Carcinoid heart disease: correlation of echocardiographic and histopathological findings

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Carcinoid heart disease: correlation of echocardiographic and histopathological findings.

To cite: Miles LF, Leong T, McCall P, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2014207732 DESCRIPTION A 41-year-old man presented to an anaesthetic preassessment clinic with a metastatic neuroendocrine tumour and clinical features of carcinoid syndrome for consideration of hepatic resection. He gave a history of worsening exertional dyspnoea and peri...

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Carcinoid heart disease. Clinical and echocardiographic spectrum in 74 patients.

BACKGROUND The carcinoid syndrome is a rare cause of acquired valvular heart disease. Although the typical echocardiographic features of carcinoid heart disease are well recognized, this large series provides new information about unusual manifestations of the disease as well as the role of Doppler echocardiography. METHODS AND RESULTS Between 1980 and 1989, 132 patients with carcinoid syndro...

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Echocardiographic and biochemical evaluation of the development and progression of carcinoid heart disease.

OBJECTIVES To study the applicability of a newly developed echocardiographic scoring system in the assessment of carcinoid valvular heart disease. BACKGROUND We investigated prospectively the development, progression and regression of carcinoid valvular heart disease in patients with carcinoid syndrome by serial echocardiography, correlating these features with urinary 5-HIAA levels and clini...

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Carcinoid heart disease.

The patient, C.P., is a 59-year-old woman who was diagnosed with metastatic carcinoid of the terminal ileum in May 2003. In June 2003, she underwent an extensive resection including hemicolectomy, cholecystectomy, distal pancreatectomy, and splenectomy with metastatic disease in her pancreas, mesentery, and liver. She had been treated with octreotide, everolimus, oxaliplatin, and multiple hepat...

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Carcinoid heart disease.

Carcinoid tumors are relatively rare neuroendocrine malignancies most commonly originating from enterochromaffin cells in the gastrointestinal tract. The incidence is 1 in 100 000 of the general population.1 They usually grow slowly over years, commonly causing no symptoms at all until they become large or have metastasized. Carcinoid tumors of midgut origin may secrete large amounts of vasoact...

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ژورنال

عنوان ژورنال: Case Reports

سال: 2014

ISSN: 1757-790X

DOI: 10.1136/bcr-2014-207732