Hizawa K, Iida M, Yao T, Aoyagi K, Fujishima M
Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
J Clin Pathol. 1997 Sep;50(9):771-4. doi: 10.1136/jcp.50.9.771.
To clarify a clinical entity of juvenile polyposis of the stomach compared with generalised juvenile gastrointestinal polyposis.
The clinicopathological features of juvenile polyposis dominantly involving the stomach at initial presentation were reviewed in 12 patients (three new patients and nine from the literature). These were compared with 29 cases of generalised juvenile gastrointestinal polyposis.
There were three men and nine women with juvenile polyposis of the stomach, aged 10-63 years. Hypoproteinaemia was present in nine patients, anaemia in seven, and a family history of intestinal polyposis in seven. No patient presented with a congenital abnormality. During the observation period, two patients developed colonic juvenile polyps. Gastric polyps invariably affected the antrum and extended to the fundus, eventually becoming more numerous, larger, and more pedunculated. Ten patients required gastrectomy for associated malignancy or uncontrolled protein losing gastropathy. Histological examinations of the resected specimens demonstrated neoplastic tissue arising from juvenile polyps in four of the 12 patients. Atypism in these mixed polyps varied from adenoma to well or moderately differentiated adenocarcinoma.
Juvenile polyposis of the stomach has malignant potential, and may be a separate entity from generalised juvenile gastrointestinal polyposis.
明确胃幼年性息肉病相较于全身性幼年性胃肠道息肉病的临床实体。
回顾了12例初诊时以胃幼年性息肉病为主的患者(3例新患者和9例文献报道患者)的临床病理特征。将这些患者与29例全身性幼年性胃肠道息肉病患者进行比较。
胃幼年性息肉病患者中男性3例,女性9例,年龄10 - 63岁。9例患者存在低蛋白血症,7例贫血,7例有肠道息肉病家族史。无患者有先天性异常。在观察期内,2例患者出现结肠幼年性息肉。胃息肉总是累及胃窦并延伸至胃底,最终数量增多、体积增大且带蒂息肉增多。10例患者因相关恶性肿瘤或无法控制的蛋白丢失性胃病而行胃切除术。对切除标本的组织学检查显示,12例患者中有4例幼年性息肉出现肿瘤组织。这些混合性息肉的异型性从腺瘤到高分化或中分化腺癌不等。
胃幼年性息肉病具有恶性潜能,可能是与全身性幼年性胃肠道息肉病不同的独立实体。