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1.
Korean Circulation Journal ; : 442-448, 1997.
Article in Korean | WPRIM | ID: wpr-22124

ABSTRACT

BACKGROUND: Cardiac myxomas are rare benign tumors of the heart. Although cardiac myxomas are histologically benign, they may be lethal because of their strategic position. Most cases are sporadic, but rare familial occurrence has been described. PATIENTS AND RESULTS: The left atrial myxoma with cerebral embolism was diagnosed in the 21 year old female and the left atrial myxoma with acromegaly due to pituirary adenoma was subsequently diagnosed in her 19 year old male sibling. The myxoma in the male patient was successfully excised. CONCLUSION: Echocardiography can be used effectively in the diagnosis of atrial myxoma, detection of its possible recurrence, and screening other members of the family.


Subject(s)
Female , Humans , Male , Young Adult , Acromegaly , Adenoma , Diagnosis , Echocardiography , Heart , Intracranial Embolism , Mass Screening , Myxoma , Recurrence , Siblings
2.
Journal of the Korean Society of Echocardiography ; : 202-207, 1996.
Article in Korean | WPRIM | ID: wpr-741273

ABSTRACT

Cardiac myxoma is a rare tumor and occurs sporadically as isolated lesions in the left atrium of middle aged women. However, familial occurrence of the neoplasm has been described to comparison of certain clinical and pathologic features among patients who have nonfamilial cardiac myxona with those of patients who have familial cardiac myxoma showed statistically significant differences. Several case reports described that a familial occurrence of this tumor, also that these are associated skin lesions as well as other endocrine tumor. This so called complex of syndrome form of cardiac myxoma and the familial form have characteristics that distinguish them from the sporadic form. Nonfamilial cardiac myxoma was a disorder of middle aged women, usually occurred in the left atrium as a single tumor and had no particular associated conditions. On the other hand, familial cardiac myxoma was a disorder of young men, was less commonly in the left atrium, was often multicentric, and was occasionally associated with unusual or rare conditions and a tendency for recurrence. Therefore, for these patients, we recommand a thorough search for multiple tumors at operation, close postoperative follow-up, and careful screening of family members. Our findings of atrial myxoma in a brother and a sister associated with pigmented skin lesions strongly suggest a tendency to familial occurrence.


Subject(s)
Female , Humans , Male , Middle Aged , Follow-Up Studies , Hand , Heart Atria , Mass Screening , Myxoma , Recurrence , Siblings , Skin
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