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postmortem magnetic resonance imaging in the diagnosis of congenital pneumonia
Tumanova UN1 Lyapin VM1, Bychenko VG1, Schegolev AI12, Sukhikh GT1
1 Kulakov Research Center for Obstetrics, Gynecology and Perinatology, Moscow, Russia
2 Pirogov Russian National Research Medical University, Moscow, Russia
Congenital pneumonia is one of the leading causes of neonatal deaths. In this work we assess the possibility of using postmortem magnetic resonance imaging for the diagnosis of congenital pneumonia. The study was conducted on 21 neonate bodies. Before the autopsy, MRI scanning was performed on the Magnetom Verio 3T system (Siemens, Germany) in T1 and T2 standard modes. The resulting images were used to analyze signal intensities of lung tissue, pleural fluid and air. Airiness index was computed as the ratio of pleural fluid signal intensity to lung tissue signal intensity. Then, the autopsy was performed. Based on the histological analysis results, the main and the control groups were formed. The bodies of 9 neonates who had died from congenital pneumonia were included into the main group; the control group consisted of 12 dead neonates with no signs of pneumonia. On T1-weighted images, the signal intensity from the lungs of the infants with congenital pneumonia was higher by 26.5 % in the left lung and 12.9 % in the right lung, compared to the controls (p >0.05). On T2-weighted images, the corresponding figures were 23.7 and 31.2 % (p >0.05). The sensitivity of the method is 77.8 %, specificity is 75.0 % and diagnostic efficacy is 76.2 %.
Keywords: congenital pneumonia, lung, postmortem magnetic resonance imaging, autopsy, airiness index
Correspondence should be addressed: Uliana Tumanova
ul. Akademika Oparina, d. 4, Moscow, Russia, 117997; [email protected]
Received: 17.08.2016 Accepted: 23.08.2016
посмертная мрт для диагностики врожденной пневмонии
У. Н. Туманова1 ^ В. М. Ляпин1, В. Г. Быченко1, А. И. Щеголев1'2, Г. Т. Сухих1
1 Научный центр акушерства, гинекологии и перинатологии имени академика В. И. Кулакова, Москва
2 Российский национальный исследовательский медицинский университет имени Н. И. Пирогова, Москва
Врожденная пневмония — одна из основных причин гибели детей в неонатальном периоде. В работе оценена возможность применения посмертной магнитно-резонансной томографии для диагностики врожденной пневмонии на аутопсийном материале. Исследовали тела 21 умершего новорожденного. До аутопсии проводили МРТ-исследование на аппарате 3T Magnetom Verio (Siemens, Германия) в стандартных Т1 и Т2 режимах. На томограммах анализировали интенсивность сигнала от ткани легких, плевральной жидкости и воздуха и рассчитывали показатель воздушности — отношение интенсивности сигнала от жидкости в плевральной полости к интенсивности сигнала от ткани легких. Затем проводили патологоанатомическое вскрытие и по результатам изучения гистологических препаратов все наблюдения разделили на две группы: в основную группу включили тела 9 новорожденных, умерших от врожденной пневмонии, в группу сравнения — тела 12 умерших новорожденных без признаков пневмонии. Интенсивность сигнала от ткани легких новорожденных с врожденной пневмонией была выше аналогичного показателя в группе сравнения: на 26,5 и 12,9 % в левом и правом легком соответственно на Т1-взве-шенных изображениях (p >0,05) и на 23,7 и 31,2 % — на Т2-взвешенных изображениях (p >0,05). Чувствительность описанного метода составила 77,8 %, специфичность — 75,0 %, диагностическая эффективность — 76,2 %.
Ключевые слова: врожденная пневмония, легкое, посмертная магнитно-резонансная томография, аутопсия, показатель воздушности
Для корреспонденции: Туманова Ульяна Николаевна
117997, г. Москва, ул. Академика Опарина, д. 4; [email protected]
Статья поступила: 17.08.2016 Статья принята к печати: 23.08.2016
Congenital pneumonia is an acute inflammatory condition of the respiratory zone caused by an antenatal or/and intrapartum infection and manifesting itself clinically and radiographically within the first 72 hours after birth [1]. Improvements in diagnostic techniques and treatment approaches contribute to better survival of affected neonates, but death rate still remains relatively high. According to research data [2], congenital pneumonia is diagnosed worldwide in 10-38 % of stillborn and 20-63 % of liveborn babies who subsequently die. In Russia, congenital pneumonia accounted for 0.43 % of all intrauterine
deaths and was also the primary cause of death of 8.7 % of infants in the early (0-6 days) neonatal period in 2010, as reported by the Federal Service for State Statistics [3]. In 2014, those figures were 0.35 % and 8.34 %, respectively [4].
