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佩-杰综合征:肿瘤形成风险增加。

Peutz-Jeghers syndrome: an increased risk of neoplasia.

作者信息

Leal A S, Leal C S, Gonzaga R A

出版信息

Arq Gastroenterol. 1986 Apr-Jun;23(2):104-7.

PMID:3566569
Abstract

A family with Peutz-Jeghers syndrome is reported, colonic involvement having been demonstrated on several affected members. Of the 50 members of the family about whom we could get informations, 21 had the characteristic cutaneous lesions (and usually had had some manifestation of the intestinal disease). Our first patient had a colonic carcinoma, and we could detect at least another colonic carcinoma in the family. A third attained member of the family was known to have died from "throat cancer". The most frequent clinical manifestations of this family patients are intussusception related abdominal crisis of colicky pain and rectorrhagy. In Peutz-Jeghers syndrome, there is a slight increase in the risk of malignancy, and digestive cancer can arise from coexistent adenomas, from cancerous changes of hamartomas, or "de novo", i.e., appear on previously normal mucosa.

摘要

报道了一个患有黑斑息肉综合征的家族,在几名患病成员中发现有结肠受累情况。在我们能够获取信息的该家族50名成员中,21人有特征性皮肤损害(且通常有肠道疾病的某些表现)。我们的首例患者患有结肠癌,并且我们在该家族中至少还检测到另外一例结肠癌。已知该家族的第三名成年成员死于“喉癌”。该家族患者最常见的临床表现是与肠套叠相关的腹部绞痛和便血。在黑斑息肉综合征中,恶性肿瘤风险略有增加,消化癌可源于并存的腺瘤、错构瘤的癌变或“新发”,即在先前正常的黏膜上出现。

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1
[Peutz-Jeghers syndrome. Cases at the Mannheim clinic over 25 years].
Langenbecks Arch Chir. 1995;380(1):43-52. doi: 10.1007/BF00184415.

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