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[内分泌性动脉高血压。嗜铬细胞瘤]

[Endocrine arterial hypertension. Pheochromocytoma].

作者信息

Telles E C, Machado F S, Bicho M P, Rego F, Almeida G, Amram S

出版信息

Acta Med Port. 1989 Jan-Feb;2(1):41-5.

PMID:2672701
Abstract

The authors emphasize some embryologic features of the chromaffin tissue as a basis of understanding of both the physiopathologic and clinical aspects of Pheochromocytoma. The appropriate sequence of diagnostic procedures was established in order to obtain clinical, biochemical and anatomical evidence of the tumor. It was concluded that an early diagnosis is mandatory in order to plan a curative surgical therapeutic approach. The embryologic and biochemical understanding of the Pheochromocytoma, in the context of the neuroendocrine tumors, allows a better rationale both for the diagnosis and therapy of this condition.

摘要

作者强调嗜铬组织的一些胚胎学特征,以此作为理解嗜铬细胞瘤生理病理和临床方面的基础。为了获得肿瘤的临床、生化和解剖学证据,确立了适当的诊断程序顺序。得出的结论是,为了规划治愈性手术治疗方案,早期诊断是必不可少的。在神经内分泌肿瘤的背景下,对嗜铬细胞瘤的胚胎学和生化理解为这种疾病的诊断和治疗提供了更好的理论依据。

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