The major technique for the postmortem diagnosis of congenital pneumonia is autopsy. However, morphological analysis is often impeded by false positive results of lung float test performed at autopsy and by a weak inflammatory response in premature babies or upon treatment with antibiotics [5, 6]. Here, radiography is usually an alternative.
Computed tomography (CT) is considered the major radiographic technique used to diagnose pulmonary pathologies [7-9]. Postmortem CT is also quite effective in the assessment of lung conditions and determining cause of death in adults [10]. However, lungs of dead fetuses and neonates are not visible on unenhanced CT [11]. Parallel to CT, magnetic resonance imaging (MRI) is being increasingly used to detect pulmonary pathologies [12]. For example, bronchial pneumonia previously diagnosed during a CT scan was detected later by MRI in 21 out of 22 adults, and the efficacy of this technique was relatively high: sensitivity of 95 %, specificity of 88 %, positive prognostic value of 95 % [13]. MRI proved to be an effective diagnostic tool in the examination of 30 children (3-19 years of age) who had already been diagnosed with pneumonia based on the X-ray test [14]. The researchers concluded that MRI could be used as an alternative to X-ray or CT for the detection of pneumonia foci no smaller than 1 cm in size in the absence of calcification [13, 14]. Since MRI produces images in any projection and the patient is not exposed to radiation, it can be recommended for the dynamic assessment of pneumonia progression. Leutner et al. [15] demonstrated that MRI is more effective in diagnosing necrotizing pneumonia, compared to enhanced CT. MRI also proved highly effective in the differential diagnosis of causes of stillbirths and neonatal deaths [16, 17] and was successfully used to determine time of intrauterine fetal death by evaluating lung morphology [18, 19].
The aim of this work was to study a possibility of using postmortem MRI for diagnosing congenital pneumonia in autopsy material.
METHODS
We studied 21 dead neonates. Six to fifteen hours after infants had been pronounced dead but prior to autopsy, the bodies were scanned in standard T1 and T2 modes on 3T Magnetom Verio scanner (Siemens, Germany) set up to a field of view of 300 mm and a flip angle of 180°. T1-mode settings were as follows: slice thickness of 0.9 mm, repetition time of 1, 900 ms, echo time of 2.2 ms. T2-mode settings were as follows: slice thickness of 1 mm, repetition time of 3,200 ms, echo time of 410 ms. Using sagittal T1- and T2-weighted images, we measured signal intensity (SI) in the following regions of interest (ROI): the largest possible section of the right and left lung that did not contain big elements of the bronchovascular bundle, region of air in the area close to the anterior abdominal wall and in the pleural fluid. Then, an original airiness index (AI) was calculated for the right and left lungs as the ratio of the SI value of the pleural fluid to the SI value of the lung tissue. Because MR signal intensity within a given body region changes non-linearly and depends on a number of factors (distance from the scanner's isocenter, magnetic field homogeneity, physical properties of the surrounding tissues, etc.), to study its absolute value alone would be incorrect. We believe that airiness index allows minimizing or even eliminating measurement error related to the performance of an individual scanner.
After MRI scan, autopsy was performed followed by the analysis of hematoxylin- and eosin-stained histological slices. Based on the autopsy results, two groups were formed: group (the main experimental group) included bodies of 9 neonates who had died of congenital pneumonia 2 h 12 min to 36.5 days after birth; group II (the comparison group) included bodies of 12 neonates with no signs of pneumonia who had died 2 h 7 min to 24 days after birth. The bodies, the right lung and the left lung were weighted. The weight ratio of both lungs to the
body was calculated.
Statistical processing was done using Statistica 8.0 software (StatSoft, USA). Mean values, standard deviations and a coefficient of variation were computed for each measured parameter. Differences were considered significant with p <0.05. Using the obtained results, we calculated sensitivity, specificity and diagnostic efficacy of postmortem MRI in the diagnosis of congenital pneumonia.
The study was approved by the Biomedical Research Ethics Committee of Kulakov Research Center for Obstetrics, Gynecology and Perinatology (Protocol 25 dated June 22, 2012).
RESULTS
Morphological analysis of autopsy material obtained from the comparison group established that left lung weight varied from 2.1 to 36.5 g (coefficient of variation was 95.4 %) and right lung weight varied from 0.3 to 24.2 g (coefficient of variation was 50.9 %) (table 1). Mean weight of the left, right and both lungs was 10.8 ± 10.8, 11.5 ± 6.1 and 22.3 ± 14.6 g, respectively. Histological samples of lung tissue had signs of hypoplasia (in bodies with congenital diaphragmatic hernia) (fig. 1A), atelectases and dystelectases.
In neonates who had died of pneumonia, the weights of the left and right lungs were 4.1 to 42.7 g (coefficient of variation was 44.9 and 40.1 %, respectively) (table 1). Mean weights were 19.6 ± 9.3 and 24.1 ± 10.2 g, respectively; mean weight of both lungs was 45.9 ± 17.7 g. This indicates that all values were 1.8-2.1 times higher than in the comparison group (p <0.05). The weight ratio of both lungs to the body was 2.4 times higher in the experimental group (p <0.05). Histological samples obtained from group I showed signs of pneumonia manifested as weak monocyte/macrophage infiltration. (fig. 1B).
