• Nie Znaleziono Wyników

Right-sided atrial tumour in a patient with abdominal neoplasm

N/A
N/A
Protected

Academic year: 2022

Share "Right-sided atrial tumour in a patient with abdominal neoplasm"

Copied!
1
0
0

Pełen tekst

(1)

www.kardiologiapolska.pl

Kardiologia Polska 2014; 72, 9: 843; DOI: 10.5603/KP.2014.0176 ISSN 0022–9032

Studium przypadku / CliniCal Vignette

Right-sided atrial tumour in a patient with abdominal neoplasm

Guz prawego przedsionka u chorej z nowotworem w obrębie jamy brzusznej Małgorzata Chlabicz

1

, Anna Lisowska

1

, Małgorzata Knapp

1

, Bożena Sobkowicz

1

, Tomasz Hirnle

2

1Department of Cardiology, Medical University in Bialystok, Bialystok, Poland

2Department of Cardiac Surgery, Medical University in Bialystok, Bialystok, Poland

A 47-year-old woman was admitted to hospital due to a loud diastolic murmur of the whole heart. One month earlier, she had been diagnosed with a huge abdominal tumour (130 mm × 119 mm × 290 mm), which probably came from the uterus, with metastases in the lungs, hence the patient was prepared for surgery. Her past medical history was negative for any cardiopulmonary disease. On admission, the electrocardiogram demonstrated sinus tachycardia and incomplete right bundle branch block. Transthoracic echocardiography revealed big, mobile masses with a maximum dimension of 20 mm × 60 mm attached to the tricuspid valve leaflets with moderate tricuspid regurgitation, without obstruction of the valve orifice (Figs. 1A, B). Magnetic resonance imaging confirmed irregular, mobile masses which were attached to the tricuspid valve leaflets from atrial and ventricular sites, with one of them prolapsing into the right ventricle (Fig. 1C). Both lungs presented with diffuse tumours, the largest in the tenth segment of the left lung with dimensions of 20 mm × 20 mm, suggestive of metastatic lesions. To broaden the diagnosis, trans-thoracic fine needle aspiration of the lung under computed tomography (CT) guidance was performed, however histopathology revealed only histiocytes and inflammatory cells. The patient was consulted by a heart surgeon and a gynaecologist. Based on performed diagnostic resets, a metastatic tumour was suspected. At first the patient underwent abdominal tumour resection and the sections showed a histologically benign tumour — cotylenoid dissecting leiomyoma, an extremely rare variant of uterine leiomyoma. The patient was admitted again to our department for clinical evaluation. CT pulmonary angiography revealed peripheral pulmonary embolism, which might suggest cardiac thrombus. Secondly cardiac surgery was performed — excision of tumour and tricuspid val- vuloplasty through the right minithoracotomy. Intraoperatively, a large tumour which was attached to the right atrium near the annulus of the tricuspid valve with 4 branches entangled into the chordae tendineae, was found (Fig. 1D). The tumour branches measured 10 mm × 50 mm,

16 mm × 45 mm, 8 mm × 66 mm, and 14 mm × 100 mm (Fig. 1E). Postoperative course was uneventful. Histopathological examination revealed myxoma. Primary tumours of the heart are extremely rare entities, with about half of these being cardiac myxomas. They are most com- monly of left atrial origin (85% to 90%), less commonly right atrial (10% to 12%).

Our case presents two different benign tumours — cotylenoid dissecting leio- myoma and cardiac myxoma, which is an extremely rare phenomenon. Before the gynaecological surgery, we were convinced that the patient had abdominal neoplasm with metastases in the lungs and heart.

Then we expected thrombus in the right atrium with concomitant pulmonary em- bolism. Finally, the tumour turned out to be a cardiac myxoma. It was a long and complicated diagnostics. However, so far we have not established the nature of the changes in the lungs.

Address for correspondence:

Anna Lisowska, MD, PhD, Department of Cardiology, Medical University in Bialystok, ul. Skłodowskiej-Curie 24 A, 15–276 Białystok, Poland, tel: +48 85 74 68 656, fax: +48 85 74 68 604, e-mail: anlila@poczta.onet.pl

Conflict of interest: none declared

Figure 1. A, B. Two-dimensional transthoracic echocardiogram in the 4-cham- ber view demonstrating a large, mobile right atrial (RA) tumour; C. Magnetic resonance imaging scan of the heart with masses, which were prolapsed into the right ventricle (RV); D. Large RA tumour during cardiac surgery excision, with branches entangled into the chordae tendineae; E. The large tumour removed from the RA; LA — left atrium; LV — left ventricle

A C

D E

B

Cytaty

Powiązane dokumenty

The TNM modification proposed by Dulguerov and Cal- caterrain [5] is also used: T1 – tumour involves the nasal cavity and/or sinuses (except the sphenoid sinus), ethmoid cells, T2

Cellular angiofibroma is microsco- pically characterised by mesenchymal spindle-shaped cells, thick-walled blood vessels of small and medium diameter and intracellular substance..

Uwzględniając całość przebiegu klinicznego (ujemny wynik PET/CT i całkowitą rezolucję zmiany pod wpływem leczenia przeciwkrzepliwego, przy braku cech przeciążenia prawej

W tomo- grafii komputerowej klatki piersiowej uwidoczniono rozsiane guzki w obu płucach interpretowane przez radiologa jako możliwe zmiany przerzutowe.. Nasunęło to

Several factors suggested the diagnosis of intra- vascular large B-cell lymphoma: advanced age, potentially pri- mary heart tumour, short medical history, aggressive course, and

W badaniu wykluczono zatoro- wość płucną, potwierdzono obecność dodatkowej struktury w świetle żyły głównej dolnej i w prawym przedsionku, ale całość obrazu nie pozwoliła

Therefore, a followed-up CT scan of the abdomen showed, as well as the metastatic changes within the liver, a well- vascularised jejunal tumour suspected to be the primary focus of

Intratesticular cellular angiofibroma — a rare benign tumour: case report and literature review.. NOWOTWORY J