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Relevant bibliographies by topics / Spindle Cell Tumor

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Academic literature on the topic 'Spindle Cell Tumor'

Author: Grafiati

Published: 3 June 2025

Last updated: 19 July 2025

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Journal articles on the topic "Spindle Cell Tumor"

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Singh Jatin Bhatt, Aparajita. "Case Report on Spindle Cell Tumor." International Journal of Science and Research (IJSR) 12, no. 6 (2023): 2959–61. http://dx.doi.org/10.21275/mr23426075734.

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Mizutani, Kenichi, Motona Kumagai, Akane Aikawa, et al. "Nasal spindle cell tumor with rhabdomyoblastic features: A rare and diagnostically difficult case." SAGE Open Medical Case Reports 8 (January 2020): 2050313X2096409. http://dx.doi.org/10.1177/2050313x20964090.

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Nasal spindle cell rhabdomyosarcoma is very rare. The tumor is sometimes confused with other spindle cell tumors. We herein report a case of nasal spindle cell tumor in a 62-year-old woman. The patient first presented herself to a medical doctor’s office after an episode of left epistaxis. An intranasal tumor was found and resected. The tumor was composed of spindle cells, and she was diagnosed with desmoid-type fibromatosis. Five years after the initial episode, an intranasal tumor was found again. The tumor showed a fascicular growth pattern with high cellularity and was predominantly compos

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Grebenkin, E. V., Sh V. Malhanov, D. Y. Agibalov, G. O. Rukhadze, I. R. Kryuchkov, and V. V. Fedotov. "Mucin-poor mucinous tubular and spindle cell kidney cancer and clear cell renal cell carcinoma: a rare clinical case." Urology Herald 11, no. 2 (2023): 164–70. http://dx.doi.org/10.21886/2308-6424-2023-11-2-164-170.

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Mucinous tubular and spindle cell carcinoma of the kidney is a rare low-grade malignant tumour and accounts for less than 1% of all renal neoplasms. The classic morphological structure of the tumor is represented by three elements: spindle cells, ducts and myxoid or mucinous stroma. This tumor is indolent with a low risk of metastasis and a favorable outcome. However, cases with relapses, metastases to regional lymph nodes, and distant metastases, which were mainly characterised by high nuclear atypia, sarcomatoid transformation and other atypical morphological features are described in the li

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Wehrle, Chase J., J. Will Daigle, Asad Ullah, Suash Sharma, Edmond F. Ritter, and Edward J. Kruse. "Atypical Spindle Cell Lipomatous Lesion Resected From Patient With History of CLL." American Surgeon 86, no. 9 (2020): 1208–11. http://dx.doi.org/10.1177/0003134820933601.

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Atypical spindle cell lipomatous neoplasm, also known as well-differentiated spindle cell liposarcoma, represents a newly discovered entity of adipocytic tumors. Recent research has shown this tumor variant to be more related to spindle cell lipoma, rather than the originally hypothesized atypical lipomatous tumor spectrum. Here we present a case of a 58-year-old man with a history of chronic lymphocytic leukemia with an enlarging mass on the posterior left shoulder, initially hypothesized to be a benign lipoma. However, magnetic resonance imaging showed a large, multiseptated, heterogeneous m

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Dardick, Irving, and Peter Rippstein. "Subcutaneous Metastatic Spindle Cell Tumor." Ultrastructural Pathology 11, no. 5-6 (1987): 745–50. http://dx.doi.org/10.3109/01913128709048462.

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Mariño-Enriquez, Adrian, Alessandra F. Nascimento, Azra H. Ligon, Cherwei Liang, and Christopher D. M. Fletcher. "Atypical Spindle Cell Lipomatous Tumor." American Journal of Surgical Pathology 41, no. 2 (2017): 234–44. http://dx.doi.org/10.1097/pas.0000000000000770.

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Maurya, Vivek, Girish Motwani, and Ankit Jaiswal. "Benign Spindle Cell Tumor of Flexor Tendon Sheath of Toe: A Rare Case Report." Journal of Orthopaedic Case Reports 15, no. 5 (2025): 146–50. https://doi.org/10.13107/jocr.2025.v15.i05.5590.

