Pulmonary Tumor Thrombotic Microangiopathy Caused by a Parotid Tumor: Early Antemortem Diagnosis and Long-term Survival

Pulmonary tumor thrombotic microangiopathy (PTTM) is a high-mortality disease that is difficult to diagnose clinically. Our patient was an 80-year-old woman who came to us due to symptoms of increasing dyspnea. A clinical evaluation showed that she had hypoxemia and pulmonary arterial hypertension w...

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Veröffentlicht in:Internal Medicine 2017/01/01, Vol.56(1), pp.67-71
Hauptverfasser: Toyonaga, Haruka, Tsuchiya, Michiko, Sakaguchi, Chikara, Ajimizu, Hitomi, Nakanishi, Yosuke, Nishiyama, Seiya, Morikawa, Noboru, Hayashi, Yasuyuki, Nagasaka, Yukio, Yasui, Hiroshi
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Sprache:eng
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Zusammenfassung:Pulmonary tumor thrombotic microangiopathy (PTTM) is a high-mortality disease that is difficult to diagnose clinically. Our patient was an 80-year-old woman who came to us due to symptoms of increasing dyspnea. A clinical evaluation showed that she had hypoxemia and pulmonary arterial hypertension without any abnormalities in the major pulmonary arteries, bronchi, or alveoli. A lung perfusion scan showed multiple wedge-shaped perfusion defects. Further examination revealed adenocarcinoma in her right parotid gland with metastasis to the submandibular lymph nodes. We diagnosed her to have PTTM caused by a parotid tumor. The patient survived for 11 months with chemotherapy. An early antemortem diagnosis by minimally invasive examinations will help PTTM patients to survive longer.
ISSN:0918-2918
1349-7235
DOI:10.2169/internalmedicine.56.7439