Pancreatic glucagonoma with metastasis followed up for 15 years: A case report / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 621-624, 2023.
Article
en Zh
| WPRIM
| ID: wpr-994369
Biblioteca responsable:
WPRO
ABSTRACT
To explore the clinical characteristics, diagnosis, and management of pancreatic glucagonoma, a retrospective analysis of the clinical data and diagnostic algorithm of a patient with pancreatic glucagonoma was conducted, along with literature review. Pancreatic glucagonoma is a rare neuroendocrine tumor that originates from the pancreatic alpha cells. The main manifestations of glucagonoma syndrome(GS) include necrolytic migratory erythema, diabetes, anemia, and other systemic involvement. Early diagnosis of GS is challenging and crucial. Early identification and recognition of skin lesions contribute to timely diagnosis and treatment of the disease. Surgical resection is an effective treatment modality for glucagonoma.
Texto completo:
1
Base de datos:
WPRIM
Idioma:
Zh
Revista:
Chinese Journal of Endocrinology and Metabolism
Año:
2023
Tipo del documento:
Article