Dergiler / Eastern Journal of Medicine / 2013 / Cilt: 18 Sayı: 4

Recurrent left atrial myxoma: A case report

Sayfa
214–216
Yayın Tarihi
2014-03-14
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We present this case because of its recurrence and accompany with idiopathic thrombocytopenic purpura.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Cardiac myxomas are the most common primary cardiac tumors.
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Temel Bulgular & Veri: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.
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Sonuç & Katkı:We present this case because of its recurrence and accompany with idiopathic thrombocytopenic purpura.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Left atrium · myxoma · recurrence

Abstract

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.

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Bu Makaleye Atıf Yap

Ekici, B., Tanındı, A., Sahin, M., Apaydın, Z., Töre, H. (2014). Recurrent left atrial myxoma: A case report. Eastern Journal of Medicine, Cilt: 18 Sayı: 4, 214–216. https://ajindex.com/articles/984915

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Kaynakça (6)

  1. 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.
  2. Dell'amore A, Albertini A, Lamarra M. Twenty years experience in oncologic surgery for primary cardiac tumors. G Chir 2013; 34: 106-111.
  3. 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
  4. 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.
  5. 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.
  6. Yavuz S, Eris C, Sezen M, et al. Recurrent multiple cardiac myxomas. Bratisl Lek Listy 2010; 111: 5495