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Introduction: Spindle cell tumors are tumors consisting of spindle cells that are long and slender cells when viewed under a microscope. Their incidence is low and usually benign in nature, although it may turn malignant rarely. Histopathological diagnosis is gold-standard for diagnosis although Fine needle aspiration cytology (FNAC) and magnetic resonance imaging (MRI) may help in narrowing down the diagnosis pre-operatively. Complete tumor excision is the mainstay for managing these tumors. Case Report: A 15-year-old male presented to our outpatient department with complaints of pain and swe

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Nistal, Manuel, Pilar Gonzalez-Peramato, Alvaro Serrano, Miguel Reyes-Mugica, and Mariana M. Cajaiba. "Primary Intratesticular Spindle Cell Tumors: Interdigitating Dendritic Cell Tumor and Inflammatory Myofibroblastic Tumor." International Journal of Surgical Pathology 19, no. 1 (2008): 104–9. http://dx.doi.org/10.1177/1066896908323505.

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Nimmagadda, Moorthy N. L., Vithaleswar M. Rao, Padmaja S., and Harshini Reddy. "Spindle cell sarcoma of sphenoid bone." International Journal of Research in Medical Sciences 5, no. 11 (2017): 5072. http://dx.doi.org/10.18203/2320-6012.ijrms20174974.

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Primary bone tumors involving skull are extremely rare and they constitute 0.8% of all bone tumors. The common tumors that are seen in skull base include fibrous dysplasia, giant cell tumor, chordoma, ossifying fibroma, angiosarcoma. We report a rare case of spindle cell sarcoma arising from right sphenoid bone in a 70-year-old male which presented as unilateral defective vision with mild proptosis.

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Kanteti, A. P., and E. Martinez Duarte. "A Rare Case of Dedifferentiated Solitary Fibrous Tumor." American Journal of Clinical Pathology 154, Supplement_1 (2020): S42. http://dx.doi.org/10.1093/ajcp/aqaa161.089.

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Abstract Casestudy: Dedifferentiated solitary fibrous tumor is a rare malignant subtype of the common benign mesenchymal neoplasm with fibroblastic differentiation known as solitary fibrous tumor (SFT). These account for less than 2% of all soft masses; and about 20% of SFTs turn aggressive. They feature bland spindle cells creating a classic “pattern-less pattern” in collagenous stroma with prominent staghorn vessels. They can dedifferentiate into a biphasic tumor with low grade areas that are spindle cell rich and high-grade areas with epithelioid cells, mitotic figures and necrosis. Here we

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Dissertations / Theses on the topic "Spindle Cell Tumor"

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Knezevich, Stevan Robert. "Molecular characterization of pediatric spindle cell tumors." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape4/PQDD_0021/NQ48668.pdf.

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Borysova, Meghan E. K. "Novel roles for B-Raf in mitosis and cancer." [Tampa, Fla] : University of South Florida, 2009. http://purl.fcla.edu/usf/dc/et/SFE0002899.

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NICOLAI, ALICE. "Anti-neoplastic effects of novel compounds on human head & neck squamous carcinoma cell lines." Doctoral thesis, 2022. http://hdl.handle.net/11573/1614138.

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Human head and neck squamous cell carcinomas (HNSCC) are the sixth most frequent cancers worldwide, characterized by recurrent metastasis and drug resistance. Aiming to develop a different and new therapy approach, we first analysed some novel synthesized aminopyrimidine compounds on several cancer cell lines, including HNSCC. These compounds were found to be good cancer cell proliferation inhibitors, especially a N-benzyl counterpart of RDS 3442, the reference molecule that in our earlier research demonstrated to be a promising negative regulator acting on tumor cell proliferation. Afterwards

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Books on the topic "Spindle Cell Tumor"

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Theeler, Brett J., and Mark R. Gilbert. Primary Central Nervous System Tumors. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0129.

