Syndrome cardiac myxoma: More than just a sporadic event

American Heart Journal

Volumn 114, Issue 4 PART 1, 1987, Pages 886-889

  Vatterott, Pierce J ^a,b,c   Seward, James B ^a,b,c   Vidaillet, Humberto J ^a,b,c   Daniel Su, W P ^a,b,c   Oftedahl, Gary L ^a,b,c  

^a MAYO CLINIC ROCHESTER   (United States)

^b MAYO CLINIC   (United States)

^c Olmsted Medical Group   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; DIAGNOSIS; HEART; HEART MYXOMA; HUMAN; THERAPY;

ADULT; CASE REPORT; FEMALE; HEART NEOPLASMS; HUMAN; MYOCARDIUM; MYXOMA; SYNDROME;

EID: 0023619203     PISSN: 00028703     EISSN: 10976744     Source Type: Journal    
DOI: 10.1016/0002-8703(87)90798-8     Document Type: Article

References (12)

1. NAME syndrome (nevi, atrial myxoma, myxoid neurofibroma, ephelides): a new and unrecognized subset of patients with cardiac myxoma
2. The complex of myxomas, spotty pigmentation, and endocrine overactivity
3. Differences between nonfamilial and familial cardiac myxoma
4. The significance of multiple, recurrent, and “complex” cardiac myxomas
5. “Syndrome myxoma”: a subset of patients with cardiac myxoma associated with pigmented skin lesions and peripheral and endocrine neoplasms
6. Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine overactivity
7. Multiple lentigenes syndrome: complex comprising multiple lentigenes, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities of genitalia, retardation of growth, sensorineural deafness, and autosomal dominant hereditary pattern
8. Familial atrial myxoma
9. A syndrome of various cutaneous pigmented lesions, myxoid neurofibromata and atrial myxoma: the NAME syndrome
10. Mucocutaneous lentigines, cardiomucocutaneous myxomas, and multiple blue nevi: the “LAMB” syndrome
11. Primary cardiac tumors: experience with 30 consecutive patients since the introduction of two-dimensional echocardiography