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Case Study
Spindle Cell Rhabdomyosacoma of Uterus: A Case Study
Dae Woon Kim, Jung Hwan Shin, Ho Jung Lee, Young Ok Hong, Jong Eun Joo, Eun Kyung Kim
Korean J Pathol. 2013;47(4):388-391.   Published online August 26, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.4.388
  • 8,118 View
  • 57 Download
  • 10 Crossref
AbstractAbstract PDF

Uterine rhabdomyosarcoma (RMS) typically presents as a mixed epithelial and mesenchymal tumors. Pure RMSs of the female genital tract are uncommon. Spindle cell variant of RMS is a rare morphologic subtype of embryonal RMS and mostly occurs in the paratesticular region of children. Here, we present a case of uterine spindle cell RMS in a 76-year-old woman. The tumor, 20×15×7 cm in size, was highly necrotic and adherent to the colon and rectum. Tumor cells were mostly spindle-shaped, and isolated rhabdomyoblasts were scattered. Immunohistochemical stains for myoglobin and myo-D1 showed diffuse positivity for tumor cells. The patient died only of disease three months after diagnosis.

Citations

Citations to this article as recorded by  
  • A rare adult case of primary uterine rhabdomyosarcoma with mixed pattern: a clinicopathological & immunohistochemical study with literature review
    Nehal K.H. Kamel, Eiman Adel Hasby
    Diagnostic Pathology.2024;[Epub]     CrossRef
  • Embryonal rhabdomyosarcoma of the uterine corpus: a clinicopathological and molecular analysis of 21 cases highlighting a frequent association with DICER1 mutations
    Jennifer A. Bennett, Zehra Ordulu, Robert H. Young, Andre Pinto, Koen Van de Vijver, Eike Burandt, Pankhuri Wanjari, Rajeev Shah, Leanne de Kock, William D. Foulkes, W. Glenn McCluggage, Lauren L. Ritterhouse, Esther Oliva
    Modern Pathology.2021; 34(9): 1750.     CrossRef
  • Vaginal embryonal rhabdomyosarcoma in young woman: A case report and literature review
    Lalya Issam, Laatitioui Sana, Essadi Ismail, El Omrani Abdelhamid, Khouchani Mouna
    Archives of Cancer Science and Therapy.2020; 4(1): 034.     CrossRef
  • Is fertility-preservation safe for adult non-metastatic gynecologic rhabdomyosarcoma patients? Systematic review and pooled survival analysis of 137 patients
    Maha AT Elsebaie, Zeinab Elsayed
    Archives of Gynecology and Obstetrics.2018; 297(3): 559.     CrossRef
  • Spindle cell sarcoma – a rare diagnosis
    SK Kathpalia, Manju Mehrotra, Pinky Jena, Archana H Deshpande
    Women's Health.2018;[Epub]     CrossRef
  • Malignant mesenchymal tumors of the uterus – time to advocate a genetic classification
    Birgit Rommel, Carsten Holzmann, Jörn Bullerdiek
    Expert Review of Anticancer Therapy.2016; 16(11): 1155.     CrossRef
  • Human rhabdomyosarcoma cells express functional pituitary and gonadal sex hormone receptors: Therapeutic implications
    AGATA PONIEWIERSKA-BARAN, GABRIELA SCHNEIDER, WENYUE SUN, AHMED ABDELBASET-ISMAIL, FREDERIC G. BARR, MARIUSZ Z. RATAJCZAK
    International Journal of Oncology.2016; 48(5): 1815.     CrossRef
  • Primary third ventricular tumor in an 18‐year‐old man
    Tianping Yu, Mengni Zhang, Qiao Zhou, Jing Gong, Ling Nie, Xueqin Chen, Ni Chen
    Neuropathology.2015; 35(6): 599.     CrossRef
  • Rhabdomyosarcoma of vulva in a young lady
    Tapesh Bhattacharyya, Firuza D. Patel, Radhika Srinivasan, Bhavana Rai, Pradeep Saha, R. Nijhawan
    Journal of Cancer Research and Therapeutics.2015; 11(3): 650.     CrossRef
  • Uterine sarcoma in a 14year-old girl presenting with uterine rupture
    Jane Özcan, Özlem Dülger, Latif Küpelioğlu, Ali İhsan Gönenç, Aynur Erşahin
    Gynecologic Oncology Reports.2014; 10: 44.     CrossRef
Case Report
Well-Differentiated Thymic Carcinoma, Spindle Cell Type, Arising from Anterior Mediastinum: A case report.
Hun Kyung Lee, Yeong Jin Choi, Seok Jin Kang, Byung Kee Kim, Sun Moo Kim, Sang In Shim
Korean J Pathol. 1995;29(6):800-803.
  • 1,501 View
  • 12 Download
AbstractAbstract PDF
Well differentiated thymic carcinoma(WDTC) was recently separated from cortical thymoma. It is characterized by a predominance of epithelial cells with usually low mitotic rate, an epidermoid differentiation with slight to moderate cytologic atypia and lobular growth pattern. In recent reports, an uncommon spindle cell variant of WDTC, which is composed of spindle shaped epithelial cells, has been described. We investigated an unusual case of WDTC consisted of purely spindle shaped epithelial cells in a 66-year-old female. Radiologically, the well demarcated mass was located in the anterior mediastinum with focal invasion into the surrounding left upper lung. The tumor, 10 x 8 x 5 cm, was encapsulated with thin fibrous tissue and showed a pale yellow solid and lobulated cut surface. Microscopically, it consisted of solid sheets of purely spindle shaped epithelial cells with mild atypism, a low mitotic rate and focal epidennoid differentiation.

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