Academic literature on the topic 'Pleomorphic malignant fibrous histiocytoma'

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Journal articles on the topic "Pleomorphic malignant fibrous histiocytoma"

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Fletcher, Christopher D. M. "Pleomorphic Malignant Fibrous Histiocytoma." American Journal of Surgical Pathology 16, no. 3 (1992): 213–28. http://dx.doi.org/10.1097/00000478-199203000-00001.

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M Kiran, M., M. Karaman, F. Hatipoglu, and Y. Koc. "Malignant fibrous histiocytoma in a dog: a case report." Veterinární Medicína 50, No. 12 (2012): 553–57. http://dx.doi.org/10.17221/5665-vetmed.

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In this report, a case of malignant fibrous histiocytoma involving skin, lungs, kidneys, pancreas and mediastinal lymph node was described. Microscopically, the tumor classified as storiform-pleomorphic type malignant fibrous histiocytoma.
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Martha, Lilia Tena-Suck, Sánchez-Garibay Carlos, and Salinas-Lara Citlaltepelt. "Intracranial Pleomorphic Malignant Fibrous Histiocytoma, Associated to Systemic Lupus Erythematous: A Case Report." British Journal of Medicine & Medical Research 21, no. 9 (2017): 1–9. https://doi.org/10.9734/BJMMR/2017/32743.

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<strong>Background:</strong> Pleomorphic Malignant Fibrous histiocytoma (MFH) is a rare neoplasms of the soft tissue and bone composed of fibroblastic and histiocytic components with mitosis figures, nuclear pleomorphism and anaplasia. <strong>Case Presentation:</strong> We presented a rare case of MFH in 44 year old woman with history of systemic erythematosus lupus and seizures. Treated with prednisone. The cerebral TAC showed a temporal mass. Craniotomy was performed and the examination of the biopsy sample revealed a giant, pleomorphic and atypical cells. Immunohistochemical analysis showe
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Bajaj, Anubha. "The Vascular Swirls- Angiomatoid Fibrous Histiocytoma." Journal of Clinical and Diagnostic Pathology 1, no. 3 (2021): 15–23. http://dx.doi.org/10.14302/issn.2689-5773.jcdp-20-3648.

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Angiomatoid fibrous histiocytoma (AFH) is an exceptional, soft tissue neoplasm of indeterminate lineage and intermediate malignancy associated with minimal localized tumour reoccurrence and infrequent distant metastasis. Preliminarily contemplated to be a variant or derivative of malignant fibrous histiocytoma or undifferentiated pleomorphic sarcoma or an unusual fibrohistiocytic sarcoma, angiomatoid fibrous histiocytoma predominantly incriminates young po pulation and superficial sites although several extra-somatic sites can be implicated.
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Bajaj, Anubha. "The Vascular Swirls- Angiomatoid Fibrous Histiocytoma." Journal of Clinical and Diagnostic Pathology 1, no. 3 (2021): 15–23. http://dx.doi.org/10.14302/issn.2689-5773.jcdp-20-3648.

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Angiomatoid fibrous histiocytoma (AFH) is an exceptional, soft tissue neoplasm of indeterminate lineage and intermediate malignancy associated with minimal localized tumour reoccurrence and infrequent distant metastasis. Preliminarily contemplated to be a variant or derivative of malignant fibrous histiocytoma or undifferentiated pleomorphic sarcoma or an unusual fibrohistiocytic sarcoma, angiomatoid fibrous histiocytoma predominantly incriminates young po pulation and superficial sites although several extra-somatic sites can be implicated.
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ÖZEN, Η., S. DAĞ, E. KARAKURT, and E. BÜYÜK. "Malignant fibrous histiocytoma in a budgerigar (Melopsittacus undulatus)." Journal of the Hellenic Veterinary Medical Society 71, no. 3 (2020): 2407. http://dx.doi.org/10.12681/jhvms.25105.

