Pulmonary Tumor Thrombotic Microangiopathy Diagnosed Antemortem and Treated with Combination Chemotherapy

被引:53
|
作者
Kayatani, Hiroe [1 ]
Matsuo, Kiyoshi [1 ]
Ueda, Yusuke [1 ]
Matsushita, Mizuho [1 ]
Fujiwara, Keiichi [1 ]
Yonei, Toshiro [1 ]
Yamadori, Ichiro [2 ]
Shigematsu, Hisayuki [3 ]
Andou, Akio [3 ]
Sato, Toshio [1 ]
机构
[1] Natl Hosp Org Okayama Med Ctr, Dept Resp Med, Okayama, Japan
[2] Natl Hosp Org Okayama Med Ctr, Dept Clin Pathol, Okayama, Japan
[3] Natl Hosp Org Okayama Med Ctr, Dept Chest Surg, Okayama, Japan
关键词
pulmonary tumor thrombotic microangiopathy; cancer of unknown primary; pulmonary hypertension; combination chemotherapy; ENDOTHELIAL GROWTH-FACTOR; CELL-CARCINOMA; TISSUE FACTOR; HYPERTENSION; STOMACH;
D O I
10.2169/internalmedicine.51.7682
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 29-year-old man developed a persistent dry cough. Chest high-resolution computed tomography (HRCT) revealed centrilobular ultrafine granular shadows scattered in all lung fields. A lung biopsy with video-assisted thoracoscopic surgery revealed findings compatible with pulmonary tumor thrombotic microangiopathy (PTTM). However, the primary tumor was not identified. Combination chemotherapy with S-1 and cisplatin decreased his cough and improved the chest HRCT findings. The illness, however, gradually became difficult to control. He eventually developed pulmonary hypertension and died. Typically, an antemortem diagnosis of PTTM cannot be made. In this case, the diagnosis of PTTM and combination chemotherapy improved the chest HRCT findings, respiratory symptoms, and prognosis.
引用
收藏
页码:2767 / 2770
页数:4
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