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失代偿性肺心病作为成人起病型肌病的首发表现。

Decompensated cor pulmonaleas the first manifestation of adult-onset myopathy.

作者信息

Kurz D, Aguzzi A, Scherer T A

机构信息

Department of Internal Medicine and Division of Pulmonary Diseases, Triemli City Hospital, Zurich, Switzerland.

出版信息

Respiration. 1998;65(4):317-9. doi: 10.1159/000029285.

Abstract

A 46-year-old white female was admitted for decompensated cor pulmonale (CP). It had not interfered with her daily activities and she had not experienced shortness of breath, fatigue or muscle weakness prior to the onset of right heart failure. A thorough investigation revealed severe generalized muscle weakness with restrictive chest bellows disease and secondary CP (mean pressure in the pulmonary artery 60 mm Hg). After having refused respiratory support the patient died a few days after admission. The muscle biopsy was consistent with adult-onset acid-maltase deficiency. This is a rare case of metabolic myopathy presenting as decompensated CP without previous symptoms of muscle weakness. This condition can easily be treated with nocturnal ventilatory support, improving the quality and length of life.

摘要

一名46岁的白人女性因失代偿性肺心病(CP)入院。在此之前,该病并未影响她的日常活动,在右心衰竭发作前,她也未曾经历过呼吸急促、疲劳或肌肉无力。全面检查发现严重的全身性肌肉无力,伴有限制性胸壁疾病和继发性CP(肺动脉平均压60毫米汞柱)。在拒绝呼吸支持后,患者入院几天后死亡。肌肉活检结果与成人起病型酸性麦芽糖酶缺乏症相符。这是一例罕见的代谢性肌病,表现为失代偿性CP,此前并无肌肉无力症状。这种情况可通过夜间通气支持轻松治疗,从而提高生活质量并延长寿命。

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