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In this report, a case of malignant fibrous histiocytoma in a budgerigar (Melopsittacus undulatus) is described. At necropsy, a tumorous subcutaneous mass was noted to be located under the right wing at the level of humerus in a budgerigar. On microscopic examination, the tumor was composed of pleomorphic cells having mostly round to oval large nucleus. Presence of occasional bands composed of fibroblastoid cells were noted. Occasional giant cells and mitotic figures were also observed. Based on the microscopic findings, a diagnosis of malignant fibrous histiocytoma was made. The present case
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Letayf, Sonia Lopez, Ana María Cano Valdez, Beatriz Catalina Aldape Barrios, and Gerardo Jasso Romero. "Pleomorphic Undifferentiated Sarcoma (Malignant Fibrous Histiocytoma)." Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 119, no. 3 (2015): e164. http://dx.doi.org/10.1016/j.oooo.2014.07.275.

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Dilek, T. U. K., S. Dilek, O. Pata, C. Tataroglu, and E. Tok. "Malignant fibrous histiocytoma of the ovary: a case report." International Journal of Gynecologic Cancer 16, Suppl 1 (2006): 352–56. http://dx.doi.org/10.1136/ijgc-00009577-200602001-00062.

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Malignant fibrous histiocytoma is the most common type of soft tissue sarcoma in adults. Primary malignant fibrous histiocytoma of the ovary is extremely rare, with only three previously reported cases. We reported a rare and uncommon localization of malignant fibrous histiocytoma in a 22-year-old woman. She was referred for adjuvant chemotherapy to our center with the diagnosis of storiform-pleomorphic malignant fibrous histiocytoma. A left adnexal mass was detected by computed tomography of the lower abdomen. Therefore, we decided to perform reoperation for debulking, and left salpingo-oophe
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Nguyen, Austin, Adam Vaudreuil, Paul Haun, Gabriel Caponetti, and Christopher Huerter. "Clinical Features and Treatment of Fibrous Histiocytomas of the Tongue: A Systematic Review." International Archives of Otorhinolaryngology 22, no. 01 (2017): 094–102. http://dx.doi.org/10.1055/s-0037-1602819.

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Introduction Benign fibrous histiocytomas are common lesions of the skin that rarely affect the tongue. Such cases are available in the literature exclusively as case reports. Similarly, malignant fibrous histiocytoma, now classified as undifferentiated pleomorphic sarcoma, is exceedingly rare in the tongue and not fully understood. Objectives This study systematically reviews the available literature discussing the clinical and pathological features of malignant and benign fibrous histiocytomas. Data Synthesis A total of 20 cases were included in this review. Patient-level data were extracted
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., Shubham, Ashokan Ravi, and Haridarshan S. J. "Anterior abdominal wall spindle cell tumour - atypical fibrous histiocytoma: a rare presentation." International Surgery Journal 5, no. 10 (2018): 3450. http://dx.doi.org/10.18203/2349-2902.isj20184109.

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Atypical fibrous histiocytoma is a rare and a distinct variant of cutaneous fibrous histiocytoma which can be misdiagnosed as sarcoma. It is mainly composed of a mixture of fibroblastic and histiocytic cells, especially found in the skin (dermatofibroma), particularly in the limbs. It is quite uncommon and is difficult to distinguish from a malignant lesion. Due to the lack of clear cut predictive morphological patterns and due to the suspicion of malignancy, complete surgical excision is recommended. Provided that atypical fibrous histiocytoma is treated by complete excision, a benign outcome
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Dissertations / Theses on the topic "Pleomorphic malignant fibrous histiocytoma"

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Fröhner, Michael, Andreas Manseck, Michael Haase, Oliver W. Hakenberg, and Manfred P. Wirth. "Locally Recurrent Malignant Fibrous Histiocytoma: A Rare and Aggressive Genitourinary Malignancy." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-133923.

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Objective: In this study, 22 cases of locally recurrent urological malignant fibrous histiocytoma were reviewed considering therapeutic options, follow-up and prognosis. Patients and Methods: In the available literature on this topic we identified 19 cases of locally recurrent genitourinary malignant fibrous histiocytoma. Three additional cases are discussed, primarily arising from the kidney, the bladder and the paratesticular region. Results: The prognosis of locally recurrent urological malignant fibrous histiocytoma was found to be extraordinarily poor. Only 2 of 22 patients have survived
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Fröhner, Michael, Andreas Manseck, Michael Haase, Oliver W. Hakenberg, and Manfred P. Wirth. "Locally Recurrent Malignant Fibrous Histiocytoma: A Rare and Aggressive Genitourinary Malignancy." Karger, 1999. https://tud.qucosa.de/id/qucosa%3A26499.

