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Relevant bibliographies by topics / Desmoid tumor

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Academic literature on the topic 'Desmoid tumor'

Author: Grafiati

Published: 1 February 2025

Last updated: 31 July 2025

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Journal articles on the topic "Desmoid tumor"

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Ramonaitė, Justė, Gabija Imbrasaitė, Alfredas Smailys, Mindaugas Stravinskas, and Vėtra Markevičiūtė. "THE NEED FOR MULTIPLE SURGERIES FOR FREQUENT DESMOID TUMOR RECURRENCE." Health Sciences 33, no. 5 (2023): 39–43. http://dx.doi.org/10.35988/sm-hs.2023.176.

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Desmoid tumors are very rare mesenchymal neoplasms with an estimated incidence of 3 per 100 soft tissue tumor cases. They are locally invasive, aggressive and cause significant complications. The treatment modalities of desmoids include surgery, radiotherapy, chemotherapy, hormonal therapy. Currently there is no gold standard and neither therapy is effective for high recurrence (25‑77%) desmoid tumors. Desmoid tumors also have the capacity for self-limitation and, therefore, no treatment other than observation is possible expecting spontaneous regression. Treatment options for desmoid tumors a

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Khandelwal, Niranjan, Mandeep Garg, Nidhi Prabhakar, and Divya Dahiya. "Desmoid Tumor: Rare Abdominal Wall Lump in a Multiparous Woman." Journal of Postgraduate Medicine, Education and Research 52, no. 1 (2018): 31–33. http://dx.doi.org/10.5005/jp-journals-10028-1271.

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ABSTRACT Background Desmoids are rare tumors. Abdominal wall desmoids are more common in women of reproductive age, especially postpartum women. Here we present a case of desmoid tumor in a 37-year-old multiparous woman, who came with the complaint of a slowly growing painless abdominal lump. Case report A 37-year-old multiparous female presented with the complaint of a gradually increasing, painless abdominal lump. On physical examination, a well-defined, firm, mobile mass was palpated in the suprapubic region. Ultrasound revealed a homogeneous hypoechoic lesion in the right anterolateral abd

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Koshariya, Mahim, Samir Shukla, Zuber Khan, et al. "Giant Desmoid Tumor of the Anterior Abdominal Wall in a Young Female: A Case Report." Case Reports in Surgery 2013 (2013): 1–4. http://dx.doi.org/10.1155/2013/780862.

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Desmoid tumors (also called desmoids fibromatosis) are rare slow growing benign and musculoaponeurotic tumors. Although these tumors have a propensity to invade surrounding tissues, they are not malignant. These tumors are associated with women of fertile age, especially during and after pregnancy. We report a young female patient with a giant desmoid tumor of the anterior abdominal wall who underwent primary resection. The patient had no history of an earlier abdominal surgery. Preoperative evaluation included abdominal ultrasound, computed tomography, and magnetic resonance imaging. The hist

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MINAMI, YUSUKE, SEIICHI MATSUMOTO, KEISUKE AE, et al. "The Clinical Features of Multicentric Extra-abdominal Desmoid Tumors." Cancer Diagnosis & Prognosis 1, no. 4 (2021): 339–43. http://dx.doi.org/10.21873/cdp.10045.

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Background: Extra-abdominal desmoid tumors often occur in the necks, shoulder, chest wall, back, arm, buttock, thigh and leg. Multicentric extra-abdominal desmoids are rather rare and seem to have other clinical features. The aim of our study was to investigate clinical features, especially multicentric occurrence of extra-abdominal desmoid tumors. Patients and Methods: A total of 135 patients diagnosed with extra-abdominal desmoid were enrolled in this study from January 2005 to December 2019 at the Cancer Institute Hospital of The Japanese Foundation for Cancer Research. The operative proced

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Salas, Sébastien, Armelle Dufresne, Binh Bui, et al. "Prognostic Factors Influencing Progression-Free Survival Determined From a Series of Sporadic Desmoid Tumors: A Wait-and-See Policy According to Tumor Presentation." Journal of Clinical Oncology 29, no. 26 (2011): 3553–58. http://dx.doi.org/10.1200/jco.2010.33.5489.

