Raras
Buscar doenças, sintomas, genes...
Hemossiderose pulmonar, idiopática
ORPHA:99931CID-10 · E83.1+CID-11 · CB04.30OMIM 178550DOENÇA RARA

Uma doença respiratória causada por sangramentos repetidos e espalhados nos saquinhos de ar dos pulmões, sem uma causa aparente e que afeta principalmente crianças. A maioria dos pacientes apresenta anemia, tosse e manchas nos pulmões, visíveis em radiografias de tórax.

Mantido por Agente Raras·Colaborar como especialista →

Introdução

O que você precisa saber de cara

📋

Uma doença respiratória causada por sangramentos repetidos e espalhados nos saquinhos de ar dos pulmões, sem uma causa aparente e que afeta principalmente crianças. A maioria dos pacientes apresenta anemia, tosse e manchas nos pulmões, visíveis em radiografias de tórax.

Pesquisas ativas
1 ensaio
3 total registrados no ClinicalTrials.gov
Publicações científicas
538 artigos
Último publicado: 2026

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
Unknown
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.0
Europe
Início
Childhood
🏥
SUS: Sem cobertura SUSScore: 0%
CID-10: E83.1+
Você se identifica com essa condição?
O Raras está aqui pra te apoiar — com ou sem diagnóstico

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🫁
Pulmão
12 sintomas
🩸
Sangue
2 sintomas
❤️
Coração
2 sintomas
🫃
Digestivo
2 sintomas
📏
Crescimento
1 sintomas
🫘
Rins
1 sintomas

+ 12 sintomas em outras categorias

Características mais comuns

90%prev.
Anemia ferropriva
Muito frequente (99-80%)
55%prev.
Hemoptise
Frequente (79-30%)
55%prev.
Palidez
Frequente (79-30%)
55%prev.
Tosse
Frequente (79-30%)
55%prev.
Fadiga
Frequente (79-30%)
55%prev.
Opacificação em vidro fosco na TC de alta resolução pulmonar
Frequente (79-30%)
35sintomas
Muito frequente (1)
Frequente (7)
Ocasional (19)
Muito raro (2)
Sem dados (6)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 35 características clínicas mais associadas, ordenadas por frequência.

Anemia ferroprivaIron deficiency anemia
Muito frequente (99-80%)90%
HemoptiseHemoptysis
Frequente (79-30%)55%
PalidezPallor
Frequente (79-30%)55%
TosseCough
Frequente (79-30%)55%
FadigaFatigue
Frequente (79-30%)55%

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico538PubMed
Últimos 10 anos120publicações
Pico202220 papers
Linha do tempo
2026Hoje · 2026🧪 2017Primeiro ensaio clínico📈 2022Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

🧬

Nenhum gene associado encontrado

Os dados genéticos desta condição ainda estão sendo catalogados.

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
2Fase 21
1Fase 11
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 2 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Hemossiderose pulmonar, idiopática

🗺️

Selecione um estado ou use sua localização para ver resultados.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

🟢 Recrutando agora

1 pesquisa recrutando participantes. Converse com seu médico sobre a possibilidade de participar.

Outros ensaios clínicos

3 ensaios clínicos encontrados, 1 ativos.

Distribuição por fase
Ver todos no ClinicalTrials.gov
🧪 Está conduzindo uma pesquisa?
Divulgue para pacientes e familiares que acompanham esta doença.
Divulgar pesquisa →

Publicações mais relevantes

Timeline de publicações
123 papers (10 anos)
#1

[Clinical, imaging, and pathological features of diffuse alveolar filling diseases].

Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases2026 Mar 12

Diffuse alveolar filling disease (DAFD) is characterized by diffuse lesions in both lungs caused by the abnormal filling of bilateral alveolar spaces (and sometimes the terminal bronchioles) with substances such as water, blood, lipids, inflammatory cells, pathogens, or tumor cells. Clinically, it is characterized mainly by dyspnea and hypoxemia, while imaging examinations reveal diffuse ground-glass opacities or consolidation shadows in both lungs. In the early stage, lung volume generally remains unchanged, but pulmonary interstitial fibrosis may occur in the advanced stage. Typical diseases included in this category are pulmonary alveolar proteinosis (PAP), diffuse alveolar hemorrhage (DAH), idiopathic pulmonary hemosiderosis (IPH), and pneumocystis pneumonia (PCP). While these diseases share certain similarities in clinical symptoms, imaging features, and pathological manifestations, each has its own distinct characteristics. Bronchoalveolar lavage fluid (BALF) detection and lung biopsy are the main confirmatory diagnostic methods. As a newly proposed concept, DAFD and diffuse interstitial lung diseases (DILD) both belong to diffuse parenchymal lung diseases (DPLD). The formal proposal of this new concept is of great significance for the diagnosis and differential diagnosis of DPLD. 弥漫性肺泡填充性疾病(DAFD)是指双侧肺泡腔被水、血液、类脂、炎性渗出物、病原微生物或肿瘤细胞等物质异常填充所导致的双肺弥漫性病变。临床以呼吸困难、低氧血症为主要表现,影像学可见双肺弥漫性磨玻璃影或实变影,晚期可能出现肺间质纤维化。典型疾病包括肺泡蛋白沉着症(PAP)、弥漫性肺泡出血(DAH)、特发性肺含铁血黄素沉着症(IPH)及肺孢子菌肺炎(PCP)等,各类疾病在症状、影像学特征及病理表现上既相似又各具特点。支气管肺泡灌洗液检测和肺活检是其主要的确诊方法。DAFD与弥漫性间质性肺病(DILD)同属弥漫性实质性肺病(DPLD),这个新概念的提出对DPLD的诊断和鉴别诊断具有重要的意义。.

#2

The role of arterial embolization in pediatric Idiopathic Pulmonary Hemosiderosis: a case report and literature review.

Respiratory medicine case reports2026

Idiopathic Pulmonary Hemosiderosis is a rare life-threatening disorder, characterized by recurrent episodes of Diffuse Alveolar Hemorrhage. Currently, there are still many unresolved questions concerning its actual etiopathogenesis and, consequently, the most appropriate treatment to adopt. Through our case report we aim to highlight the role of angiography in identifying the presence of abnormal pulmonary collaterals as a possible cause of therapeutic failure. Although further studies are needed and even if it remains unclear if they are simultaneous problems or causative of one another, embolization of abnormal pulmonary arteries appears to play an important role in cases of Idiopathic Pulmonary Hemosiderosis unresponsive to conventional therapies and presenting severe side effects due to immunosuppression. After an extensive literature review, we found only two studies supporting our hypothesis; to our knowledge, this is the first case in Western world.

#3

Idiopathic Pulmonary Hemosiderosis Characterized by Recurrent Infections and Anemia.

Clinical laboratory2026 Jan 01

Idiopathic pulmonary hemosiderosis (IPH) is a rare condition characterized by recurrent alveolar bleeding, hemosiderin deposition, and pulmonary fibrosis, predominantly affecting children. Its diagnosis and management are complex. A case involving a 3-year-old female patient with iron deficiency anemia and recurrent pneumonia was analyzed supported by laboratory and imaging investigations. Clinical symptoms included nausea, fever, and pallor. Initial evaluations indicated moderate anemia (HGB 73 g/L) and signs of infection, with imaging revealing diffuse ground-glass opacities. Following the exclusion of other conditions, a diagnosis of IPH was established, and comprehensive treatment resulted in notable clinical improvement. This case underscores the importance of multidisciplinary collaboration in diagnosing and managing IPH, particularly in pediatric patients, to enhance outcomes and quality of life.

#4

Idiopathic Pulmonary Hemosiderosis in a Child Diagnosed by Transbronchial Cryobiopsy.

Pediatric pulmonology2026 Feb
#5

Age at disease onset is an independent risk factor for physical growth of children with idiopathic pulmonary hemosiderosis.

