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1.
Am J Med Sci ; 363(5): 452-455, 2022 05.
Article in English | MEDLINE | ID: mdl-35134372

ABSTRACT

Lipoid pneumonia occurs due to the accumulation of lipids within the lung tissue. Autopsy series have reported an incidence of 1.0-2.5% in adult and 8.8% in children. Lipoid pneumonia can be from an exogeneous or an endogenous source. Exogenous lipoid pneumonia is often associated with aspiration of fatty materials, whereas endogenous lipoid pneumonia is associated with an accumulation of lipid-rich debris from destroyed alveolar cells. We describe a 75-year-old man who presented with spiculated lung nodules found incidentally on abdominal CT. Reviews of systems were positive for weight loss, and a history of constipation. A PET/CT revealed spiculated nodules with positive fluorodeoxyglucose (FDG) uptakes. A wedge resection was performed with histopathologic findings consistent with exogenous lipoid pneumonia with granulomatous reaction. We report clinical, radiological, and pathological features of exogenous lipoid pneumonia secondary to chronic aspiration mimicking invasive adenocarcinoma. A high index of suspicion for exogenous lipoid pneumonia should be maintained, especially when evaluating patients with abnormal chest radiographic findings and risk factors for aspirations.


Subject(s)
Pneumonia, Lipid , Positron Emission Tomography Computed Tomography , Adult , Aged , Child , Fluorodeoxyglucose F18 , Humans , Lung/pathology , Male , Pneumonia, Lipid/complications , Pneumonia, Lipid/etiology , Risk Factors
2.
Chest ; 156(6): e117-e120, 2019 12.
Article in English | MEDLINE | ID: mdl-31812209

ABSTRACT

CASE PRESENTATION: A 65-year-old man was referred for evaluation of several years of chest congestion and cough productive of yellow sputum as well as recently noted abnormalities on chest imaging. He denied dyspnea, weight loss, fevers, chills, or hemoptysis. He had no history of systemic illness, pneumonia, other respiratory illness, gastroesophageal reflux, or sinusitis. He had a remote smoking history. He worked as a railroad conductor and had occupational exposure to asbestos, as well as to other uncharacterized dusts and fumes. The patient spent most of his life in Washington and California and regularly traveled through the California Central Valley. Other travel history included trips to Southeast Asia, Iceland, and Europe in the remote past. The patient had one dog but no exposure to other animals. His only medication was loratadine, taken daily for allergic rhinitis. He applied petroleum jelly to his nares nightly to moisturize his nasal passages.


Subject(s)
Emollients/adverse effects , Mycobacterium Infections, Nontuberculous/diagnostic imaging , Petrolatum/adverse effects , Pneumonia, Lipid/chemically induced , Aged , Cough/etiology , Humans , Male , Mycobacterium Infections, Nontuberculous/complications , Mycobacterium chelonae , Nasal Cavity , Pneumonia, Lipid/complications , Pneumonia, Lipid/diagnostic imaging , Respiratory Aspiration/complications , Respiratory Aspiration/diagnostic imaging , Sputum , Tomography, X-Ray Computed
3.
Beijing Da Xue Xue Bao Yi Xue Ban ; 50(5): 921-923, 2018 Oct 18.
Article in Chinese | MEDLINE | ID: mdl-30337759

ABSTRACT

Lipoid pneumonia (LP) is an uncommon form of pneumonia that is characterized by the presence of intra-alveolar lipid and lipid-laden macrophages on microscopy. It categorized as exogenous lipoid pneumonia (ExLP) and endogenous lipoid pneumonia (EnLP). Exogenous lipoid pneumonia caused by inhalation of liposuction substances (animal fat, vegetable oil, or mineral oil), mostly, in adult cases, they were medicines for constipation or rhinopharyngitis. Most of these patients showed mild clinical manifestations, and chronic medical condition. There were reports of lipoid pneumonia being successfully treated with corticosteroids, immunoglobulins and whole lung lavage. We report a case of exogenous lipoid pneumonia characterized by high fever and acute medical condition. A 77-year-old woman with hypertension and diabetes mellitus, accepted paraffin oil treatment for "incomplete intestinal obstruction", then, an accident of aspiration happened, as she went through the history of coughing while eating, followed by persistent hyperthermia and increases of white blood cells (WBC). Chest CT showed progressive ground-glass opacities, accompanied with fusion of consolidation, her sputum etiological examination was negative, and the therapy of broad-spectrum antibiotic was invalid. The patient was subjected to bronchofibroscopy with bronchoalveolar lavage (BAL). The bronchoalveolar lavage fluid (BALF) appeared colorless and transparent, and did not show a milky appearence. Total cell count of the BALF was 2.0×109 cell/mL, including 7.2% macrophages and 92.8% neutrophils. Cultures of the BALF were negative for bacterial, fungal, and mycobacterial pathogens. The BALF cytologic findings showed vacuolated lipid-laden macrophages (Oil Red O staining). These findings revealed exogenous lipoid pneumonia. There were reports of lipoid pneumonia being successfully treated with corticosteroids, immunoglobulins, and whole-lung lavage. So this patient was treated with methylprednisolone 120 mg/d for 3 days and 80 mg/d for 6 days, at the same time, immunoglobulins was given to infusion, but the daily peak temperature of the patients fluctuated between 38 and 39 degrees. Then, whole lung lavage was performed 28 days after admission. Unfortunately, acute pulmonary edema occurred during the operation, as the tracheal intubation problems, and 6 days later, the patient died at last. The clinical manifestations of exogenous lipid pneumonia vary greatly, from asymptomatic to life-threatening symptoms, and as febrile low fever is the main manifestation, but hyperthermia may also be the remarkable presentation.


