1.A Case of Statin-Induced Interstitial Pneumonitis due to Rosuvastatin.
Se Yong KIM ; Se Jin KIM ; Doran YOON ; Seung Wook HONG ; Sehhoon PARK ; Chan Young OCK
Tuberculosis and Respiratory Diseases 2015;78(3):281-285
Statins lower the hyperlipidemia and reduce the incidence of cardiovascular events and related mortality. A 60-year-old man who was diagnosed with a transient ischemic attack was started on acetyl-L-carnitine, cilostazol, and rosuvastatin. After rosuvastatin treatment for 4 weeks, the patient presented with sudden onset fever, cough, and dyspnea. His symptoms were aggravated despite empirical antibiotic treatment. All infectious pathogens were excluded based on results of culture and polymerase chain reaction of the bronchoscopic wash specimens. Chest radiography showed diffuse ground-glass opacities in both lungs, along with several subpleural ground-glass opacity nodules; and a foamy alveolar macrophage appearance was confirmed on bronchoalveolar lavage. We suspected rosuvastatin-induced lung injury, discontinued rosuvastatin and initiated prednisolone 1 mg/kg tapered over 2weeks. After initiating steroid therapy, his symptoms and radiologic findings significantly improved. We suggest that clinicians should be aware of the potential for rosuvastatin-induced lung injury.
Acetylcarnitine
;
Bronchoalveolar Lavage
;
Chemically-Induced Disorders
;
Cough
;
Dyspnea
;
Fever
;
Humans
;
Hydroxymethylglutaryl-CoA Reductase Inhibitors
;
Hyperlipidemias
;
Incidence
;
Ischemic Attack, Transient
;
Lung
;
Lung Diseases, Interstitial*
;
Lung Injury
;
Macrophages, Alveolar
;
Middle Aged
;
Mortality
;
Polymerase Chain Reaction
;
Prednisolone
;
Radiography
;
Thorax
;
Rosuvastatin Calcium
2.Clinical analysis of heterozygous ABCA3 mutations in children.
Xiujuan XU ; Enmei LIU ; Zhengxiu LUO ; Jian LUO ; Zhou FU
Chinese Journal of Pediatrics 2014;52(4):244-247
OBJECTIVETo investigate the association of ATP-binding cassette transporter A3 (ABCA3) gene mutations with severe neonatal respiratory distress syndrome (NRDS) and lung disease in children.
METHODThirty-eight children hospitalized with respiratory disorders in Children's Hospital of Chongqing Medical University from January 2010 to December 2011 were screened. Two mutations (E292V, G1221S) in the ABCA3 gene were identified. Interstitial lung disease (ILD) was present in 10 cases, NRDS was found in 23 and congenital pulmonary dysplasia in 5 cases. There were 24 males and 14 females, with an age range of 1 hour to 15 years. Genomic DNA was prepared from blood samples and sequences were analyzed by polymerase chain reaction (PCR). Clinical feature, imaging characteristics and the results of gene detection were retrospectively analyzed.
RESULTFour cases with ABCA3 gene mutations were found; 2 patients (case 2 and case 4) had the heterozygous mutation of ABCA3 E292V. One was a 3-hour-old girl and another was a 52-day-old boy, 2 patients (case 1 and case 4) had the heterozygous mutation of ABCA3 G1221S. One was a 78-day-old boy and another was a girl, 15 years and one month old. The family history was negative for respiratory disease. Three patients (case 1, 2, 4 ) had NRDS and 2 (case 1, 2) of them were premature. One patient (case 3) had normal growth and development. She was diagnosed clinically as interstitial lung disease (ILD) after admission. The clinical outcomes of 4 cases were various. Case 1 had recurrent wheezing and inhaled corticosteroid was needed. Case 2 died because she failed to wean from mechanical ventilator. Case 3 was discharged with improvement but lost to follow-up. Case 4 grows normally.
CONCLUSIONGenetic variants within ABCA3 may be the genetic causes or background of a contributor to some unexplained refractory NRDS, and chronic lung disease developed in latter childhood. Identification of ABCA3 genetic variants in NRDS infants is important to offer genetic counseling, as well as early prognosis estimation and intervention in pediatric chronic lung disease.
ATP-Binding Cassette Transporters ; genetics ; Adolescent ; Child ; Child, Preschool ; DNA Mutational Analysis ; Exons ; Female ; Heterozygote ; Humans ; Infant ; Infant, Newborn ; Lung ; diagnostic imaging ; pathology ; Lung Diseases, Interstitial ; diagnosis ; genetics ; Male ; Mutation ; genetics ; Radiography ; Respiratory Distress Syndrome, Newborn ; diagnosis ; genetics
3.Pulmonary Cryptococcosis in Rheumatoid Arthritis Patient Treated With Leflunomide.