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Purpose Desmoid tumors are mesenchymal fibroblastic/myofibroblastic proliferations with locoregional aggressiveness and high ability to recur after initial treatment. We present the results of the largest series of sporadic desmoid tumors ever published to determine the prognostic factors of these rare tumors. Patients and Methods Four hundred twenty-six patients with a desmoid tumor at diagnosis were included, and the following parameters were studied: age, sex, delay between first symptoms and diagnosis, tumor size, tumor site, previous history of surgery or trauma in the area of the primary

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Leal, Raquel Franco, Patricia V. V. Tapia Silva, Maria de Lourdes Setsuko Ayrizono, João José Fagundes, Eliane M. Ingrid Amstalden, and Cláudio Saddy Rodrigues Coy. "Desmoid tumor in patients with familial adenomatous polyposis." Arquivos de Gastroenterologia 47, no. 4 (2010): 373–78. http://dx.doi.org/10.1590/s0004-28032010000400010.

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CONTEXT: Desmoid tumors constitute one of the most important extraintestinal manifestations of familial adenomatous polyposis. The development of desmoids is responsible for increasing morbidity and mortality rates in cases of familial adenomatous polyposis. OBJECTIVES: To evaluate the occurrence of desmoid tumors in familial adenomatous polyposis cases following prophylactic colectomy and to present patient outcome. METHODS: Between 1984 and 2008, 68 patients underwent colectomy for familial adenomatous polyposis at the School of Medical Sciences Teaching Hospital, University of Campinas, SP,

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Makarenko, M. V., D. O. Govseyev, S. V. Gridchin, et al. "Desmoid tumor of the anterior abdominal wall in a female (Clinical case)." HEALTH OF WOMAN, no. 5(131) (June 30, 2018): 116–18. http://dx.doi.org/10.15574/hw.2018.131.116.

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Desmoid tumors (also called desmoids fibromatosis) are rare slow growing benign and musculoaponeurotic tumors. Although these tumors have a propensity to invade surrounding tissues, they are not malignant. These tumors are associated with women of fertile age, especially during and after pregnancy and postoperative surgeries. Our clinical case is interesting because of the rarity of the pathology and the difficulties in setting the correct diagnosis. The patient, with a history of laparoscopic myomectomy (2012), was preparing for a routine surgery for the endometrioma of the anterior abdominal

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Boceska, Zhaneta P., Katerina B. Kubelka-Sabit, and Julija Zh Zhivadinovik. "FIBROMATOSIS (DESMOID TUMOR) OF THE BREAST. Fibromatosis (tumor desmoide) de mama." Revista Argentina de Anatomía Clínica 3, no. 2 (2016): 99–105. http://dx.doi.org/10.31051/1852.8023.v3.n2.13926.

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El tumor desmoide (fibromatosis) es una entidad patológica extremadamente rara que se desarrolla de la fascia muscular y la aponeusorsis. Aunque sin potencial metastático, estos tumores son localmente muy agresivos y tienden a infiltrarse en los tejidos circundantes. Nosotros presentamos un caso de tumour desmoide de mama, que tuvo apariencias clínicas sugestivas a carcinoma. La paciente, de 56 años presentó una masa palpable de mama derecho. La citología por aspiracion con aguja fina (AGF) no detectó ninguna célula maligna, por lo que se hizo una escisión local conservadora. La paciente no re

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Murshid, Areen Abdulelah, and Hatim Q. Al-Maghraby. "Subsequent Development of Desmoid Tumor after a Resected Gastrointestinal Stromal Tumor." Case Reports in Pathology 2018 (2018): 1–5. http://dx.doi.org/10.1155/2018/1082956.

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Desmoid tumors (deep fibromatosis) of the mesentery are rare mesenchymal tumors. They are often misdiagnosed, especially with a previous history of resection for gastrointestinal stromal tumor (GIST). Immunohistochemistry can help differentiate between these two tumors. In this article, we present a case we had encountered: a Desmoid tumor developing in a patient with a history of GIST 3 years ago. It is the first case of GIST with subsequent development of Desmoid tumor to be reported in Saudi Arabia. We discuss the two entities of Desmoid tumor and GIST by comparing their definitions, clinic

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Mercier, Kelly A., and Darragh M. Walsh. "The initiation, design, and establishment of the Desmoid Tumor Research Foundation Patient Registry and Natural History Study." Rare Tumors 11 (January 2019): 203636131988097. http://dx.doi.org/10.1177/2036361319880978.

