Pediatric angiomyxofibromatous tumor of the falx cerebri with locally destructive growth into the cranial bone
Kentaro Tsuji
Department of Pathology, Jichi Medical University, Tochigi, Japan
These authors contributed equally to this work.
Search for more papers by this authorTakeo Nakaya
Department of Pathology, Jichi Medical University, Tochigi, Japan
These authors contributed equally to this work.
Search for more papers by this authorKentaro Ashizawa
Department of Pathology, Jichi Medical University, Tochigi, Japan
These authors contributed equally to this work.
Search for more papers by this authorFumihiro Arai
Department of Pediatric Neurosurgery, Jichi Children's Medical Center Tochigi, Jichi Medical University, Tochigi, Japan
Search for more papers by this authorNoriyoshi Fukushima
Department of Pathology, Jichi Medical University, Tochigi, Japan
Search for more papers by this authorAkira Gomi
Department of Pediatric Neurosurgery, Jichi Children's Medical Center Tochigi, Jichi Medical University, Tochigi, Japan
Search for more papers by this authorShintaro Sugita
Department of Surgical Pathology, Sapporo Medical University, Hokkaido, Japan
Search for more papers by this authorTadashi Hasegawa
Department of Surgical Pathology, Sapporo Medical University, Hokkaido, Japan
Search for more papers by this authorAkira Tanaka
Department of Pathology, Jichi Medical University, Tochigi, Japan
Search for more papers by this authorKentaro Tsuji
Department of Pathology, Jichi Medical University, Tochigi, Japan
These authors contributed equally to this work.
Search for more papers by this authorTakeo Nakaya
Department of Pathology, Jichi Medical University, Tochigi, Japan
These authors contributed equally to this work.
Search for more papers by this authorKentaro Ashizawa
Department of Pathology, Jichi Medical University, Tochigi, Japan
These authors contributed equally to this work.
Search for more papers by this authorFumihiro Arai
Department of Pediatric Neurosurgery, Jichi Children's Medical Center Tochigi, Jichi Medical University, Tochigi, Japan
Search for more papers by this authorNoriyoshi Fukushima
Department of Pathology, Jichi Medical University, Tochigi, Japan
Search for more papers by this authorAkira Gomi
Department of Pediatric Neurosurgery, Jichi Children's Medical Center Tochigi, Jichi Medical University, Tochigi, Japan
Search for more papers by this authorShintaro Sugita
Department of Surgical Pathology, Sapporo Medical University, Hokkaido, Japan
Search for more papers by this authorTadashi Hasegawa
Department of Surgical Pathology, Sapporo Medical University, Hokkaido, Japan
Search for more papers by this authorAkira Tanaka
Department of Pathology, Jichi Medical University, Tochigi, Japan
Search for more papers by this author
REFERENCES
- 1Medeiros F, Scheithauer BW, Oliveira AM, Gregory RS. Angiomyxofibromatous tumor of the falx cerebri. Am J Surg Pathol 2006; 30: 545–47.
- 2Sugita S, Obata M, Takebayashi S, Kikuchi T, Hasegawa T. Angiomyxomatous tumor of the falx cerebri. Pathol Int 2016; 66: 50–51.
- 3Miettinen M, Finnell V, Fetsch JF. Ossifying fibromyxoid tumor of soft parts—a clinicopathologic and immunohistochemical study of 104 cases with long-term follow-up and a critical review of the literature. Am J Surg Pathol 2008; 32: 996–1005.
- 4Kao YC, Sung YS, Zhang L et al. EWSR1 fusions with CREB family transcription factors define a novel myxoid mesenchymal tumor with predilection for intracranial location. Am J Surg Pathol 2017; 41: 482–90.
- 5Bale TA, Oviedo A, Kozakewich H et al. Intracranial myxoid mesenchymal tumors with EWSR1-CREB family gene fusions: Myxoid variant of angiomatoid fibrous histiocytoma or novel entity? Brain Pathol 2018; 28: 183–91.
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