ABSTRACT

Objective: Neuroendocrine cell hyperplasia of infancy (NEHI) is a form of childhood interstitial lung disease characterized by tachypnea, retractions, crackles, and hypoxia. The aim of this study was to report and discuss the clinical, imaging, and histopathological findings in a series of NEHI cases at a tertiary pediatric hospital, with an emphasis on diagnostic criteria and clinical outcomes. Methods: Between 2003 and 2011, 12 full-term infants were diagnosed with NEHI, based on clinical and tomographic findings. Those infants were followed for 1-91 months. Four infants were biopsied, and the histopathological specimens were stained with bombesin antibody. Results: In this case series, symptoms appeared at birth in 6 infants and by 3 months of age in the remaining 6. In all of the cases, NEHI was associated with acute respiratory infection. The most common initial chest HRCT findings were ground-glass opacities that were in the middle lobe/lingula in 12 patients and in other medullary areas in 10. Air trapping was the second most common finding, being observed in 7 patients. Follow-up HRCT scans (performed in 10 patients) revealed normal results in 1 patient and improvement in 9. The biopsy findings were nonspecific, and the staining was positive for bombesin in all samples. Confirmation of NEHI was primarily based on clinical and tomographic findings. Symptoms improved during the follow-up period (mean, 41 months). A clinical cure was achieved in 4 patients. Conclusions: In this sample of patients, the diagnosis of NEHI was made on the basis of the clinical and tomographic findings, independent of the lung biopsy results. Most of the patients showed clinical improvement and persistent tomographic changes during the follow-up period, regardless of the initial severity of the disease or type of treatment.

Keywords: Lung diseases, interstitial/diagnosis; Lung diseases, interstitial/treatment; Tomography, X-ray computed.

RESUMO

Objetivo: A hiperplasia de células neuroendócrinas do lactente (HCNEL) é uma forma de doença pulmonar intersticial da infância caracterizada por taquipneia, retrações, estertores e hipóxia. O objetivo deste estudo foi descrever e discutir os achados clínicos, histopatológicos e de imagem em uma série de casos de HCNEL em um hospital pediátrico terciário, enfatizando critérios de diagnóstico e desfechos clínicos. Métodos: Entre 2003 e 2011, 12 lactentes nascidos a termo foram diagnosticados com HCNEL, com base em critérios clínico-tomográficos e acompanhados por 1-91 meses. Quatro lactentes foram submetidos a biopsia pulmonar, e as amostras histopatológicas foram coradas com anticorpo para bombesina. Resultados: Nesta série de casos, os sintomas surgiram ao nascimento em 6 lactentes e em até 3 meses de idade nos outros 6. Em todos os casos, HCNEL estava associada com infecção respiratória aguda. Os achados iniciais em TCAR de tórax foram opacidades em vidro fosco em lobo médio e língula, em 12 pacientes, e em outras regiões medulares, em 10. O aprisionamento aéreo foi o segundo achado mais frequente, em 7 pacientes. As TCAR de controle (realizadas em 10 pacientes) revelaram resultados normais (em 1) e melhorias (em 9). Os achados de biopsia foram inespecíficos, e os resultados para bombesina foram positivos em todas as amostras. A confirmação de HCNEL baseou-se principalmente em achados clínico-tomográficos. Os sintomas melhoraram durante o seguimento (média, 41 meses). Quatro pacientes apresentaram cura clínica. Conclusões: Os achados clínico-tomográficos permitiram o diagnóstico de HCNEL nesta série de pacientes, independentemente dos resultados de biopsia pulmonar. A maioria mostrou melhora clínica e persistência das alterações tomográficas durante o seguimento, independentemente da gravidade inicial da doença ou do tipo de tratamento.

Palavras-chave: Doenças pulmonares intersticiais/diagnóstico; Doenças pulmonares intersticiais/terapia; Tomografia computadorizada por raios X.

