Araştırma Makalesi
Yıl 2013,
Cilt: 18 Sayı: 4, 214 - 216, 14.03.2014
Öz
Kaynakça
- Porapakkham P, Porapakkham P, Petchyungtong P. Cardiac myxoma: sixteen-year experience in Central Chest Institute of Thailand. J Med Assoc Thai 2012; 95: 1509-1516.
- Dell'amore A, Albertini A, Lamarra M. Twenty years experience in oncologic surgery for primary cardiac tumors. G Chir 2013; 34: 106-111.
- Manduz S, Katrancioglu N, Karahan O, Yucel O, Yilmaz MB. Diagnosis and follow up of patients with primary cardiac tumours: a single-centre experience of myxomas. Cardiovasc J Afr 2011; 22: 310-3
- Turhan S, Tulunay C, Altin T, Dincer I. Second recurrence of familial cardiac myxomas in atypical locations. Can J Cardiol 2008; 24: 715-716. Carney JA, Hruska LS, Beauchamp GD, Gordon H. Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine over activity. Mayo Clin Proc 1986; 61: 165-172. Pan L, Peng L, Jean-Gilles J, et al. Novel PRKAR1A gene mutations in Carney Complex. Int J Clin Exp Pathol 2010; 3: 545-548.
- Durgut K, Gormus N, Ozulku M, Ozergin U, Ozpinar C. Clinical features and surgical treatment of cardiac myxoma: report of 18 cases. Asian Cardiovasc Thorac Ann 2002; 10: 111-114.
- Yavuz S, Eris C, Sezen M, et al. Recurrent multiple cardiac myxomas. Bratisl Lek Listy 2010; 111: 5495
Yıl 2013,
Cilt: 18 Sayı: 4, 214 - 216, 14.03.2014
Öz
Cardiac myxomas are the most common primary cardiac tumors. A 69-year-old female patient with a history of operated left atrial myxoma 3 years ago readmitted to the hospital for evaluation of progressive dyspnea and atypical chest pain. The echocardiographic study revealed a new tumorous mass at the same localization. The tumor was resected with the underlying heart tissue by transseptal approach. Histologic analysis confirmed a recurrent myxoma. Postoperative echocardiographic examination revealed no abnormalities. We present this case because of its recurrence and accompany with idiopathic thrombocytopenic purpura.
Anahtar Kelimeler
Kaynakça
- Porapakkham P, Porapakkham P, Petchyungtong P. Cardiac myxoma: sixteen-year experience in Central Chest Institute of Thailand. J Med Assoc Thai 2012; 95: 1509-1516.
- Dell'amore A, Albertini A, Lamarra M. Twenty years experience in oncologic surgery for primary cardiac tumors. G Chir 2013; 34: 106-111.
- Manduz S, Katrancioglu N, Karahan O, Yucel O, Yilmaz MB. Diagnosis and follow up of patients with primary cardiac tumours: a single-centre experience of myxomas. Cardiovasc J Afr 2011; 22: 310-3
- Turhan S, Tulunay C, Altin T, Dincer I. Second recurrence of familial cardiac myxomas in atypical locations. Can J Cardiol 2008; 24: 715-716. Carney JA, Hruska LS, Beauchamp GD, Gordon H. Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine over activity. Mayo Clin Proc 1986; 61: 165-172. Pan L, Peng L, Jean-Gilles J, et al. Novel PRKAR1A gene mutations in Carney Complex. Int J Clin Exp Pathol 2010; 3: 545-548.
- Durgut K, Gormus N, Ozulku M, Ozergin U, Ozpinar C. Clinical features and surgical treatment of cardiac myxoma: report of 18 cases. Asian Cardiovasc Thorac Ann 2002; 10: 111-114.
- Yavuz S, Eris C, Sezen M, et al. Recurrent multiple cardiac myxomas. Bratisl Lek Listy 2010; 111: 5495
Toplam 6 adet kaynakça vardır.
Ayrıntılar
| Birincil Dil | İngilizce |
|---|---|
| Bölüm | Case Report |
| Yazarlar | |
| Yayımlanma Tarihi | 14 Mart 2014 |
| Yayımlandığı Sayı | Yıl 2013 Cilt: 18 Sayı: 4 |