Key result
Ovarian adenocarcinoma presents as severe pre-capillary pulmonary hypertension from fatal pulmonary tumor thrombotic microangiopathy.
Why the study?
Pulmonary tumour thrombotic microangiopathy is a fatal disease that is usually diagnosed post-mortem due to rare occurrences and lack of clear diagnostic guidelines.
Case Report (n=1)
Highlights the importance of considering pulmonary tumour thrombotic microangiopathy in patients with signs of pulmonary hypertension and right heart failure, as early diagnosis is essential for potentially life-prolonging treatment.
Consider PTTM in malignancy with unexplained pre-capillary PH; single case leaves open need for ante-mortem diagnostics.
BACKGROUND: Pulmonary tumour thrombotic microangiopathy (PTTM) is a fatal disease in which tumour cells embolize to the pulmonary vasculature leading to pulmonary hypertension and right heart failure. Early diagnosis is essential for timely treatment which can reduce intimal pulmonary vascular proliferation and prolong survival, improve the symptoms. Due to rare occurrences and no clear diagnostic guidelines the disorder usually is found post-mortem. We present a review of this rare disease and a case of post-mortem diagnosed pulmonary tumour thrombotic microangiopathy in a young female. CASE PRESENTATION: 51 years old woman presented with progressively worsening dyspnea, right ventricular failure signs and symptoms. Computerized tomography denied pulmonary embolism. 2D transthoracic echocardiography demonstrated right ventricle dilatation and dysfunction, severely increased systolic pulmonary pressure. Right heart catheterization revealed pre-capillary pulmonary hypertension with mean pulmonary artery pressure of 78 mmHg, pulmonary wedge pressure of 15 mmHg, reduced cardiac output to 1.78 L/min with a calculated pulmonary vascular resistance of 35 Wood units, and extremely low oxygen saturation (26%) in pulmonary artery. Because of worsening ascites, pelvic magnetic resonance imaging was performed, tumours in both ovaries were diagnosed. Due to the high operative risk, detailed tumour diagnosis surgically was not established. The patient developed progressive cardiorespiratory failure, unresponsive to optimal heart failure drug treatment. A postmortem morphology analyses revealed tumorous masses in pre-capillary lung vessels, right ventricle hypertrophy, ovary adenocarcinoma. CONCLUSIONS: An early diagnosis of PTTM is essential. Most cases are lethal due to respiratory failure progressing rapidly. Patients with a history of malignancy, symptoms and signs implying of PH should be considered of having PTTM. If detected early enough, combination of chemotherapy with specific PH therapy is believed to be beneficial in reducing intimal proliferation and prolonging survival, along with improving the symptoms.
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Neverauskaitė-Piliponienė et al. (2022) conducted a case report in Pulmonary tumour thrombotic microangiopathy (n=1). A 51-year-old woman with ovarian adenocarcinoma developed fatal pulmonary tumour thrombotic microangiopathy, diagnosed post-mortem after presenting with severe pre-capillary pulmonary hypertension.
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