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Ependymomas are rare primary central nervous system (CNS) tumors that are thought to arise from ependymal cells lining the ventricular system located throughout the CNS. Ependymomas occur in all age groups but are more common in the pediatric population. Ependymomas typically present as mass lesions within the ventricular system, brain or spinal cord parenchyma. As with most central nervous system tumors, pathologic evaluation is required for definitive diagnosis. Ependymomas are typically treated with a combination of surgery and radiotherapy although this varies depending on tumor location,

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Boriani, Stefano, Ziya L. Gokaslan, Charles G. Fisher, and Luiz Vialle. Primary Tumors. Thieme Medical Publishers, Incorporated, 2014.

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Ajithkumar, Thankamma, Ann Barrett, Helen Hatcher, and Natalie Cook. HIV related tumours. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199235636.003.0016.

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Kaposi's sarcoma (KS) is a low-grade multifocal vascular tumour associated with human herpesvirus 8 (HHV8)/Kaposi's sarcoma herpes virus (KSHV) infection.KS lesions of all epidemiological forms are similarly comprised of HHV8-positive (LNA-1 immunoreactive) spindle-shaped tumour cells, vessels, and chronic inflammatory cells. Lesions evolve from early patch, to plaque, and later tumour nodules....

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Dodds, Chris, Chandra M. Kumar, and Frédérique Servin. Neurosurgery in the elderly. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198735571.003.0009.

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The increasing provision of neurosurgery to the elderly is reviewed in this chapter. The two major areas of practice and the forms of presentation are briefly discussed. Specific issues with the elderly neurosurgical patient are then considered, including the urgency of the surgery, surgery duration, extent of the planned procedure, and management of concurrent drug therapy. Details on the common risks with hyperventilation and hypothermia are noted, and the use of more recent anaesthetic agents, remifentanil and desflurane, is covered. Spinal surgery for decompression and stabilization for ce

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Book chapters on the topic "Spindle Cell Tumor"

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Cheng, Xiaoguang, Yongbin Su, and Mingqian Huang. "Invasive Mesenchymal Malignant Spindle Cell Tumor: Case 14." In Bone Tumor Imaging. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9927-5_14.

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Mocellin, Simone. "Spindle Cell Hemangioma." In Soft Tissue Tumors. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58710-9_235.

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Mocellin, Simone. "Spindle Cell Lipoma." In Soft Tissue Tumors. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58710-9_236.

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Cinotti, Elisa, Catherine Douchet, and Franco Rongioletti. "Spindle Cell Liposarcoma." In Rare Malignant Skin Tumors. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-2023-5_40.

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Mocellin, Simone. "Spindle Cell/Sclerosing Rhabdomyosarcoma." In Soft Tissue Tumors. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58710-9_237.

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Varga, Peter Pal, and Aron Lazary. "Giant Cell Tumor." In Essentials of Spine Surgery. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-80356-8_57.

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Cheng, Xiaoguang, Yongbin Su, and Mingqian Huang. "Spindle Cell Lipoma: Case 25." In Imaging of Bone Tumors in Wrist, Hand, Ankle and Foot. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-6407-9_50.

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Masterpol, Kasia Szyfelbein, Andrea Primiani, and Lyn McDivitt Duncan. "Immunophenotype of Dermal Spindled Cell Tumors." In Atlas of Essential Dermatopathology. Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-4471-7_33.

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Laurenge, Alice, Emmanuelle Huillard, Franck Bielle, and Ahmed Idbaih. "Cell of Origin of Brain and Spinal Cord Tumors." In Advances in Experimental Medicine and Biology. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-14732-6_6.

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Yucel, Deniz, Irem Ayse Kanneci, Damla Arslantunali, Gamze Torun Kose, and Vasif Hasirci. "Spinal Cord Injury: Tissue Engineering Using Neural Stem Cells." In Tumors of the Central Nervous System, Volume 10. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5681-6_29.

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Conference papers on the topic "Spindle Cell Tumor"

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Taneja, M., M. Nashawi, D. Villafuerte, et al. "When a Tumor Is Not a Tumor: A Case of Mycobacterial Spindle Cell Pseudotumor." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a7356.