Chang Kyoo BYON ; Sang Woo YIM ; Jun Yong PARK ; Mee Sook ROH ; Sung Won LEE ; Won Tae CHUNG ; Sang Yeob LEE
Journal of the Korean Geriatrics Society 2014;18(4):232-236
Leflunomide, a disease-modifying antirheumatic drug, is effective for rheumatoid arthritis as monotherapy or combination therapy with methotrexate. The most common adverse effects are diarrhea, dyspepsia, nausea, abdominal pain, oral ulcer, hepatotoxicity, skin rash, hypertension, weight loss, and interstitial lung disease. The occurrence of pulmonary cryptococcosis in leflunomide treatment has not been reported in Korea. A 74-year-old woman was admitted to hospital due to asymptomatic pulmonary nodule. She was diagnosed rheumatoid arthritis and treated with leflunomide 5 months ago due to treatment failure with methotrexate, hydroxychloroquine, and sulfasalazine. Chest radiograph and computed tomography showed solitary pulmonary nodule in her right lower lung. Pulmonary cryptococcosis was confirmed by needle biopsy of lung stained with Gomori methenamine silver and mucicarmine. The lesion was improved after antifungal therapy for 3 months.
Abdominal Pain
;
Aged
;
Arthritis, Rheumatoid*
;
Biopsy, Needle
;
Cryptococcosis*
;
Diarrhea
;
Dyspepsia
;
Exanthema
;
Female
;
Humans
;
Hydroxychloroquine
;
Hypertension
;
Korea
;
Lung
;
Lung Diseases, Interstitial
;
Methenamine
;
Methotrexate
;
Nausea
;
Oral Ulcer
;
Radiography, Thoracic
;
Solitary Pulmonary Nodule
;
Sulfasalazine
;
Treatment Failure
;
Weight Loss
4.Clinical Characteristics of the Development of Pneumothorax in Mechanically Ventilated Patients in Intensive Care Units.
Wan Chul KIM ; Su Jin LIM ; Kyong Young KIM ; Seung Jun LEE ; Yu Ji CHO ; Yi Yeong JEONG ; Mi Jung PARK ; Kyoung Nyeo JEON ; Jong Deog LEE ; Young Sil HWANG ; Ho Cheol KIM
The Korean Journal of Critical Care Medicine 2014;29(1):13-18
BACKGROUND: Pneumothorax (PTX) can occur as a complication of positive pressure ventilation in mechanically ventilated patients. METHODS: We retrospectively reviewed the clinical characteristics of patients who developed PTX during mechanical ventilation (MV) in the intensive care unit (ICU). RESULTS: Of the 326 patients admitted (208 men and 118 women; mean age, 65.3 +/- 8.74 years), 15 (4.7%) developed PTX, which was MV-associated in 11 (3.3%) cases (6 men and 5 women; mean age, 68.3 +/- 9.12 years) and procedure-associated in 4. Among the patients with MV-associated PTX, the underlying lung diseases were acute respiratory distress syndrome in 7 patients, interstitial lung disease in 2 patients, and chronic obstructive pulmonary disease in 2 patients. PTX diagnosis was achieved by chest radiography alone in 9 patients and chest computed tomography alone in 2 patients. Nine patients were using assist-control mode MV with the mean applied positive end-expiratory pressure, 9 +/- 4.6 cmH2O and the mean tidal volume, 361 +/- 63.7 ml at the diagnosis of PTX. Two patients died as a result of MV-associated PTX and their systolic pressure was below 80 mmHg and heart rates were less than 80/min. Ten patients were treated by chest tube insertion, and 1 patient was treated by percutaneous pigtail catheter insertion. CONCLUSIONS: PTX can develop in patients undergoing MV, and may cause death. Early recognition and treatment are necessary to prevent hemodynamic compromise in patients who develop PTX.
Blood Pressure
;
Catheters
;
Chest Tubes
;
Diagnosis
;
Female
;
Heart Rate
;
Hemodynamics
;
Humans
;
Intensive Care Units*
;
Critical Care*
;
Lung Diseases
;
Lung Diseases, Interstitial
;
Male
;
Pneumothorax*
;
Positive-Pressure Respiration
;
Pulmonary Disease, Chronic Obstructive
;
Radiography
;
Respiration, Artificial
;
Respiratory Distress Syndrome, Adult
;
Retrospective Studies
;
Thorax
;
Tidal Volume
5.Findings of high resolution computerized tomography of the chest in children with interstitial lung disease.