Visual analysis of T1- and T2-weighted images obtained from both groups indicated almost identical signal intensity in both lungs, but T2-weighted images reflected the organ structure more clearly, compared to T1-weighted images (fig.2, 3). The signal from the lungs of neonates who had died of pneumonia was more intense in both scanning modes as compared to the signal from the lungs of neonates who had died of other pathologies. It was 26.5 and 12.9 % more intense for the left and right lungs, respectively, on T1-weighted images and 23.7 and 31.2 % more intense on T2-weighted images (p >0.05) (table 2). Nonuniform signal intensity within one lung was occasionally observed in the comparison group as a result of a haemorrhage (fig.4); differences in tissue brightness in the right and left lungs were due to organ compression caused by diaphragmatic hernia (fig. 5).
Mean airiness index of the left lung calculated upon the analysis of T1-weighted images of neonates who had died of pneumonia was by 44 % lower in the experimental group than in the comparison group; with the right lung, it was by 1.1 % higher (table 2). The same index calculated upon the analysis of T2-weighted images was lower for both lungs in the experimental group: by 14.3 % for the left lung and by 5.7 % for the right lung. When airiness index was calculated in the right and left lung separately, differences were statistically insignificant (p >0.05). However, if the index value obtained from T2-weighted images was less than 2.5 in both lungs of a newborn, it indicated a morphologically confirmed pneumonia in the vast majority of cases (77.8 %).
Sensitivity of the applied technique was 77.8 %, its specificity was 75.0 % and diagnostic efficacy was 76.2 %, which indicates its high diagnostic value.
Table 1. Clinical and morphological features of dead neonates
Group Case Sex Gestational age Age Body weight Weight of both lungs Right lung weight Left lung weight Weight ratio of both lungs to the body
1 F 38 5 cyT. 11 H 2080.0 43.2 22.1 21.1 0.021
2 M 33 28 cyT. 2800.0 58.6 25.2 33.4 0.021
3 M 24 5 cyT. 15 H 800.0 16.3 12.2 14.1 0.020
4 F 33 7 cyT. 14 H 2674.0 52.6 29.3 23.3 0.020
5 M 35 36 cyT. 10 H 3206.0 43.9 23.3 20.6 0.014
6 M 39 3 cyT. 4 H 3980.0 65.3 42.7 22.6 0.016
7 M 30 5 cyT. 1942.0 62.7 33.7 29.0 0.032
8 F 33 1 cyT. 1 H 2636.0 21.3 17.2 4.1 0.008
9 F 27 2 H 980.0 19.3 10.8 8.5 0.020
M ± SD 32.4 ± 4.8 10 cyT. 7 H 2344.2 ± 1018.4 45.9 ± 17.7 24.1 ± 10.2 19.6 ± 9.3 0.019 ± 0.006
10 M 40 2 H 2747.0 15.7 9.6 6.1 0.006
11 F 36 23 cyT. 15 H 1820.0 46.5 24.2 22.3 0.026
12 M 39 23 H 3538.0 13.2 6.2 7.0 0.004
13 M 35 3 cyT. 2 H 1391.0 12.6 9.4 3.2 0.009
14 F 39 2 cyT. 3740.0 17.0 14.5 2.5 0.005
15 F 39 21 H 4450.0 21.3 11.4 9.9 0.005
II 16 F 37 16 H 2310.0 10.1 7.8 2.3 0.004
17 M 40 6 H 4550.0 13.6 11.3 2.3 0.003
18 F 37 19 H 2853.0 11.5 9.4 2.1 0.004
19 M 37 4 cyT. 3182.0 36.0 17.5 18.5 0.011
20 F 39 24 cyT. 5164.0 53.1 16.6 36.5 0.010
21 F 37 1 cyT. 11 H 3770.0 17.1 0.3 16.8 0.005
M ± SD 37.9 ± 1.6 5 cyT. 10 H 3292.9 ± 1134.7 22.3 ± 14.6 11.5 ± 6.1 10.8 ± 10.8 0.008 ± 0.006
DISCUSSION
For this work, we selected pleural fluid and air as the most stable lung components with regard to their physical parameters. Signal intensity varied in the area containing pleural fluid and air. Since there were no signs of pleuritis at autopsy, such variability was probably related to different scanner settings used by different tomography specialists. The presence of fluid of non-inflammatory origin (transudate-like) in the pleural cavity is indicative of early nonspecific postmortem changes [20] and is observed in all deaths, as proved by the autopsy.