Introduction

In 2005, Deterding et al.(1) described neuroendocrine cell hyperplasia of infancy (NEHI) in a study including 15 infants with symptoms of interstitial lung disease (ILD), such as persistent tachypnea, retractions, hypoxemia, and crackles in the first year of life. The same authors had previously used the term persistent tachypnea of infancy for this condition.(2) Lung biopsies of the 15 infants showed minimal and nonspecific changes, despite prominent clinical symptoms. The only specific histopathological finding was an increase in clear cells in the distal airways, representing pulmonary neuroendocrine cells (PNECs), and this finding was confirmed by immunohistochemistry with bombesin antibody staining.(1)

PNECs are granular epithelial cells distributed in the conducting airways. They produce vasoactive substances (bombesin, calcitonin, and serotonin) that can cause bronchoconstriction, vasoactivity, epithelial differentiation, and proliferation of adjacent mesenchymal cells (smooth muscle cells and fibroblasts).(1,3) PNECs are numerous in the fetal and neonatal lung; however, their number decreases markedly in the first year of life.(1) These cells have complex functions and are involved in the differentiation and maturation of the fetal lung, neonatal adaptation, lung regeneration, and carcinogenesis.(3) PNEC hyperplasia has been reported in a variety of pediatric pulmonary disorders, as well as in adults; however, the significance of PNEC hyperplasia and the mechanisms involved are unknown.(3,4)

Fan et al.(5) recently classified NEHI as a unique form of ILD in infants. In 2007, Deutsch et al.(6) proposed a new classification system for diffuse lung diseases in children under 2 years of age. Their multicenter study was conducted in North America and described 18 new cases of NEHI with clinical and histopathological findings similar to those of the original series.

NEHI has a characteristic clinical and tomographic presentation. Clinically, infants with NEHI present tachypnea, retractions, hypoxemia, and crackles. Chest HRCT shows a characteristic pattern of ground-glass opacity (GGO) in the central regions of the lungs, especially in the middle lobe and lingula, as well as air trapping.(7,8) Recently, some centers have used the term "NEHI syndrome" to diagnose this entity, using only clinical and tomographic criteria.(9) The purpose of the present study was to report and discuss the clinical, imaging, and histopathological findings in a series of NEHI cases at a tertiary pediatric hospital with an emphasis on diagnostic criteria and clinical outcomes.

Methods

A series of 12 infants with NEHI, diagnosed by clinical and HRCT criteria or histopathological examination of lung tissue, were followed between March of 2003 and April of 2011. The infants attended a tertiary-level hospital (Hospital Infantil Albert Sabin) in the city of Fortaleza, Brazil. The study was approved by the research ethics committee of the hospital (Protocol no. 068/2010). The parents or guardians of the infants gave written informed consent.

In order to diagnose cases of NEHI, we used a standardized protocol for children under 2 years of age with clinical suspicion of childhood ILD (chILD). The chILD syndrome requires the presence of at least three of the four following criteria: respiratory symptoms (cough, rapid or difficult breathing, or exercise intolerance); signs (tachypnea at rest, adventitious sounds, retractions, clubbing, failure to thrive, or respiratory failure); hypoxemia; and diffuse abnormalities on chest X-rays or CT scans.(5,10) We excluded all of the children with ILD of a known cause or associated with systemic diseases.

The criteria for the diagnosis of NEHI were the presence of persistent tachypnea, retractions, crackles, low oxygen saturations, and HRCT findings consisting of GGO, especially in the middle lobe and lingula, associated with air trapping.(9,10)

The standardized protocol included the following variables: sex, neonatal condition, history of environmental exposure/family history, age at symptom onset, precipitating factors, initial signs and symptoms, supplemental oxygen use, histopathological findings, imaging findings, treatment, disease progression, and duration of follow-up.

