Hoff M, Kramp B
Klinik und Poliklinik für Hals-Nasen-Ohrenheilkunde, Kopf- und Halschirurgie Otto Körner, Universität Rostock.
Laryngorhinootologie. 2000 Oct;79(10):573-8. doi: 10.1055/s-2000-7673.
CASUISTRY: The case of a patient with atypical carcinoid of the larynx is reported and literature about neuroendocrine tumors of the larynx (NETL) is reviewed.
Especially terminology, histological differentiation, diagnostics and therapy are discussed.
Neuroendocrine tumors are rare and untypically located in the larynx. In spite of this they should to be known as an important differential diagnosis of a laryngeal neoplasia, because of possible malign or highly malign course. The typical localisation of neuroendocrine tumors (NET) are the gastrointestinal tract and the lung, but the clinical course differs from the one of laryngeal manifestation. This means diagnostics and therapy have to be adapted to this special disease. That's why it is important to explore the identity of these tumors scientifically. This is difficult because of the low rate of patients with this disease. The message of this report is the conclusion of the established and appeal for publications of new cases of NETL.
决疑法:报告了一例喉非典型类癌患者的病例,并对喉神经内分泌肿瘤(NETL)的相关文献进行了综述。
特别讨论了术语、组织学分化、诊断和治疗。
神经内分泌肿瘤在喉部罕见且位置不典型。尽管如此,由于其可能的恶性或高度恶性病程,它们应被视为喉肿瘤的重要鉴别诊断。神经内分泌肿瘤(NET)的典型定位是胃肠道和肺,但临床病程与喉部表现不同。这意味着诊断和治疗必须适应这种特殊疾病。因此,科学探索这些肿瘤的特性很重要。由于该病患者数量较少,这一过程颇具难度。本报告的主旨是总结已有的研究成果,并呼吁发表新的喉神经内分泌肿瘤病例。