Differences between groups with regard to airiness index were statistically insignificant, which might be due to a relatively
A -
small sample size and a need to assess lung pathology in each individual case and not in the whole group. However, we believe that AI <2.5 registered simultaneously in both lungs on T2-weighted images indicates pneumonia. This pattern was observed in 7 out of 9 cases in the experimental group. In two other cases, a higher AI was a result of concomitant pathologies: pneumothorax in case 1 and the edematous form of hemolytic disease in case 7. In the comparison group, AI was >2.5 for both lungs in 9 out of 12 cases. In three cases with airiness index <2.5 for both lungs indicating pneumonia, we detected multiple congenital defects (case 11) and false congenital diaphragmatic hernia with compression of the lungs (cases 13 and 18).
Fig. 1. Histological changes of lungs: (A) hypoplasia, (B) monocyte/macrophage pneumonia. Staining with hematoxylin and eosin, *100
Fig. 2. Coronal MR-images of a dead neonate with congenital pneumonia (the experimental group): (A) T1-weighted image, (B) T2-weighted image
Fig. 4. Coronal MR-images of a dead neonate from the comparison group with hemorrhages in both lungs in the absence of pneumonia: (A) T1-weighted image, (B) T2-weighted image
We think that airiness index allows for minimizing or eliminating measurement error related to the performance of an individual scanner and its settings.
Our results show a higher diagnostic efficacy of the applied technique as compared to the results obtained by Arthurs et al. [21], who demonstrated that sensitivity of the postmortem MRI in fetuses, newborns and children was 12.5 %, specificity was 92.6 % and the prognostic value of a positive result was 25 %. The reason here might be that the researchers visually assessed lung airiness and indurations to diagnose pneumonia. They also demonstrated that MRI diagnostic efficacy improves in older patients: the worst results (69.7 % of false negative
Fig. 3. Coronal MR-images of a dead neonate without lung pathology (the comparison group): (A) T1-weighted image, (B) T2-weighted image
Fig. 5. Sagittal MR-images of a dead neonate from the comparison group with the intact left lung and right lung compressed by a diaphragmatic hernia
results) were obtained for fetuses that had died before week 24 of gestation. On the one hand, MRI-based diagnosis of lung conditions, such as pneumonia, is a complicated clinical task; MR images of lungs are of low quality because of low proton density and a large amount of air-tissue gradients [22, 23]. On the other hand, back in the1990s Herold et al. [24] and Blum et al. [25] demonstrated moderate signal intensity on Tl-weighted images and high signal intensity on T2-weighted images of immunocompromised patients with pulmonary aspergillosis. A definite MRI advantage is its ability to measure absolute and relative lung size that to some extent reflects progression of respiratory failure [26, 27].
Table 2 . Signal Intensity and airiness Index (AI) of lungs of dead neonates
T1-weighted images T2-weighted images
Group Case Signal intensity Signal intensity
Right lung Left lung Air Fluid AI, RL AI, LL Right lung Left lung Air Fluid AI, RL AI, LL
1 128 664 6.0 515 4.0 0.8 120 330 3.0 880 7.3 2.7
2 488 750 7.0 409 0.8 0.5 330 200 6.0 300 0.9 1.5
3 538 517 9.0 379 0.7 0.7 416 345 4.5 735 1.8 2.1
4 769 530 9.0 588 0.8 1.1 330 300 3.0 720 2.2 2.4
5 566 492 6.0 293 0.5 0.6 380 290 1.0 523 1.4 1.8
I 6 688 741 11 557 0.8 0.8 521 450 4.5 1122 2.2 2.5
7 719 693 7.0 393 0.5 0.6 239 208 5.0 639 2.7 3.1
8 479 595 12 444 0.9 0.7 446 453 6.0 920 2.1 2.0
9 873 887 12 516 0.6 0.6 870 837 8.0 1120 1.3 1.3
M ± SD 583.1 ± 217.2 652.1 ± 130.6 8.8 ± 2.4 454.9 ± 95.8 1.1 ± 1.1 0.7 ± 0.2 405.8 ± 209.8 379.2 ± 193.4 4.6 ± 2.1 773.2 ± 270.1 2.4 ± 1.9 2.2 ± 0.5
10 144 72 6.0 277 1.9 3.8 195 176 3.0 590 3.0 3.4
11 938 871 9.6 736 0.8 0.8 552 465 4.0 996 2.1 2.1
12 605 564 9.0 420 0.7 0.7 119 133 3.0 500 4.2 3.8
13 624 585 7.0 430 0.7 0.7 363 365 3.0 672 1.9 1.8
14 251 569 9.0 349 1.4 0.6 251 312 3.0 690 2.7 2.2
15 477 384 10 340 0.7 0.9 265 237 3.0 598 2.3 2.5
II 16 829 866 10 573 0.7 0.7 436 456 7.0 1140 2.6 2.5
17 581 541 5.0 435 0.7 0.8 287 278 3.0 742 2.6 2.7
18 524 388 7.0 261 0.5 0.7 279 396 4.0 583 2.1 1.5
19 359 250 3.0 930 2.6 3.7 359 363 3.0 930 2.6 2.6
20 504 678 3.0 341 0.7 0.5 446 323 2.0 926 2.1 2.9
21 362 419 5.0 514 1.4 1.2 160 176 1.0 412 2.6 2.3
M ± SD 516.5 ± 225.3 515.6 ± 232.8 7.0 ± 2.6 467.2 ± 197.5 1.1 ± 0.6 1.3 ± 1.1 309.3 ± 127.0 306.7 ± 109.6 3.3 ± 1.4 731.6 ± 220.5 2.6 ± 0.6 2.5 ± 0.6
Artifacts on MR images result from lung motion during aspiration and blood pulsations, especially in newborns [28]. They are not the case in postmortem MRI; however, we have to admit that there is a problem with accurate assessment of unspecific postmortem changes related to blood redistribution and autolysis [20, 29, 30]. To improve diagnostic accuracy and provide a possibility for differential diagnosis, some authors suggest histological analysis (apart from MRI) of lung tissue samples obtained percutaneously or endoscopically [31].
