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[儿童内淋巴囊腺癌。病例报告]

[Adenocarcinoma of the endolymphatic sac in children. A case report].

作者信息

Facon F, Bruzzo M, Figarella-Branger D, Girard N, Chays A, Magnan J

机构信息

Hôpital Nord, Service d'ORL et de chirurgie cervico-faciale, chemin des bourrellys, F-13915 Marseille, France.

出版信息

Rev Laryngol Otol Rhinol (Bord). 2002;123(1):55-9.

Abstract

We report a case of an adenocarcinoma of the endolymphatic sac in a 13 years old child, which was fortuitously discovered at the time of radiological investigation of growth delay. Arising from the end of the endolymphatic sac, this rare tumour shares a similar clinic expression with other cerebellopontine angle pathologies. Radiological investigation reveals a moth eaten appearance to the posterior temporal bone and specific bony inclusions. With MRI there is an intense and/or intermediate signal on T1, a hyper signal on T2 and T1 enhancement with injection of gadolinium. Treatment is surgical and local recurrences are not uncommon. After histological confirmation, a search for Von Hippel-Lindau disease is mandatory because this tumour is not exceptional among this subset of patients. Diagnosis and therapeutic criteria will be highlighted by our case and a review of the literature.

摘要

我们报告一例13岁儿童内淋巴囊腺癌病例,该病例在生长发育迟缓的影像学检查时偶然发现。这种罕见肿瘤起源于内淋巴囊末端,与其他桥小脑角病变有相似的临床症状。影像学检查显示颞骨后部呈虫蚀样外观及特定的骨质包块。MRI检查显示T1加权像呈高信号和/或中等信号,T2加权像呈高信号,注射钆后T1加权像强化。治疗方式为手术,局部复发并不少见。组织学确诊后,必须筛查冯·希佩尔-林道病,因为在这类患者中这种肿瘤并不罕见。我们将通过该病例及文献复习强调诊断和治疗标准。

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