All of the patients underwent a complete evaluation, which included blood count, blood gas analysis, transcutaneous oximetry (at rest, during exercise, and during sleep), echocardiography with indirect measurement of pulmonary arterial pressure, measurement of serum immunoglobulin levels, sweat test, upper gastrointestinal series, serological tests for viral infections, and chest imaging (X-ray and HRCT). All of the infants were submitted to imaging tests upon diagnosis, and 10 infants had additional HRCT scans taken during follow-up visits. Regarding HRCT scans, a sequential technique with a low dose protocol (120 kV, 40 mAs) was used. All of the patients were sedated with 10% chloral hydrate (1 mL/3 kg of body weight), and images were obtained during quiet breathing. During the inspiratory phase, six to ten 1-mm slices were obtained with the patient in the supine position. From 2006 onward, CT scans in the lateral position on both sides during the expiratory phase were also obtained, as described by Lucaya et al.(11) Four to six images were obtained, resulting in twelve 1-mm slices with a 10-20-mm range. All images were reviewed in consensus by two experienced pediatric radiologists.

Initial and follow-up CT scans were used in order to identify the number of lobes involved, the lingula being considered as a separate lobe. The HRCT scans were assessed for the presence, distribution, and extension of GGOs and air trapping. The criteria for these findings are defined in the Fleischner Society Glossary of Terms.(12) Any other lung abnormalities were also investigated. The presence of air trapping was assessed only on expiratory HRCT images. The first four patients in the present series underwent chest HRCT-guided open lung biopsy with the consent of a legal guardian. Immunohistochemistry with bombesin antibody staining was performed. Pulmonary function tests were performed in cooperative patients older than 6 years of age.

The presence of GGO in the central regions of the lungs involving at least four lung lobes (including middle lobe and lingula) and associated with air trapping was considered a characteristic tomographic finding of NEHI.(9) Infants who presented involvement of fewer than four lung lobes were diagnosed by lung biopsy.

Results

All of the infants (8 males and 4 females) were born at full term. No infant had a family history of ILD, a history of environmental exposure, or a history of continued exposure to high altitude. Six patients experienced respiratory symptoms during the neonatal period that did not require oxygen therapy, and their clinical deterioration, with increased work of breathing and oxygen requirement, developed at 2-6 months of life following an episode of acute respiratory infection (ARI). In this context, ARI refers to the first episode of a probable viral infection in the upper airways. In the remaining 6 patients, ILD symptoms started at 1-3 months of age following an episode of ARI. Among the 12 infants, 8 were referred to the outpatient clinic for clarification of persistent tachypnea with a previous diagnosis of acute viral bronchiolitis, asthma, pneumonia, gastroesophageal reflux, or heart disease, and 4 were hospitalized upon diagnosis due to respiratory distress requiring oxygen therapy. All of the patients presented with tachypnea and chest retractions disproportionate to X-ray findings, but no toxemia. Only 1 infant presented with cough, although this was not a prominent complaint. Crackles were present in 7 patients and were transient in most of these patients. Wheezing was absent in all infants. Hypoxemia was present in only 5 infants, with no pulmonary hypertension or clubbing at baseline. Feeding problems (choking or regurgitation) were present in 7 patients; however, diagnostic tests revealed no aspiration syndrome in order to justify the respiratory symptoms. Among the 12 infants, 6 had difficulty in gaining weight. The anteroposterior diameter of the chest was increased (best identified from the sixth month of life onward) in 8 patients. Pectus excavatum was identified in only 1 infant. The main characteristics of the patients are summarized in Table 1.



Chest X-rays showed lung hyperinflation in 9 patients; perihilar opacities, in 5; and increased bronchovascular markings in the perihilar region, in 1. Initial HRCT scans showed GGO in the central regions of the lungs (including middle lobe and lingula) in all cases, as well as in other central regions, in 11 cases. Peripheral regions were affected in 5 patients. Air trapping, especially in the lower lobes, was the second most frequent finding, in 7 patients. Two to six lobes were affected in each patient, five or more lobes being affected in 10 cases. The only CT changes found in this series were GGO and air trapping (Figure 1). The main HRCT findings are summarized in Table 2. Mean age at initial HRCT examination was 9.4 months (range, 6-16 months). The mean interval between the first outpatient consultation and the first HRCT examination was 1 month.





