Moirangthem G S, Nepram S S, Debnath K, Singh T D, Singh L D
Department of Gastrointestinal Surgery, Regional Institute of Medical Sciences, Imphal, India.
Int Surg. 2001 Oct-Dec;86(4):252-3.
Puetz-Jegher's syndrome is an autosomal dominant hereditary disease, which is characterized by hamartomatous polyposis and mucocutaneous pigmentation mainly over the circum-oral region. Patients with Peutz-Jeghers syndrome seek medical attention whenever there are complications such as intussusception, bleeding from the polyps, etc. Occasionally, gastrointestinal tract malignancies have been reported in Peutz-Jeghers syndrome. In this paper, we report a patient with Peutz-Jeghers syndrome who had multiple complications and polyposis involving the appendix, because involvement of the appendix is extremely rare in Peutz-Jeghers syndrome.
普茨-耶格综合征是一种常染色体显性遗传性疾病,其特征为错构瘤性息肉病以及主要在口周区域的皮肤黏膜色素沉着。普茨-耶格综合征患者每当出现诸如肠套叠、息肉出血等并发症时就会寻求医疗救治。偶尔,普茨-耶格综合征中也有胃肠道恶性肿瘤的报道。在本文中,我们报告了一名患有普茨-耶格综合征的患者,该患者有多种并发症且息肉病累及阑尾,因为阑尾受累在普茨-耶格综合征中极为罕见。