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Ahmad, Zafarullah, Guido Mühlmeier, Konrad Steinestel, and Matthias Tisch. "Spindle cell lipoma as rare soft tissue tumor of the parotid gland." In 94th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1767642.

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Godse, Neal R., Sara Alsulaimani, Pablo F. Recinos, and Raj Sindwani. "Resection of an Orbital Spindle Cell Tumor via Combined Endoscopic Endonasal and Open Transorbital Approaches." In 32nd Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/s-0043-1762535.

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Wehn, Amy K., Yang Xie, John O. Schorge, and Angelique W. Whitehurst. "Abstract LB-364: The ACRBP tumor antigen normalizes mitotic spindle function to promote cancer cell proliferation." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-lb-364.

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Irakleidis, Foivos, Michael Masucci, Eleftherios Sfakianakis, Peng H. Tan, and Hazel Welch. "MODIFIED SLOW DIGESTION TECHNIQUE FOR THE ISOLATION OF PATIENT-DERIVED CELLS: AN IN VITRO MODEL FOR THE DESIGN OF BREAST CANCER-ASSOCIATED STROMA." In Abstracts from the Brazilian Breast Cancer Symposium - BBCS 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s2018.

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Objective: Highly prevalent cancer-associated fibroblasts (CAFs) are understood to play a key role in tumorigenesis. Understanding of CAFs and tumor-associated stroma is considered to be essential in novel cancer therapies. Patient-derived cells (PDCs) more closely resemble tumor microenvironment compared with commercial cell lines that are subjected to genetic and phenotypic changes. However, PDCs use can be limited by challenges in isolating high-yield viable cultures. Overcoming these challenges would benefit novel personalized cancer research. In this study, we aimed to investigate the eff

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Chopra, Seema. "Sclerosing sex cord stromal tumour of the ovary: A rare variant of ovarian neoplasms in childhood and adolescence." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685321.

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Case Report: 19 yr old unmarried girl c/o abdominal distension, loss of appetite and Irregular menstrual cycles x 5 months. USG: gross ascites, liver, Lobulated isoechoic mass in right adnexa, 7x5 cm, abutting right ovary. CA125: 1297 U/ml. FNAC Degenerated crushed cells & stromal fragments. Few scattered benign oval/spindle cells. Laparoscopy f/b laparotomy: 6 litres of straw colored asciic fluid drained. Uterus, left adnexa normal. Rt ovarian mass 6x7 cm, bilobed, arising from ovary. Solid, stuck in POD Adherent to gut. Right oophrectomy done. CA-125: 22 u/ml on day 6 post op. HPE – Scle

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Aquino, Fernanda Mabel Batista, Larissa Santos Lourenço Ferreira, Jader Rodrigues Gonçalves, Clarissa Amaral Abreu, and Maria Isabel Oliveira Silva. "DERMATOFIBROSARCOMA PROTUBERANS ON THE BREAST: A CASE REPORTED AND DISCUSSION ABOUT THE STEPS FOR YOUR DIAGNOSIS." In Scientifc papers of XXIII Brazilian Breast Congress - 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s1019.

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Introduction: Dermatofibrosarcoma Protuberans (DFSP) is a soft tissue tumor, with slow growth and low metastasis rate, but with a high chance of local recurrence. Epidemiologically, DFSP represents only 0.1% of all malignant tumors. It is more common in women aged between 30 and 50 years and the most affected site is the trunk. However, the presentation in the breast is rare. Clinically, DFSP is revealed as a slow and asymptomatic growth nodule that originates in the dermis and invades the subcutaneous tissue. The diagnosis is made by histopathology, with the result of uniform spindle cells wi

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Zardo, Bianca Ceratti, Alexandre Pedroso de Albuquerque Olmedo, Andrea Barlezze, Alan Azambuja, and Ruben Rodriguez. "Malignant tumor of the peripheral nerve sheath induced after radiotherapy for breast cancer: a case report and therapeutic approach." In XXVI Brazilian Mastology Congress. Mastology, 2024. https://doi.org/10.29289/259453942024v34s2007.

