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恶性假性贲门失弛缓症的临床表现与评估

Clinical presentation and evaluation of malignant pseudoachalasia.

作者信息

Moonka R, Patti M G, Feo C V, Arcerito M, De Pinto M, Horgan S, Pellegrini C A

机构信息

Department of Surgery, Seattle Veterans Affairs Medical Center and the University of Washington Medical Center, Seattle, WA, USA.

出版信息

J Gastrointest Surg. 1999 Sep-Oct;3(5):456-61. doi: 10.1016/s1091-255x(99)80097-3.

Abstract

Malignant pseudoachalasia can be indistinguishable from primary achalasia on routine clinical evaluation, often resulting in a delay in diagnosis. To better define the clinical features and appropriate management of this disease, the course of five patients discovered to have pseudoachalasia after being referred for a minimally invasive Heller myotomy was reviewed, as were 67 cases of pseudoachalasia previously reported in the literature. Patients with an occult malignancy tended to present with shorter durations of symptoms, greater weight loss, and at a more advanced age than patients with primary achalasia. Since contrast radiography and endoscopy frequently failed to differentiate these two diseases, persons with presumed achalasia meeting these criteria who are referred for minimally invasive surgery should undergo additional imaging to rule out an occult malignancy, since this condition cannot be reliably detected during the course of a thoracoscopic or laparoscopic esophagomyotomy.

摘要

在常规临床评估中,恶性假性贲门失弛缓症可能与原发性贲门失弛缓症难以区分,这常常导致诊断延迟。为了更好地明确这种疾病的临床特征和恰当治疗方法,我们回顾了5例在接受微创Heller肌切开术后被发现患有假性贲门失弛缓症患者的病程,以及文献中先前报道的67例假性贲门失弛缓症病例。与原发性贲门失弛缓症患者相比,隐匿性恶性肿瘤患者的症状持续时间往往更短,体重减轻更明显,且发病年龄更大。由于对比造影和内镜检查常常无法区分这两种疾病,因此,因疑似贲门失弛缓症而被转诊接受微创手术且符合这些标准的患者,应进行额外的影像学检查以排除隐匿性恶性肿瘤,因为在胸腔镜或腹腔镜食管肌切开术中无法可靠地检测出这种情况。

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