Translational pediatrics2025 Aug 31

Idiopathic pulmonary hemosiderosis (IPH), a pediatric pulmonary disorder requiring prolonged corticosteroid therapy raises concerns about growth impairment. While corticosteroid-induced stunting is well-documented, its specific impact on the height of IPH patients remains unclear. This study aimed to evaluate the impact of corticosteroid exposure on height outcomes and identify key predictors of growth restriction in children with IPH. In this retrospective cohort study, 45 IPH patients [2018-2023] were stratified into normal-stature (n=37) and short-stature (n=8) groups based on anthropometric criteria. Multivariable Cox regression and comparative analyses assessed age at onset, diagnostic delay, corticosteroid duration, nutritional parameters, pulmonary function, and growth hormone (GH) therapy efficacy. Short-stature patients demonstrated an earlier disease onset (P=0.004) and prolonged diagnostic delay (P=0.002). A younger age at onset independently predicted impaired height growth [hazard ratio (HR) =0.435, 95% confidence interval (CI): 0.206-0.920, P=0.02], while corticosteroid duration showed no association (P=0.45). Secondary analyses identified synergistic effects of anemia (P=0.02), malnutrition (P=0.045), and pulmonary fibrosis (P=0.008). GH therapy significantly improved height velocity (P<0.001) and bone metabolism markers (P<0.05). Early IPH onset, rather than corticosteroid exposure, drives growth impairment in children. Timely diagnosis, nutritional optimization, and adjunctive GH therapy may mitigate height deficits, underscoring the significance of multidisciplinary management strategies.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC444 artigos no totalmostrando 117

2026

[Clinical, imaging, and pathological features of diffuse alveolar filling diseases].

Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases
2026

The role of arterial embolization in pediatric Idiopathic Pulmonary Hemosiderosis: a case report and literature review.

Respiratory medicine case reports
2026

Idiopathic Pulmonary Hemosiderosis in a Child Diagnosed by Transbronchial Cryobiopsy.

Pediatric pulmonology
2026

Idiopathic Pulmonary Hemosiderosis Characterized by Recurrent Infections and Anemia.

Clinical laboratory
2025

Heiner syndrome and correlation with food allergy: case report.

Frontiers in allergy
2025

Back to the Diving Board: A Rare Cause of Hemoptysis in a Healthy Female Athlete.

Case reports in pulmonology
2025

Age at disease onset is an independent risk factor for physical growth of children with idiopathic pulmonary hemosiderosis.

Translational pediatrics
2025

Idiopathic pulmonary hemosiderosis: A pediatric case report.

Respiratory medicine case reports
2025

Different clinical presentations of idiopathic pulmonary hemosiderosis.

Anales de pediatria
2025

Idiopathic Pulmonary Hemosiderosis Mimicking Transfusion-Related Acute Lung Injury.

Indian journal of pediatrics
2025

Idiopathic Pulmonary Hemosiderosis Complicated by Direct Antiglobulin Test-negative Autoimmune Hemolytic Anemia.

Journal of pediatric hematology/oncology
2025

Neuropsychiatric Side Effects of Hydroxychloroquine in a Patient With Idiopathic Pulmonary Hemosiderosis.

Journal of paediatrics and child health
2025

The gut-lung axis in celiac disease: a narrative review of pulmonary manifestations and pathogenic mechanisms.

Gastroenterology and hepatology from bed to bench
2024

Clinical features and risk factors for recurrence of idiopathic pulmonary hemosiderosis in children.

BMC pulmonary medicine
2025

Pulmonary hemorrhagic syndromes.

Pediatric pulmonology
2024

Novel germline STAT3 gain-of-function mutation causes autoimmune diseases and severe growth failure.

The journal of allergy and clinical immunology. Global
2024

Diffuse alveolar hemorrhage in pediatrics: Etiologies and outcomes.

Pediatric pulmonology
2024

Idiopathic pulmonary hemosiderosis associated with Kabuki syndrome.

Immunological medicine
2024

A Rare Presentation of Late-Onset Idiopathic Pulmonary Hemosiderosis: A Case Report.

Cureus
2024

Pulmonary siderosis complicated with severe mycoplasma pneumoniae pneumonia: A case report.

Respiratory medicine case reports
2024

Cardiomyopathy in Celiac Disease: A Systematic Review.

Journal of clinical medicine
2023

Panacinar emphysema complicating idiopathic pulmonary hemosiderosis: a case report.

Oxford medical case reports
2023

Idiopathic Pulmonary Hemosiderosis. Reply.

The New England journal of medicine
2023

Idiopathic Pulmonary Hemosiderosis.

