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Erschienen in: La radiologia medica 10/2015

01.10.2015 | CHEST RADIOLOGY

Idiopathic interstitial pneumonias: do HRCT criteria established by ATS/ERS/JRS/ALAT in 2011 predict disease progression and prognosis?

verfasst von: Chiara Romei, Laura Tavanti, Paola Sbragia, Annalisa De Liperi, Laura Carrozzi, Ferruccio Aquilini, Antonio Palla, Fabio Falaschi

Erschienen in: La radiologia medica | Ausgabe 10/2015

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Abstract

Purpose

The objective of the study was to determine whether HRCT criteria for Usual Interstitial Pneumonia (UIP), possible UIP or no-UIP pattern recommended by ATS/ERS/JRS/ALAT guidelines 2011 are able to predict progression and prognosis of the disease in a group of patients with fibrotic idiopathic interstitial pneumonia (IIP).

Materials and methods

This was a retrospective study conducted with the approval of the ethics committee. Two radiologists at baseline HRCT distributed 70 patients with fibrotic IIP into three groups on the basis of the 2011 guidelines: UIP pattern (group 1), possible UIP pattern (group 2), inconsistent with UIP pattern (group 3). The different abnormalities (honeycombing, reticulation, ground-glass and traction bronchiectasis), fibrotic score (reticulation + honeycombing) and overall CT score were visually scored at baseline and during the follow-up (total HRCT 178). The mortality rate of the three groups was compared. The baseline abnormalities were then correlated with the mortality rate in the UIP group.

Results

The inter-observer agreement in the classification of the abnormalities in the three groups was almost perfect (k = 0.92). After consensus, 44 patients were classified into group 1, 13 into group 2 and 13 into group 3. During a mean follow-up of 1386 days, overall CT score, fibrotic score, honeycombing and traction bronchiectasis showed a significant progression in group 1. The mortality rate was significantly higher in group 1 (18 deaths) versus group 2 and 3 (1 death each). In group 1, baseline honeycombing rate higher than 25 %, fibrotic score higher than 30, overall CT score greater than 45 and traction bronchiectasis in more than 4 lobes defined the worst prognosis.

