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Cardiac rhabdomyoma in intrauterine life: clinical features and natural history. A case series and review of published reports.
Ital Heart J. 2002 Jan; 3(1):48-52.IH

Abstract

BACKGROUND

Fetal cardiac rhabdomyoma is very rare; despite the fact that many cases and series have been reported, the clinical presentation, the natural history and the frequency with which this pathology is associated with tuberous sclerosis complex are not well determined. The aim of this investigation was to study the clinical features and the natural history of cardiac rhabdomyoma when diagnosed during prenatal life.

METHODS

Nine cases of cardiac rhabdomyoma detected among 5276 fetal echocardiograms recorded over a 10-year period in a single center were retrospectively reviewed. Medical records and echocardiograms were studied to determine the prenatal and postnatal course and outcome.

RESULTS

The incidence of cardiac rhabdomyoma in our center was 0.17%. The gestational age at diagnosis ranged from 27 to 36 weeks. The most common reason for fetal echocardiography was an abnormal obstetric ultrasound scan (6/9 cases). In no case was there a family history of tuberous sclerosis. In one case, the tumor was single whereas in 8 cases multiple tumors were diagnosed. During prenatal life the majority of tumors were clinically silent. One fetus died of hydrops and arrhythmia. Four children presented with arrhythmia postnatally and one required surgery. At a mean follow-up of 47 months, total or partial regression was observed in 7 patients. Seven patients developed postnatal clinical signs of tuberous sclerosis.

CONCLUSIONS

Fetal cardiac rhabdomyomas are often benign and have a tendency to regress, but their prognosis is guarded due to very frequent association with arrhythmias and tuberous sclerosis. During prenatal counseling, it is of utmost importance to inform the future parents of the virtually constant perspective of tuberous sclerosis complex.

Authors+Show Affiliations

Division of Cardiology, Hospital Casa del Sole, Palermo, Italy. spipiton@neomedia.itNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

11899590

Citation

Pipitone, Salvatore, et al. "Cardiac Rhabdomyoma in Intrauterine Life: Clinical Features and Natural History. a Case Series and Review of Published Reports." Italian Heart Journal : Official Journal of the Italian Federation of Cardiology, vol. 3, no. 1, 2002, pp. 48-52.
Pipitone S, Mongiovì M, Grillo R, et al. Cardiac rhabdomyoma in intrauterine life: clinical features and natural history. A case series and review of published reports. Ital Heart J. 2002;3(1):48-52.
Pipitone, S., Mongiovì, M., Grillo, R., Gagliano, S., & Sperandeo, V. (2002). Cardiac rhabdomyoma in intrauterine life: clinical features and natural history. A case series and review of published reports. Italian Heart Journal : Official Journal of the Italian Federation of Cardiology, 3(1), 48-52.
Pipitone S, et al. Cardiac Rhabdomyoma in Intrauterine Life: Clinical Features and Natural History. a Case Series and Review of Published Reports. Ital Heart J. 2002;3(1):48-52. PubMed PMID: 11899590.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Cardiac rhabdomyoma in intrauterine life: clinical features and natural history. A case series and review of published reports. AU - Pipitone,Salvatore, AU - Mongiovì,Maurizio, AU - Grillo,Roberto, AU - Gagliano,Sergio, AU - Sperandeo,Velio, PY - 2002/3/20/pubmed PY - 2002/10/3/medline PY - 2002/3/20/entrez SP - 48 EP - 52 JF - Italian heart journal : official journal of the Italian Federation of Cardiology JO - Ital Heart J VL - 3 IS - 1 N2 - BACKGROUND: Fetal cardiac rhabdomyoma is very rare; despite the fact that many cases and series have been reported, the clinical presentation, the natural history and the frequency with which this pathology is associated with tuberous sclerosis complex are not well determined. The aim of this investigation was to study the clinical features and the natural history of cardiac rhabdomyoma when diagnosed during prenatal life. METHODS: Nine cases of cardiac rhabdomyoma detected among 5276 fetal echocardiograms recorded over a 10-year period in a single center were retrospectively reviewed. Medical records and echocardiograms were studied to determine the prenatal and postnatal course and outcome. RESULTS: The incidence of cardiac rhabdomyoma in our center was 0.17%. The gestational age at diagnosis ranged from 27 to 36 weeks. The most common reason for fetal echocardiography was an abnormal obstetric ultrasound scan (6/9 cases). In no case was there a family history of tuberous sclerosis. In one case, the tumor was single whereas in 8 cases multiple tumors were diagnosed. During prenatal life the majority of tumors were clinically silent. One fetus died of hydrops and arrhythmia. Four children presented with arrhythmia postnatally and one required surgery. At a mean follow-up of 47 months, total or partial regression was observed in 7 patients. Seven patients developed postnatal clinical signs of tuberous sclerosis. CONCLUSIONS: Fetal cardiac rhabdomyomas are often benign and have a tendency to regress, but their prognosis is guarded due to very frequent association with arrhythmias and tuberous sclerosis. During prenatal counseling, it is of utmost importance to inform the future parents of the virtually constant perspective of tuberous sclerosis complex. SN - 1129-471X UR - https://www.unboundmedicine.com/medline/citation/11899590/Cardiac_rhabdomyoma_in_intrauterine_life:_clinical_features_and_natural_history__A_case_series_and_review_of_published_reports_ L2 - https://medlineplus.gov/fetalhealthanddevelopment.html DB - PRIME DP - Unbound Medicine ER -