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1.
2.
James E. Salter Jr. Donald Gibson Nelson G. Ord ez Bruce Mackay 《Ultrastructural pathology》1995,19(4):305-310
A 7-cm anterior mediastinal tumor in an 80-year-old woman was found by light and electron microscopy to be a neuroblastoma. Immunoreactivity for neuron-specific enolase, synaptophysin, and chromogranin supported the diagnosis. Neuroblastoma is an uncommon tumor in adults and we are not aware of a previous report of such a tumor in a patient of this age. 相似文献
3.
The aortic nipple, a small “pseudotumor” adjacent to the aortic arch, is the left superior intercostal vein. In our series
of 40 patients it was demonstrated in six; all had a right upper thoracic mass and four had a superior vena caval syndrome.
Coronal magnetic resonance, images (MRI) of the thorax were superior to all other imaging methods in demonstrating the nipple.
It is concluded that in patients with masses in the right upper chest, coronal MR chest examinations are valuable in demonstrating
an aortic nipple, a sign of impending present superior vena caval or innominate, vein obstruction. 相似文献
4.
目的探讨原发纵隔囊肿影像表现特征,提高影像诊断的准确率。方法回顾性分析经手术病理证实且资料完整的42例原发纵隔囊肿的影像学表现。所有病例均摄胸部后前位与侧位片,胸部CT平扫29例,其中15例行增强扫描,胸部MRI平扫6例。观察病变的部位、大小、形态、密度(信号)、边缘、壁及其厚度、邻近结构。每一病种均分为影像征象典型与不典型2类。结果病变位于前纵隔28例,中、后纵隔各7例。上纵隔9例,中纵隔24例,下纵隔9例。支气管囊肿9例,囊性淋巴管瘤4例,胸腺囊肿11例,心包囊肿5例,成熟性囊性畸胎瘤13例。影像征象典型38例,不典型4例。结论90%的纵隔囊肿,根据CT、MRI显示的病变部位与内部密度、信号特征,可做出正确的影像诊断;不典型者确诊仍依靠手术病理。 相似文献
5.
本科手术治疗纵隔软组织肿瘤23例,占同期手术治疗纵隔肿瘤390例的5.9%,年龄35岁以下者17例,占73.9%。男女之比为4.8:1(19/4),本病的临床及X线表现缺乏特异性,确诊有赖于术后病理学检查。本组中良性肿瘤15例(65.2%),恶性肿瘤8例(34.8%),手术治疗24例次,肿瘤切除率为91.7%(22/24),手术为首选的治疗方法。 相似文献
6.
A 23-year-old male patient who had no history of any previous medical illness was noted to have a widened mediastinum on chest X-ray undertaken as part of a routine medical evaluation. A computer tomographic (CT) scan confirmed the widened mediastinum to be due to a double superior vena cava (SVC). No further investigations were undertaken. The patient was noted to be well when re-assessed 3 years later. 相似文献
7.
Takanori Hirose Tadashi Hasegawa Kunihiko Seki Peng Yang Toshiaki Sano Hiroshi Morizumi Masaru Tsuyuguchi 《Ultrastructural pathology》1996,20(5):451-456
A case is reported of atypical glomus tumor occurring in the posterior inferior mediastinum of a 26-year-old woman complaining of severe back pain. The tumor was composed of atypical small, round tumor cells with scattered mitotic figures. In addition to sheet-like, diffuse proliferation of the tumor cells, some areas of the tumor contained small “glo-moid” cells arranged in organoid and hemangiopericytoma-like patterns. Immunohistochemically, many tumor cells were positive for muscle-type actins and a few cells were focally positive for desmin. Ultrastructural studies revealed smooth muscle features of tumor cells, that is, pinocytotic vesicles, external laminas, dense plaques, and occasional thin filaments with dense bodies. The patient remained well for 5 years and 4 months after the operation without additional radiation and chemotherapy. The tumor was diagnosed as an atypical, or low-grade malignant, glomus tumor morphologically. It seems important to recognize the presence of this type of tumor in sites other than extremities and to differentiate it from other malignant small, round cell tumors. 相似文献
8.
An unusual case of malignant peripheral nerve sheath tumor (MPNST) arising in the posterior mediastinum of a 59-year-old man is reported. Histopathologically, the tumor showed an admixture of a dense proliferation of small round cells resembling a primitive neuroectodermal tumor (PNET) and a pleomorphic spindle cell sarcomatous area. Abortive rosettes, primitive neural tube-like structures, and a few glandular structures were found in the small round cell area. Small round cells were immunoreactive for neural cell adhesion molecule and synaptophysin, but were not immunoreactive for MIC2 and neuron-specific enolase. Pleomorphic spindle cells were occasionally arranged in a storiform pattern and were diffusely immunoreactive for S-100 protein. The MPNST of small round cell type is distinguishable from PNET by its negative immunoreactivity for MIC2, and the present tumor is assumed to be derived from primitive neuroectodermal cells in the peripheral nerve capable of bidirectional (neuron and Schwann cell) differentiation. 相似文献
9.
Kuba H Sato N Uchiyama A Nakafusa Y Mibu R Yoshida K Kuroiwa K Tanaka M 《Surgery today》1999,29(4):375-377
We herein describe a patient with mediastinal lymph node metastases which occurred after both a primary sigmoid colon cancer
and metachronous ovarian metastasis had been resected. The most likely route of metastases to the mediastinum in this case
is the paravertebral venous plexus probably connected to the ovarian metastasis, or so-called remetastasis. This case illustrates
that the mediastinum is thus a possible metastatic site in patients with colon cancer. Surgeons should therefore pay attention
to the mediastinum as well as the lung fields when checking chest X-ray films during a follow-up of patients after a resection
of colon cancer. 相似文献
10.