Conclusion

HRCT classification based on 2011 guidelines showed high accuracy in stratifying fibrotic changes because in our study UIP, possible UIP and inconsistent with UIP pattern seem to be correlated with different disease progression and mortality rate.
Literatur
1.
Zurück zum Zitat American Thoracic Society; European Respiratory Society (2000) Idiopathic pulmonary fibrosis: diagnosis and treatment: international consensus statement. Am J Respir Crit Care Med 161:646–664CrossRef American Thoracic Society; European Respiratory Society (2000) Idiopathic pulmonary fibrosis: diagnosis and treatment: international consensus statement. Am J Respir Crit Care Med 161:646–664CrossRef
2.
Zurück zum Zitat American Thoracic Society; European Respiratory Society (2002) American Thoracic Society/European Respiratory Society international multidisciplinary consensus classification of idiopathic interstitial pneumonias. Am J Respir Crit Care Med 165:277–304CrossRef American Thoracic Society; European Respiratory Society (2002) American Thoracic Society/European Respiratory Society international multidisciplinary consensus classification of idiopathic interstitial pneumonias. Am J Respir Crit Care Med 165:277–304CrossRef
3.
Zurück zum Zitat Travis WD, Costabel U, Hansell DM, King TE Jr, Lynch DA, Nicholson AG, Ryerson CJ, Ryu JH, Selman M, Wells AU, Behr J, Bouros D, Brown KK, Colby TV, Collard HR, Cordeiro CR, Cottin V, Crestani B, Drent M, Dudden RF, Egan J, Flaherty K, Hogaboam C, Inoue Y, Johkoh T, Kim DS, Kitaichi M, Loyd J, Martinez FJ, Myers J, Protzko S, Raghu G, Richeldi L, Sverzellati N, Swigris J, Valeyre D, ATS/ERS Committee on Idiopathic Interstitial Pneumonias (2013) An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med 188:733–748CrossRefPubMed Travis WD, Costabel U, Hansell DM, King TE Jr, Lynch DA, Nicholson AG, Ryerson CJ, Ryu JH, Selman M, Wells AU, Behr J, Bouros D, Brown KK, Colby TV, Collard HR, Cordeiro CR, Cottin V, Crestani B, Drent M, Dudden RF, Egan J, Flaherty K, Hogaboam C, Inoue Y, Johkoh T, Kim DS, Kitaichi M, Loyd J, Martinez FJ, Myers J, Protzko S, Raghu G, Richeldi L, Sverzellati N, Swigris J, Valeyre D, ATS/ERS Committee on Idiopathic Interstitial Pneumonias (2013) An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med 188:733–748CrossRefPubMed
4.
Zurück zum Zitat Flaherty KR, Toews GB, Travis WD, Colby TV, Kazerooni EA, Gross BH, Jain A, Strawderman RL, Paine R, Flint A, Lynch JP III, Martinez FJ (2002) Clinical significance of histological classification of idiopathic interstitial pneumonia. Eur Respir J 19:275–283CrossRefPubMed Flaherty KR, Toews GB, Travis WD, Colby TV, Kazerooni EA, Gross BH, Jain A, Strawderman RL, Paine R, Flint A, Lynch JP III, Martinez FJ (2002) Clinical significance of histological classification of idiopathic interstitial pneumonia. Eur Respir J 19:275–283CrossRefPubMed
5.
Zurück zum Zitat Bjoraker JA, Ryu JH, Edwin MK, Myers JL, Tazelaar HD, Schroeder DR, Offord KP (1998) Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 157:199–203CrossRefPubMed Bjoraker JA, Ryu JH, Edwin MK, Myers JL, Tazelaar HD, Schroeder DR, Offord KP (1998) Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 157:199–203CrossRefPubMed
6.
Zurück zum Zitat Hansell DM (2013) Classification of diffuse lung diseases: why and how. Radiology 268:628–640CrossRefPubMed Hansell DM (2013) Classification of diffuse lung diseases: why and how. Radiology 268:628–640CrossRefPubMed
7.