The New England journal of medicine
2023

Idiopathic Pulmonary Hemosiderosis: The Great Hemolytic Anemia Mimicker.

Cureus
2023

Leflunomide Is Safe and Effective for the Induction and Maintenance of Idiopathic Pulmonary Hemosiderosis Remission.

Pediatric allergy, immunology, and pulmonology
2024

An Adult Case of Idiopathic Pulmonary Hemosiderosis Associated with Pulmonary Fibrosis and Emphysematous Change.

Internal medicine (Tokyo, Japan)
2023

Determining the threshold for azathioprine use in recurrent diffuse alveolar hemorrhage in idiopathic pulmonary hemosiderosis.

The American journal of the medical sciences
2023

Idiopathic pulmonary hemosiderosis and stroke secondary to protein C deficiency in a child with Down syndrome: a case report.

Journal of medical case reports
2023

Fatal Invasive Aspergillosis in a Child with Idiopathic Pulmonary Hemosiderosis.

Turkish archives of pediatrics
2023

Lane-Hamilton Syndrome in an Adult With Down Syndrome: A Case Report.

Cureus
2023

Diffuse alveolar hemorrhage in children with interstitial lung disease: Determine etiologies!

Pediatric pulmonology
2022

Rituximab in Idiopathic Pulmonary Hemosiderosis in Children: A Novel and Less Toxic Treatment Option.

Pharmaceuticals (Basel, Switzerland)
2023

The role of flexible bronchoscopy in the diagnostic pathway of children with unexplained peripheral eosinophilia.

Pediatrics international : official journal of the Japan Pediatric Society
2023

Updates in idiopathic pulmonary hemosiderosis in 2022: A state of the art review.

Pediatric pulmonology
2022

Assessment of type I interferon signatures in undifferentiated inflammatory diseases: A Japanese multicenter experience.

Frontiers in immunology
2022

Celiac disease and idiopathic pulmonary hemosiderosis: a literature review of the Lane-Hamilton syndrome.

Postgraduate medicine
2021

Place of bronchoscopy in the diagnostics and follow-up of patients with idiopathic pulmonary hemosiderosis.

Folia medica
2022

Late presentation of lane-hamilton syndrome in a 33 year old female: A case report.

International journal of applied &amp; basic medical research
2022

The Spectrum of Autoantibodies in Adult Patients With Idiopathic Pulmonary Hemosiderosis: A Brief Review of the Literature.

Cureus
2022

An Infant With Interstitial Lung Disease of Rare Cause.

Chest
2022

Liposteroid Therapy for Idiopathic Pulmonary Hemosiderosis: A Scoping Review of the Literature.

Prague medical report
2022

Comparative Analysis of Adult Patients With Idiopathic Pulmonary Hemosiderosis and Lane-Hamilton Syndrome: A Systematic Review of the Literature in the Period 1971-2022.

Cureus
2022

Strike while the iron is hot: diagnosis of pediatric idiopathic pulmonary hemosiderosis.

Blood
2022

Recurrence of idiopathic pulmonary hemosiderosis in adults with childhood onset: A case report and literature review.

Respiratory investigation
2022

A 49-year-old man with ischemic cardiomyopathy and persistent hemoptysis for eighteen months.

The American journal of the medical sciences
2022

Proposed Pathogenesis of Diffuse Alveolar Hemorrhage in Idiopathic Pulmonary Hemosiderosis.

Lung
2022

Rare causes of anemia in children: Two cases of idiopathic pulmonary hemosiderosis.

Respiratory medicine case reports
2022

Idiopathic pulmonary hemosiderosis: A mimic of severe COVID-19 pneumonia.

Pediatrics international : official journal of the Japan Pediatric Society
2022

Adult patients with idiopathic pulmonary hemosiderosis: a comprehensive review of the literature.

Clinical rheumatology
2022

Association between idiopathic pulmonary hemosiderosis and celiac disease in pediatric patients: A scoping review of the literature over the past 50 years.

Pediatric pulmonology
2022

Prevalence of autoantibodies in pediatric patients with idiopathic pulmonary hemosiderosis: a scoping review of the literature in the period 1980-2021.

Clinical rheumatology
2021

The etiology, clinical profile, and outcome of diffuse alveolar hemorrhage in children: a ten-year single-center experience.