The first 4 patients included in the present series underwent lung biopsy, 3 of whom under 10 months of age and 1 of whom at 51 months. The histopathological findings demonstrated normal alveolar structures without any fibrosis. Slightly enlarged peribronchial lymphocyte aggregates were seen in 3 cases. Immunohistochemistry showed a significant number of bombesin-positive cells in the walls of the small airways consistent with neuroendocrine cells.

Most of our cases (n = 7) required no oxygen therapy. Only 2 of the 5 hypoxemic infants required continuous oxygen therapy. One patient required overnight oxygen therapy for 24 months. Three infants received oxygen therapy only overnight or during episodes of ARI. Therapy was performed with oxygen to maintain oxygen saturation greater than 92%, measured by transcutaneous oximetry. Five infants were treated with systemic corticosteroids: oral corticosteroids, in 2; monthly methylprednisolone pulse therapy, in 2; and oral corticosteroids and hydroxychloroquine plus methylprednisolone pulse therapy, in 1 (the patient with the most severe disease in the series). The mean duration of systemic corticosteroid therapy was 15 months (range, 8-29 months). Prior use of bronchodilators and oral corticosteroids was common; however, clinical response was unsatisfactory. Five infants received no specific treatment except for antireflux medication in order to mitigate regurgitation or vomiting.

All of the infants showed progressive clinical improvement and, after 24 months of age, none depended on oxygen therapy. No patient was hospitalized due to respiratory problems or recurrent wheezing. During the follow-up period, none of the patients experienced pulmonary hypertension or clubbing. Most patients showed persistent retractions, resolution of crackles, and reduction in anteroposterior chest diameter with age. Difficulty in gaining weight persisted in 4 of the 6 infants with that initial complaint. Pulmonary function tests (performed in 3 patients) showed mild obstructive respiratory pattern in 2 and severe obstructive respiratory pattern in 1 patient with a major thoracic deformity. Follow-up HRCT scans performed in 10 patients showed persistence of GGO in 9 patients, mainly in the middle lobe and lingula, and air trapping, in 5 patients, predominantly in the lower lobes. The number of affected lobes decreased during the follow-up period, and changes were less intense overall (Figure 2 and Table 2). The mean time from initial HRCT to follow-up HRCT examinations was 36 months (range, 4-72 months). Complete tomographic and clinical resolution was achieved in 1 patient, whose HRCT scans displayed initial involvement of the lingula and right middle lobe and areas of air trapping. Three patients had complete clinical resolution, despite still showing functional and CT alterations. Clinical and CT improvement was not correlated with any type of treatment, although the most symptomatic cases showed a greater number of affected lobes on initial CT scans. Only 1 infant, who presented with respiratory dysfunction at 2 months and who was 11 months old at the end of the study period, continued to receive oxygen therapy during sleep due to young age and relatively recent diagnosis. All of the patients were alive at the end of the study period (mean age, 50 months; range, 11-100 months) and showed improvement of the thoracic deformity (increased anteroposterior chest diameter). Eight patients continued to show mild respiratory dysfunction, and 4 patients achieved clinical cure. No patient in our series was lost to follow-up. The mean duration of the follow-up period was 41 months (range, 1-91 months).



Discussion

In the last decade, NEHI was described as an ILD that exclusively affected infants, with characteristic clinical findings (tachypnea, retractions, hypoxemia, and crackles) and tomographic findings (GGO in the central regions of the lungs, especially in the middle lobe and lingula, and air trapping), and good prognosis(9,10,13); similar results were found in our case series, only differing in the need for oxygen therapy, which was lower than in previous reports.