As postmortem MRI efficacy largely depends on the scanner type and its settings, special protocols should be elaborated considering scanner types, operating modes and corresponding software. Taylor et al. [32] inferred the necessity of using different protocols when analyzing the bodies of dead fetuses and infants.
CONCLUSIONS
Postmortem magnetic resonance imaging is effective in the detection of congenital pneumonia in stillborn babies and neonates who die shortly after birth. To verify the pathology, specific parameters of lung tissue on MR images are less important than a ratio of signal intensity in lung tissue to fluid signal intensity (pleural fluid in our case) on T2-weighted images. This ratio, or the airiness index, allows minimizing the impact of scanner settings on the procedure outcome. Differences in the airiness index between the studied groups of babies who died of congenital pneumonia and those who died of other causes were statistically insignificant because of a small sample size. A study with a larger sample may prove our hypothesis that airiness index less than 2.5 for both lungs on T2-weighted images can be used to diagnose congenital pneumonia.
References
1. Grebennikov VA, lonov OM, Mostovoy AV, Ovsyannikov DYu, Degtyarev DN. Dykhatel'nye rasstroystva. In: Volodin NN, editor. Neonatologiya: natsional'noe rukovodstvo. Moscow: GEOTAR-Media; 2009. p. 246-92. Russian.
2. Duke T. Neonatal pneumonia in developing countries. Arch Dis Child Fetal Neonatal Ed. 2005; 90 (3): F211-9.
3. Shchegolev Al, Tumanova UN, Frolova OG. [Regional features of stillbirth in the Russian Federation]. In: Mezhregional'naya nauchno-prakticheskaya konferentsiya s mezhdunarodnym
uchastiem "Aktual'nye voprosy sudebno-meditsinskoy ekspertizy i ekspertnoy praktiki v regional'nykh byuro sudebno-meditsinskoy ekspertizy na sovremennom etape"; 2013 Nov 21-22; Ryazan, Russia. Ryazan; 2013. p. 163-9. Russian
4. Shchegolev Al, Tumanova UN, Shuvalova MP, Frolova OG. Vrozhdennaya pnevmoniya kak prichina perinatal'noy smerti v Rossiyskoy Federatsii. Neonatologiya: novosti, mneniya, obuchenie 2016; 2: 61-6. Russian.
5. Khrushchelevski E, Shperl'-Zeyfridova G, Chervakov VF, editors.
Sektsiya trupov plodov i novorozhdennykh. Moscow: Medgiz; 1962. p. 224. Russian.
6. Sorokin AF. Pnevmonii novorozhdennykh. In: Ivanovskaya TE, Leonova LV, editors. Patologicheskaya anatomiya bolezney ploda i rebenka. Moscow: Meditsina; 1989. p. 208-10. Russian.
7. Vishnevskiy AA, Karmazanovskiy GG, Kokov LS, Bykov GA, Borisov VV, Shchegolev AI. Sovremennye vozmozhnosti diagnostiki v torakal'noy khirurgii. Khirurgiya. Zhurnal imeni N. I. Pirogova. 2003; 3: 92-5. Russian.
8. Verschakelen JA, De Wever W. Computed tomography of the lung. A pattern approach. Berlin: Springer-Verlag; 2007.
9. Tyurin IE. Novye gorizonty torakal'noy khirurgii. Poliklinika. 2013; 5 (1): 12-7. Russian.
10. Michiue T, Sakurai T, Ishikawa T, Oritani S, Maeda H. Quantitative analysis of pulmonary pathophysiology using postmortem computed tomography with regard to the cause of death. Forensic Sci Int. 2012; 220 (1-3): 232-8.
