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Original Report |
1 Department of Radiology, Toki Municipal General Hospital, 703-24 Tokitsuguchi,
Tokitsu-cho, Toki, Gifu 509-5193 Japan.
2 Department of Radiology, Shiga University of Medical Science, Ohtsu, Shiga
520-2192 Japan.
3 Department of Radiology, Nagoya University School of Medicine, Nagoya, Aichi
466-8550 Japan.
Received February 6, 2002;
accepted after revision April 5, 2002.
Address correspondence to S. Otake.
Abstract
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CONCLUSION. Osteophytes of the thoracic vertebrae appear to cause focal fibrosis in the adjacent pulmonary tissue.
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The purpose of our study was to determine whether osteophytes of the thoracic vertebrae cause focal fibrosis in the subpleural region. We assessed the relationship among the focal interstitial opacity, the osteophyte, and the patient's age; examined the reversibility of the change by imaging the patient in the prone position; and correlated the CT findings with histology in postmortem cases.
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To exactly match the sex distribution and age range of cases in our study, we reviewed CT images of patients whose sex and age matched those of patients with osteophytes and selected 100 patients without osteophytes as a control group. Therefore, the control group also included 68 men and 32 women (ages range, 45-85 years; mean ± SD, 69 ± 9 years). The patients whose CT images revealed abnormalities in addition to focal interstitial opacities adjacent to the osteophytes or who had histories of pulmonary diseases were excluded from our study. CT scans of 200 patients obtained in the supine position were retrospectively reviewed.
Prospective CT Study Performed with Patients in Prone Position
To determine whether focal interstitial opacity was dependent on gravity,
CT examinations were prospectively performed from April to May 2001, with
patients in the prone position in seven consecutive patients (two men and five
women; age range, 57-89 years; mean ± SD, 71 ± 11 years). The
patients had osteophytes with a thickness of more than 5 mm and focal
interstitial opacities adjacent to the osteophytes. Informed consent was
obtained from all patients before enrollment in the study, which was approved
by the institutional review committee.
Histologic Correlation in Postmortem Cases
To correlate CT findings with histology, we obtained specimens of the right
lungs from five patients with osteophytes having a thickness of more than 5 mm
and focal interstitial opacities adjacent to the osteophytes from autopsies of
patients who had died in 2000 and 2001. This group included four men and one
woman (age range, 69-84 years; mean ± SD, 76 ± 6 years). H and
E, azan, and elastica Masson stains were used to examine the specimens.
CT Protocol
CT was performed with a helical CT scanner (Xvision/GX; Toshiba Medical
Systems, Tokyo, Japan) using the following parameters: 120 kV; 200 mA; width
of X-ray beam, 10 mm; table speed, 10 mm/sec; breath-hold after full
inspiration for one scan, 8 sec; number of scans required to cover the entire
lungs, 4; section thickness, 10 mm; section interval, 10 mm; field of view,
320 mm; reconstruction matrix, 512x512; bone algorithm, window center of
-500 H and window width of 1600 H. CT images were analyzed by two
board-certified radiologists who were experienced in interpreting chest CT
scans. Final interpretation of all CT images was determined by consensus.
Statistical Analysis
The relationship among focal interstitial opacity, presence and thickness
of the osteophyte, and patient's age was assessed by using a chi-square test.
A p value of less than 0.05 was considered statistically
significant.
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The incidence of focal interstitial opacities increased with the thickness of the osteophytes (Table 1). A significant difference was found between the thickness of the osteophytes and the incidence of focal interstitial opacities (p = 0.039). No significant difference was found between the patient's age and the incidence of focal interstitial opacities or between the patient's age and the thickness of the osteophytes.
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CT Findings of Patients Imaged in the Prone Position
Of the seven patients in the prospective study, four showed the reticular
pattern and three showed the linear pattern on prior CT performed with the
patient in the supine position. On the CT examinations performed in the prone
position, findings in all seven patients were identical to findings in those
performed in the supine position. These results suggest that these changes
were irreversible (Fig.
3A,3B).
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Histologic Findings
Macroscopically, the pleura that was attached to the osteophyte was white
and hard, and a collapse of the alveolar spaces with a relatively uniform
thickness in the subpleural region was seen. In the collapsed area, the
collagen fibers were markedly increased and the elastic fibers were slightly
increased; this finding was consistent with fibrosis (Fig.
4A,4B,4C,4D,4E).
These results were seen in all the five postmortem cases.
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Histologic examination showed that focal interstitial opacity was fibrosis. On the CT examinations performed with patients in the prone position, focal interstitial opacities did not disappear, a finding that suggests irreversible changes. In the retrospective study, focal interstitial opacities were noted in 45% of the patients with osteophytes; however, none were noted in the patients without osteophytes. These findigns suggest that the focal interstitial opacity was caused by direct compression from the osteophyte. A significant difference was found between the thickness of the osteophyte and the incidence of focal interstitial opacity. The thick osteophyte seems to compress the pulmonary tissue severely. These findings suggest that the cause of focal interstitial opacity is mechanical stress from the osteophyte. On the other hand, no significant difference between the patient's age and focal interstitial opacity was seen, possibly because of the lack of significant difference between the patient's age and the thickness of the osteophyte.
Our study suggests that mechanical compression by the osteophyte causes focal fibrosis in the adjacent pulmonary tissue. Protrusion of the osteophyte may also cause the collapse of the subpleural alveolar space chronically and the subsequent formation of collagen and elastic fibers in the alveolar septa. In addition, the abnormal blood circulation or abnormal ventilation caused by the mechanical compression may contribute to fibrosis formation. However, because it is difficult to fully explain the mechanism of fibrosis, further studies are needed. An animal model might provide the best means for the further study.
Both reticular and linear patterns were seen on CT images. No explanation for the two patterns could be established. The amount of the increased collagen and elastic fibers and their distribution in the 10-mm section thickness may be one explanation.
On routine chest CT performed with patients in the supine position, dependent density is seen in the posterior regions of both lungs as a result of volume loss in the dependent lung. Dependent density also can be seen in the anterior portion of the vertebrae. However, such density disappears in images obtained with patients in the prone position and, therefore, the change that the density represents is considered reversible [2]. Focal interstitial opacities shown in our study did not disappear in the images obtained with patients in the prone position. This finding that suggests that the changes are irreversible and different from those in dependent density.
The differential diagnosis includes early interstitial pneumonia, collagen vascular disease, asbestosis, and chronic pneumonia in the periphery [3,4,5]. In early interstitial pneumonia and asbestosis, the subpleural curvilinear shadow is noted bilaterally in the subpleural region. Focal fibrosis in our study is shown only in the subpleural region adjacent to the osteophyte. The changes after pneumonia usually show a segmental or subsegmental distribution. Therefore, the differentiation of focal fibrosis adjacent to the osteophyte from these diseases is not difficult.
All osteophytes were found on the right side of the lower thoracic vertebrae in our study. Consequently, focal fibrosis was noted only in the right lung. If the osteophyte developed on the left side because of the rightward elongation of the descending aorta, we speculate that focal fibrosis might form in the left lung.
On the basis of our limited cases, focal fibrosis adjacent to osteophytes of the thoracic vertebrae appears to be caused by compression from the osteophyte. This change should not be confused with other types of lung disorders.
Acknowledgments
We thank Hiroshi Oda for his assistance with the CT examinations, Fumio
Matsubara for his help in the statistical analysis, Hiroaki Ozawa and Fusae
Hayashi for their assistance with histologic correlation, Hitomi Hayashi for
her secretarial assistance, and Phyllis S. Bergman for her editorial
assistance.
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