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佩-吉综合征中的癌症问题。

Cancer problem in Peutz-Jeghers syndrome.

作者信息

Taheri Diana, Afshar-Moghadam Noushin, Mahzoni Parvin, Eftekhari Amin, Hashemi Seyed Mozafar, Emami Mohammad Hasan, Fesharakizadeh Mehdi, Ghasemi-Basir Hamid Reza

机构信息

Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Adv Biomed Res. 2013 Mar 30;2:35. doi: 10.4103/2277-9175.109721. eCollection 2013.

Abstract

Peutz-Jeghers syndrome is a rare autosomal dominantly inherited condition, characterized by the presence of hamartomatous gastrointestinal polyps and mucocutaneous pigmentation. Patients with this syndrome can be associated with other neoplasms such as ovarian neoplasms known as sex-cord tumor with annular tubules that are associated in one third of the cases with this syndrome and other types of malignancies. We report a 42-year-old woman with a history of Peutz-Jeghers Syndrome and bilateral breast cancer that presented with abnormal uterine bleeding. Total abdominal hysterectomy with bilateral salpino-oophorectomy was done and an ovarian sex cord tumor with annular tubules was incidentally diagnosed. By reviewing literatures and in agreement with previous studies we suggest routine screening for malignancies in patients with Peutz-Jeghers syndrome.

摘要

黑斑息肉综合征是一种罕见的常染色体显性遗传疾病,其特征为存在错构瘤性胃肠道息肉和黏膜皮肤色素沉着。该综合征患者可能与其他肿瘤相关,如卵巢肿瘤,即环状小管性性索瘤,在三分之一的病例中与该综合征相关,以及其他类型的恶性肿瘤。我们报告一名42岁有黑斑息肉综合征病史且患有双侧乳腺癌的女性,她出现了异常子宫出血。进行了全腹子宫切除术及双侧输卵管卵巢切除术,术中偶然诊断出环状小管性卵巢性索瘤。通过文献回顾并与先前研究一致,我们建议对黑斑息肉综合征患者进行恶性肿瘤的常规筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/013c/3748667/3dc9414ffe8c/ABR-2-35-g001.jpg

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