Zurück zum Zitat Peikert T, Daniels CE, Beebe TJ, Meyer KC, Ryu JH, Interstitial Lung Diseases Network of the American College of Chest Physicians (2008) Assessment of current practice in the diagnosis and therapy of idiopathic pulmonary fibrosis. Respir Med 102(9):1342–1348CrossRefPubMed Peikert T, Daniels CE, Beebe TJ, Meyer KC, Ryu JH, Interstitial Lung Diseases Network of the American College of Chest Physicians (2008) Assessment of current practice in the diagnosis and therapy of idiopathic pulmonary fibrosis. Respir Med 102(9):1342–1348CrossRefPubMed
8.
Zurück zum Zitat Diette GB, Scatarige JC, Haponik EF, Merriman B, Fisherman EK (2005) Do high-resolution CT findings of usual interstitial pneumonitis obviate lung biopsy? Views of pulmonologists. Respiration 72:134–141CrossRefPubMed Diette GB, Scatarige JC, Haponik EF, Merriman B, Fisherman EK (2005) Do high-resolution CT findings of usual interstitial pneumonitis obviate lung biopsy? Views of pulmonologists. Respiration 72:134–141CrossRefPubMed
9.
Zurück zum Zitat Utz JP, Ryu JH, Douglas WW, Tazelaar HD, Myers JL, Allen MS, Schroeder DR (2001) High short term mortality following lung biopsy for usual interstitial pneumonia. Eur Respir J 17:175–179CrossRefPubMed Utz JP, Ryu JH, Douglas WW, Tazelaar HD, Myers JL, Allen MS, Schroeder DR (2001) High short term mortality following lung biopsy for usual interstitial pneumonia. Eur Respir J 17:175–179CrossRefPubMed
10.
Zurück zum Zitat Yuksel M, Ozyurtkan MO, Bostanci K, Ahiskali R, Kodalli N (2006) Acute exacerbation of interstitial fibrosis after pulmonary resection. Ann Thorac Surg 82:336–338CrossRefPubMed Yuksel M, Ozyurtkan MO, Bostanci K, Ahiskali R, Kodalli N (2006) Acute exacerbation of interstitial fibrosis after pulmonary resection. Ann Thorac Surg 82:336–338CrossRefPubMed
11.
Zurück zum Zitat Collard HR, King TE Jr, Bartelson BB, Vourlekis JS, Schwarz MI, Brown KK (2003) Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 168:538–542CrossRefPubMed Collard HR, King TE Jr, Bartelson BB, Vourlekis JS, Schwarz MI, Brown KK (2003) Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 168:538–542CrossRefPubMed
12.
Zurück zum Zitat Flaherty KR, Mumford JA, Murray S, Kazerooni EA, Gross BH, Colby TV, Travis WD, Flint A, Toews GB, Lynch JP III, Martinez FJ (2003) Prognostic implication of physiologic and radiographic changes in idiopathic interstitial pneumonia. Am J Respir Crit Care Med 168:543–548CrossRefPubMed Flaherty KR, Mumford JA, Murray S, Kazerooni EA, Gross BH, Colby TV, Travis WD, Flint A, Toews GB, Lynch JP III, Martinez FJ (2003) Prognostic implication of physiologic and radiographic changes in idiopathic interstitial pneumonia. Am J Respir Crit Care Med 168:543–548CrossRefPubMed
13.
Zurück zum Zitat Flaherty KR, Thwaite EL, Kazerooni EA, Gross BH, Toews GB, Colby TV, Travis WD, Mumford JA, Murray S, Flint A, Lynch JP III, Martinez FJ (2003) Radiological versus histological diagnosis in UIP and NSIP: survival implications. Thorax 53:143–148CrossRef Flaherty KR, Thwaite EL, Kazerooni EA, Gross BH, Toews GB, Colby TV, Travis WD, Mumford JA, Murray S, Flint A, Lynch JP III, Martinez FJ (2003) Radiological versus histological diagnosis in UIP and NSIP: survival implications. Thorax 53:143–148CrossRef
14.
Zurück zum Zitat Mura M, Porretta MA, Bargagli E, Sergiacomi G, Zompatori M, Sverzellati N, Taglieri A, Mezzasalma F, Rottoli P, Saltini C, Rogliani P (2012) Predicting survival in newly diagnosed idiopathic pulmonary fibrosis: a 3-year prospective study. Eur Respir J 40(1):101–109CrossRefPubMed Mura M, Porretta MA, Bargagli E, Sergiacomi G, Zompatori M, Sverzellati N, Taglieri A, Mezzasalma F, Rottoli P, Saltini C, Rogliani P (2012) Predicting survival in newly diagnosed idiopathic pulmonary fibrosis: a 3-year prospective study. Eur Respir J 40(1):101–109CrossRefPubMed
