2023年4月10日 · Peutz-Jeghers polyp is a hamartomatous polyp associated with Peutz-Jeghers syndrome that is characterized by papillary architecture with arborizing compact bundles of smooth muscle

2023年7月26日 · Peutz-Jeghers syndrome (PJS) is a condition that causes polyps to form inside your body and dark-colored spots to appear on your face, hands, feet and elsewhere. Both the polyps and the spots are benign (noncancerous). Still, having PJS substantially increases your cancer risk. Cleveland Clinic is a non-profit academic medical center.

2018年4月25日 · Peutz-Jeghers polyp, abbreviated PJP, is an uncommon hamartomous gastrointestinal polyp. It is usually associated with Peutz-Jeghers syndrome. Features: [1] [2] Peutz-Jeghers syndrome is autosomal dominant. Altered gene: STK11. Features: [3] Melanocytic macules. Lips, buccal mucosa, and digits. Multiple Peutz-Jeghers polyps.

PJS 主要以兩方面來表現症狀,包括皮膚黏膜黑色素沉著以及腸胃道多發性息肉( 缺陷瘤)。 1. 皮膚黏膜黑色素沉著: 肛門周圍。 黑色素沈著通常在出生後的第一年到第二年內發生,隨著年齡增長,斑點的大小和數量會. 增加,顏色也會漸漸變深成為黑色斑點,直到青春期後可能逐漸消退,除了頰部黏膜上的斑點。 PJS. 的皮膚黏膜黑色素沉著可能會被誤認為雀斑(ephelides)。 然而,與PJS的斑點不同的是,雀斑通常在. 鼻孔和嘴附近較稀疏,出生時並不存在,並且不會出現在頰部黏膜上。 ( 圖二. 圖 …

2023年7月17日 · Juvenile polyposis (JPS) is an autosomal dominant inherited condition that presents with hamartomatous polyps of the small intestine due to mutations in the BMPR1A, SMAD4, or ENG genes; however, dermatological findings of PJS are not appreciated.

波伊茨-耶格综合征[1] （Peutz–Jeghers syndrome，PJS）又译 珀茨－傑格斯症候群，意译为 色素沉着-息肉综合征 、 黑斑息肉综合征 、 黑斑息肉病 （pigment spot polyposis），是一种家族性黏膜皮肤色素沉着并胃肠道息肉病，属 常染色体 显性 遗传疾病；主要表现为面部、口唇周围皮肤和颊黏膜的色素沉着，以及胃肠道多发性 错构瘤 性息肉；内镜下可见大小及形态不一的息肉，小肠最多见，结肠次之 [2]:857，每25,000至300,000人中大概有1人发病 [3]。 波伊茨-耶格综合征 …

Peutz–Jeghers syndrome (often abbreviated PJS) is an autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis). [2] .

Patients with Peutz-Jeghers syndrome (PJS) have characteristic GI hamartomatous polyps, mucocutaneous pigmentation and predisposition to GI, breast, and other cancers. The prevalence of PJS is between 1/8,300 and 1/29,000. A full description with …

2012年9月17日 · Peutz-Jeghers syndrome is an autosomal dominant condition characterized by hamartomatous polyps (Peutz-Jeghers polyps) of the gastrointestinal tract and mucocutaneous freckling. The syndrome is associated with significant morbidity and mortality.

Peutz–Jeghers syndrome (PJS) is a rare hereditary condition characterized by mucocutaneous pigmentation and Peutz–Jeghers hamartomatous polyps, predominantly affecting the small intestine (Figure 1) [1, 2]. The diagnostic clinical criteria for Peutz–Jeghers syndrome are shown in Table 1 [3, 4, 5].