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Desmoid tumors are locally invasive sarcoma, affecting 5–6 individuals out of 1,000,000 per year. The desmoid tumors have high rates of recurrence after resection and can lead to significant deterioration of the quality of life of patients. There is a need for a better understanding of the desmoid tumors’ patient experience from first symptoms through diagnosis, disease monitoring, and clinical treatment options. With the National Organization of Rare Disorders, the Desmoid Tumor Research Foundation Natural History Study was designed to be collected through the registry. This article describes

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Dissertations / Theses on the topic "Desmoid tumor"

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Braumandl, Karin [Verfasser], та Florian [Gutachter] Haller. "Untersuchungen zu β-Catenin hinsichtlich des Mutationsstatus, sowie klinisch-pathologischer Eigenschaften in aggressiver Fibromatose (Desmoid-Tumor) / Karin Braumandl ; Gutachter: Florian Haller". Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2017. http://d-nb.info/1125715448/34.

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Gantzer, Justine. "Integrative multi-omics characterization of mesenchymal tumors." Electronic Thesis or Diss., Strasbourg, 2024. http://www.theses.fr/2024STRAJ056.

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Ce travail de thèse s’articule autour de trois projets indépendants dont le but est de mieux caractériser trois tumeurs mésenchymateuses grâce à une approche multi-omique intégrative.Les tumeurs thoraciques indifférenciées SMARCA4-déficientes (SMARCA4-UT), initialement « sarcomes » semblaient répondre aux inhibiteurs de point de contrôle immunitaire (ICIs) comme d’autres tumeurs SWI/SNF déficientes, sans qu’aucune caractérisation de leur microenvironnement tumoral (TME) ne soit faite pour le comprendre. Grâce à des immunomarquages et à une analyse transcriptomique, nous avons mis en évidence u

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Dufresne, Armelle. "Une étude des voies de signalisation impliquées dans la carcinogénèse et le traitement des fibromatoses agressives." Phd thesis, Université Claude Bernard - Lyon I, 2014. http://tel.archives-ouvertes.fr/tel-01058194.

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Les fibromatoses agressives sont des tumeurs conjonctives rares, pouvant envahir les structures adjacentes parfois de manière très agressive et responsables de fréquentes récidives loco-régionales mais dépourvues de potentiel métastatique. Leur évolution est imprévisible. Actuellement, la stratégie de leur prise en charge est remise en cause et ces tumeurs sont de plus en plus souvent surveillées à leur diagnostic. En cas de tumeur évolutive, les traitements systémiques disponibles sont multiples mais d'efficacité variable. Aucun facteur pronostique de récidive ou d'évolutivité spontanée et au

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Kotilingam, Dhanasekaran Douglas Tommy C. Ford Charles Erwin Rodin Andrei S. "Prognostic factors in desmoid tumors." 2008. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1457520.

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Books on the topic "Desmoid tumor"

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Litchman, Charisse, ed. Desmoid Tumors. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-1685-8.

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Litchman, Charisse. Desmoid Tumors. Springer Science+Business Media B.V., 2011.

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Litchman, Charisse. Desmoid Tumors. Springer, 2014.

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Sri-Ram, Kesavan, Anthony Mcgrath, Eric Yeung, et al. Benign tumours of soft tissues. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.002003.

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♦ Ganglion cyst♦ Intramuscular myxoma♦ Myositis ossificans♦ Nodular fasciitis♦ Haemangioma♦ Lipoma♦ Cavernous lymphangioma♦ Glomus tumour♦ Neurofibroma♦ Desmoid tumour♦ Elastofibroma♦ Schwannoma♦ Synovial chondromatosis.

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Denys, Hannelore. B-Catenin Target Genes in Desmoid Tumors. Leuven Univ Pr, 2002.

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6

Chambers, Anne. Eleanor, Countess of Desmond: A Heroine of Tudor Ireland. Wolfhound Press (IE), 1986.

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Tejpar, Sabine. Analysis of Wnt: Catenin Signaling in Desmoid Tumors (Acta Biomedica Lovaniensia, 237). Leuven Univ Pr, 2001.

