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Superior caval vein syndrome and cardiac inflammatory myofibroblastic tumour in an infant

Published online by Cambridge University Press:  18 April 2023

Bernardo Mussi Soares Open the ORCID record for Bernardo Mussi Soares [Opens in a new window] ,
Andressa Mussi Soares  and
Vera Demarchi Aiello Open the ORCID record for Vera Demarchi Aiello [Opens in a new window]
Bernardo Mussi Soares
Affiliation:
Fundacao Tecnico-Educacional Souza Marques Escola de Medicina Souza Marques, Rio de Janeiro 21310-310, Brazil
Andressa Mussi Soares
Affiliation:
Hospital Evangelico de Cachoeiro de Itapimirim, Cachoeiro DE Itapemirim, ES, Brazil
Vera Demarchi Aiello*
Affiliation:
Laboratory of Pathology, Heart Institute (InCor), University of Sao Paulo School of Medicine, Sao Paulo, Brazil
*
Author for correspondence: Vera Demarchi Aiello, Laboratory of Pathology, Heart Institute (InCor), University of Sao Paulo School of Medicine, Sao Paulo, Brazil. E-mail: vdaiello@gmail.com
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Abstract

The inflammatory myofibroblastic tumour, although very rare, must be considered in the differential diagnosis of intracardiac masses in children as it has systemic implications. We present a case of an infant whose diagnosis was suspected on clinical basis and echocardiogram, but the anatomopathological analysis with immunohistochemical study was essential for the conclusion of the histological type and orientation of the clinical follow-up.

Keywords

Cardiac myofibroblastic tumourinfantechocardiogramimmunohistochemical study
Type
Brief Report
Information
Cardiology in the Young , Volume 33 , Issue 7 , July 2023 , pp. 1226 - 1228
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Copyright
© The Author(s), 2023. Published by Cambridge University Press

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References

Umiker, WO, Iverson, LC. Postinflammatory ‘‘Tumors’’ of the lung: report of four cases simulating xanthoma, fibroma, or plasma cell tumor. J Thorac Surg 1954; 28: 55–63.CrossRefGoogle ScholarPubMed
Brunn, H. Two interesting benign lung tumors of contradictory histopathology: remarks on the necessity for maintaining the chest tumor registry. J Thorac Surg 1939; 9: 119–131.10.1016/S0096-5588(20)32030-4CrossRefGoogle Scholar
Al, Eilers, Nazarullah, AN, Shipper, ES, et al. Cardiac inflammatory myofibtoblastic tumor: a comprehensive review of the literature. Word J Pediatr Congenit Heart Surg 2014; 5: 556–562.Google Scholar
Becker, AE. Primary heart tumors in the pediatric age group: a review of salient pathologic features relevant for clinicians. Pediatr Cardiol 2000; 21: 317–323.CrossRefGoogle ScholarPubMed
Butany, J, Dixit, V, Leong, SW, Daniel, LB, Mezody, M, David, TE. Inflammatory myofibroblastic tumor with valvular involvement: a case report and review of the literature. Cardiovasc Pathol 2007; 16: 359–364.CrossRefGoogle ScholarPubMed
Li, L, Cerilli, LA, Wick, MR. Inflamatory pseudotumor (myofibroblastic tumor) of the heart. Ann Diagn 2002; 6: 116–121.10.1053/adpa.2002.32380CrossRefGoogle Scholar
Andersen, ND, DiBernardo, LR, Linardic, CM, Camitta, MGW, Lodge, AJ. Recurrent inflammatory myofibroblastic tumor of the heart. Circulation 2012; 125: 2379–2381.CrossRefGoogle ScholarPubMed
Cina, SJ, Smialek, JE, Burke, AP, Virmani, R, Hutchins, GM. Primary cardiac tumors causing sudden death: a review of the literature. Am J Forensic Med Pathol 1996; 17: 271–281.10.1097/00000433-199612000-00001CrossRefGoogle ScholarPubMed
Mull, CC, Dahdah, NS, Scarfone, RJ. Cerebral and coronary embolization of a valvular tumor. Pediatr Cardiol 2002; 23: 71–73.CrossRefGoogle ScholarPubMed
Mizia-Malarz, A, Sobol-Milejska, G, Buchwald, J, Wo¿, H. Inflammatory myofibroblastic tumor of the heart in the infant: review of the literature. J Pediatr Hematol Oncol 2016; 38: e298–e302.CrossRefGoogle ScholarPubMed