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Articles by Jun Nishio
Chondromyxoid Fibroma: An Updated Review
Keywords: Chondromyxoid fibroma chondroblastoma phosphaturic mesenchymal tumor chondrosarcoma osteosarcoma GRM1 COL12A1 review Introduction Chondromyxoid fibroma (CMF) is a rare benign cartilaginous tumor first described by Jaffe and Lichtenstein (1) in 1948. It belongs to the chondrogenic tumor group according to the latest World Health Organization (WHO) classification of soft tissue and bone tumors (2). The etiology of this peculiar tumor is unknown.
Acral Angioleiomyoma With Tumoral Calcinosis: A Rare Case Report and Literature Review
Keywords: Angioleiomyoma tumoral calcinosis calcification foot Introduction Angioleiomyoma, also known as vascular leiomyoma, is a distinctive benign soft-tissue tumor originating from the smooth muscle layer of blood vessels (1). According to the latest World Health Organization classification of soft-tissue tumors, it belongs to the group of pericytic (perivascular) tumors (2). Angioleiomyoma comprises about 4.4% of all benign soft-tissue tumors and 0.2% of all tumors of the foot and ankle (3).
Calcifying Aponeurotic Fibroma: A Review and Update
Keywords: Calcifying aponeurotic fibroma calcified chondroid mesenchymal neoplasm lipofibromatosis fibronectin 1 epidermal growth factor fusion gene review Introduction Calcifying aponeurotic fibroma (CAF), formerly known as juvenile aponeurotic fibroma, is a rare benign but locally aggressive mesenchymal tumor first described by Keasbey in 1953 (1).
Bizarre Parosteal Osteochondromatous Proliferation Revisited
Keywords: Bizarre parosteal osteochondromatous proliferation Nora lesion subungual exostosis florid reactive periostitis osteochondroma COL1A1 COL1A2 review Introduction Bizarre parosteal osteochondromatous proliferation (BPOP), formerly known as Nora lesion, is a rare benign surface-based bone lesion first described in detail by Nora et al. (1) in 1983. Meneses et al. (2) subsequently described the largest series of 65 cases that became the basis of further understanding of this disease.
Superficial Angiomyxoma Revisited
Keywords: Superficial angiomyxoma cutaneous myxoma superficial acral fibromyxoma deep (aggressive) angiomyxoma myxofibrosarcoma PRKAR1A review Introduction Superficial angiomyxoma (SAM), also known as cutaneous myxoma, is an uncommon benign mesenchymal tumor first properly described by Allen et al. (1) in 1988. It may be sporadic or related to Carney complex (2-4). The exact etiology of SAM is unknown.
Fibroma of Tendon Sheath Revisited
Keywords: Fibroma of tendon sheath desmoplastic fibroblastoma tenosynovial giant cell tumor nodular fasciitis USP6 review Introduction Fibroma of tendon sheath (FTS) is a rare benign soft-tissue tumor first described in detail by Geschickter and Copeland (1) in 1949. Chung and Enzinger (2) subsequently described the largest series of 138 cases that became the basis of our understanding of this disease.
Atypical Spindle Cell/Pleomorphic Lipomatous Tumor: A Review and Update
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
Keratin-Positive Giant Cell-Rich Tumor: A Review and Update
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
Giant Cell Tumor of Soft Tissue: An Updated Review
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
Intramuscular Hybrid Nerve Sheath Tumor of the Thigh: Case Report and Literature Review
Key Words: Hybrid nerve sheath tumor intramuscular schwannoma neurofibroma magnetic resonance imaging Hybrid nerve sheath tumor (HNST) is a recently recognized soft-tissue tumor with combined features of more than one type of conventional benign peripheral nerve sheath tumors. It usually presents as a painless, subcutaneous/dermal mass and often affects young adults, with no sex predilection (1). Pain or neurological deficit is uncommon unless the tumor reaches a certain size.
Recent Advances in the Diagnosis, Pathogenesis, and Management of Myxoinflammatory Fibroblastic Sarcoma
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
Giant Cell Tumor of the Acromion: Case Report and Literature Review
Key Words: Giant cell tumor of bone acromion scapula shoulder H3-3A Giant cell tumor of bone (GCTB) is an intermediate, locally aggressive but rarely metastasizing neoplasm. It accounts for 4-5% of all primary bone tumors and typically affects the ends (epiphyses) of long bones (1). GCTB may occur at any age but has a peak incidence in the third and fourth decades of life, with a slight female predominance. Pain is the most common symptom.
Biology and Management of High-Grade Myxofibrosarcoma: State of the Art and Future Perspectives
1. Introduction Myxoid soft tissue sarcomas (STSs) represent a heterogeneous group of mesenchymal neoplasms characterized by a predominantly myxoid stroma, including myxofibrosarcoma (MFS) [1]. MFS is a common type of STS that primarily arises in the extremities of elderly patients. It belongs to the fibroblastic/myofibroblastic tumor group according to the 2020 World Health Organization Classification of Soft Tissue Tumors [2].
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