Xin-Yu YUAN ; Chun-Ju ZHOU ; Guang-Min NONG ; Xiu-Yun LIU ; Rong-Yan HUANG ; Shun-Ying ZHAO ; Zhi-Min CHEN ; De-Yu ZHAO ; En-Mei LIU ; Li DENG ; Yue-Jie ZHENG ; Ji-Rong LU ; Yun-Xiao SHANG ; Hai-Ling ZHANG ; Yun PENG ; Ji-Zhen ZOU ; Hui-Zhong CHEN
Chinese Journal of Contemporary Pediatrics 2012;14(4):310-313
6.An Adult Case of Chronic Active Epstein-Barr Virus Infection with Interstitial Pneumonitis.
Eun Jeong JOO ; Young Eun HA ; Dong Sik JUNG ; Hae Suk CHEONG ; Yu Mi WI ; Jae Hoon SONG ; Kyong Ran PECK
The Korean Journal of Internal Medicine 2011;26(4):466-469
Chronic active Epstein-Barr virus (CAEBV) infection is characterized by persistent infectious mononucleosis-like symptoms, an unusual pattern of Epstein-Barr virus (EBV) antibodies, detection of the EBV genome in affected tissues or peripheral blood, and chronic illness that cannot be attributed to any other known disease. This is the first reported Korean case of an immunocompetent adult with CAEBV-associated interstitial pneumonitis. A 28-year-old female was admitted with a fever that persisted for 3 weeks. She had multiple lymphadenopathy, hepatosplenomegaly, pancytopenia, and elevated serum aminotransferase levels. Serology for antibodies was positive and chest computed tomography showed diffuse ground glass opacities in both lungs. Histopathology of the lung tissue showed lymphocyte infiltration, and EBV DNA was detected in those lymphocytes using in situ hybridization with an EBV-encoded RNA probe. After 1 month of hospitalization, she improved without specific treatment.
Adult
;
Chronic Disease
;
Epstein-Barr Virus Infections/complications/*pathology/radiography
;
Female
;
*Herpesvirus 4, Human
;
Humans
;
Immunocompetence
;
Lung Diseases/etiology/pathology
;
Lung Diseases, Interstitial/etiology/*pathology/radiography
7.Comparison of Usual Interstitial Pneumonia and Nonspecific Interstitial Pneumonia: Quantification of Disease Severity and Discrimination between Two Diseases on HRCT Using a Texture-Based Automated System.
Sang Ok PARK ; Joon Beom SEO ; Namkug KIM ; Young Kyung LEE ; Jeongjin LEE ; Dong Soon KIM
Korean Journal of Radiology 2011;12(3):297-307
OBJECTIVE: To evaluate the usefulness of an automated system for quantification and discrimination of usual interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP). MATERIALS AND METHODS: An automated system to quantify six regional high-resolution CT (HRCT) patterns: normal, NL; ground-glass opacity, GGO; reticular opacity, RO; honeycombing, HC; emphysema, EMPH; and consolidation, CONS, was developed using texture and shape features. Fifty-four patients with pathologically proven UIP (n = 26) and pathologically proven NSIP (n = 28) were included as part of this study. Inter-observer agreement in measuring the extent of each HRCT pattern between the system and two thoracic radiologists were assessed in 26 randomly selected subsets using an interclass correlation coefficient (ICC). A linear regression analysis was used to assess the contribution of each disease pattern to the pulmonary function test parameters. The discriminating capacity of the system between UIP and NSIP was evaluated using a binomial logistic regression. RESULTS: The overall ICC showed acceptable agreement among the system and the two radiologists (r = 0.895 for the abnormal lung volume fraction, 0.706 for the fibrosis fraction, 0.895 for NL, 0.625 for GGO, 0.626 for RO, 0.893 for HC, 0.800 for EMPH, and 0.430 for CONS). The volumes of NL, GGO, RO, and EMPH contribute to forced expiratory volume during one second (FEV1) (r = 0.72, beta values, 0.84, 0.34, 0.34 and 0.24, respectively) and forced vital capacity (FVC) (r = 0.76, beta values, 0.82, 0.28, 0.21 and 0.34, respectively). For diffusing capacity (DLco), the volumes of NL and HC were independent contributors in opposite directions (r = 0.65, beta values, 0.64, -0.21, respectively). The automated system can help discriminate between UIP and NSIP with an accuracy of 82%. CONCLUSION: The automated quantification system of regional HRCT patterns can be useful in the assessment of disease severity and may provide reliable agreement with the radiologists' results. In addition, this system may be useful in differentiating between UIP and NSIP.
Female
;
Humans
;
Idiopathic Pulmonary Fibrosis/pathology/radiography
;
Logistic Models
;
Lung Diseases, Interstitial/pathology/*radiography
;
Male
;
Middle Aged
;
Pattern Recognition, Automated/*methods
;
Respiratory Function Tests
;
Severity of Illness Index
;
*Tomography, X-Ray Computed
8.Interstitial Pneumonitis in a Patient with Chronic Hepatitis C and Chronic Renal Failure on Interferon Therapy.
