Update of pathological diagnosis of pulmonary neuroendocrine tumor.
- Author:
Xiaodong TENG
1
;
Ming ZHAO
2
;
Maode LAI
3
Author Information
1. Department of Pathology, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
2. Department of Pathology, Zhejiang Provincial People's Hospital, Hangzhou 310014, China.
3. School of Basic Medical Sciences, Zhejiang University School of Medicine, Hangzhou 310058, China.
- Publication Type:Journal Article
- MeSH:
Carcinoid Tumor;
diagnosis;
pathology;
Diagnosis, Differential;
Humans;
Hyperplasia;
Lung Neoplasms;
diagnosis;
pathology;
Neuroendocrine Tumors;
classification;
diagnosis;
pathology
- From:
Journal of Zhejiang University. Medical sciences
2016;45(1):36-44
- CountryChina
- Language:Chinese
-
Abstract:
Pulmonary neuroendocrine tumors are common in pathological practice and its pathological classification and histological grading are not exactly the same as that of those in the digestive tract and pancreas. In 2015 edition of World Health Organization classification, pulmonary neuroendocrine tumors are classified as carcinoid tumors (including typical carcinoid and atypical carcinoid), small cell lung carcinoma, large cell neuroendocrine carcinoma, and precursor lesion diffuse idiopathic neuroendocrine cell hyperplasia; each category has distinctive morphological and immunohistochemical features. The morphologic features including growth patterns and cytological appearances are keys for the diagnosis of neuroendocrine tumor, and immunohistochemical findings are also critical for its diagnosis. Furthermore, the diagnostic criteria vary for different types of specimen. In this article, we present a concise review and summary of the update of clinicopathological characterizations of pulmonary neuroendocrine tumor, with an emphasis on its diagnostic criteria and differential diagnosis.