Idiopathic pulmonary hemosiderosis: challenges of differential diagnosis

Idiopathic pulmonary hemosiderosis (IPH) is a rare disease of unclear etiology that belongs to interstitial lung diseases and is characterized by a triad of symptoms: hemoptysis, iron deficiency anemia, and diffuse interstitial changes on computed tomography (CT) of the chest cavity. IPH can occur at any age, but the disease develops in childhood in 80% of cases, more often before 10 years of age. A significant proportion of pulmonary hemosiderosis cases in this age group remain undiagnosed. The purpose of the study is to demonstrate a clinical case illustrating the features of differential diagnosis and therapy of IPH during the COVID-19 pandemic. Conclusion. An 8-year-old girl was diagnosed with IPH based on fever, shortness of breath, weakness, and severe iron-deficient anemia. The chest CT scan revealed diffuse interstitial ground-glass opacity in lungs. The lung biopsy revealed hemosiderin deposits and hemosiderophages in the alveolar lumens. Treatment with systemic glucocorticoids (SGC) and azathioprine was effective. The patient was followed for 3 years.

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Publication Details

Journal
PULMONOLOGIYA
Published
2024-12-26
DOI
https://doi.org/10.18093/0869-0189-2024-4444
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
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article

Idiopathic pulmonary hemosiderosis: challenges of differential diagnosis

M. F. Dubko, Ольга Федоровна Позднякова, Yu.V. Peshekhonova, Svetlana I. Petrova et al.
PULMONOLOGIYA
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Idiopathic pulmonary hemosiderosis: challenges of differential diagnosis

M. F. Dubko, Ольга Федоровна Позднякова, Yu.V. Peshekhonova, Svetlana I. Petrova, Л. А. Желенина, Elena P. Fedotova, А. А. Кузнецова, O. L. Krasnogorskaya, Yu. B. Klyukhina, Maria V. Kuropatenko, Mikhail Mikhaylovich Kostik, Natalia M. Solomatina, I. I. Grafskaya, A. A. Bukovskaya
article en

Abstract

Idiopathic pulmonary hemosiderosis (IPH) is a rare disease of unclear etiology that belongs to interstitial lung diseases and is characterized by a triad of symptoms: hemoptysis, iron deficiency anemia, and diffuse interstitial changes on computed tomography (CT) of the chest cavity. IPH can occur at any age, but the disease develops in childhood in 80% of cases, more often before 10 years of age. A significant proportion of pulmonary hemosiderosis cases in this age group remain undiagnosed. The purpose of the study is to demonstrate a clinical case illustrating the features of differential diagnosis and therapy of IPH during the COVID-19 pandemic. Conclusion. An 8-year-old girl was diagnosed with IPH based on fever, shortness of breath, weakness, and severe iron-deficient anemia. The chest CT scan revealed diffuse interstitial ground-glass opacity in lungs. The lung biopsy revealed hemosiderin deposits and hemosiderophages in the alveolar lumens. Treatment with systemic glucocorticoids (SGC) and azathioprine was effective. The patient was followed for 3 years.

PULMONOLOGIYAVol. 35(6)
Institute of Experimental Medicine (RU), Saint Petersburg State Pediatric Medical University (RU)
Good health and well-being
Openalex Percentile: Top 57%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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