11. Fedoseeva VK, Tumanova UN, Lyapin VM, Voevodin SM, Shchegolev AI. Vozmozhnosti ispol'zovaniya mul'tispiral'noy komp'yuternoy tomografii v posmertnoy diagnostike patologii plodov i novorozhdennykh. Rossiyskiy elektronnyy zhurnal luchevoy diagnostiki. 2013; 3 (S2): 448. Russian.
12. Puderbach M, Kauczor HU. Can lung MR replace lung CT? Pediatr Radiol. 2008; 38 Suppl 3: S439-51.
13. Eibel RP, Herzog O, Dietrich C, Rieger H, Ostermann M, Reiser S, et al. Nachweis von pneumonischen Infiltraten mit der MRT. Radiologe. 2006; 46: 267-74. German.
14. Rupprecht T, Böwing B, Kuth R, Deimling M, Rascher W, Wagner M. Steady-state free precession projection MRI as a potential alternative to the conventional chest X-ray in pediatric patients with suspected pneumonia. Eur Radiol. 2002; 12 (11): 2752-6.
15. Leutner CC, Gieseke J, Lutterbey G, Kuhl C K, Glasmacher A, Wardelmann E, et al. MR-imaging of pneumonia in immunocompromised patients: comparison with helical CT. AJR Am J Roentgenol. 2000; 175 (2): 391-7.
16. Barber JL, Sebire NJ, Chitty LS, Taylor AM, Arthurs OJ. Lung aeration on post-mortem magnetic resonance imaging is a useful marker of live birth versus stillbirth. Int J Legal Med. 2015; 129 (3): 531-6.
17. Tumanova UN, Bychenko VG, Lyapin VM, Voevodin SM, Shchegolev AI, Sukhikh GT, inventors. Kulakov Research Center for Obstetrics, Gynecology and Perinatology, assignee. Sposob differentsial'noy diagnostiki mertvorozhdennogo i smerti novorozhdennogo posle rozhdeniya. Patent. RU 2577454 2015 Jun 18. Russian.
18. Lally PJ, Arthurs O, Addison S, Alavi A, Sebire NJ, Taylor A, et al. Estimating maceration severity using whole body magnetic resonance T2 relaxometry. Arch Dis Child Fetal Neonatal. 2014; (S1): A92-3.
19. Tumanova UN, Lyapin VM, Voevodin SM, Shchegolev AI, Sukhikh GT. Postmortem MRI to determine the time of intrauterine fetal death. Vichows Archiv. 2015; 467 (S1): 27.
20. Tumanova UN, Shchegolev AI. Nespetsificheskie posmertnye
izmeneniya, vyyavlyaemye pri komp'yuterno-tomograficheskom issledovanii. In: Mezhdunarodnaya konferentsiya "Kriminali-sticheskoe soprovozhdenie rassledovaniya prestupleniy: problemy i puti ikh resheniya"; 2016 Feb 19; Moscow, Russia. Moscow; 2016. p. 525-9. Russian.
21. Arthurs OJ, Thayyil S, Olsen OE, Addison S, Wade A, Jones R, et al. Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children. Eur Radiol. 2014; 24: 2876-84.
22. Bankier AA, O'Donnell CR, Mai VM, Storey P, De Maertelaer V, Edelman RR, et al. Impact of lung volume on MR signal intensity changes of the lung parenchyma. J Magn Reson Imaging. 2004; 20 (6): 961-6.
23. Ciet P, Tiddens HAWM, Wielopolski PA, Wild JM, Lee EY, et al. Magnetic resonance imaging in children: common problems and possible solutions for lung and airways imaging. Pediatr Radiol. 2015; 45 (13): 1901-5.
24. Herold CJ, Mostbeck G, Kramer J, Schwarzinger I, Wrba F, Haller J, et al. Invasive pulmonary aspergillosis: radiologic and magnetic resonance tomographic characteristics. Rofo. 1990; 153 (5): 569-74.
25. Blum U, Windfuhr M, Buitrago-Tellez C, Sigmund G, Herbst EW, Langer M. Invasive pulmonary aspergillosis. MRI, CT and plain radiographic findings and their contribution for early diagnosis. Chest. 1994; 106 (4): 1156-61.
26. Thayyil S, Schievanoa S, Robertson NJ, Jones R, Chitty LS, Sebire NJ, et al. A semi-automated method for non-invasive internal organ weight estimation by post-mortem magnetic resonance imaging in fetuses, newborns and children. Eur J Radiol. 2009; 72: 321-6.
27. Tumanova UN, Bychenko VG, Liapin VM, Voevodin SM, Shchegolev AI. [Congenital Diaphragmatic Hernia in a Newborn: MRI - Pathomorphological Comparisons]. Medical Visualization. 2014; 4: 72-83. Russian.