15.
Zurück zum Zitat Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, Colby TV, Cordier JF, Flaherty KR, Lasky JA, Lynch DA, Ryu JH, Swigris JJ, Wells AU, Ancochea J, Bouros D, Carvalho C, Costabel U, Ebina M, Hansell DM, Johkoh T, Kim DS, King TE Jr, Kondoh Y, MyersJ Müller NL, Nicholson AG, Richeldi L, Selman M, Dudden RF, Griss BS, Protzko SL, Schünemann HJ, ATS/ERS/JRS/ALAT Committee on Idiopathic Pulmonary Fibrosis (2011) An officialATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 183:788–824CrossRefPubMed Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, Colby TV, Cordier JF, Flaherty KR, Lasky JA, Lynch DA, Ryu JH, Swigris JJ, Wells AU, Ancochea J, Bouros D, Carvalho C, Costabel U, Ebina M, Hansell DM, Johkoh T, Kim DS, King TE Jr, Kondoh Y, MyersJ Müller NL, Nicholson AG, Richeldi L, Selman M, Dudden RF, Griss BS, Protzko SL, Schünemann HJ, ATS/ERS/JRS/ALAT Committee on Idiopathic Pulmonary Fibrosis (2011) An officialATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 183:788–824CrossRefPubMed
16.
Zurück zum Zitat Raghu G, Lynch D, Godwin JD, Webb R, Colby TV, Leslie KO, Behr J, Brown KK, Egan JJ, Flaherty KR, Martinez FJ, Wells AU, Shao L, Zhou H, Pedersen PS, Sood R, Montgomery AB, O’Riordan TG (2014) Diagnosis of idiopathic pulmonary fibrosis with high-resolution CT in patients with little or no radiological evidence of honeycombing: secondary analysis of a randomised, controlled trial. Lancet Respir Med 2:277–284CrossRefPubMed Raghu G, Lynch D, Godwin JD, Webb R, Colby TV, Leslie KO, Behr J, Brown KK, Egan JJ, Flaherty KR, Martinez FJ, Wells AU, Shao L, Zhou H, Pedersen PS, Sood R, Montgomery AB, O’Riordan TG (2014) Diagnosis of idiopathic pulmonary fibrosis with high-resolution CT in patients with little or no radiological evidence of honeycombing: secondary analysis of a randomised, controlled trial. Lancet Respir Med 2:277–284CrossRefPubMed
17.
Zurück zum Zitat Shin KM, Lee KS, Chung MP, Bae YA, Kim TS, Chung MJ (2008) Prognostic determinants among clinical, thin-section CT, and histopathologic findings for fibrotic idiopathic interstitial pneumonias: tertiary hospital study. Radiology 249(1):328–337CrossRefPubMed Shin KM, Lee KS, Chung MP, Bae YA, Kim TS, Chung MJ (2008) Prognostic determinants among clinical, thin-section CT, and histopathologic findings for fibrotic idiopathic interstitial pneumonias: tertiary hospital study. Radiology 249(1):328–337CrossRefPubMed
18.
Zurück zum Zitat Schmidt SL, Sundaram B, Flaherty KR (2009) Diagnosing fibrotic lung disease: when is high resolution computed tomography sufficient to make a diagnosis of idiopathic pulmonary fibrosis? Respirology 14(7):934–939CrossRefPubMed Schmidt SL, Sundaram B, Flaherty KR (2009) Diagnosing fibrotic lung disease: when is high resolution computed tomography sufficient to make a diagnosis of idiopathic pulmonary fibrosis? Respirology 14(7):934–939CrossRefPubMed
19.
Zurück zum Zitat Lee HY, Lee KS, Jeong YJ, Hwang JH, Kim HJ, Chung MP, Han J (2012) High-resolution CT findings in fibrotic idiopathic interstitial pneumonias with little honeycombing: serial changes and prognostic implications. AJR Am J Roentgenol 199(5):982–989CrossRefPubMed Lee HY, Lee KS, Jeong YJ, Hwang JH, Kim HJ, Chung MP, Han J (2012) High-resolution CT findings in fibrotic idiopathic interstitial pneumonias with little honeycombing: serial changes and prognostic implications. AJR Am J Roentgenol 199(5):982–989CrossRefPubMed
20.
Zurück zum Zitat Altman DG (1991) Practical Statistics for Medical Research. Chapman & Hall, London Altman DG (1991) Practical Statistics for Medical Research. Chapman & Hall, London
