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首页> 外文期刊>Case Reports & Clinical Practice Review >A Case of Carcinoid Syndrome Due to Malignant Metastatic Carcinoid Tumor with Carcinoid Heart Disease Involving Four Cardiac Valves
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A Case of Carcinoid Syndrome Due to Malignant Metastatic Carcinoid Tumor with Carcinoid Heart Disease Involving Four Cardiac Valves

机译:恶性转移类癌伴类癌性心脏病累及四个心脏瓣膜的类癌综合征1例

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Objective: Rare diseaseBackground: Carcinoid tumor, benign, low-grade malignant, and high-grade malignant, can be associated with the release of vasoactive substances that cause symptoms including cutaneous flushing, diarrhea, and bronchospasm. In 50–60% of patients with carcinoid syndrome, the vasoactive substances cause fibrosis of the pulmonary and tricuspid heart valves which lead to regurgitation and right-sided heart failure. The right side of the heart is usually affected because monoamine oxidases in the lungs usually inactivate the vasoactive substances.Case Report: A 62-year-old woman presented with a four-month history of diarrhea and abdominal discomfort. The patient had bilateral pelvic masses and elevated serum CA125 and an elevated urinary 5-hydroxyindoleacetic acid (5-HIAA). Total abdominal hysterectomy (TAH) and bilateral salpingo-oophorectomy (BSO) identified a prima-ry appendiceal carcinoid tumor with bilateral ovarian metastases. Post-operatively, a computed tomography (CT) scan showed cardiomegaly. Transthoracic echocardiography showed morphologic changes that affected all four heart valves, consistent with carcinoid heart disease but without a patent foramen ovale (PFO). The pa-tient was evaluated for valve replacement surgery, but surgery was not performed due to the degree of heart failure.Conclusions: This report describes a rare case of carcinoid heart disease with involvement of all four cardiac valves, but without the presence of a PFO, possibly due to a large amount of vasoactive substances in the patient’s circu-lation, as supported by the patient’s elevated urinary 5-HIAA. This rare presentation highlights the importance of early diagnosis and treatment with tumor resection and, if possible, Cardiac valve replacement to prevent irreversible heart failure.
机译:目的:罕见病背景:类癌,良性,低度恶性和高度恶性,可能与血管活性物质的释放有关,这些物质引起包括皮肤潮红,腹泻和支气管痉挛的症状。在50-60%的类癌综合征患者中,血管活性物质引起肺和三尖瓣心脏纤维化,从而导致反流和右侧心力衰竭。心脏的右侧通常会受到影响,因为肺中的单胺氧化酶通常会使血管活性物质失活。病例报告:一名62岁的女性出现了四个月的腹泻和腹部不适史。该患者双侧骨盆肿块,血清CA125升高,尿中5-羟吲哚乙酸(5-HIAA)升高。全腹子宫切除术(TAH)和双侧输卵管卵巢切除术(BSO)确定了具有双侧卵巢转移的原发性阑尾类癌。术后,计算机断层扫描(CT)扫描显示心脏肥大。经胸超声心动图显示影响所有四个心脏瓣膜的形态变化,与类癌性心脏病一致,但无卵圆孔未闭(PFO)。对患者进行了瓣膜置换手术的评估,但由于心力衰竭的程度而未进行手术。结论:本报告描述了罕见的类癌性心脏病,其中全部四个心脏瓣膜均受累,但没有PFO,可能是由于患者尿中5-HIAA升高支持了患者循环中大量血管活性物质。这种罕见的表现突出了早期诊断和肿瘤切除术的治疗的重要性,如果可能的话,心脏瓣膜置换术可以预防不可逆的心力衰竭。

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