Locally advanced thymic carcinoma with direct pericardial extension and atrial clot diagnosed with endoscopic ultrasound: A case report

A 31-years-old white male presented with progressive right-sided chest pain and hemoptysis for 2 weeks. Physical exam revealed reduced breath sounds in the right lower lobe. Computed tomography (CT) scan of the chest demonstrated a 5.8 3 4.9 3 4.5 cm bulky right subcarinal paraesophageal posterior mediastinal mass engulfing the bronchus intermedius and extending through the pulmonary vein into the body of the left atrium. Positron emission tomography scan demonstrated intense fluorodeoxyglucose activity in the mass suggesting malignancy. Abdominal and pelvic CT showed no metastasis or lymph nodes. A CT-guided biopsy was suggestive of basaloid lung carcinoma though thymic carcinoma could not be ruled out. EUS revealed a 4.0 3 4.8 cm mass abutting the left atrium along with a 1.8 3 2.5 cm intra-atrial thrombus (Fig. 1). A subcarinal lymph node measuring 3.0 3 1.8 cm was also seen. EUS-FNA cytology of the subcarinal lymph node revealed lymphocytes and CAM5.2, CD5-positive neoplastic cells. The patient underwent induction chemotherapy followed by right thoracotomy with resection of paraesophageal mass, complete thoracic lymphadenectomy, right lower lobectomy, and partial left atriaectomy with subsequent reconstruction of left atrium with myocardial patch. Biopsy from resected tissue showed a lobulated epithelial tumor involving the lung and myocardium (Figs. 2a and b). Most of the tumor exhibited a basaloid histology with foci and small nests of keratinization reminiscent of Hassal’s corpuscles and had lymphocytic infiltration. Immunoperoxidase stains were positive for cytokeratin (Fig. 2c) and p63 but negative for CD5, CD57, CD117, CD20, CD45, TTF-1, CAE, CEA, S-100, chromogranin, NSE, and CAM5.2. Pathologic examination was consistent with thymic carcinoma. He subsequently underwent concurrent chemoradiotherapy though chemotherapy had to be discontinued halfway through the treatment course due to increased toxicity. He had complete relief of symptoms and was leading an active life at the time of last follow-up 2 years after treatment. Follow-up CT scans were negative for metastatic disease.

[1]  K. Takabe,et al.  Thymic neoplasm: a rare disease with a complex clinical presentation. , 2013, Journal of thoracic disease.

[2]  G. Wilding,et al.  Tumour eosinophilia combined with an immunohistochemistry panel is useful in the differentiation of type B3 thymoma from thymic carcinoma , 2011, International journal of experimental pathology.

[3]  A. Ochiai,et al.  Immunohistochemical differential diagnosis between thymic carcinoma and type B3 thymoma: diagnostic utility of hypoxic marker, GLUT-1, in thymic epithelial neoplasms , 2009, Modern Pathology.

[4]  I. Eltoum,et al.  Agreement between Rapid Onsite and Final Cytologic Interpretations of EUS-guided FNA Specimens: Implications for the Endosonographer and Patient Management , 2006, The American Journal of Gastroenterology.

[5]  A. Larghi,et al.  EUS-guided fine needle tissue acquisition by using high negative pressure suction for the evaluation of solid masses: a pilot study. , 2005, Gastrointestinal endoscopy.

[6]  R. Tsuchiya,et al.  Immunohistochemical KIT (CD117) expression in thymic epithelial tumors. , 2005, Chest.

[7]  Y. Tamaki,et al.  The role of radiotherapy for thymic carcinoma. , 2004, Japanese journal of clinical oncology.

[8]  J. Pruim,et al.  Oesophageal endoscopic ultrasound with fine needle aspiration improves and simplifies the staging of lung cancer , 2004, Thorax.

[9]  I. Waxman,et al.  Clinical Impact of On-Site Cytopathology Interpretation on Endoscopic Ultrasound-Guided Fine Needle Aspiration , 2003, American Journal of Gastroenterology.

[10]  L. Sobin,et al.  Histological Typing of Tumours of the Thymus , 1999, World Health Organization. International Histological Classification of Tumours.

[11]  J. Rosai,et al.  CD5 labeling of thymic carcinomas and other nonlymphoid neoplasms. , 1998, American journal of clinical pathology.

[12]  J. Jett,et al.  Primary mediastinal tumors. Part 1: tumors of the anterior mediastinum. , 1997, Chest.