Glucagonoma syndrome with severe erythematous rash A rare case report

Glucagonoma syndrome with severe erythematous rash A rare case report
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胰高血糖素瘤综合征伴严重红斑皮疹罕见病例报告

DOI:
10.1097/md.0000000000017158
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发表时间:
2019
期刊:
影响因子:
1.6
通讯作者:
Zhao Jian Guo
Zhao Jian Guo
中科院分区:
医学4区
文献类型:
--
作者:
Wang Zhen Xia;Wang Fei;Zhao Jian Guo

文献摘要

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干预措施:2017年行胰体尾切除加脾切除术。结果:术后皮损消失。经过随访,目前未见复发。教训:临床医生应根据典型的初始症状考虑胰高血糖素瘤的诊断。早期诊断对于提供更好的预后非常重要。多学科方法对不可切除的转移性肿瘤患者有效。
Interventions:The distal pancreatectomy plus splenectomy was performed in 2017.Outcomes:The skin lesions disappeared after surgery. She was followed up and showed no recurrence until now.Lessons:Clinicians should consider the diagnosis of glucagonoma according to the typical initial symptoms. Early diagnosis is very important to provide a better prognosis. A multidisciplinary approach is effective in patients with unresectable metastatic tumors.