Pulmonary hypertension associated with pulmonary occlusive vasculopathy after allogeneic bone marrow transplantation

被引:55
作者
Seguchi, M
Hirabayashi, N
Fujii, Y
Azuno, Y
Fujita, N
Takeda, K
Sato, Y
Nishimura, M
Yamada, K
Oka, Y
机构
[1] Yamaguchi Univ, Sch Med, Dept Internal Med 3, Total Care Unit, Ube, Yamaguchi 755, Japan
[2] Yamaguchi Univ, Sch Med, Div Blood Transfus, Ube, Yamaguchi 755, Japan
[3] Nagoya First Red Cross Hosp, Dept Pathol, Nagoya, Aichi, Japan
[4] Yamaguchi Rosai Hosp, Dept Internal Med, Onoda, Japan
关键词
D O I
10.1097/00007890-200001150-00030
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Pulmonary vasculature abnormalities, including pulmonary veno-occlusive disease, have been demonstrated in marrow allograft recipients. However, it is often difficult to make a correct diagnosis of pulmonary lesions. Methods. An open lung biopsy was performed on a patient who developed severe pulmonary hypertension after bone marrow transplantation for T-cell lymphoma. Results. An open lung biopsy specimen demonstrated pulmonary arterial occlusion due to intimal fibrosis and veno-occlusion. The most striking alteration was partial to complete occlusion of the small arteries by fibrous proliferation of the intima. Conclusion. High-dose preparative chemotherapy and radiation before transplantation are thought to have contributed to the development of vasculopathy in this patient, because arterial occlusion by intimal fibrosis and atypical veno-occlusion are often associated with lung injury due to chemoradiation. An open lung biopsy is essential for diagnosing pulmonary vascular disease presenting signs compatible with posttransplantation pulmonary hypertension.
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收藏
页码:177 / 179
页数:3
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