21.
Zurück zum Zitat Armitage P, Berry G (1994) Statistical methods in Medical Research, 3rd edn. Blackwell, Oxford Armitage P, Berry G (1994) Statistical methods in Medical Research, 3rd edn. Blackwell, Oxford
22.
Zurück zum Zitat Siegel S (1956) Nonparametric statistics for the behavioral sciences. McGraw-Hill, New York Siegel S (1956) Nonparametric statistics for the behavioral sciences. McGraw-Hill, New York
23.
Zurück zum Zitat Dwyer JH, Feinleib M (1992) Introduction to statistical models for longitudinal observation. In: Dwyer JH, Feinleib M, Lippert P, Hoffmeister H (eds) Statistical. Models for Longitudinal Studies of Health. Oxford University Press, New York, pp 3–48 Dwyer JH, Feinleib M (1992) Introduction to statistical models for longitudinal observation. In: Dwyer JH, Feinleib M, Lippert P, Hoffmeister H (eds) Statistical. Models for Longitudinal Studies of Health. Oxford University Press, New York, pp 3–48
24.
Zurück zum Zitat Cox DR, Oakes D (1984) Analysis of Survival Data. Chapman & Hall, London Cox DR, Oakes D (1984) Analysis of Survival Data. Chapman & Hall, London
25.
Zurück zum Zitat Galvin JR, Frazier AA, Franks TJ (2010) Collaborative radiologic and histopathologic assessment of fibrotic lung disease. Radiology 255(3):692–706CrossRefPubMed Galvin JR, Frazier AA, Franks TJ (2010) Collaborative radiologic and histopathologic assessment of fibrotic lung disease. Radiology 255(3):692–706CrossRefPubMed
26.
Zurück zum Zitat Sverzellati N, Calabrò E, Chetta A, Concari G, Larici AR, Mereu M, Cobelli R, De Filippo M, Zompatori M (2007) Visual score and quantitative CT indices in pulmonary fibrosis: relationship with physiologic impairment. Radiol Med 112(8):1160–1172 Epub 2007 Dec 13CrossRefPubMed Sverzellati N, Calabrò E, Chetta A, Concari G, Larici AR, Mereu M, Cobelli R, De Filippo M, Zompatori M (2007) Visual score and quantitative CT indices in pulmonary fibrosis: relationship with physiologic impairment. Radiol Med 112(8):1160–1172 Epub 2007 Dec 13CrossRefPubMed
27.
Zurück zum Zitat Edey AJ, Devaraj AA, Barker RP, Nicholson AG, Wells AU, Hansell DM (2011) Fibrotic idiopathic interstitial pneumonias: HRCT findings that predict mortality. Eur Radiol 21(8):1586–1593CrossRefPubMed Edey AJ, Devaraj AA, Barker RP, Nicholson AG, Wells AU, Hansell DM (2011) Fibrotic idiopathic interstitial pneumonias: HRCT findings that predict mortality. Eur Radiol 21(8):1586–1593CrossRefPubMed
28.
Zurück zum Zitat Johkoh T, Müller NL, Cartier Y, Kavanagh PV, Hartman TE, Akira M, Ichikado K, Ando M, Nakamura H (1999) Idiopathic interstitial pneumonias: diagnostic accuracy of thin-section CT in 129 patients. Radiology 211(2):555–560CrossRefPubMed Johkoh T, Müller NL, Cartier Y, Kavanagh PV, Hartman TE, Akira M, Ichikado K, Ando M, Nakamura H (1999) Idiopathic interstitial pneumonias: diagnostic accuracy of thin-section CT in 129 patients. Radiology 211(2):555–560CrossRefPubMed
29.
Zurück zum Zitat Thomeer M, Demedts M, Behr J, Buhl R, Constabel U et al (2008) Multidisciplinary interobserved agreement in the diagnosis of idiopathic pulmonary fibrosis. Eur Respir J 31:585–591CrossRefPubMed Thomeer M, Demedts M, Behr J, Buhl R, Constabel U et al (2008) Multidisciplinary interobserved agreement in the diagnosis of idiopathic pulmonary fibrosis. Eur Respir J 31:585–591CrossRefPubMed
30.
Zurück zum Zitat Sverzellati N, De Filippo M, Bartalena T, Piciucchi S, Zompatori M (2010) High-resolution computed tomography in the diagnosis and follow-up of idiopathic pulmonary fibrosis. Radiol Med 115(4):526–538CrossRefPubMed Sverzellati N, De Filippo M, Bartalena T, Piciucchi S, Zompatori M (2010) High-resolution computed tomography in the diagnosis and follow-up of idiopathic pulmonary fibrosis. Radiol Med 115(4):526–538CrossRefPubMed
