年前均患有急性旋毛虫病,从急性寄生虫感染到出现缓慢进展的神经肌肉综合征的时间分别为21、13、35、26和16年。在活检标本中,存在典型的进行性神经源性肌萎缩的形态学和酶组织化学变化;此外,还检测到包被但仍活的酶阳性寄生虫和局灶性肌炎的征象。讨论了“慢性”旋毛虫病与“退行性”神经肌肉疾病之间可能的发病关系。
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