Previous reports of NEHI also found a male predominance, and most subjects were born full term and presented the first symptoms by 15 months of age.(1,6,14) Similarly, all infants in the present series were born full term and most were male; however, 50% presented symptoms in the neonatal period, showing an earlier onset of the disease in relation to other series. The early presentation of the illness observed in the present series suggests that a possible genetic cause is involved in its pathogenesis, since familial cases have been described in the literature.(14) Disease symptoms were associated with or aggravated by ARI. In fact, ARI might have precipitated the onset of NEHI or aggravated existing symptoms. It is possible that NEHI results from an interaction of genetic or environmental factors, including viral infections. Other authors have reported that acute viral bronchiolitis was associated with the onset of symptoms in infants with surfactant protein C mutation (a type of chILD), but rarely with NEHI.(14-16) Other ILDs can produce symptoms in the neonatal period in full-term infants, such as surfactant dysfunction, especially of ABCA3 mutations and, in some cases, of surfactant protein C mutations.(15,17,18) Mutations in these proteins might cause clinical findings that cannot be easily differentiated from other benign forms of ILD in infants, such as NEHI.

Most of the infants in the present series did not require continuous oxygen therapy, despite the early development of symptoms and persistence of retractions. This less severe phenotypic presentation has not been described in previous series.(1,14,19) Recently, Lukkarinen et al.(20) has described a series of 9 cases of NEHI, and only 33% of the patients presented with hypoxia. Clinical manifestations (such as difficulty in gaining weight and feeding problems) are common, and nonspecific complaints are frequently seen in various forms of chILD. These symptoms are probably due to respiratory distress, especially in young infants, and usually improve with age. An important clinical feature, observed in almost 70% of our patients but not previously reported, is increased anteroposterior chest diameter, suggesting an obstructive disorder. Although our patients presented with a picture suggestive of airway disease (hyperinflation on chest X-ray and increased anteroposterior diameter of the chest), chest auscultation was normal or revealed "Velcro" type crackles, consistent with ILD. During follow-up, some infants experienced progressive improvement in symptoms that evolved to complete resolution, whereas the majority of the cases showed persistent mild respiratory dysfunction. Our findings corroborate those in other series and show that NEHI is a pediatric interstitial disorder with a good prognosis and long duration.(1,6,14,19) It is not known whether NEHI is a self-limited childhood disease or whether it is related to other diseases in adults, such as diffuse idiopathic pulmonary neuroendocrine cell hyperplasia.(4,21) A longer follow-up period is required in order to determine the natural evolution of NEHI. The most severely affected infants in our sample received systemic corticosteroids but showed no improvement in clinical response. Improvement seemed to occur with age, especially after 2 years of age, rather than as a result of a specific treatment. Because NEHI lacks inflammatory characteristics, patients are unlikely to benefit from anti-inflammatory drugs. Hence, the last patients in our series received no corticosteroid therapy.

The functional assessment of the children in our series revealed an obstructive pattern without bronchodilator response. Recently, Kerby et al.(22) have described a pattern of significant pulmonary obstruction and air trapping in young children with a clinical and tomographic diagnosis of NEHI, confirmed or not by lung biopsy. Clinical improvement with age is likely associated with functional improvement. Studies based on larger series of NEHI patients might help clarify the relationship between initial functional severity and clinical or radiological improvement.

