Cardiac myxomas make up approximately 50% of all benign cardiac tumors and represented 86% of all surgically treated cardiac tumors. Most of them originated from the left atrium, in some cases from both of atria. We report a case of male patient with biatrial myxomas and other extra-cardiac involvement: hypophyseal adenoma, enlargement of thyroid gland, tubular adenoma polyp of colon and bilateral large cell calcifying Sertoli cell tumor (LCCSCT) of testis. These findings led to the diagnosis of Carney's complex, which is a syndrome with multiple neoplasias, cardiac myxomas, lentigines, and endocrine abnormalities. A genetic test confirm this diagnosis. was revealed and resected the left atrial myxoma. This tumor was of identic consistence, 6 × 5 × 3 cm, attached to the free wall of the atrium by a small stalk 3 × 1 cm. The diagnosis of bilateral atrial myxomas was confirmed by histologic studies (Fig. 2). We assumed association between the endocrine abnormalities-hypophyseal adenoma, struma nodosa and benign tumors (bilateral LCCSCT of testis and biatrial tumor), and therefore we signed this patient with Carney complex. Carney complex is an autosomal dominant condition most commonly caused by mutations in the PRKAR1A gene on chromosome 17q23-q24. In our patient mutation c.491-492delTG/p.V164Dfs*5 in exon 4 of PRKAR1A gene was identified and the diagnosis of Carney complex was confirmed (Fig. 3). The patient was discharged in good condition. Keywords DiscussionAlthough primary tumors of the heart are rare, the myxoma is the most frequent benign primary heart tumor as it accounts for 0.3% of open-heart surgery. 4) Cardiac myxomas usually appear as a sporadic isolated condition in the left atrium of middle-aged women with no other coincidental pathology. A small percentage of primary cardiac tumors have familial penetrance. Recurrence is more frequent in patients with the family history of myxoma, and familial myxomas frequently appear et early ages, with atypical and multicentric location. 5) In 1985, Carney and others described in young people a special complex group of cardiac myxomas associated to a distinctive complex pathology, giving identity to the There is a marked familial trend (52%), a high incidence of recurrence (20%). 6) The most frequent extra-cardiac involvements are pigmented skin lesions, cutaneous myxomas, adrenal cortical disease, myxoid mammary fibroadenoma, pituitary adenoma, melanotic schwannomas, thyroid disease and male patients with testes tumors. The diagnosis is made when two or more of these criteria are present. The myxom in CNC is usually in left atrium, biatrial myxomas are rare. The four chambers of the heart should be examined at surgery for typical myxoma locations, right atriotomy and combined superior-transseptal approach improve exposure of the cavities. In our patient, the tumor size and attachment were identified by echocardiogram, and a safe and efficient transseptal incision was achieved. Myxoma is known to recur in 30%-70% of patients with familial myxomas. Close follo...
The article presents a case study of a 37-year-old male who was admitted to the Acute Cardiology Unit of our hospital with suspicion of acute coronary syndrome. By invasive imaging examination, acute coronary syndrome was ruled out, but as a secondary finding a foreign body was found in the pericardium - a broken needle that had travelled to the heart after intravenous heroin administration into the right femoral vein, which was also confirmed on a computed tomography scan. Because of a developing pericardial tamponade, surgical intervention and the extraction of the foreign body was indicated.
V článku popisujeme prípad re-expanzného pľúcneho edému (RPE), ktorý sa rozvinul po odstránení mediastinálneho tumoru. Re-expanzný pľúcny edém je raritná komplikácia spojená s liečbou skolabovaných pľúc pri pneumotoraxe, veľkom množstve pleurálneho výpotku alebo tumoru. Rizikovými faktormi pre vznik RPE sú: dlhšie trvanie atelektázy pľúc (viac ako tri dni), rozsah intratorakálnej lézie, strata surfaktantu, vek pacienta. Pre nejednoznačnú patofyziológiu je liečba náročná, a preto RPE je spojená s vysokou mortalitou. Terapia vyžaduje dôsledný a komplexný manažment pacienta.
Direct tumour extension into the right atrium in thyroid cancer is extremely uncommon. We report the case of an 80-year-old woman with echocardiography diagnosed in the right atrial mass. A large thyroid tumour with extension into the right jugular vein (JV), the superior vena cava (SVC) fi lling the right atrium was revealed by magnetic resonance imaging (MRI). Percutaneous fi ne-needle aspiration biopsy led to carcinoma being strongly suspected. The massive intravascular invasion and age of the patient contra-indicated surgical resection.
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