31.
Zurück zum Zitat Sumikawa H, Johkoh T, Fujimoto K, Arakawa H, Colby TV, Fukuoka J, Taniguchi H, Kondoh Y, Kataoka K, Ogura T, Baba T, Ichikado K, Gyobu T, Yanagawa M, Honda O, Tomiyama N (2014) Pathologically proved nonspecific interstitial pneumonia: CT pattern analysis as compared with usual interstitial pneumonia CT Pattern. Radiology 272(2):549–556CrossRefPubMed Sumikawa H, Johkoh T, Fujimoto K, Arakawa H, Colby TV, Fukuoka J, Taniguchi H, Kondoh Y, Kataoka K, Ogura T, Baba T, Ichikado K, Gyobu T, Yanagawa M, Honda O, Tomiyama N (2014) Pathologically proved nonspecific interstitial pneumonia: CT pattern analysis as compared with usual interstitial pneumonia CT Pattern. Radiology 272(2):549–556CrossRefPubMed
32.
Zurück zum Zitat Best AC, Meng J, Lynch AM, Bozic CM, Miller D, Grunwald GK, Lynch DA (2008) Idiopathic pulmonary fibrosis: physiologic tests, quantitative CT indexes, and CT visual scores as predictors of mortality. Radiology 246(3):935–940CrossRefPubMed Best AC, Meng J, Lynch AM, Bozic CM, Miller D, Grunwald GK, Lynch DA (2008) Idiopathic pulmonary fibrosis: physiologic tests, quantitative CT indexes, and CT visual scores as predictors of mortality. Radiology 246(3):935–940CrossRefPubMed
33.
Zurück zum Zitat Sumikawa H, Johkoh T, Colby TV, Ichikado K, Suga M, Taniguchi H, Kondoh Y, Ogura T, Arakawa H, Fujimoto K, Inoue A, Mihara N, Honda O, Tomiyama N, Nakamura H, Muller NL (2008) Computed tomography findings in pathological usual interstitial pneumonia. Relation to survival. Am J Respir Crit Care Med 177:433–439CrossRefPubMed Sumikawa H, Johkoh T, Colby TV, Ichikado K, Suga M, Taniguchi H, Kondoh Y, Ogura T, Arakawa H, Fujimoto K, Inoue A, Mihara N, Honda O, Tomiyama N, Nakamura H, Muller NL (2008) Computed tomography findings in pathological usual interstitial pneumonia. Relation to survival. Am J Respir Crit Care Med 177:433–439CrossRefPubMed
34.
Zurück zum Zitat Lynch DA, Godwin JD, Safrin S, Starko KM, Hormel P, Brown KK, Raghu G, King TE Jr, Bradford WZ, Schwartz DA, Webb WR (2005) High-resolution computed tomography in idiopathic pulmonary fibrosis. Diagnosis and prognosis. Am J Respir Crit Care Med 172:488–493CrossRefPubMed Lynch DA, Godwin JD, Safrin S, Starko KM, Hormel P, Brown KK, Raghu G, King TE Jr, Bradford WZ, Schwartz DA, Webb WR (2005) High-resolution computed tomography in idiopathic pulmonary fibrosis. Diagnosis and prognosis. Am J Respir Crit Care Med 172:488–493CrossRefPubMed
35.
Zurück zum Zitat Misumi S, Lynch DA (2006) Idiopathic pulmonary fibrosis/usual interstitial pneumonia: imaging diagnosis, spectrum of abnormalities, and temporal progression. Proc Am Thorac Soc 3(4):307–314CrossRefPubMed Misumi S, Lynch DA (2006) Idiopathic pulmonary fibrosis/usual interstitial pneumonia: imaging diagnosis, spectrum of abnormalities, and temporal progression. Proc Am Thorac Soc 3(4):307–314CrossRefPubMed
Metadaten
Titel
Idiopathic interstitial pneumonias: do HRCT criteria established by ATS/ERS/JRS/ALAT in 2011 predict disease progression and prognosis?
verfasst von
Chiara Romei
Laura Tavanti
Paola Sbragia
Annalisa De Liperi
Laura Carrozzi
Ferruccio Aquilini
Antonio Palla
Fabio Falaschi
Publikationsdatum
01.10.2015
Verlag
Springer Milan
Erschienen in
La radiologia medica / Ausgabe 10/2015
Print ISSN: 0033-8362
Elektronische ISSN: 1826-6983
DOI
https://doi.org/10.1007/s11547-015-0526-0

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