28. Liszewski MC, Hersman FW, Altes TA, Ohno Y, Ciet P, Warfield SK, et al. Magnetic resonance imaging of pediatric lung parenchyma, airways, vasculature, ventilation, and perfusion: state of the art. Radiol Clin N Am. 2013; 51 (4): 555-82.
29. Dubrova SE, Vishnyakova MV, Kinle AF, Filimonov BA. [Features of computed tomography autopsy: the problem of interpretation of specific and nonspecific artifacts]. Diagnostic radiology and radiotherapy. 2016; 1: 25-40. Russian.
30. Tumanova UN, Shchyogolev AI. [Postmortem Magnetic Resonance Tomography of Fetuses and Newborns]. Medical Visualization. 2015; 5: 128-36. Russian.
31. Sebire NJ, Weber MA, Thayyil S, Mushtaq I, Taylor A, Chitty LS. Minimally invasive perinatal autopsies using magnetic resonance imaging and endoscopic postmortem examination ("keyhole autopsy"): feasibility and initial experience. J Matern Fetal Neonatal Med. 2012; 25 (5): 513-8.
32. Taylor AM, Sebire NJ, Ashworth MT, Schievano S, Scott RJ, Wade A, et al. Postmortem Cardiovascular Magnetic Resonance Imaging in Fetuses and Children: A Masked Comparison Study With Conventional Autopsy. Circulation. 2014; 129 (19): 1937-44.
Литература
1. Гребенников В. А., Ионов О. М., Мостовой А. В., Овсянников Д .Ю., Дегтярев Д. Н. Дыхательные расстройства. В кн.: Володин Н. Н., редактор. Неонатология: национальное руководство. М.: ГЭОТАР-Медиа, 2009. с. 246-92.
2. Duke T. Neonatal pneumonia in developing countries. Arch Dis Child Fetal Neonatal Ed. 2005; 90 (3): F211-9.
3. Щеголев А. И., Туманова У. Н., Фролова О. Г. Региональные особенности мертворождаемости в Российской Федерации. В сб.: Межрегиональная научно-практическая конференция с международным участием «Актуальные вопросы судебно-медицинской экспертизы и экспертной практики в региональных бюро судебно-медицинской экспертизы на современном этапе»; 21-22 ноября 2013 г.; Рязань, Россия. Рязань; 2013. c. 163-9.
Щеголев А. И., Туманова У. Н., Шувалова М. П., Фролова О. Г. Врожденная пневмония как причина перинатальной смерти в Российской Федерации. Неонатология: новости, мнения, обучение. 2016; 2: 61-6.
Хрущелевски Э., Шперль-Зейфридова Г., Черваков В. Ф., редакторы. Секция трупов плодов и новорожденных. М.: Мед-гиз; 1962. с. 224.
Сорокин А. Ф. Пневмонии новорожденных. В книге: Ивановская Т. Е., Леонова Л. В., редакторы. Патологическая анатомия болезней плода и ребенка. М.: Медицина; 1989. с. 208-10.
Вишневский А. А., Кармазановский Г. Г., Коков Л. С., Быков Г. А., Борисов В. В., Щеголев А. И. Современные возможности диагностики в торакальной хирургии. Хирургия.
Журнал имени Н. И. Пирогова. 2003; 3: 92-5. 21.
8. Verschakelen JA, De Wever W. Computed tomography of the lung. A pattern approach. Berlin: Springer-Verlag; 2007.
9. Тюрин И. Е. Новые горизонты торакальной хирургии. Поликлиника. 2013; 5 (1): 12-7. 22.
10. Michiue T, Sakurai T, Ishikawa T, Oritani S, Maeda H. Quantitative analysis of pulmonary pathophysiology using postmortem computed tomography with regard to the cause of death. Forensic Sci Int. 2012; 220 (1-3): 232-8. 23.
11. Федосеева В. К., Туманова У. Н., Ляпин В. М., Воеводин С. М., Щеголев А. И. Возможности использования мультиспираль-ной компьютерной томографии в посмертной диагностике патологии плодов и новорожденных. Российский электрон- 24. ный журнал лучевой диагностики. 2013; 3 (S2): 448.
12. Puderbach M, Kauczor HU. Can lung MR replace lung CT? Pediatr Radiol. 2008; 38 Suppl 3: S439-51.
13. Eibel RP, Herzog O, Dietrich C, Rieger H, Ostermann M, 25. Reiser S, et al. Nachweis von pneumonischen Infiltraten mit der MRT. Radiologe. 2006; 46: 267-74. German.
14. Rupprecht T, Böwing B, Kuth R, Deimling M, Rascher W, Wagner M. Steady-state free precession projection MRI as a 26. potential alternative to the conventional chest X-ray in pediatric patients with suspected pneumonia. Eur Radiol. 2002; 12 (11): 2752-6.
