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Professional Technical IVT

Neuroendocrine Cell Hyperplasia of Infancy

Pronunciation: noo-roh-EN-doh-krin sel HY-per-play-zhuh

Also written as: NEHI — Neuroendocrine Cell Hyperplasia of Infancy

A form of childhood interstitial lung disease characterised by persistent tachypnoea, hypoxaemia, and crackles in infancy, associated with increased pulmonary neuroendocrine cells.

Full Definition

Neuroendocrine cell hyperplasia of infancy (NEHI) is a benign, non-progressive chILD disorder primarily affecting term infants during the first year of life. It is characterised by increased numbers of bombesin-immunoreactive neuroendocrine cells in the distal airways. Chest CT shows pathognomonic ground-glass opacification in the right middle lobe and lingula. Unlike many chILD conditions, NEHI does not require lung biopsy for diagnosis when clinical and CT findings are typical; however, editors reviewing diagnostic criteria manuscripts must verify that CT characterisation and clinical criteria are both reported. Most infants improve with age without specific therapy.

Usage

Usage note: Some authors use 'persistent tachypnoea of infancy' as a synonym; editors should query authors on intended usage and ensure consistency throughout.

In Context

  • "High-resolution CT demonstrating ground-glass opacity in the right middle lobe and lingula supported a clinical diagnosis of neuroendocrine cell hyperplasia of infancy." — Radiology report
  • "The author used 'persistent tachypnoea of infancy' interchangeably with NEHI; the editor queried whether the two terms were being used synonymously or as distinct entities." — Manuscript peer-review query

Also known as

NEHI persistent tachypnoea of infancy

Don't confuse with

pulmonary interstitial glycogenosis chILD

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