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Objective: In this study, 22 cases of locally recurrent urological malignant fibrous histiocytoma were reviewed considering therapeutic options, follow-up and prognosis. Patients and Methods: In the available literature on this topic we identified 19 cases of locally recurrent genitourinary malignant fibrous histiocytoma. Three additional cases are discussed, primarily arising from the kidney, the bladder and the paratesticular region. Results: The prognosis of locally recurrent urological malignant fibrous histiocytoma was found to be extraordinarily poor. Only 2 of 22 patients have survive
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Besson, René. "Malignant fibrous histiocytoma : revue de la littérature à propos d'une observation à localisation sinusienne." Saint-Etienne, 1989. http://www.theses.fr/1989STET6241.

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Hussenet, Thomas. "Toward the identification of oncogenes by high resolution mapping of gene amplifications of the 3q25-qter region in malignant fibrous histiocytoma and squamous cell carcinoma." Strasbourg 1, 2005. https://publication-theses.unistra.fr/public/theses_doctorat/2005/HUSSENET_Thomas_2005.pdf.

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L’approche de clonage positionnel a été appliquée à la cartographie haute résolution des aberrations du chromosome 3 dans différents types tumoraux afin d’identifier de nouveaux candidats oncogènes du bras long du chromosome 3 (3q), amplifiés et sur-exprimés en conséquence. Une première partie a été dédiée aux Fibro-Histiocytomes Malins (MFH). Des amplicons chevauchants du locus 3q28 ont été caractérisés dans une lignée cellulaire et deux tumeurs de MFH. A ce locus, nous avons identifié un oncogène candidat, hsa-miR-28, codant pour un microARN ainsi que trois de ses cibles, impliquées dans la
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Palmer, Jessica Lynn. "Molecular genetic characterization of pediatric malignant fibrous histiocytoma." Thesis, 1997. http://hdl.handle.net/2429/6575.

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Cytogenetic and molecular genetic studies were performed on a pleiomorphic sarcoma diagnosed as malignant fibrous histiocytoma (MFH), removed from the heart of a 15 year old girl. MFH is the most common soft tissue sarcoma in adults, however, it is extremely rare in the pediatric population. Accurate pathologic classification of MFH is difficult because these primitive sarcomas lack recognizeable features of differentiation using conventional pathological techniques. Recently, analysis of chromosomal alterations in human malignancies has revealed that recurring genetic changes are often
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Books on the topic "Pleomorphic malignant fibrous histiocytoma"

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Bhumbra, Rej S., Panagiotis D. Gikas, Sammy Hanna, Jakub Jagiello, and Stephen R. Cannon. Malignant tumours of soft tissues. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.002004.

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♦ Malignant vascular tumours of soft tissue♦ Synovial sarcoma♦ Malignant peripheral nerve sheath tumours♦ Rhabdomyosarcoma♦ Leiomyosarcoma♦ Epithelioid sarcoma♦ Clear cell sarcoma♦ Malignant fibrous histiocytoma♦ Chordoma.
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Ajithkumar, Thankamma, Ann Barrett, Helen Hatcher, and Natalie Cook. Bone tumours and soft tissue sarcomas. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199235636.003.0012.

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Primary malignant tumours of bone are rare and comprise a large number of histological subtypes. • The most common are osteosarcoma, Ewing's family of tumours, and chondrosarcoma. Each of these has further subgroups which will be discussed in detail under their subheadings.• The remaining subgroups are exceptionally rare and include the presentation of spindle cell sarcoma of bone e.g. malignant fibrous histiocytoma (MFH), within the bone as a primary lesion. MFH of bone is treated as other primary bone tumours (Bramwell et al. 1999)....
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Cassidy, Jim, Donald Bissett, Roy A. J. Spence OBE, Miranda Payne, and Gareth Morris-Stiff. Malignancy of unknown primary. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199689842.003.0026.

