| Literature DB >> 27300020 |
Antonio García Escudero1, Enrique Rodríguez Zarco1, Juan Carlos Girón Arjona2, María José Ríos Moreno3, Katherine Gallardo Rodríguez1, Ana Vallejo Benítez1, Ricardo González Cámpora1.
Abstract
DIPNECH is characterized by neuroendocrine cell hyperplasia, tumorlets, and eventually carcinoid tumors. Although it is regarded by some authors as a preneoplastic condition, this issue is controversial. New pathologic criteria have recently been proposed for the diagnosis of DIPNECH, and a subgroup of carcinoid tumors expressing developing neural transcription factors (DNTFs), with clinicopathologic features similar to those of DIPNECH, has been recognized. This paper reports on the clinical and pathological findings in three cases of DIPNECH and investigates the expression of three DNTFs (TTF1, ASCL1, and POU3F2). All patients were female, with a mean age of 63 years, and all lesions were located in the periphery of the lung. In two cases, typical carcinoids were associated with a spindle-cell component. All neuroendocrine proliferations were DNTF positive. The morphologic (spindle-cell component), phenotypic (DNTF expression), and clinicopathologic (peripheral tumors, female predominance) similarities suggest that DIPNECH may be a preneoplastic lesion for peripheral carcinoids.Entities:
Keywords: DIPNECH; Developing neural transcription factors; Lung neuroendocrine tumors; Pathology; Preneoplastic lesion
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Year: 2016 PMID: 27300020 DOI: 10.1007/s00428-016-1962-5
Source DB: PubMed Journal: Virchows Arch ISSN: 0945-6317 Impact factor: 4.064