Salgueiro Fábio Rêgo, Cunha Paulo, Miranda Diana, Pereira Tatiana, Pontes Filipa, Monteiro Joana, Caetano Ana
Medical Oncology Department, Portuguese Oncology Institute of Coimbra Francisco Gentil, Coimbra, Portugal.
Internal Medicine Department, Coimbra University Hospital Centre, Coimbra, Portugal.
Eur J Case Rep Intern Med. 2021 Feb 26;8(3):002224. doi: 10.12890/2021_002224. eCollection 2021.
Thymic clear cell carcinoma is the most uncommon subtype of thymic carcinoma, with 20 cases reported worldwide.
We present the case of a 61-year-old female with dyspnoea and chest pain for 2 days. Computed tomography (CT) angiography showed pulmonary thromboembolism and the existence of mediastinal and bilateral hilar lymphadenopathy, the largest infracarinal with an inferior axis of 25 mm, and also, micronodules on the left pulmonary parenchyma. The patient was admitted for aetiological assessment and underwent anticoagulant therapy. After a month, she had an ischaemic stroke, the sequelae of which proved to be fatal. The autopsy showed a mass in the superior-anterior mediastinum, with dimensions of 11×8×6 cm, corresponding to a thymus signet ring cell primary carcinoma. The immunohistochemistry study revealed that this mass was positive for AE1/AE3, CK5/6 and CK7.
The clinical, morphological and immunophenotypic diversity of this tumour makes its diagnosis a difficult multidisciplinary challenge, which requires a high level of clinical knowledge and accurate imaging and histological investigation.
Thymic clear cell carcinoma is a very rare entity with an aggressive and nonspecific clinical behaviour.There are no defined diagnostic criteria, although diagnosis could be established with histologic/cytology analysis.There are no clear guidelines for treatment, which can include highly invasive surgery and chemotherapy or radiation therapy.
胸腺透明细胞癌是胸腺癌最罕见的亚型,全球仅报道过20例。
我们报告一例61岁女性患者,出现呼吸困难和胸痛2天。计算机断层扫描(CT)血管造影显示存在肺血栓栓塞以及纵隔和双侧肺门淋巴结肿大,最大的隆突下淋巴结短径为25mm,同时左肺实质有微小结节。该患者因病因评估入院并接受了抗凝治疗。一个月后,她发生了缺血性中风,其后遗症被证明是致命的。尸检显示上纵隔前部有一个肿块,大小为11×8×6cm,为胸腺印戒细胞原发性癌。免疫组化研究显示该肿块对AE1/AE3、CK5/6和CK7呈阳性。
该肿瘤的临床、形态学和免疫表型多样性使其诊断成为一项具有挑战性的多学科难题,这需要高水平的临床知识以及准确的影像学和组织学检查。
胸腺透明细胞癌是一种非常罕见的实体,具有侵袭性和非特异性临床行为。虽然可通过组织学/细胞学分析确诊,但尚无明确的诊断标准。对于其治疗也没有明确的指南,治疗方法可能包括高侵袭性手术以及化疗或放疗。