Desquamative interstitial pneumonia: A case report

Introduction. Desquamative interstitial pneumonia is one of the rarest idiopathic interstitial pneumonias and the rarest form of smoking-related interstitial lung diseases. It was first described by Liebow in 1965. Histologically, it is characterized by the presence of eosinophilic macro...

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Main Authors: Lovrenski Aleksandra, Eri Živka, Tegeltija Dragana, Kašiković-Lečić Svetlana, Panjković Milana
Format: Article
Language:English
Published: Serbian Medical Society 2014-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2014/0370-81791410602L.pdf
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author Lovrenski Aleksandra
Eri Živka
Tegeltija Dragana
Kašiković-Lečić Svetlana
Panjković Milana
author_facet Lovrenski Aleksandra
Eri Živka
Tegeltija Dragana
Kašiković-Lečić Svetlana
Panjković Milana
author_sort Lovrenski Aleksandra
collection DOAJ
description Introduction. Desquamative interstitial pneumonia is one of the rarest idiopathic interstitial pneumonias and the rarest form of smoking-related interstitial lung diseases. It was first described by Liebow in 1965. Histologically, it is characterized by the presence of eosinophilic macrophages uniformly filling airspaces which often contain a finely granular light-brown pigment that does not stain for hemosiderin. The alveolar walls are usually mildly thickened by fibrous tissue and infiltrated by a moderate number of lymphocytes. Case Outline. Our patient was a 56-year-old male, heavy smoker, with bilateral lung infiltrations of unknown etiology and several months of discomfort in the form of dry cough and shortness of breath. Lung function tests showed a moderate restrictive ventilation disorder and a severe reduction of diffusing capacity. Since bronchoscopic specimens did not reveal lung lesion etiology, an open lung biopsy of the lower left pulmonary lobe was performed, and based on the obtained surgical material the pathohistologically diagnosis of desquamative interstitial pneumonia was established. The patient was started on corticosteroid and immunosuppressive therapy, and he ceased smoking. At the last control examination, two years after the onset of symptoms, the patient was feeling well, and high-resolution computed tomography (HRCT) scan of the thorax showed regression of pathological changes. Conclusion. Although, as in our case, the majority of DIP patients improve on treatment, some patients still develop progressive irreversible fibrosis despite therapy.
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spelling doaj.art-105f4a63b2d947c28142aa0a354f1b112022-12-21T19:57:54ZengSerbian Medical SocietySrpski Arhiv za Celokupno Lekarstvo0370-81792014-01-011429-1060260610.2298/SARH1410602L0370-81791410602LDesquamative interstitial pneumonia: A case reportLovrenski Aleksandra0Eri Živka1Tegeltija Dragana2Kašiković-Lečić Svetlana3Panjković Milana4Institute for Pulmonary Diseases of Vojvodina, Center for Pathology, Sremska KamenicaInstitute for Pulmonary Diseases of Vojvodina, Center for Pathology, Sremska KamenicaInstitute for Pulmonary Diseases of Vojvodina, Center for Pathology, Sremska KamenicaInstitute for Pulmonary Diseases of Vojvodina, Clinic for Tuberculosis and Granulomatous Diseases, Sremska KamenicaInstitute for Pulmonary Diseases of Vojvodina, Center for Pathology, Sremska KamenicaIntroduction. Desquamative interstitial pneumonia is one of the rarest idiopathic interstitial pneumonias and the rarest form of smoking-related interstitial lung diseases. It was first described by Liebow in 1965. Histologically, it is characterized by the presence of eosinophilic macrophages uniformly filling airspaces which often contain a finely granular light-brown pigment that does not stain for hemosiderin. The alveolar walls are usually mildly thickened by fibrous tissue and infiltrated by a moderate number of lymphocytes. Case Outline. Our patient was a 56-year-old male, heavy smoker, with bilateral lung infiltrations of unknown etiology and several months of discomfort in the form of dry cough and shortness of breath. Lung function tests showed a moderate restrictive ventilation disorder and a severe reduction of diffusing capacity. Since bronchoscopic specimens did not reveal lung lesion etiology, an open lung biopsy of the lower left pulmonary lobe was performed, and based on the obtained surgical material the pathohistologically diagnosis of desquamative interstitial pneumonia was established. The patient was started on corticosteroid and immunosuppressive therapy, and he ceased smoking. At the last control examination, two years after the onset of symptoms, the patient was feeling well, and high-resolution computed tomography (HRCT) scan of the thorax showed regression of pathological changes. Conclusion. Although, as in our case, the majority of DIP patients improve on treatment, some patients still develop progressive irreversible fibrosis despite therapy.http://www.doiserbia.nb.rs/img/doi/0370-8179/2014/0370-81791410602L.pdfdesquamative interstitial pneumoniainterstitial lung diseasesmokingsmokersmacrophagessmoking-related interstitial lung disease
spellingShingle Lovrenski Aleksandra
Eri Živka
Tegeltija Dragana
Kašiković-Lečić Svetlana
Panjković Milana
Desquamative interstitial pneumonia: A case report
Srpski Arhiv za Celokupno Lekarstvo
desquamative interstitial pneumonia
interstitial lung disease
smoking
smokers
macrophages
smoking-related interstitial lung disease
title Desquamative interstitial pneumonia: A case report
title_full Desquamative interstitial pneumonia: A case report
title_fullStr Desquamative interstitial pneumonia: A case report
title_full_unstemmed Desquamative interstitial pneumonia: A case report
title_short Desquamative interstitial pneumonia: A case report
title_sort desquamative interstitial pneumonia a case report
topic desquamative interstitial pneumonia
interstitial lung disease
smoking
smokers
macrophages
smoking-related interstitial lung disease
url http://www.doiserbia.nb.rs/img/doi/0370-8179/2014/0370-81791410602L.pdf
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AT erizivka desquamativeinterstitialpneumoniaacasereport
AT tegeltijadragana desquamativeinterstitialpneumoniaacasereport
AT kasikoviclecicsvetlana desquamativeinterstitialpneumoniaacasereport
AT panjkovicmilana desquamativeinterstitialpneumoniaacasereport