Eun Jung KANG ; Dong Kyun KIM ; Seong Ran JEON ; Hyun Sook CHOI ; Soung Won JEONG ; Jae Young JANG ; Joon Seong LEE ; Soo Taek UH
The Korean Journal of Gastroenterology 2011;58(1):47-52
After 4-months of alpha interferon (IFN-alpha), a 64-year old woman with chronic hepatitis C developed a cough and dyspnea and showed diffuse infiltrative opacities on her chest X-ray. Her symptoms persisted after stopping the IFN-alpha therapy. Pulmonary function testing revealed a reduced forced vital capacity. High-resolution computed tomography of the lung showed peripheral and peribronchovascular ground glass attenuation and consolidation associated with reticulation. Bronchoalveolar lavage was performed for further evaluation and showed a lymphocyte level of 8.2%, an uncommon finding in IFN-alpha-induced interstitial pneumonitis. We performed a lung biopsy to diagnose her disease and it suggested interstitial pneumonitis. This was considered to be due to the immunomodulatory effects of INF-alpha. Although rare, any sign of significant pulmonary involvement should be evaluated.
Antiviral Agents/*adverse effects/therapeutic use
;
Bronchoalveolar Lavage
;
Female
;
Hepatitis C, Chronic/complications/*drug therapy
;
Humans
;
Interferon-alpha/*adverse effects/therapeutic use
;
Kidney Failure, Chronic/complications
;
Lung Diseases, Interstitial/*chemically induced/pathology/radiography
;
Middle Aged
;
Respiratory Function Tests
;
Tomography, X-Ray Computed
9.A Case of Multicentric Castleman's Disease Having Lung Lesion Successfully Treated with Humanized Anti-interleukin-6 Receptor Antibody, Tocilizumab.
Tomoaki HIGUCHI ; Takashi NAKANISHI ; Kunio TAKADA ; Mitsuyo MATSUMOTO ; Makoto OKADA ; Hideyuki HORIKOSHI ; Kimihiro SUZUKI
Journal of Korean Medical Science 2010;25(9):1364-1367
This report presents the case of a patient demonstrating multicentric Castleman's disease (MCD) with a lung lesion that was successfully treated with an anti-interleukin-6 receptor antibody, tocilizumab in combination with corticosteroid and tacrolimus. A 43-yr-old female with abnormal shadows on a chest X-ray was referred to the hospital for further examination. She was diagnosed as having MCD based on the characteristic pathology of inguinal lymph node, lung lesions, laboratory data, and undifferentiated arthritis. Corticosteroid and rituximab therapy did not fully ameliorate the symptoms; thus, the therapeutic regimen was changed to include tocilizumab, oral corticosteroid and tacrolimus. This regimen resulted in clinical remission and the dose of tocilizumab and corticosteroid could be tapered. Tocilizumab in combination with corticosteroid and tacrolimus may therefore be a beneficial treatment regimen for lung lesions associated with MCD.
Adrenal Cortex Hormones/therapeutic use
;
Adult
;
Antibodies, Monoclonal/*therapeutic use
;
Drug Therapy, Combination
;
Female
;
Giant Lymph Node Hyperplasia/*diagnosis/drug therapy/radiography
;
Humans
;
Immunosuppressive Agents/therapeutic use
;
Lung Diseases, Interstitial/*drug therapy/pathology
;
Lymph Nodes/pathology
;
Receptors, Interleukin-6/antagonists & inhibitors
;
Tacrolimus/therapeutic use
;
Tomography, X-Ray Computed
10.Interstitial Lung Disease Associated with Combination Chemotherapy of Oxaliplatin, 5-Fluorouracil, and Leucovorin.
Sul PARK ; Jae Jin JUNG ; Goeng Bae KIM ; Hyung Sik YOON ; Sang Hun KO ; Jae Ee KO ; Yeun Seun LEE
The Korean Journal of Gastroenterology 2010;55(5):340-343
Oxaliplatin with 5-fluorouracil plus leucovorin (FOLFOX) has become the standard treatment in patients with colorectal cancer. Among known toxicities induced by oxaliplatin, hematological, gastrointestinal and neurological toxicities are common. However, acute pulmonary toxicity associated with oxaliplatin is unusual. One case of interstitial lung disease associated with the FOLFOX protocol is reported here.
Aged
;
Antineoplastic Agents/*adverse effects/therapeutic use
;
Antineoplastic Combined Chemotherapy Protocols
;
Colorectal Neoplasms/drug therapy
;
Fluorouracil/*adverse effects/therapeutic use
;
Humans
;
Leucovorin/*adverse effects/therapeutic use
;
Lung Diseases, Interstitial/chemically induced/*etiology/radiography
;
Male
;
Organoplatinum Compounds/*adverse effects/therapeutic use

Result Analysis
Print
Save
E-mail