D'costa Grace Francis, Agale Shubhangi Vinayak, Pandya Bhanumati Sumant, Surase Sanjay Gajanan
Department of Pathology, Grant Medical College, Mumbai.
Indian J Pathol Microbiol. 2007 Oct;50(4):768-70.
A 29 year female presented with epigastric pain with bilious vomiting since 1 1/2 years. This patient was diagnosed as a case of Peutz-Jegher's syndrome based on evidence of the characteristic mucocutaneous pigmentation which was present since birth and intestinal hamartomatous polyposis. There was an associated unilateral ovarian cystadenoma which is a rare association and which highlights the importance of a gynaecologic examination in female patients with Peutz-Jegher's syndrome.
一名29岁女性自1年半前开始出现上腹部疼痛并伴有胆汁性呕吐。根据自出生以来就存在的特征性黏膜皮肤色素沉着以及肠道错构瘤性息肉病的证据，该患者被诊断为佩-吉综合征。患者还伴有单侧卵巢囊腺瘤，这种情况较为罕见，凸显了对佩-吉综合征女性患者进行妇科检查的重要性。