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Eleanor, Countess of Desmond: Captivating Tale of the Forgotten Heroine of the Tudor Wars in Ireland. M.H. Gill & Co. U. C., 2011.

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Book chapters on the topic "Desmoid tumor"

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Clark, Sue. "Desmoid Tumor." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27841-9_1578-2.

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Clark, Sue. "Desmoid Tumor." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-46875-3_1578.

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Clark, Sue. "Desmoid Tumor." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-16483-5_1578.

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Olvi, Liliana G., and Eduardo Santini-Araujo. "Periosteal Desmoid." In Tumors and Tumor-Like Lesions of Bone. Springer London, 2015. http://dx.doi.org/10.1007/978-1-4471-6578-1_52.

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Olvi, Liliana G., Isabela W. da Cunha, Eduardo Santini-Araujo, and Ricardo K. Kalil. "Periosteal Desmoid." In Tumors and Tumor-Like Lesions of Bone. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-28315-5_55.

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Campanacci, Laura. "Desmoid Fibroma." In Diagnosis of Musculoskeletal Tumors and Tumor-like Conditions. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-29676-6_14.

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Gruber-Moesenbacher, Ulrike. "Desmoid Tumor, Lung." In Encyclopedia of Pathology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-69263-0_258.

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Van Dellen, Melissa. "Desmoid Tumor, Pleural." In Encyclopedia of Pathology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-66796-6_352.

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Weiss, Aaron R., Anthony Montag, and Stephen X. Skapek. "Desmoid Tumor in Children and Adolescents: The Influence of Age." In Desmoid Tumors. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1685-8_11.

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Cheng, Xiaoguang, Yongbin Su, and Mingqian Huang. "Desmoid-Type Fibromatosis: Case 10." In Bone Tumor Imaging. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9927-5_10.

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Conference papers on the topic "Desmoid tumor"

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Itty, R., H. Chieng, J. Sung, L. Foulke, and A. Chopra. "A Pleural Rarity: Desmoid Tumor." 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.a6767.

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Braun, Alexcia Camila, Fernando Campos, Emne Ali Abdallah, et al. "Abstract LB060: Circulating tumor cells in desmoid tumors." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-lb060.

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Al-Jazrawe, Mushriq, Steven Xu, Qingxia Wei, Raymond Poon, and Benjamin Alman. "Abstract 5897: Single cell-derived analysis of desmoid tumors for studying tumor-stroma interactions." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-5897.

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Tanaka, N., M. Okuda, K. Fukuda, and Y. Kato. "A Case of Chest-Wall Desmoid Tumor with Clip Marking for Treatment." 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.a5838.

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Rodrigues Silva Catalá, Heloísa, Andressa Higa Shinzato, Alcânia Walburga de Souza Pereira, et al. "DESMOID TUMOR AS A DIAGNOSTIC OF GREATER TROCHANTERIC PAIN SYNDROME - CASE REPORT." In Congresso Brasileiro de Reumatologia 2020. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2020.17174.

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Rosenberg, Laura M., Monica M. Bertagnolli, and Nancy L. Cho. "Abstract 3794: Sorafenib suppresses desmoid tumor growth and invasion via inhibition of ERK signaling." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-3794.

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Gomez, M., and R. Mehta. "440 Desmoid tumor of the breast after mastectomy for breast cancer, a case report." In IGCS 2020 Annual Meeting Abstracts. BMJ Publishing Group Ltd, 2020. http://dx.doi.org/10.1136/ijgc-2020-igcs.381.

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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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Khudari, Husameddin El, Arsalan Nadeem, Meghana Muppuri, and Rakesh Varma. "Strategic Debulking and Neuropraxia Mitigation in CT-Guided Cryoablation of Rectus Sheath Desmoid Tumor: A Case Report." In PAIRS 2024 Annual Congress. Thieme Medical and Scientific Publishers Pvt. Ltd., 2024. http://dx.doi.org/10.1055/s-0044-1785997.

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Park, Changhee, Kum-Hee Yun, Sanghoon Song, et al. "Abstract 2250: Genomic and transcriptomic analyses of desmoid tumor reveals enrichment of transforming growth factor beta responsive signature." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-2250.

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Reports on the topic "Desmoid 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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