Key result
Gastric cancer presents as fatal rapidly progressive pulmonary hypertension driven by pulmonary tumor thrombotic microangiopathy.
Why the study?
Pulmonary tumor thrombotic microangiopathy involves pulmonary hypertension from microscopic tumor emboli of peripheral pulmonary arteries, with a need to report a rapidly exacerbating presentation linked to gastric cancer.
Case Report (n=1)
Pulmonary tumor thrombotic microangiopathy (PTTM) should be considered as an oncologic emergency in patients with carcinoma of unknown primary presenting with rapidly progressive pulmonary hypertension and shock when pulmonary embolism is ruled out.
BACKGROUND: Pulmonary tumor thrombotic microangiopathy (PTTM) is a condition that involves the development of pulmonary hypertension due to the presence of microscopic tumor emboli of the peripheral pulmonary arteries. Here, we report a case of rapidly exacerbating PTTM associated with gastric cancer that was identified postmortem through pathological autopsy. CASE PRESENTATION: A 52-year-old Asian woman who experienced anterior chest pain while coughing visited the orthopedic department of the Gifu University Hospital. She was diagnosed as having multiple osteolytic bone metastases throughout her body and was subsequently scheduled to undergo combined positron emission tomography and computed tomography (CT) to search for a primary lesion. However, 4 days after her visit to the orthopedic department, she was unable to stand up and thus visited the emergency department. At the time of admission, physical examination results revealed that she had a percutaneous oxygen saturation level of 90% (on room air) and cyanosis and that she was in a state of hemodynamic shock. Laboratory test results revealed elevated levels of fibrin degradation products and D-dimer in her blood. Chest CT results were normal. She was admitted to the hospital's general ward for follow-up but soon entered a gradually worsening state of shock and respiratory failure. Electrocardiography revealed findings associated with right heart strain; however, contrast-enhanced CT did not reveal the presence of pulmonary embolism. She was admitted to the intensive care unit and was treated for pulmonary hypertension; however, 45 h after her arrival at the hospital, she died of respiratory failure. A pathological autopsy revealed the presence of gastric cancer, tumor microemboli, and fibrous intimal thickening of the peripheral arteries of both lungs; thus, a diagnosis of PTTM was made. CONCLUSIONS: In patients with carcinoma of unknown primary site and pulmonary hypertension with pulmonary embolism ruled out by CT, emergency physicians and intensivists must consider the possibility of PTTM, which represents an oncologic emergency, and initiate chemotherapy administration as soon as possible.
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Kamidani et al. (2021) conducted a case report in Pulmonary tumor thrombotic microangiopathy (PTTM) (n=1). Gastric cancer was evaluated on Mortality. A 52-year-old woman with gastric cancer developed rapidly progressive pulmonary hypertension and died of respiratory failure, with postmortem autopsy revealing pulmonary tumor thrombotic microangiopathy.
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