15. Leutner CC, Gieseke J, Lutterbey G, Kuhl C K, Glasmacher A, Wardelmann E, et al. MR-imaging of pneumonia in 27. immunocompromised patients: comparison with helical CT. AJR
Am J Roentgenol. 2000; 175 (2): 391-7.
16. Barber JL, Sebire NJ, Chitty LS, Taylor AM, Arthurs OJ. Lung aeration on post-mortem magnetic resonance imaging is a useful 28. marker of live birth versus stillbirth. Int J Legal Med. 2015; 129 (3): 531-6.
17. Туманова У. Н., Быченко В. Г., Ляпин В. М., Воеводин С. М., Щеголев А. И., Сухих Г. Т., авторы. Научный центр акушер- 29. ства, гинекологии и перинатологии имени В. И. Кулакова, патентообладатель. Способ дифференциальной диагностики мертворожденного и смерти новорожденного после рождения. Патент РФ №2577454 от 18.06.2015. 30.
18. Lally PJ, Arthurs O, Addison S, Alavi A, Sebire NJ, Taylor A, et al. Estimating maceration severity using whole body magnetic resonance T2 relaxometry. Arch Dis Child Fetal Neonatal. 2014; 31. (S1): A92-3.
19. Tumanova UN, Lyapin VM, Voevodin SM, Shchegolev AI, Sukhikh GT. Postmortem MRI to determine the time of intrauterine fetal death. Vichows Archiv. 2015; 467 (S1): 27.
20. Туманова У. Н., Щеголев А. И. Неспецифические посмертные 32. изменения, выявляемые при компьютерно-томографическом исследовании. В сборнике: Международная конференция «Криминалистическое сопровождение расследования преступлений: проблемы и пути их решения»; 19 февраля 2016 г.; Москва, Россия. М.; 2016. с. 525-9.
Arthurs OJ, Thayyil S, Olsen OE, Addison S, Wade A, Jones R, et al. Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children. Eur Radiol. 2014; 24: 2876-84.
Bankier AA, O'Donnell CR, Mai VM, Storey P, De Maertelaer V, Edelman RR, et al. Impact of lung volume on MR signal intensity changes of the lung parenchyma. J Magn Reson Imaging. 2004; 20 (6): 961-6.
Ciet P, Tiddens HAWM, Wielopolski PA, Wild JM, Lee EY, et al. Magnetic resonance imaging in children: common problems and possible solutions for lung and airways imaging. Pediatr Radiol. 2015; 45 (13): 1901-5.
Herold CJ, Mostbeck G, Kramer J, Schwarzinger I, Wrba F, Haller J, et al. Invasive pulmonary aspergillosis: radiologic and magnetic resonance tomographic characteristics. Rofo. 1990; 153 (5): 569-74.
Blum U, Windfuhr M, Buitrago-Tellez C, Sigmund G, Herbst EW, Langer M. Invasive pulmonary aspergillosis. MRI, CT and plain radiographic findings and their contribution for early diagnosis. Chest. 1994; 106 (4): 1156-61.
Thayyil S, Schievanoa S, Robertson NJ, Jones R, Chitty LS, Sebire NJ, et al. A semi-automated method for non-invasive internal organ weight estimation by post-mortem magnetic resonance imaging in fetuses, newborns and children. Eur J Radiol. 2009; 72: 321-6.
Туманова У. Н., Быченко В. Г., Ляпин В.М., Воеводин С. М., Щеголев А. И. Врожденная диафрагмальная грыжа у новорожденного: МРТ - патоморфологические сопоставления. Медицинская визуализация. 2014; 4: 72-83. Liszewski MC, Hersman FW, Altes TA, Ohno Y, Ciet P, Warfield SK, et al. Magnetic resonance imaging of pediatric lung parenchyma, airways, vasculature, ventilation, and perfusion: state of the art. Radiol Clin N Am. 2013; 51 (4): 555-82. Дуброва С. Э., Вишнякова М. В., Кинле А. Ф., Филимонов Б. А. Особенности компьютерной томографии трупа: проблема интерпретации специфических и неспецифических артефактов. Лучевая диагностика и терапия. 2016; 1: 25-40. Туманова У. Н., Щеголев А. И. Посмертная магнитно-резонансная томография плодов и новорожденных. Медицинская визуализация. 2015; 5: 128-36.
Sebire NJ, Weber MA, Thayyil S, Mushtaq I, Taylor A, Chitty LS. Minimally invasive perinatal autopsies using magnetic resonance imaging and endoscopic postmortem examination ("keyhole autopsy"): feasibility and initial experience. J Matern Fetal Neonatal Med. 2012; 25 (5): 513-8.
Taylor AM, Sebire NJ, Ashworth MT, Schievano S, Scott RJ, Wade A, et al. Postmortem Cardiovascular Magnetic Resonance Imaging in Fetuses and Children: A Masked Comparison Study With Conventional Autopsy. Circulation. 2014; 129 (19): 1937-44.
