Rupture of bronchogenic cyst in the pericardium with high carbohydrate antigen 19-9 production

Norifumi Takeda , Jun Nakajima , Namie Yamada , Yukio Hiroi , Yasunobu Hirata , Ryozo Nagai
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引用次数: 2

Abstract

Mediastinal bronchogenic cysts are frequently detected incidentally in adults. Here, we present a unique case of atypical clinical course of bronchogenic cyst beneath the carina, which ruptured into the pericardium. We could not diagnose definitely at initial admission, even though the massive pericardial fluid was exudative with high carbohydrate antigen (CA) 19-9 production. The fluid cytology was negative for malignancy. Five years later, the regrown and unruptured bronchogenic cyst caused atrial fibrillation by impinging on the heart with a high level of serum CA19-9. After resection of the CA19-9-enriched cyst by thoracoscopic surgery, he was discharged without recurrence of atrial fibrillation or any chest symptoms, and the serum CA19-9 level decreased to within the normal range. Differential diagnosis of cytology negative pericardial effusion with high CA19-9 production may be difficult, however, intrapericardial rupture of bronchogenic cyst should be considered in some patients.

心包内支气管源性囊肿破裂伴高碳水化合物抗原19-9产生
成人纵隔支气管囊肿常被偶然发现。在这里,我们提出一个独特的病例,不典型的临床过程的支气管囊肿在隆突下,破裂进入心包。入院时虽有大量渗出的心包液,并有高碳水化合物抗原(CA) 19-9的产生,但仍不能明确诊断。液体细胞学检查为恶性阴性。5年后,再生的未破裂的支气管源性囊肿冲击心脏引起心房颤动,血清CA19-9水平较高。经胸腔镜手术切除富含CA19-9的囊肿后,患者出院,无房颤复发及任何胸部症状,血清CA19-9水平降至正常范围。细胞学阴性伴高CA19-9生成的心包积液可能难以鉴别诊断,然而,在一些患者中应考虑支气管源性囊肿心包内破裂。
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