Subject(s)
Bronchoalveolar Lavage , Pneumonia, Lipid , Adult , Aged , Bronchoalveolar Lavage Fluid , Female , Humans , Mineral Oil , Pneumonia, Lipid/complications , Pneumonia, Lipid/diagnosis , Pneumonia, Lipid/therapy , Tomography, X-Ray Computed
4.
BMJ Case Rep ; 20182018 Jul 06.
Article in English | MEDLINE | ID: mdl-29982176

ABSTRACT

A young female vaper presented with insidious onset cough, progressive dyspnoea on exertion, fever, night sweats and was in respiratory failure when admitted to hospital. Clinical examination was unremarkable. Haematological tests revealed only thrombocytopenia, which was long standing, and her biochemical and inflammatory markers were normal. Chest radiograph and high-resolution CT showed diffuse ground-glass infiltrates with reticulation. She was initially treated with empirical steroids and there was improvement in her oxygenation, which facilitated further tests. Since the bronchoscopy and high-volume lavage was unyielding, a video-assisted thoracoscopicsurgical biopsy was done later and was suggestive of lipoid pneumonia. The only source of lipid was the vegetable glycerine found in e-cigarette (EC). Despite our advice to quit vaping, she continued to use EC with different flavours and there is not much improvement in her clinical and spirometric parameters.


Subject(s)
Electronic Nicotine Delivery Systems , Lung/diagnostic imaging , Pneumonia, Lipid/complications , Respiratory Insufficiency/etiology , Vaping/adverse effects , Adult , Anti-Inflammatory Agents , Bronchoalveolar Lavage , Female , Flavoring Agents/adverse effects , Glycerol/adverse effects , Humans , Lung/pathology , Pneumonia, Lipid/diagnostic imaging , Pneumonia, Lipid/drug therapy , Prednisolone/administration & dosage , Propylene Glycols/adverse effects , Respiratory Insufficiency/drug therapy , Tomography, X-Ray Computed
7.
Conn Med ; 80(2): 91-5, 2016 Feb.
Article in English | MEDLINE | ID: mdl-27024980

ABSTRACT

INTRODUCTION: Lipoid pneumonia is a rare, underdiagnosed disorder, and its combined presentation with sarcoidosis is even more unusual. METHODS: This paper presents a case in which both lipoid pneumonia and sarcoidosis were present, and includes the relevant literature review on lipoid pneumonia. RESULTS: Lipoid pneumonia may be acute or chronic in its presentation, resulting from exogenous or endogenous factors, or classified as idiopathic, with its precise incidence unknown. Radiographic changes maybe variable, but typically include lower lobe consolidation. Pathologic changes consist of an inflammatory giant cell reaction around lipid-related empty vacuoles and giant cell granulomas. Treatment in the case of exogenous lipoid pneumonia consists of removal of the offending oil ingestion. However, in endogenous lipoid pneumonia, treatment is aimed at the underlying cause, as there is no standard treatment. Repeated bronchoalveolar lavage, corticosteroids, and surgical resection have been used as therapies. The course of the disease is usually not progressive.


Subject(s)
Bronchoalveolar Lavage , Glucocorticoids/therapeutic use , Pneumonectomy , Pneumonia, Lipid/complications , Pneumonia, Lipid/therapy , Sarcoidosis/complications , Adult , Humans , Male , Pneumonectomy/methods , Pneumonia, Lipid/diagnostic imaging , Radiography , Treatment Outcome
8.
Clin Respir J ; 10(2): 246-9, 2016 Mar.
Article in English | MEDLINE | ID: mdl-25103284

ABSTRACT

Pulmonary alveolar proteinosis (PAP) is an under-reported and under-diagnosed condition, with a high percentage of cases found on autopsy or late stage disease. The etiology of PAP includes genetic, primary (anti-granulocyte-macrophage colony-stimulating factor antibodies) and secondary (oncologic, rheumatologic, infectious, chemical and immunologic) causes. Here, we present the first reported pediatric case of endogenous lipoid pneumonia and non-specific interstitial pneumonitis preceding the development of PAP.


Subject(s)
Lung Diseases, Interstitial/diagnosis , Pneumonia, Lipid/diagnosis , Pulmonary Alveolar Proteinosis/diagnosis , Adolescent , Diagnosis , Fatal Outcome , Female , Granulocyte-Macrophage Colony-Stimulating Factor/metabolism , Humans , Lung Diseases, Interstitial/complications , Pneumonia, Lipid/complications , Pulmonary Alveolar Proteinosis/etiology
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