Primary atypical teratoid/rhabdoid tumor of the optic nerve: a rare entity in an exceptional location

被引:3
作者
Mahdi, Youssef [1 ,2 ]
Kharmoum, Jinane [1 ,2 ]
Alouan, Amal [2 ,3 ]
Elouarradi, Hakima [2 ,3 ]
Elkhiyat, Iman [1 ,2 ]
Maher, Mustapha [1 ,2 ]
Benchrif, Moulay Zahid [2 ,3 ]
Kili, Amina [2 ,4 ]
Daoudi, Rajae [2 ,3 ]
Cherradi, Nadia [1 ,2 ]
机构
[1] Ibn Sina Univ Hosp, Special Hosp, Dept Pathol, Rabat, Morocco
[2] Mohammed V Souissi Univ, Fac Med & Pharm, Rabat, Morocco
[3] Ibn Sina Univ Hosp, Special Hosp, Dept Ophthalmol, Rabat, Morocco
[4] Ibn Sina Univ Hosp, Pediat Hematol & Oncol Ctr, Rabat, Morocco
来源
DIAGNOSTIC PATHOLOGY | 2015年 / 10卷
关键词
Rhabdoid; Atypical teratoid; Optic nerve; NATIONAL-WILMS-TUMOR; STUDY-PATHOLOGY-CENTER; RHABDOID TUMORS; EXPERIENCE; HSNF5/INI1; CHILDHOOD; MUTATIONS; NEOPLASMS; KIDNEY;
D O I
10.1186/s13000-015-0284-2
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Atypical teratoid/rhabdoid tumors are rare and highly malignant central nervous system tumors. They have no specific radiological features and often present several histological components that make a problem in differential diagnosis with medulloblastoma and primitive neuroectodermal tumors. We present the case of a newborn girl complained of a gradual proptosis of the left eye secondary to an expansive lesional process of the optic nerve. The location at the optic nerve, reported only twice in the literature, and an exclusive rhabdoid appearance on biopsy added additional differential diagnosis problems. The proptosis worsened and the infant died few days after two cycles of chemotherapy.
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页数:5
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