1.Cardiac rhabdomyoma: a report of two cases.
Sang Rock CHO ; Yong Jin KIM ; Joon Ryang RHO ; Kyung Phill SUH
The Korean Journal of Thoracic and Cardiovascular Surgery 1991;24(11):1138-1143
No abstract available.
Rhabdomyoma*
2.Cardiac rhabdomyoma in the neonate: A case report.
Sung Dong PARK ; Jae Hong PARK ; Jun Ho MUN ; Wook Su AHN ; Yong HUR ; Byoung Yul KIM ; Jeong Ho LEE
The Korean Journal of Thoracic and Cardiovascular Surgery 1993;26(10):804-807
No abstract available.
Humans
;
Infant, Newborn*
;
Rhabdomyoma*
3.Rhabdomyoma of Inferior Rectus Muscle Manifesting as Vertical Eye Movement Limitation
Ji Min KWON ; Jae Hwan KWON ; Soo Jung LEE
Korean Journal of Ophthalmology 2019;33(4):397-398
No abstract available.
Eye Movements
;
Rhabdomyoma
4.Tetralogy of Fallot associated with a Cardiac Rhabdomyoma in a Infant.
Chan Uhng JOO ; Hyun Seup SIM ; Eun Kyung CHOI ; Min Ho KIM
Korean Circulation Journal 2001;31(6):588-591
No abstract available.
Humans
;
Infant*
;
Rhabdomyoma*
;
Tetralogy of Fallot*
6.Left Ventricular Rhabdomyoma with Tuberous Sclerosis: A Report of one case.
Sang Ho MOON ; Pil Won SEO ; Seongsik PARK ; Soo Bin YIM ; Sam Hyun KIM
The Korean Journal of Thoracic and Cardiovascular Surgery 2002;35(6):467-470
The most common primary heart tumor in infants is the rhabdomyoma.It is known that tuberous sclerosis is found in half of the patients with cardiac rhabdomyoma. Because the prognosis of this tumor associated with subaortic stenosis is poor,the surgical intervention is indicated.We report one case of left ventricular rhabdomyoma with tuberous sclerosis.
Constriction, Pathologic
;
Heart Neoplasms
;
Humans
;
Infant
;
Prognosis
;
Rhabdomyoma*
;
Tuberous Sclerosis*
7.A Case of Fetal Cardiac Rhabdomyoma with Tuberous Sclerosis.
Ki Cheol KIL ; Su Mi KIM ; Jae Eun HA ; Sun young NAM ; Ki Sung RYU ; Young LEE
Korean Journal of Perinatology 2009;20(4):390-394
Fetal cardiac tumors are a rare condition and are histologically benign. Cardiac rabdomyoma is the most common cardiac tumor and may be associated with tuberous sclerosis. Clinical follow-up including monitoring of fetal well-being is warranted as long as the fetus remains asymptomatic and there is no evidence for hydrops fetalis. If obstruction to blood flow and/or early fetal compromise is noted, then the decision of whether to deliver early must be made. We report a case of fetal cardiac tumor diagnosed by antenatal ultrasonography and diagnosed as tuberous sclerosis with brain MRI scanning after birth.
Brain
;
Fetus
;
Follow-Up Studies
;
Heart Neoplasms
;
Hydrops Fetalis
;
Magnetic Resonance Imaging
;
Parturition
;
Rhabdomyoma
;
Tuberous Sclerosis
8.Tetralogy of Fallot Associated with Multiple Cardiac Rhabdomyomas: case report.
Hee Suk JUNG ; Won Kyoung JHANG ; Tae Jin YUN
The Korean Journal of Thoracic and Cardiovascular Surgery 2009;42(6):770-773
Rhabdomyoma has been reported to be the most common type of cardiac tumors in fetuses and children, and multiple cardiac rhabdomyomas almost certainly signify the association with tuberous sclerosis. We report here on a case of Tetralogy of Fallot (ToF) that was associated with multiple rhabdomyomas and tuberous sclerosis. A two-year-old boy, who had undergone systemic-pulmonary shunt during the neonatal period, received total correction of his ToF after the complete regression of the cardiac tumor. The postoperative course was uneventful, and he has been follow-up for 2 months. The boy is currently in an excellent condition.
Child
;
Fetus
;
Follow-Up Studies
;
Heart Neoplasms
;
Humans
;
Rhabdomyoma
;
Tetralogy of Fallot
;
Tuberous Sclerosis
9.A Case of Primary Cardiac Fibroma.
Woo Seon SEO ; Chi Sook MON ; Min Young HER ; Hyun Sung LEE ; Sang Min LEE ; Jae Ho LEE ; Sang Bong LEE ; Soo Ryong JUNG ; Kil Hyun CHO ; Dae Gyung KIM ; Doo Il KIM ; Dong Soo KIM
Journal of the Korean Society of Echocardiography 2003;11(1):31-34
Primary cardiac tumors in infancy and childhood are rare, with fibromas being the second most common tumor after rhabdomyomas. Although cardiac fibromas are characteristically benign intramural tumors, they may exhibit expansile growth resulting in obstruction, valvular dysfunction, as well as other problems so early diagnosis and successful surgical excision are important. We experienced a case of cardiac fibroma in right ventricle that diagnosed by transthoracic echocardiography, chest CT, open heart tissue biopsy etc.
Biopsy
;
Early Diagnosis
;
Echocardiography
;
Fibroma*
;
Heart
;
Heart Neoplasms
;
Heart Ventricles
;
Rhabdomyoma
;
Tomography, X-Ray Computed
10.Rhabdomyomatous Mesenchymal Hamartoma Presenting as a Midline Mass on a Chin.
Hyeonwoo KIM ; Jee Hyeok CHUNG ; Ha Min SUNG ; Sukwha KIM
Archives of Craniofacial Surgery 2017;18(4):292-295
A 17-month-old boy was evaluated for a midline mass on his chin. The mass was anchored to the mentalis muscle with a stalk-like structure. The pathological diagnosis of the mass was rhabdomyomatous mesenchymal hamartoma. This is the first report of rhabdomyomatous mesenchymal hamartoma presenting as a midline chin mass in Korean pediatric patients.
Chin*
;
Diagnosis
;
Hamartoma*
;
Head and Neck Neoplasms
;
Humans
;
Infant
;
Male
;
Mandibular Neoplasms
;
Rhabdomyoma
;
Soft Tissue Neoplasms