| Literature DB >> 27790306 |
Lei Chen1, Lu Fang1, Zhiqi Liu1, Dexin Yu1, Daming Wang1, Yi Wang1, Dongdong Xie1, Jie Min1, Demao Ding1, Tao Zhang1, Ci Zou1, Zhiqiang Zhang1.
Abstract
Adrenal germ cell tumour is very rare. We report a case of a 59-year-old woman who presented with right flank discomfort. The laboratory examinations were normal and the chest computed tomography (CT) showed right pleural effusion. The abdominal CT scan revealed a large mass on the right adrenal gland. The patient underwent an adrenalectomy. Histopathologic examination and immunohistochemical findings were consistent with mixed germ cell tumour. Three months later following the operation, the patient was admitted to our hospital again with chest tightness and shortness of breath. The chest CT showed right pleural effusion recurrence and enlargement of mediastinal lymph nodes and right hilar lymph nodes. The patient had right supraclavicular lymphadenectasis on physical examination. Fine needle aspiration cytology from the supraclavicular lymph nodes showed groups of malignant tumour cells. The patient died within 6 months postoperatively. In this case, the lymph node pathway played an important role in the metastatic procedure.Entities:
Year: 2016 PMID: 27790306 PMCID: PMC5065414 DOI: 10.5489/cuaj.2904
Source DB: PubMed Journal: Can Urol Assoc J ISSN: 1911-6470 Impact factor: 1.862