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Bone and soft tissue malignancies describes a large group of sarcomas, some of which require highly specialist management, including osteosarcoma, Ewing’s sarcoma, and rhabdomyosarcoma, so that referral to an appropriate multidisciplinary team (MDT) is mandatory. Limb conserving surgery combined with pre- and postoperative chemotherapy is curative in the majority of osteosarcomas, and similar approach which may include local radiotherapy also holds for Ewing’s. Other primary bone tumours are reviewed including malignant fibrous histiocytoma, chondrosarcoma, chordoma, solitary plasmacytoma, and
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Book chapters on the topic "Pleomorphic malignant fibrous histiocytoma"

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Benati, Elisa. "Malignant fibrous histiocytoma (pleomorphic undifferentiated sarcoma)." In Diagnosing the Less Common Skin Tumors. CRC Press, 2019. http://dx.doi.org/10.1201/9781315100555-33.

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Rongioletti, Franco. "Atypical Fibroxanthoma/Undifferentiated Pleomorphic Sarcoma (Superficial Malignant Fibrous Histiocytoma)." In Rare Malignant Skin Tumors. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-2023-5_33.

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Brennan, Murray F., Cristina R. Antonescu, Kaled M. Alektiar, and Robert G. Maki. "Undifferentiated Pleomorphic Sarcoma (UPS) (Malignant Fibrous Histiocytoma (MFH) and Myxofibrosarcoma)." In Management of Soft Tissue Sarcoma. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-41906-0_7.

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Brennan, Murray F., Cristina R. Antonescu, and Robert G. Maki. "Undifferentiated Pleomorphic Sarcoma (UPS; Malignant Fibrous Histiocytoma: MFH) and Myxofibrosarcoma." In Management of Soft Tissue Sarcoma. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5004-7_7.

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Zimmermann, Arthur. "Malignant Fibrous Histiocytoma of the Liver: A Neoplasm of the Undifferentiated High-Grade Pleomorphic Sarcoma Group." In Tumors and Tumor-Like Lesions of the Hepatobiliary Tract. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26587-2_71-1.

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Zimmermann, Arthur. "Malignant Fibrous Histiocytoma of the Liver: A Neoplasm of the Undifferentiated High-Grade Pleomorphic Sarcoma Group." In Tumors and Tumor-Like Lesions of the Hepatobiliary Tract. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26956-6_71.

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De Schepper, A. M. A., and H. R. M. Degryse. "Malignant Fibrous Histiocytoma." In Magnetic Resonance Imaging of Bone and Soft Tissue Tumors and Their Mimics. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0997-7_18.

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Campanacci, Mario. "Malignant Fibrous Histiocytoma." In Bone and Soft Tissue Tumors. Springer Vienna, 1999. http://dx.doi.org/10.1007/978-3-7091-3846-5_67.

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Campanacci, Mario. "Malignant Fibrous Histiocytoma." In Bone and Soft Tissue Tumors. Springer Vienna, 1999. http://dx.doi.org/10.1007/978-3-7091-3846-5_7.

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Mocellin, Simone. "Malignant Fibrous Histiocytoma." In Soft Tissue Tumors. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58710-9_165.

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Conference papers on the topic "Pleomorphic malignant fibrous histiocytoma"

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Zaaqoq, Akram M., and Lawrence S. Goldstein. "Unusual Presentation Of Malignant Fibrous Histiocytoma." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a3830.

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Read, Richard N., and Brian Casserly. "Primary Malignant Fibrous Histiocytoma Of The Heart Presenting As Acute Pulmonary Embolism." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a1910.

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Boparai, S., A. M. R. G. Sharma, N. A. Siddiqui, and R. C. Holladay. "Rare Case of Primary Pulmonary Myxoid Angiomatoid Malignant Fibrous Histiocytoma with Concern for Metastasis: A Diagnostic and Therapeutic Challenge." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a4933.

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Reports on the topic "Pleomorphic malignant fibrous histiocytoma"

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Abdominal bleeding due to ruptured primary hepatic malignant fibrous histiocytoma. Science Repository OÜ, 2019. http://dx.doi.org/10.31487/j.scr.2019.01.004.

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