Myotonic dystrophy type 1 and pseudo-obstruction in a child with smooth muscle α-actin deficiency and eosinophilic myenteric plexitis.

Gloria Pelizzo, Valeria Calcaterra, Vincenzo Villanacci, Giovanni Battista Mura, Gabrio Bassotti
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引用次数: 5

Abstract

Myotonic dystrophy (MD) frequently involves the gastrointestinal tract, where it can manifest as chronic intestinal pseudo-obstruction (CIPO), particularly in adults. This manifestation is quite uncommon in children. We report the case of a 12-year-old boy with MD type 1 and CIPO, in which a pathologic assessment revealed an association with smooth muscle α-actin deficiency in the external muscular layer of the ileum, and with features of eosinophilic plexitis and eosinophilic muscle infiltration in the colon. In this peculiar case, the clinical aspects of CIPO might have been due to the involvement of several neuromuscular mechanisms.

Abstract Image

Abstract Image

平滑肌α-肌动蛋白缺乏和嗜酸性肌丛炎患儿的1型强直性肌营养不良和假性梗阻。
肌强直性营养不良(MD)常累及胃肠道,表现为慢性肠假性梗阻(CIPO),尤其是成人。这种表现在儿童中很少见。我们报告一例12岁的MD 1型男孩和CIPO,病理评估显示其与回肠外肌层平滑肌α-肌动蛋白缺乏有关,并伴有嗜酸性神经丛炎和结肠嗜酸性肌肉浸润。在这个特殊的病例中,CIPO的临床表现可能是由于几个神经肌肉机制的参与。
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