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在一名低血糖患者中发现与胰岛素瘤并存的胰腺囊性胰高血糖素瘤。

Cystic pancreatic glucagonoma in contact with insulinoma found in a hypoglycemic patient.

作者信息

Yagihashi S, Yagihashi N, Nagai K

机构信息

First Department of Pathology, Hirosaki University School of Medicine, Japan.

出版信息

Pathol Res Pract. 1992 Aug;188(6):751-6. doi: 10.1016/S0344-0338(11)80173-1.

Abstract

Cystic glucagonoma in contact with insulinoma was found in the pancreas of a 28-year-old female patient with characteristic hypoglycemic syndrome. Among six tumors in total detected in the tail of the resected pancreas, the largest solid tumor (2.5 cm in diameter) consisted mostly of insulin-containing cells with conspicuous amyloid deposition. Contiguous to this tumor, the second largest nodule, measuring 1.8 cm in diameter, showed cystic changes and consisted of glucagon-containing cells. High concentration of immunoreactive glucagon was demonstrated in the cystic fluid. In addition to the cystic changes of endocrine pancreatic tumors, simultaneous occurrence of glucagonoma in contact with insulinoma appears to be extremely rare and repeated episodes of hypoglycemia may contribute to its pathogenesis.

摘要

在一名患有典型低血糖综合征的28岁女性患者的胰腺中发现了与胰岛素瘤相邻的囊性胰高血糖素瘤。在切除的胰腺尾部总共检测到的六个肿瘤中,最大的实性肿瘤(直径2.5厘米)主要由含胰岛素的细胞组成,有明显的淀粉样沉积。与这个肿瘤相邻的第二大结节,直径1.8厘米,呈现囊性变化,由含胰高血糖素的细胞组成。囊液中显示出高浓度的免疫反应性胰高血糖素。除了内分泌胰腺肿瘤的囊性变化外,胰高血糖素瘤与胰岛素瘤同时出现似乎极为罕见,反复发生的低血糖可能与其发病机制有关。

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