B超诊断先天性无睑裂囊性眼临床分析(附2例报告)

报告 2例先天性无险裂囊性眼的B超图像,例 1左眼球前后径 28.2 mm,横径 31.3 mm,未见角膜、前房、虹膜及晶体回声,整个眼球均为暗区;例2右眼球均为暗区,前后径16.6 mm,未见角膜、前房、虹膜及晶体回声,眼球前外方另见13.8 mm×9.1 mm 的暗区。并对其发病机理与B超图像的关系进行讨论。     

Tumor-Like Meniscal Cyst

A 50-year-old woman presented with a 5-year history of mild pain in her right knee, which had increased over the last 2 years. A palpable mass over the anterolateral aspect of the knee was obvious and the last 3 months she was experiencing locking episodes with consequent knee effusion. The differential diagnosis was driven between meniscal cyst, pigmented villonodular synovitis, synovial sarcoma, synovial chondromatosis, and aneurysm. After a diagnostic arthroscopy, the lesion was excised by a limited lateral arthrotomy. The pathologic findings revealed a synovial cyst. Intra-articular synovial cysts are uncommon, nonsymptomatic, and mostly incidental findings on magnetic resonance imaging (MRI) and arthroscopy. This lateral meniscus synovial cyst (2.5 × 2.5 cm) was enlarged within the intracondylar notch and produced disabling knee symptoms. The peculiarity of this lesion was the tumor-like appearance: its large size, the progress of symptoms, and the multilobulated, nonhomogenous signal on the MRI scan. One year postoperatively, the patient is asymptomatic and the MRI obtained at 6 months revealed no remnant of the fully excised cyst.     

Teratoma tongue: Case report and review of literature

Teratomas are true neoplasms composed of tissues from all three germinal layers and may exhibit variable levels of maturity. They have an unknown origin and eccentric microscopic appearance. Teratomas arising from the oral cavity are rare in the newborn; only 22 cases have been reported in the literature. We describe a female neonate with an oral teratoma originating from the tongue that was successfully treated with surgery.     

Neuroimaging in Pineal Tumors

BACKGROUND AND PURPOSE: The authors report radiological findings in 11 tumors in the pineal region, which were histologically diagnosed as germinomas, pineocytomas pineoblastomas, ependymomas, teratomas, and astrocytomas. METHODS: Computed tomography (CT) was performed in seven patients and magnetic resonance imaging (MRI) was performed in all patients. RESULTS: CT showed a solid or solid/cystic mass with variable contrast enhancement. MRI showed a heterogeneous mass, with hypointense signal on T1 and iso/hyperintense signal on T2-weighted images (WI) and gadolinium enhancement. Extension to adjacent structures occurred in five patients and spread through the cerebral spinal fluid (CSF) in two. CONCLUSIONS: Pineal region tumors have no pathognomonic imaging pattern. MRI and CT are complementary in diagnosis and are important to determine localization, extension, and meningeal spread.     

腹腔镜胆囊切除术后残株胆囊及胆囊管结石

目的探讨腹腔镜胆囊切除术后残株胆囊／胆囊管结石的原因、诊断、处理及预防方法。方法回顾总结我院 1992-2005年间收治的8例腹腔镜胆囊切除术后残株胆囊／胆囊管结石病例的临床资料。结果 8例病人术前经B超、MRI、 ERCP检查确诊后,均经再次手术治愈。残株胆囊结石2例;残株胆囊管结石6例,其中2例合并胆总管结石;2例行残余胆囊切除术,6例行残株胆囊管切除、其中4例附加胆总管切开探查和／或取石、T型管引流。随访1．1-13年,效果良好。结论判断失误是腹腔镜胆囊切除术后残株胆囊结石的主要原因,过长的炎性及畸形的胆囊管残留是腹腔镜胆囊切除术后残株胆囊管结石的主要原因;其症状和体征类似于结石性胆囊炎、合并胆管结石时可有黄疸;B超、CT、ERCP等检查可确诊;再次手术切除(或取出)残株胆囊／胆囊管(结石)是有效可靠的治疗方法;娴熟的腹腔镜技术、术中胆道造影、正确掌握中转开腹指征以及丰富的胆道外科经验是预防其发生的关键。     

Extended total arch replacement for type B aortic dissection with ascending aneurysm following healed aortic dissection

We describe a case of type B aortic dissection with large ascending aortic aneurysm occurring 12.8 years after aortic root replacement (Cabrol procedure) in a non-Marfan patient with cystic medial necrosis of the aorta. We have successfully performed an extended total aortic arch replacement using a four-branched graft through the “L-indsion” approach (a combination of a left anterior thoracotomy and upper half median sternotomy). Of note, a histological specimen from the aneurysmal ascending aortic wall revealed “healed aortic dissection” with fibrous tissue replacing the media and intima in addition to multiple foci of cystic medial necrosis.     

多房性囊性肾瘤的影像学表现与病理对照

目的 提高对多房性囊性肾瘤的影像学的认识。资料与方法 报告2例经手术病理证实，且临床与影像学资料完整的多房性囊性肾瘤。分析其B超、IVU、CT、MRI检查所见征象，并与手术、病理所见对照，结合文献复习，对多房性囊性肾瘤作深入讨论。结果 影像学表现为肾区单发、多房性囊性病灶；囊肿边界清楚，与肾盏不相通，肾脏被挤压变薄，未受累区的肾脏正常；囊内容均匀或不均匀；囊间隔的密度比正常肾实质低，分隔完全且厚薄不一，可强化，但强化程度不及正常的肾组织。术后病理证实为多房性囊性肾瘤。结论 CT、MRI最能反映多房性囊性肾瘤的病理基础，是术前诊断该病的最佳方法。术前完善的影像学检查对该病的治疗方案及预后至关重要。     

肺囊肿样病变的X线诊断

作者报道28例经手术及病理证实的肺部囊性病变,其中21例为先天性,7例为后天性.x线表现可分为:①单发气囊腔.②多发性气囊腔.③单发液囊腔.④单或多发液气囊腔,内有液平面.⑤肺隔离症.讨论了形成机理以及与肺结核,肺脓肿,肺癌,转移性肺肿瘤,肺包虫囊肿等的x线鉴别诊断