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Aiko Kurisaki-Arakawa

Researcher at Juntendo University

Publications -  18
Citations -  333

Aiko Kurisaki-Arakawa is an academic researcher from Juntendo University. The author has contributed to research in topics: Sarcoma & Solitary fibrous tumor. The author has an hindex of 10, co-authored 18 publications receiving 267 citations.

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Distinct clinicopathological features of NAB2-STAT6 fusion gene variants in solitary fibrous tumor with emphasis on the acquisition of highly malignant potential

TL;DR: In this article, the authors examined variations of the NAB2-STAT6 fusion gene in 40 cases of SFT using formalin-fixed, paraffin-embedded tissues and secondary genetic alterations of tumor protein p53 (TP53),, platelet-derived growth factor receptor, β polypeptide (PDGFRB), and telomerase reverse transcriptase (TERT) promoters.
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In Japanese patients with papillary thyroid carcinoma, TERT promoter mutation is associated with poor prognosis, in contrast to BRAF V600E mutation

TL;DR: In PTCs, telomerase activation by TERT promoter mutation might be more important than alternative lengthening of telomere maintenance by immunohistochemical staining for ATRX and DAXX.
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Microsatellite instability and mismatch repair protein expressions in lymphocyte‐predominant breast cancer

TL;DR: Tests on triple‐negative breast cancers with a high density of tumor‐infiltrating lymphocytes found that MSI‐H tumors were absent in TIL‐high breast cancers, and examination of MMR proteins and PD‐L1 expression may merit further studies to yield predictive information for identifying patients who are likely to benefit from ICI.
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A case of dedifferentiated solitary fibrous tumor in the pelvis with TP53 mutation

TL;DR: A case of dedifferentiated SFT arising within the pelvis of a 70-year-old Japanese woman identifies a possible role of p53 dysfunction in the dedifferentiation process of SFT as reported in other sarcomas.
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Deeply located low-grade fibromyxoid sarcoma with FUS-CREB3L2 gene fusion in a 5-year-old boy with review of literature.

TL;DR: This case presented with an intramuscular tumor in the region of the gastrocnemius, the first case of deep LGFMS arising in a child younger than 5 years of age and still alive with no evidence of the disease 4 months after diagnosis.