Left atrial cavernous haemangioma presenting with cardiac tamponade in a patient with Cowden syndrome

Cowden syndrome (CS) is a rare disorder characterised by multiple non-cancerous, tumour-like growths called hamartomas. The syndrome is associated with the development of cancer of the breast, endometrium, kidneys, skin and rarely the brain. We report a rare case of symptomatic cardiac haemangioma in a patient with CS. A 54-year-old woman with CS presented with dyspnoea and orthopnoea in the setting of cardiac tamponade. Echocardiography revealed a large haemopericardium and tamponade physiology, secondary to a pericardial mass. The patient underwent urgent cardiopulmonary bypass with removal of the mass. Histopathology confirmed a benign cavernous haemangioma. We postulate that tumours involving the heart/pericardium may be an additional manifestation of CS. This case further highlights the necessity to consider pericardial/cardiac manifestations in patients with hamartomatous syndromes who present with cardiorespiratory symptoms, so that opportunistic investigation and treatment may be instituted.

[1]  S. Padhi,et al.  Pericardial Haemangioma: A Common Tumour in an Unusual Location: Case Report and Review of Literature. , 2017, Journal of clinical and diagnostic research : JCDR.

[2]  이명구,et al.  Robbins and Cotran Pathologic basis of disease , 2017 .

[3]  Y. Umekita,et al.  Tumor-to-tumor metastases in Cowden’s disease: an autopsy case report and review of the literature , 2015, Diagnostic Pathology.

[4]  Liang Ma,et al.  Cardiac Hemangioma: A Comprehensive Analysis of 200 Cases. , 2015, The Annals of thoracic surgery.

[5]  Jon C. Aster,et al.  Robbins & Cotran Pathologic Basis of Disease , 2014 .

[6]  E. Swisher,et al.  Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria. , 2013, Journal of the National Cancer Institute.

[7]  S. Martinez-Jiménez,et al.  Primary pericardial tumors. , 2013, Radiographics : a review publication of the Radiological Society of North America, Inc.

[8]  David Moher,et al.  The CARE Guidelines: Consensus-based Clinical Case Reporting Guideline Development , 2013, Journal of Medical Case Reports.

[9]  W. Frishman,et al.  Cardiac and Pericardial Tumors , 2012, Cardiology in review.

[10]  F. Patanè,et al.  Right atrial lipoma in patient with Cowden syndrome. , 2010, Interactive cardiovascular and thoracic surgery.

[11]  P. Burger,et al.  Lhermitte-Duclos Disease: A Report of 31 Cases with Immunohistochemical Analysis of the PTEN/AKT/mTOR Pathway , 2005, Journal of neuropathology and experimental neurology.

[12]  T. Horinouchi,et al.  Recurrent pericardial tamponade from atrial hemangioma. , 2004, The Annals of thoracic surgery.

[13]  William R Sellers,et al.  The biology and clinical relevance of the PTEN tumor suppressor pathway. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[14]  C Eng,et al.  PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. , 1999, Human molecular genetics.

[15]  C. Woods,et al.  Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations , 1999, European Journal of Human Genetics.

[16]  B. Brodwater,et al.  Case report. Pericardial hemangioma. , 1996, Journal of computer assisted tomography.