The histopathological findings in infants who underwent lung biopsy showed mild histological abnormalities, and immunohistochemistry showed a significant number of bombesin-positive cells, consistent with neuroendocrine cells, which is similar to the findings described in the original report.(1) Unlike the minor changes described in the original histopathological findings, Young et al.(19) found inflammation in plaques or pulmonary fibrosis in a series of infants with NEHI. In the same study, the authors examined the distribution and frequency of neuroendocrine cells in NEHI and in other lung diseases, and they demonstrated that, despite the significant prominence of neuroendocrine cells in NEHI, the finding was not specific for the diagnosis. The extensive inter- and intrasubject variability in the number of neuroendocrine cells in typical cases of NEHI and the potential for overlapping with other lung diseases suggest that a clinical, radiological, and pathological correlation is required for the diagnosis of NEHI. Recently, guidelines for the histological diagnosis of NEHI have been developed.(23)

Brody et al.(9) showed that GGO in the central regions of the lungs is a characteristic finding on chest HRCT in infants with NEHI, with a sensitivity of 78% and a specificity of 100%. Five or more lobes were affected in 83% of cases in our series, and the middle lobe and the lingula were affected in all of the cases. Similarly to the findings of Brody et al.(9), mosaic or diffuse air trapping was the second most common finding on chest HRCT. The presence of these tomographic findings in infants with symptoms suggestive of ILD has led to the establishment of a diagnosis of "NEHI syndrome". In the present series, all of the infants met the clinical and tomographic criteria for the diagnosis of NEHI, allowing us to dispense with lung biopsy in most cases.

There is still considerable discussion about the need for lung biopsy in children with probable NEHI, although most of the authors currently dispense with biopsies in typical cases of NEHI.(9,13,19,22,24) The need for diagnostic lung biopsy in cases suspected of NEHI is currently reserved for significantly symptomatic patients or those with no characteristic clinical or tomographic findings (Figure 3).



To the best of our knowledge, no published report to date has included a description of follow-up CT scans of patients with NEHI. In most of our cases, tomographic changes persisted, although to a lesser degree, regardless of clinical improvement, age, and length of follow-up.

The present study has some limitations, including the small sample size. Despite the small number of patients included, our sample of 12 infants with NEHI might seem relatively large for a single institution, considering the rarity of the disease. Another limitation was the lack of a radiological follow-up protocol. In order to avoid unnecessary radiation, radiological protocols for NEHI should be standardized. The lack of functional evaluation in infants was another limitation of our study, given that the characteristic functional pattern observed in the disease (significant pulmonary obstruction and air trapping) could be added to the typical tomographic findings in an attempt to corroborate the noninvasive diagnosis of NEHI.

In conclusion, we suggest that NEHI can be diagnosed on the basis of clinical and radiological findings. The presence of persistent tachypnea, retractions, crackles, and low oxygen saturation in a infant without auscultatory findings suggestive of airway disease, as well as tomographic findings of GGO in the central regions of the lungs, involving at least four lobes, especially the middle lobe and lingula, associated with air trapping, is highly suggestive of NEHI. In such circumstances, lung biopsy should be avoided.

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* Study carried out at the Hospital Infantil Albert Sabin, Fortaleza, Brazil.
Correspondence to: Vivianne Calheiros Chaves Gomes. Rua Desembargador Leite Albuquerque, 1060, apto. 1100, Aldeota, CEP 60150-150, Fortaleza, CE, Brasil.
Tel. 55 85 3261-1578. Fax: 55 85 3261-1578. E-mail: vccgomes@terra.com.br
Financial support: None.
Submitted: 11 March 2013. Accepted, after review: 6 September 2013.



About the authors

Vivianne Calheiros Chaves Gomes
Pediatric Pulmonologist. Hospital Infantil Albert Sabin, Fortaleza, Brazil.

Mara Cristina Coelho Silva
Pediatric Pulmonologist. Hospital Infantil Albert Sabin, Fortaleza, Brazil.

José Holanda Maia Filho
Radiologist. Hospital Infantil Albert Sabin, Fortaleza, Brazil.

Pedro Daltro
Doctoral Student in Radiology. Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.

Simone Gusmão Ramos
Pathologist. University of São Paulo at Ribeirão Preto School of Medicine, Ribeirão Preto, Brazil.

Alan S. Brody
Radiologist. Cincinnati Children's Hospital, Cincinnati (OH) USA.

Edson Marchiori
Associate Professor of Radiology. Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.