WordNet

of or relating to interstices
not caused by a specific agent; used also of staining in making microscope slides; "nonspecific enteritis"
inflammation of the lungs; caused by a virus or an allergic reaction

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1. 非特異的間質性肺炎 nonspecific interstitial pneumonia
2. 特発性間質性肺炎：臨床症状および病理 idiopathic interstitial pneumonias clinical manifestations and pathology
3. シェーグレン症候群関連間質性肺疾患：管理と予後 interstitial lung disease associated with sjogrens syndrome management and prognosis
4. 皮膚筋炎および多発性筋炎における間質性肺疾患：治療 interstitial lung disease in dermatomyositis and polymyositis treatment
5. 未分化型の全身性リウマチ性（結合組織）疾患およびオーバーラップ症候群 undifferentiated systemic rheumatic connective tissue diseases and overlap syndromes

αvβ6 integrin may be a potential prognostic biomarker in interstitial lung disease.

Saini G1, Porte J2, Weinreb PH3, Violette SM3, Wallace WA4, McKeever TM5, Jenkins G2.
The European respiratory journal.Eur Respir J.2015 Aug;46(2):486-94. doi: 10.1183/09031936.00210414. Epub 2015 Mar 5.
Idiopathic pulmonary fibrosis (IPF) and fibrotic nonspecific interstitial pneumonitis are progressive interstitial lung diseases (ILDs) with limited treatment options and poor survival. However, the rate of disease progression is variable, implying there may be different endotypes of disease. We hyp
PMID 25745053

Serum metalloproteinases 1 and 7 in the diagnosis of idiopathic pulmonary fibrosis and other interstitial pneumonias.

Morais A1, Beltrão M2, Sokhatska O2, Costa D3, Melo N4, Mota P4, Marques A4, Delgado L5.
Respiratory medicine.Respir Med.2015 Aug;109(8):1063-8. doi: 10.1016/j.rmed.2015.06.003. Epub 2015 Jun 12.
INTRODUCTION: Accurate diagnosis of idiopathic pulmonary fibrosis (IPF) has important therapeutic and prognostic implications and would be greatly aided by reliable diagnostic biomarkers as IPF has sometimes overlapping features with other interstitial lung diseases (ILD).OBJECTIVES: To explore the
PMID 26174192

Drug-Related Pneumonitis During Mammalian Target of Rapamycin Inhibitor Therapy: Radiographic Pattern-Based Approach in Waldenström Macroglobulinemia as a Paradigm.

Nishino M1, Boswell EN2, Hatabu H2, Ghobrial IM2, Ramaiya NH2.
The oncologist.Oncologist.2015 Jul 23. pii: theoncologist.2015-0033. [Epub ahead of print]
BACKGROUND: This study determined the frequency of drug-related pneumonitis during mammalian target of rapamycin (mTOR) inhibitor therapy in Waldenström macroglobulinemia patients and investigated the imaging characteristics and radiographic patterns of pneumonitis.MATERIALS AND METHODS: A total of
PMID 26205737

Morimoto Konosuke,Janssen William J.,Terada Mayumi
Respiratory Medicine 106(12), 1800-1803, 2012-12
… Rationale: Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrosing interstitial pneumonia. … Methods: Efferocytosis, was evaluated using Wright-Giemsa stained cell preparations isolated from the bronchoalveolar lavage (BAL) fluid of patients with IPF (n = 5), nonspecific interstitial pneumonitis (n = 6), cryptogenic organizing pneumonia (n = 4) and eosinophilic pneumonia (EP) (n = 5). …
NAID 120005230378

BAL Fluid Concentrations of Cytokines in Patients with Nonspecific Interstitial Pneumonia, Usual Interstitial Pneumonia, Collagen Vascular Disease Associated with Interstitial Pneumonia, and Sarcoidosis

Fukushima Fumiya,Hirata Hiroyuki,Tatewaki Masamitsu,Fukushima Yasutsugu,Sugiyama Kumiya,Fukuda Takeshi
Dokkyo journal of medical sciences 39(3), 161-172, 2012-10-25
… However, their individual roles in idiopathic interstitial pneumonitis (IIP) and inthe other types of interstitial pneumonitis (IP), including collagen vascular disease associated interstitialpneumonitis (CVD-IP), remain unknown. …
NAID 110009493151