Literature DB >> 10865004

Primary heart tumors in the pediatric age group: a review of salient pathologic features relevant for clinicians.

A E Becker1.   

Abstract

Because primary tumors of the heart in infants and children are extremely rare, most knowledge is based on collections of case reports rather than large cohort studies. The types of heart tumors encountered in the pediatric age group differ from those seen in adults. In the latter, cardiac myxomas are by far the most common tumor; in infants and children the most common primary tumor of the heart is the rhabdomyoma. Spontaneous regression of these tumors has been well established so that surgical intervention is no longer indicated unless there are clinical manifestations from the heart. There is a high incidence of associated tuberous sclerosis. Any intracavitary mass in infants is suggestive for a cardiac rhabdomyoma unless otherwise proven. The second most common tumor in this age group is cardiac fibroma. These tumors probably represent hamartomatous lesions and this has led to a strategy in which radical surgical excision is not indicated if the procedure endangers postoperative heart function. Cardiac myxomas are of interest in this age group because of their familial occurrence as part of the myxoma syndrome. Other types of primary heart tumors occur, including malignant variants, but all are exceedingly rare. It is because of the sporadic nature of these tumors that treatment and insights into prognosis are based largely on case documentations and analogies from similar tumors originating elsewhere.

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Year:  2000        PMID: 10865004     DOI: 10.1007/s002460010071

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  31 in total

1.  Surgical removal of a rhabdomyoma in a neonate as rescue therapy.

Authors:  C Schreiber; M Vogt; M Kostolny; T Günther; R Lange
Journal:  Pediatr Cardiol       Date:  2006 Jan-Feb       Impact factor: 1.655

2.  Cardiac tumors in infants and children: study of 120 operated patients.

Authors:  Kyle J Bielefeld; James H Moller
Journal:  Pediatr Cardiol       Date:  2012-06-27       Impact factor: 1.655

3.  Actin isoform expression patterns in adult extracardiac and cardiac rhabdomyomas indicate a different cell of origin.

Authors:  Christina C Westhoff; Katharina Schoner; Sylvia Hartmann; Andreas M Sesterhenn; Roland Moll
Journal:  Virchows Arch       Date:  2017-01-14       Impact factor: 4.064

4.  Case report: surgical resection of right ventricular cardiac fibroma in an adult patient.

Authors:  Hirohisa Ikegami; Anthony Lemaire; Subhashini Gowda; Billie Fyfe; Mahmoud Ali; Mark J Russo; Leonard Y Lee
Journal:  J Cardiothorac Surg       Date:  2021-05-20       Impact factor: 1.637

5.  Incidental Finding of a Cardiac Mass on Abdominal CT Scan.

Authors:  Javaria Ahmad; Bader S Alshammari; Faisal Nabi
Journal:  Methodist Debakey Cardiovasc J       Date:  2017 Oct-Dec

Review 6.  Shedding light on inflammatory pseudotumor in children: spotlight on inflammatory myofibroblastic tumor.

Authors:  Lillian M Lai; M Beth McCarville; Patricia Kirby; Simon C S Kao; Toshio Moritani; Eve Clark; Kousei Ishigami; Armita Bahrami; Yutaka Sato
Journal:  Pediatr Radiol       Date:  2015-05-12

7.  Cardiac rhabdomyoma in familial tuberous sclerosis.

Authors:  Amit Kumar Chaurasia; S Harikrishnan; S Bijulal; Dinesh Choudhary; Ja Tharakan
Journal:  J Cardiovasc Thorac Res       Date:  2013-06-27

8.  Cardiac Fibroma with Ventricular Tachycardia: An Unusual Clinical Presentation of Nevoid Basal Cell Carcinoma Syndrome.

Authors:  Alyssa L Ritter; Eric J Granquist; V Ramesh Iyer; Kosuke Izumi
Journal:  Mol Syndromol       Date:  2018-05-19

9.  Successful resection of a primary cardiac fibroma in a neonate: report of a case.

Authors:  Xian-Gang Yan; Bing Jia; Bing-Xue Zhu; Xi-Hong Hu
Journal:  Surg Today       Date:  2013-05-15       Impact factor: 2.549

Review 10.  Syndrome-Associated Tumors by Organ System.

Authors:  Raul S Gonzalez; Nicole D Riddle
Journal:  J Pediatr Genet       Date:  2016-03-09
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