Hemangioma of the right ventricular outflow tract

Kann, Brian R.; Kim, William J; Cilley, Jonathan H.; Marra, Steven; DelRossi, Anthony J.

doi:10.1016/s0003-4975(00)01616-7

Cited by 14 publications

(8 citation statements)

References 5 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Bu tümörlerin doğal seyri oldukça değişkendir. Tamamen uykuda ve klinik olarak sessiz seyredebilir veya bir süre sonra prolifere olabilirler (6). Genel inanış tüm kardiyak kapak tümörlerinin rezeke edilmesi yönündedir (2, 7).…”

Section: Discussionunclassified

Triküspid Kapağın Hemanjiomu

Diken¹,

Yalçınkaya²,

Hanedan³

et al. 2016

Kocatepe Tıp Dergisi

View full text Add to dashboard Cite

ÖZETOldukça nadir görülen lezyonlar olan kalp kapak tümörleri kalbin primer neoplastik oluşum-larının %10 kadarını oluşturmaktadırlar. Literatürde triküspid kapakta yer alan hemanjioma oldukça nadir rastlanmaktadır. Olgumuz olan 17 yaşında erkek hasta perimembranöz ventriküler septal defekt nedeniyle opere edilirken triküspid kapağın anterior leafletinde 7 x 5 mm boyutlarında bir lezyon saptanarak eksize edilmiş ve patolojisi benign vasküler proliferasyon; hemanjiom olarak rapor edilmiştir. Bu olguyu literatürde nadir rastlanması ve özellikle konjenital operasyonlarda eşlik edebilecek patolojiler açısından inspeksiyonun önemini vurgulamak amacıyla sunmaktayız. Anahtar Kelimeler: Triküspit kapak, hemanjiyom, neoplazi ABSTRACTCardiac valve tumors are rare, accounting for less than 10% of all primary cardiac tumors. Hemangiomas of the tricuspid valve are rarely documented in the literature. A 7 x 5 mm lesion was determined and resected during the operation of a 17-year-old male who underwent surgery for perimembranous ventricular septal defect and documented as benign vascular proliferation; hemangioma in the pathology report. We report this case because of it's rarity and to demostrate the importance of inspection for the lesions which can especially accompany to congenital cardiac diseases.

show abstract

Section: Discussionunclassified

Triküspid Kapağın Hemanjiomu

Diken¹,

Yalçınkaya²,

Hanedan³

et al. 2016

Kocatepe Tıp Dergisi

View full text Add to dashboard Cite

show abstract

“…Obstruction and ventricular arrhythmias are predominant symptoms of right ventricular outflow tract hemangioma. [3][4][5][6][7] Surgical resection is often the preferred treatment option for cardiac hemangioma. The relationship of right atrial hemangioma with right coronary artery and sinoatrial node has to be considered prior to surgical removal.…”

Section: Discussionmentioning

confidence: 99%

Obstructive Right Ventricular Outflow Tract Hemangioma in an Adolescent

Sharma¹,

Hsu²,

Weinstein³

2011

Congenital Heart Disease

View full text Add to dashboard Cite

Cardiac tumors are rare in children, but they are being diagnosed with increasing frequency and great accuracy with wide array of imaging modalities. Cardiac rhabdomyoma and myxoma are the most common tumors in children and adults, respectively. Cardiac hemangiomas comprise about 2.8% of all primary cardiac tumors and fewer than 100 cases have been reported in the literature. We report a successful resection of cardiac hemangioma in the right ventricular outflow tract in an adolescent, presented with moderate to severe obstruction.

show abstract

“…5 Moreover, they are usually found on the lateral wall of the left ventricle, free wall of the right ventricle, or interventricular septum. 6 Histologically, there are 3 categories of cardiac hemangiomas: (1) cavernous hemangioma typified by dilated thinwalled vessels; (2) capillary hemangioma distinguished by small capillary-like vessels; and (3) arteriovenous hemangioma characterized by dysplastic and malformed arteries and veins. Histological examination of resected hemangioma is often able to identify elements of all categories interspersed with fibrous tissue.…”

Section: Ainsworth Et Al Vt Caused By LV Tumormentioning

confidence: 99%

A Bloody Mass

et al. 2012

View full text Add to dashboard Cite

A n active, physically fit, and previously healthy 23-year-old man is referred by his family physician to a cardiology clinic with a several-month history of progressively worsening episodes of palpitations associated with dyspnea. He reports experiencing brief episodes almost hourly and describes the palpitations as being extremely rapid and the rhythm as regular.Dr Salehian: Palpitations as a chief complaint are a common issue routinely assessed by family physicians, general internists, emergency department physicians, and cardiologists. The differential diagnosis in such patients is broad and often not related to a primary cardiac issue or arrhythmia. Broadly, symptoms of palpitations may be related to cardiac arrhythmia or structural heart disease, medications, recreational drugs and alcohol, metabolic disorders, high output states, or psychiatric conditions. To help to determine the etiology of the patient's symptoms, a thorough history, physical examination, and basic laboratory investigations are necessary to help to determine which further investigations are required.The patient reports mild dyspnea with the episodes but denies associated syncope or presyncope, chest discomfort, nausea, or vomiting. The palpitations are not precipitated by exertion, and there are no other identifiable aggravating factors. He is unaware of any physical activity limitations, exertional symptoms, or features suggestive of congestive heart failure. There is no drug or alcohol use and absence of a family history of early coronary artery disease, congenital heart disease, dysrhythmia, or sudden cardiac death. He also denies recent infectious symptoms. On physical examination, he is afebrile, with a blood pressure of 116/72 mm Hg, heart rate of 68 bpm, and respiratory rate of 14 breaths per minute. There is no adenopathy noted, and the jugular venous pressure is not elevated. Carotid upstroke is normal without any bruits. On cardiac examination, apical impulse is not easily palpable, and no obvious heaves or thrills are felt. On auscultation, first and second heart sounds are normal, with no extra heart sounds, murmurs, or rubs. Lungs are clear to auscultation with no adventitious sounds. Abdomen is soft, and organomegaly is not detected. Peripheral pulses are all normal. There is no peripheral edema detected in his extremities. All blood work, including complete blood count, electrolytes, and thyroid function studies, is within normal limits.Dr Salehian: In this patient, there are no significant worrisome features in the history or physical examination to suggest a sinister arrhythmia as the cause of his symptoms. Basic blood work is reassuringly normal as well. Although not completely ruled out by a benign history, absence of certain features is encouraging. For example, symptoms are not precipitated by exercise (catecholaminergic polymorphic ventricular tachycardia [VT], hypertrophic obstructive cardiomyopathy), and there is no history suggestive of underlying cardiomyopathy (nonischemic or ischemic cardiomyopathy) and no fa...

show abstract

Hemangioma of the right ventricular outflow tract

Cited by 14 publications

References 5 publications

Triküspid Kapağın Hemanjiomu

Triküspid Kapağın Hemanjiomu

Obstructive Right Ventricular Outflow Tract Hemangioma in an Adolescent

A Bloody Mass

Contact Info

Product

Resources

About