1.Clinical characteristics of 6 children with idiopathic interstitial pneumonia.
Meng CHEN ; Rui Zhu WANG ; Fan Qing MENG ; Qiao Qiao FANG ; De Yu ZHAO
Chinese Journal of Pediatrics 2022;60(9):930-934
Objective: To analyze the clinical characteristics and prognosis of 6 children with idiopathic interstitial pneumonia (IIP). Methods: This retrospective study analyzed the clinical manifestations, examinations, treatment and prognosis of 6 children with IIP who were hospitalized in Children's Hospital of Nanjing Medical University from January 2015 to March 2020. Results: Of the 6 children, 2 were males and 4 were females, aged 4.8 to10.6 years. All children had a subacute onset, and presented with cough, shortness of breath and cyanosis. The lung high-resolution CT (HRCT) showed diffuse patchiness in bilateral lung fields in all the children and reticular pattern in 2 cases. Pulmonary function test found moderate to severe mixed defect in 5 children. Lung biopsy was performed in 4 children. All of the 6 children were treated with systemic glucocorticoids, of whom 2 cases had additional inhaled glucocorticoids. Four children were finally diagnosed as cryptogenic organizing pneumonia (COP), whose lung HRCT return to normal in 1-11 months. Two children were finally diagnosed as nonspecific interstitial pneumonia (NSIP), and had long-term residual fibrosis on lung HRCT. The 6 children were followed up for 1 year to 6 years and 5 months after discontinuation of systemic glucocorticoids, and all had no recurrence. Conclusions: The clinical characteristics of IIP in children are subacute onset presented with cough, shortness of breath, cyanosis and diffuse patchiness in bilateral lungs on HRCT. The common subtypes of IIP in children are COP and NSIP. Systemic glucocorticoid is effective for IIP in children and there is a good prognosis overall.
Child
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Cough/etiology*
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Cryptogenic Organizing Pneumonia
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Cyanosis/pathology*
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Dyspnea/pathology*
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Female
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Glucocorticoids/therapeutic use*
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Humans
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Idiopathic Interstitial Pneumonias/pathology*
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Lung/pathology*
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Male
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Retrospective Studies
2.Clinicopathologic analysis of organizing pneumonia in elderly autopsies.
Fang FANG ; Feng-Ru LIN ; Hui-Zhang LI
Chinese Journal of Pathology 2004;33(2):113-116
OBJECTIVETo study the clinicopathologic characteristics of organizing pneumonia of the autopsies in elder and to analyze the possible underlying etiologic factors.
METHODSNinety-five cases of organizing pneumonia were found from 635 elderly autopsy reports of the Beijing Hospital since 1980. The morphologic and imaginal features were analyzed.
RESULTSThe foci of organizing pneumonia in our series were often small, patchy, scattered and adjacent to other lung lesion. There were, however, some variations in cases with different underlying conditions. The conditions associated with organizing pneumonia, as detected in our series, were: (1) 36 cases with suppurative inflammation, lung abscesses and chronic relapsing pneumonia; (2) 17 cases with fungal or viral infection; (3) 16 cases with aspiration pneumonia; (4) 5 cases with radiation pneumonia. We observed that it was not uncommon for organizing pneumonia coexisting with atelectasis and chronic pleuritis. The image of organizing pneumonia was varied.
CONCLUSIONSOrganizing pneumonia is a common finding in autopsies of the elder. It occurs in association with many diseases and the basic pathologic changes are similar. All of which represent secondary phenomenon. Possible etiologic factors include infection (due to bacteria, fungi or virus), aspiration and radiation. The possibility of organizing pneumonia should be considered if the shadow of lung is undisappeared in imagin.
Aged ; Cryptogenic Organizing Pneumonia ; etiology ; pathology ; Humans ; Lung ; diagnostic imaging ; pathology ; Lung Abscess ; complications ; pathology ; Lung Diseases, Fungal ; complications ; pathology ; Middle Aged ; Pneumonia, Aspiration ; complications ; pathology ; Radiography ; Retrospective Studies
3.Acute Fibrinous and Organizing Pneumonia Following Hematopoietic Stem Cell Transplantation.
Sang Min LEE ; Jae Jung PARK ; Sun Hee SUNG ; Yookyung KIM ; Kyoung Eun LEE ; Yeung Chul MUN ; Soon Nam LEE ; Chu Myong SEONG
The Korean Journal of Internal Medicine 2009;24(2):156-159
A 60-year-old man presented with cough, sputum, and dyspnea. He had a history of acute myeloid leukemia and hematopoietic stem cell transplantation with chronic renal failure. Chest CT scans showed miliary nodules and patchy consolidations. Histological examination revealed numerous fibrin balls within the alveoli and thickening of the alveolar septum, both of which are typical pathological features of acute fibrinous and organizing pneumonia (AFOP). We report the first case of AFOP following allogeneic hematopoietic stem cell transplantation.
Acute Disease
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Anti-Bacterial Agents/therapeutic use
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Biopsy
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Cryptogenic Organizing Pneumonia/etiology/pathology
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Fatal Outcome
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Glucocorticoids/administration & dosage
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Hematopoietic Stem Cell Transplantation/*adverse effects
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Hemoptysis/etiology
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Humans
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Leukemia, Myeloid, Acute/*surgery
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Lung Diseases/*etiology/pathology
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Male
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Middle Aged
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Pleural Effusion/etiology
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Pulse Therapy, Drug
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Radiography, Thoracic
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Respiratory Insufficiency/etiology
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Tomography, X-Ray Computed