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Introduction: We present the case of patient I.R., a 69-year-old woman, who was diagnosed with invasive ductal carcinoma of the breast in June 2014. She underwent breast-conserving surgery, radiotherapy, and hormone therapy. After nine years, magnetic resonance imaging revealed a mass in the thoracoabdominal region. Subsequent examinations identified a solid nodule in the right breast. A biopsy diagnosed a spindle cell neoplasm. In June 2023, she underwent a right mastectomy with chest wall reconstruction. The pathological examination revealed a malignant tumor of the peripheral nerve sheath i

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Belluco, Rosana Zabulon Feijó, Júllia Eduarda Feijó Belluco, Ana Elisa de Freitas Souza, et al. "Desmoid breast fibromatosis occurring after reconstructive surgery simulating carcinoma: A rare case report." In Brazilian Breast Cancer Symposium 2023. Mastology, 2023. http://dx.doi.org/10.29289/259453942023v33s1050.

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Introduction: Desmoid fibromatosis is a rare tumor, representing less than 0.2% of all breast tumors, characterized by clonal fibroblastic deep soft tissue, locally aggressive growth and high incidence of recurrence (between 24% and 77% in 10 years). It is associated with trauma or surgical procedures of the breast and presents similary to breast carcinoma. Diagnostic criteria are histological, and breast imaging techniques are non-specific. The treatment is surgical with complete excision and safety margin, varying according to the studies, from 0.5 to 3 cm to avoid recurrences, which, when t

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Ramalho, Tarciane Campos, Rafael Victor Moita Minervino, IsaIbela Campos Ramalho, Jean Fabricio de Lima Pereira, and Og Arnaud Rodrigues. "METAPLASTIC CARCINOMA OF THE BREAST WITH CHONDROID-TYPE MESENCHYMAL DIFFERENTIATION: A CASE REPORT." In XXIV Congresso Brasileiro de Mastologia. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s1055.

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Metaplastic breast carcinoma (MpBC) is a rare and morphologically diverse group of tumors in which a variable proportion or the entire tumor is composed of nonglandular epithelium or mesenchymal cells. It is defined by the histological presence of at least two cellular types, typically epithelial and mesenchymal components. It is composed of ductal, squamous, and/or chondroid, and spindle elements, with squamous cell carcinoma being the most frequent histological subtype. MpBC represents 0.2%–5% of all breast cancers and it is very aggressive. This type of breast cancer is typically triplenega

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Reports on the topic "Spindle Cell Tumor"

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Tran, Emily, Jasmine J. Park, Nandini N. Kulkarni, and Vinay S. Gundlapalli. Left Facial Primary Leiomyosarcoma Misdiagnosed as Atypical Fibroxanthoma and Immunochemical Markers Relevant to Diagnosis: A Case Report. Science Repository, 2024. http://dx.doi.org/10.31487/j.ajscr.2023.04.03.

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Soft tissue sarcomas are relatively rare neoplasms of mesenchymal origin that generally make up less than 2% of all adult malignant neoplasms. Atypical fibroxanthoma is a benign soft tissue tumor often confused with malignant variants of similar tumors such as leiomyosarcoma due to similar staining markers and cell morphology. We report a case of a 70-year-old caucasian male who initially presented with a 2 cm exophytic left facial lesion that was misdiagnosed as atypical fibroxanthoma upon biopsy. The patient underwent a wide local excision of the growing 11 cm mass and immediate reconstructi

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Estevez-Ordonez, Dagoberto, Matthew Jarrell, Travis Atchley, Nick Laskay, Mark Hadley, and Mohommad Hamo. Systematic Review of Spinal Glial Tumors. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.4.0085.

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Review question / Objective: Does the extent of resection of intramedullary spinal cord astrocytomas affect oncologic and neurologic outcomes? Condition being studied: Intramedullary spinal cord tumors, which are a class of tumors arising from the cells from within the spinal cord. Study designs to be included: Randomized clinical trials, clinical and observational studies, and case series with available abstracts and published as full-scale original articles, brief reports in peer-reviewed academic journals or descriptive publications on surgical techniques with no restriction on language or

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