Georgacopulo P, Azzolini P, Franchella A, Riccipetitoni G
Minerva Med. 1981 Dec 8;72(49):3309-14.
Megacolon must be considered as a diagnosis in any case of intractable constipation also in the adult. Besides the Hirschsprung's disease and the idiopathic megacolon, which have no apparent organic cause, many other pathologic conditions may produce a marked dilatation of the large bowel. The differential diagnosis depends, after a valuation of the clinical and radiologic features, also from enzymatic, histologic and functional tests. The Hirschsprung's disease can be observed after the infancy in: 1) Patients in whom diagnosis is made only in adult age; 2) Patients with a diagnosis made in infancy or childhood, with moderate symptoms, treated with a conservative methods, who are getting worse; 3) Adult relapsers after a previous inadequate operation. Group II also includes the patients who need an emergency operation, because of a perforation or a volvolus of a dilatated loop. We report three cases of adult Hirschsprung's disease and two adult "idiopathic megacolon". The patients with aganglionic megacolon were admitted to our Hospital respectively for an abdominal palpable mass, a volvolus and incontinence. The two patients with idiopathic megacolon showed the same clinical picture of those with Hirschsprung's disease. We choose a surgical therapy in all five patients, with good long-term results.
在任何难治性便秘病例中,即使是成人,也必须考虑巨结肠的诊断。除了无明显器质性病因的先天性巨结肠和特发性巨结肠外,许多其他病理状况也可能导致大肠明显扩张。在评估临床和放射学特征后,鉴别诊断还取决于酶学、组织学和功能检查。先天性巨结肠可在婴儿期后出现于以下情况:1)仅在成年期才确诊的患者;2)婴儿期或儿童期确诊、症状较轻、采用保守方法治疗但病情恶化的患者;3)先前手术不充分后复发的成人患者。第二组还包括因扩张肠袢穿孔或扭转而需要紧急手术的患者。我们报告了3例成人先天性巨结肠病例和2例成人“特发性巨结肠”病例。无神经节巨结肠患者分别因腹部可触及肿块、肠扭转和大便失禁入住我院。两名特发性巨结肠患者表现出与先天性巨结肠患者相同的临床症状。我们对所有5例患者均采用了手术治疗,长期效果良好。