Translational pediatrics
2022

Puzzling (IRIDA-Like and Hemolytic) Anemia in a Child With Idiopathic Pulmonary Hemosiderosis.

Journal of pediatric hematology/oncology
2021

Children with Heiner Syndrome: A Single-Center Experience.

Children (Basel, Switzerland)
2021

Short Review of Liposteroid: A Novel Targeted Glucocorticoid Preparation for Treatment of Autoimmune and Inflammatory Diseases.

Prague medical report
2021

Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia.

The Indian journal of radiology &amp; imaging
2022

Differentiation of idiopathic pulmonary hemosiderosis from rheumatologic and autoimmune diseases causing diffuse alveolar hemorrhage: establishing a diagnostic approach.

Clinical rheumatology
2021

Coincidence or connection? A patient with concurrent Lane Hamilton Syndrome and idiopathic membranous nephropathy.

Respiratory medicine case reports
2022

Lung transplant to manage end-stage lung disease due to idiopathic pulmonary hemosiderosis: A review of the literature.

Respiratory investigation
2021

Diffuse alveolar hemorrhage in children with trisomy 21.

Pediatric rheumatology online journal
2021

Diffuse alveolar haemorrhage with suspected idiopathic pulmonary hemosiderosis and decrease in lung diffusing capacity and chronic respiratory failure.

BMJ case reports
2021

Pulmonary Nocardia infection in a child with idiopathic pulmonary hemosiderosis.

BMC pulmonary medicine
2021

Is It Time to Call Idiopathic Pulmonary Hemosiderosis by the Correct Name: Immune-Mediated Pulmonary Hemosiderosis?

The American journal of the medical sciences
2021

Risk factors for recurrent pulmonary exacerbation in idiopathic pulmonary hemosiderosis.

Pediatric pulmonology
2021

Idiopathic pulmonary hemosiderosis: A state of the art review.

Respiratory medicine
2021

Idiopathic pulmonary hemosiderosis: a review of the treatments used during the past 30 years and future directions.

Clinical rheumatology
2021

Idiopathic Pulmonary Hemosiderosis Associated with Emphysematous Change in an Adult Who Underwent Lung Transplantation.

Internal medicine (Tokyo, Japan)
2020

Diffuse alveolar hemorrhage in infants: Report of five cases.

Respiratory medicine case reports
2020

Possible association of idiopathic pulmonary hemosiderosis with rheumatoid arthritis: A case report.

Experimental and therapeutic medicine
2020

Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis.

Respiratory medicine case reports
2020

Idiopathic pulmonary hemosiderosis - A rare cause of chronic anemia.

Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace
2021

Aggressive corticosteroid treatment in childhood idiopathic pulmonary hemosiderosis with better outcome.

Journal of the Formosan Medical Association = Taiwan yi zhi
2020

Successful Liposteroid Therapy for a Recurrent Idiopathic Pulmonary Hemosiderosis with Down Syndrome.

Case reports in pediatrics
2020

Cobalamin C deficiency presenting with diffuse alveolar hemorrhage and pulmonary microangiopathy.

Pediatric pulmonology
2020

Idiopathic Pulmonary Hemosiderosis as a Mimic of Pulmonary Vasculitis: A Case Report and Review of the Literature.

Current allergy and asthma reports
2020

Thoracotomy Wound Dehiscence After Lung Transplant Is an Effective Surgical Solution: A Case Report.

Transplantation proceedings
2019

Early diagnosis of idiopathic pulmonary hemosiderosis using gastric lavage.

Pediatrics international : official journal of the Japan Pediatric Society
2020

Childhood diffuse parenchymal lung diseases: We need a new classification.

The clinical respiratory journal
2019

[Diffuse alveolar hemorrhage in children].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
2019

Cryobiopsy in the diagnosis of idiopathic pulmonary hemosiderosis: a case report.

Journal of thoracic disease
2019

Extracorporeal Membrane Oxygenation for Diffuse Alveolar Hemorrhage Caused by Idiopathic Pulmonary Hemosiderosis: A Case Report and a Review of the Literature.

