Combined morphological, immunohistochemical and genetic analyses of medulloepithelioma in the posterior cranial fossa. Issue 2 (3rd October 2017)

• Record Type: Journal Article
• Authors: Kusakabe, Kosuke; Kohno, Shohei; Inoue, Akihiro; Seno, Toshimoto; Yonezawa, Sachiko; Moritani, Kyoko; Mizuno, Yosuke; Kurata, Mie; Kitazawa, Riko; Tauchi, Hisamichi; Watanabe, Hideaki; Iwata, Shinji; Hirato, Junko; Kunieda, Takeharu
• Is Part Of: Neuropathology. Volume 38:Issue 2(2018)
• Page Start: 179
• Page End: 184
• Publication Date: 2017-10-03
• Subjects: C19MC microRNA cluster -- medulloepithelioma -- multilayered rosettes -- pediatric central nervous system tumor -- posterior cranial fossa; Nervous system -- Diseases -- Periodicals; Nervous system -- Pathophysiology -- Periodicals; 616.8047
• DOI: 10.1111/neup.12431
• Languages: English
• ISSNs: 0919-6544

Abstract

Abstract : Medulloepithelioma is a rare and highly malignant primitive neuroectodermal tumor that usually occurs in childhood. The diagnosis of this entity required only morphological analysis until the World Health Organization classification of central nervous system (CNS) tumors was revised, and now genetic analysis is necessary. We report a case of medulloepithelioma in the posterior cranial fossa that was diagnosed by both morphological and genetic analyses based on this classification. A 10‐month‐old girl was admitted to our hospital with consciousness disturbance and vomiting. Neuroimaging revealed a partially calcified mass and cyst formation in the posterior cranial fossa. Partial resection of the tumor was performed and histological findings revealed multilayered rosettes with LIN28A staining, but genetic analysis showed no amplification of the C19MC microRNA cluster at 19q14.32. Therefore, we diagnosed the tumor as medulloepithelioma belonging to other CNS embryonal tumors. The patient was immediately treated with systemic high‐dose chemotherapy. Follow‐up neuroimaging 10 months later showed no signs of recurrence. Medulloepitheliomas are difficult to diagnose by routine HE staining and require combined morphological, immunohistochemical and genetic analyses to provide an accurate diagnosis.