Case report: Atypical spindle cell/pleomorphic lipomatous tumor masquerading as a myxoid liposarcoma or intramuscular myxoma

被引:5
作者
Ichikawa, Jiro [1 ]
Kawasaki, Tomonori [2 ]
Imada, Hiroki [3 ]
Kanno, Satoshi [2 ]
Taniguchi, Naofumi [1 ]
Ashizawa, Tomoyuki [1 ]
Haro, Hirotaka [1 ]
机构
[1] Univ Yamanashi, Interdisciplinary Grad Sch Med, Dept Orthopaed Surg, Chuo, Yamanashi, Japan
[2] Saitama Med Univ Int Med Ctr, Dept Pathol, Saitama, Hidaka, Japan
[3] Saitama Med Univ, Saitama Med Ctr, Dept Pathol, Kawagoe, Saitama, Japan
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
基金
日本学术振兴会;
关键词
atypical spindle cell; pleomorphic lipomatous tumor; differential diagnosis; magnetic resonance imaging; histopathology; immunohistochemistry; fluorescence in situ hybridization; CELL LIPOMA;
D O I
10.3389/fonc.2022.1033114
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Atypical spindle cell/pleomorphic lipomatous tumors (ASPLTs) were recently categorized as benign lipomatous tumors. However, accurate and complete preoperative diagnosis of ASPLTs may be difficult. Furthermore, diagnosis based on magnetic resonance imaging (MRI) findings is uncertain because of the varying ratios of the fat component within the tumor. Here, we report a case of ASPLT masquerading as a myxoid tumor. Although MRI findings were consistent with a myxoid liposarcoma, needle biopsy findings suggested a myxoma, and we performed marginal resection. Histopathological findings revealed infiltrating spindle cells with atypia. In addition, immunohistochemistry (IHC) showed positive staining for CD34 and heterogeneous retinoblastoma deficiency, and fluorescence in situ hybridization (FISH) showed no amplification of mouse double minute 2 homolog and no rearrangement of FUS or EWSR1. When MRI and histopathological findings suggest a myxoid tumor, IHC and FISH should be considered and performed for a precise and accurate diagnosis.
引用
收藏
页数:7
相关论文
共 44 条
  • [41] Soft tissue tumor with BRAF and NRAS mutations sharing features with NTRK-rearranged spindle cell neoplasm: A case report expanding the spectrum of spindle cell tumor with kinase gene alterations
    Kakuda, Yuko
    Kato, Ikuma
    Kawata, Takuya
    Goto, Keisuke
    Ito, Kan
    Satake, Ryo
    Toki, Shunichi
    Murata, Hideki
    Wasa, Junji
    Katagiri, Hirohisa
    Takahashi, Mitsuru
    Nagashima, Takeshi
    Mori, Taro
    Oda, Yoshinao
    Sugino, Takashi
    Yamaguchi, Ken
    PATHOLOGY INTERNATIONAL, 2025, 75 (01) : 40 - 45
  • [42] Solitary fibrous tumor of the liver - A case report, review of the literature and differential diagnosis of spindle cell lesions of the liver
    Bejarano, PA
    Blanco, R
    Hanto, DW
    INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 1998, 6 (02) : 93 - 100
  • [43] RAF1-rearranged Spindle Cell Mesenchymal Tumor With Calcification and Heterotopic Ossification: A Case Report and Review of Literature
    Cordier, Fleur
    Loontiens, Siebe
    Van der Meulen, Joni
    Lapeire, Lore
    van Ramshorst, Gabrielle H.
    Sys, Gwen
    Van Dorpe, Jo
    Creytens, David
    INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2024, 32 (01) : 133 - 139
  • [44] Uterine Leiomyoma-Like Inflammatory Myofibroblastic Tumor Without Myxoid Matrix or Inflammatory Cell Infiltration: A Case Report of a Potential Diagnostic Pitfall
    Zhou, Ning
    Li, Tao
    Yang, Li
    Chen, Liqiao
    Fu, Yangyan
    Chen, Ying
    INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2024, 32 (04) : 767 - 771