Journal of pediatric intensive care
2020

Autoimmunity and Delayed Diagnosis in Pediatric Idiopathic Pulmonary Hemosiderosis.

Journal of pediatric hematology/oncology
2019

Early Initiation of Steroid-sparing Drugs in Idiopathic Pulmonary Hemosiderosis.

Indian pediatrics
2019

Fatal case of Hajdu-Cheney syndrome with idiopathic pulmonary hemosiderosis.

Pediatrics international : official journal of the Japan Pediatric Society
2019

A different clinical presentation of Heiner syndrome: The case of diffuse alveolar hemorrhage causing massive hemoptysis and hematemesis.

Respiratory medicine case reports
2018

Severe iron-deficiency anemia as initial manifestation of pulmonary hemosiderosis in a child.

Einstein (Sao Paulo, Brazil)
2018

Diffuse pulmonary small nodular and patchy infiltrates on chest X-ray with hemoptysis: TB or not TB?-a call for scale up of respiratory medicine services in African TB high burden countries: a case of idiopathic pulmonary hemosiderosis.

The Pan African medical journal
2019

Clinical characteristics and prognosis of idiopathic pulmonary hemosiderosis in pediatric patients.

The Journal of international medical research
2018

Recurrent idiopathic pulmonary hemosiderosis after long-term remission presented with Sjogren's syndrome: Idiopathic no more?

Respiratory medicine case reports
2018

Liposteroid and methylprednisolone combination therapy for a case of idiopathic lung hemosiderosis.

Respiratory medicine case reports
2019

Pulmonary Hemorrhage in Children: Etiology, Clinical Profile and Outcome.

Indian journal of pediatrics
2019

Respiratory Distress and Severe Anemia in a Child With Idiopathic Pulmonary Hemosiderosis.

Journal of pediatric hematology/oncology
2017

[Diffuse alveolar hemorrhage in 4 girls].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
2017

Idiopathic pulmonary hemosiderosis: Hemorrhagic flare after 6 years of remission.

Revista portuguesa de pneumologia
2017

Methylprednisolone pulse therapy rescued life-threatening pulmonary hemorrhage due to idiopathic pulmonary hemosiderosis.

The American journal of emergency medicine
2017

Idiopathic Pulmonary Hemosiderosis Mimicking Iron Deficiency Anemia: A Delayed Diagnosis?

Hematology reports
2017

Idiopathic Pulmonary Hemosiderosis in a Child with Recurrent Macrophage Activation Syndrome Secondary to Systemic Juvenile Idiopathic Arthritis.

Case reports in pediatrics
2017

Corticosteroid in Combination with Leflunomide and Mesenchymal Stem Cells for Treatment of Pediatric Idiopathic Pulmonary Hemosiderosis.

Journal of tropical pediatrics
2016

[Idiopathic pulmonary hemosiderosis with dendriform pulmonary ossification].

Biomedica : revista del Instituto Nacional de Salud
2016

Severe Alveolar Hemorrhage - What's in it for the Gastroenterologist?

Journal of gastrointestinal and liver diseases : JGLD
2017

A Case of Idiopathic Pulmonary Hemosiderosis Presenting With Signs and Symptoms Mimicking Hemolytic Anemia.

Journal of pediatric hematology/oncology
2016

Unusual presentation: Concurrent IgA deficiency and idiopathic pulmonary hemosiderosis.

Pediatric pulmonology
2016

Cor triatriatum sinister: a rare underlying cause of pulmonary hemosiderosis.

SpringerPlus
2016

[Analysis of the etiology of hemoptysis and its diagnosis and treatment in 106 cases].

Zhonghua er ke za zhi = Chinese journal of pediatrics
2017

Idiopathic pulmonary hemosiderosis in adults: review of cases reported in the latest 15 years.

The clinical respiratory journal
2015

Severe Respiratory Distress in a Child with Pulmonary Idiopathic Hemosiderosis Initially Presenting with Iron-Deficiency Anemia.

Case reports in pulmonology
2015

Advances in pediatrics in 2014: current practices and challenges in allergy, gastroenterology, infectious diseases, neonatology, nutrition, oncology and respiratory tract illnesses.

Italian journal of pediatrics
2015

Idiopathic pulmonary hemosiderosis complicated by Down syndrome.

Pediatrics international : official journal of the Japan Pediatric Society
2015

Association of Celiac Disease With Idiopathic Pulmonary Hemosiderosis; Lane Hamilton Syndrome.

Iranian journal of pediatrics
2015

Decreased VEGF Level Is Associated with Elevated Ferritin Concentration in Bronchoalveolar Lavage Fluid of Children with Interstitial Lung Diseases.

Respiration; international review of thoracic diseases
2016

Idiopathic Pulmonary Hemosiderosis Presenting as Anemia, Failure to Thrive, and Jaundice in a Toddler.

Pediatric emergency care
2015

A physician survey reveals differences in management of idiopathic pulmonary hemosiderosis.

Orphanet journal of rare diseases
2015

Idiopathic Pulmonary Hemosiderosis With Allergic Asthma Diagnosis in a Pediatric Patient.

Journal of pediatric hematology/oncology
2015

Idiopathic pulmonary hemosiderosis presenting in an adult: A case report and review of the literature.

Lung India : official organ of Indian Chest Society
2015

Unexplained childhood anaemia: idiopathic pulmonary hemosiderosis.

Hong Kong medical journal = Xianggang yi xue za zhi
2015

A young man with hemoptysis: Rare association of idiopathic pulmonary hemosiderosis, celiac disease and dilated cardiomyopathy.

Lung India : official organ of Indian Chest Society
Ver todos os 444 no EuropePMC

Associações

Organizações que acompanham esta doença — pra ter apoio e orientação

Ainda não temos associações cadastradas para Hemossiderose pulmonar, idiopática.

É de uma associação que acompanha esta doença? Fale com a gente →

Comunidades

Grupos ativos de quem convive com esta doença aqui no Raras

Ainda não existe comunidade no Raras para Hemossiderose pulmonar, idiopática

Pacientes, familiares e cuidadores se organizam em comunidades pra compartilhar experiências, fazer perguntas e se apoiar. Você pode ser o primeiro.

Tire suas dúvidas

Perguntas, dicas e experiências compartilhadas aqui na página

Participe da discussão

Faça login para postar dúvidas, compartilhar experiências e interagir com especialistas.

Fazer login

Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

Referências e fontes

Bases de dados externas citadas neste artigo

Publicações científicas

Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.

  1. [Clinical, imaging, and pathological features of diffuse alveolar filling diseases].
    Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases· 2026· PMID 41820048mais citado
  2. The role of arterial embolization in pediatric Idiopathic Pulmonary Hemosiderosis: a case report and literature review.
    Respiratory medicine case reports· 2026· PMID 41732710mais citado
  3. Idiopathic Pulmonary Hemosiderosis Characterized by Recurrent Infections and Anemia.
    Clinical laboratory· 2026· PMID 41543088mais citado
  4. Idiopathic Pulmonary Hemosiderosis in a Child Diagnosed by Transbronchial Cryobiopsy.
    Pediatric pulmonology· 2026· PMID 41725300mais citado
  5. Age at disease onset is an independent risk factor for physical growth of children with idiopathic pulmonary hemosiderosis.
    Translational pediatrics· 2025· PMID 40949900mais citado
  6. Bilateral Lung Transplantation for Lymphangioleiomyomatosis With Secondary Pulmonary Hemosiderosis: A Case Report.
    Case Rep Pathol· 2026· PMID 41953042recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:99931(Orphanet)
  2. OMIM OMIM:178550(OMIM)
  3. MONDO:0008346(MONDO)
  4. GARD:6763(GARD (NIH))
  5. Busca completa no PubMed(PubMed)
  6. Q1052626(Wikidata)

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Hemossiderose pulmonar, idiopática
Compêndio · Raras BR

Hemossiderose pulmonar, idiopática

ORPHA:99931 · MONDO:0008346
Prevalência
Unknown
CID-10
E83.1+ · Distúrbios do metabolismo de minerais
CID-11
Ensaios
1 ativos
Início
Childhood
Prevalência
0.0 (Europe)
MedGen
UMLS
C0020807
EuropePMC
Wikidata
Papers 10a
DiscussaoAtiva

Nenhuma novidade ainda. O agente esta monitorando.

0membros
0novidades