Gotowe bibliografie tematyczne / Rare fibroblastic neoplasm

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Gotowa bibliografia na temat „Rare fibroblastic neoplasm”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Rare fibroblastic neoplasm"

Córdoba-Fernández, Antonio, José María Juárez-Jiménez, José Mazuecos-Blanca, and Matilde Illanes-Moreno. "A Report of a Rare Case of Myxoinflammatory Fibroblastic Sarcoma." Journal of the American Podiatric Medical Association 100, no. 6 (2010): 497–501. http://dx.doi.org/10.7547/1000497.

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Myxoinflammatory fibroblastic sarcoma of the soft tissues is a rare low-grade tumor of uncertain origin that most often occurs on the extremities of adults. The tumor predominantly involves the subcutaneous tissues of the hands and feet. Despite being a rare neoplasm, owing to its varied histologic appearance, myxoinflammatory fibroblastic sarcoma should be differentiated from various benign and malignant soft-tissue lesions. Myxoinflammatory fibroblastic sarcoma has been well described in pathology journals but not in the surgical literature. We report a case of myxoinflammatory fibroblastic

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Lee, Eun Sun. "Malignant Solitary Fibrous Tumor of Ileum with Intussusception." Korean Journal of Abdominal Radiology 5, no. 1 (2021): 77–80. http://dx.doi.org/10.52668/kjar.2021.00038.

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Solitary fibrous tumor (SFT) is rare mesenchymal neoplasm of fibroblastic or myofibroblastic origin. Especially, extrapleural SFT is known to be extremely rare. Here, we report a case of malignant SFT of ileum, resulting in small bowel intussusception in a 74-year-old female patient.

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Rynda, Artemiy, Viktor Olyushin, Yuliya Zabrodskaya, and Dmitriy Rostovtsev. "METASTASIS PRIMARY MYXOFIBROSARCOMA FROM THE HEART OF IN BRAIN. CASE REPORT." Problems in oncology 65, no. 3 (2019): 467–74. http://dx.doi.org/10.37469/0507-3758-2019-65-3-467-474.

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Background: myxofibrosarcoma is rare a fibroblastic neoplasm with myxoid matrix. Objective: to show rare case of heart myxofibrosarcoma with brain metastasis. Materials and methods: 52-year-old women, clinical manifestations were headaches, left hemiparesis, intellection-amnestic disorder. Results: radical operation with intraoperative photodynamic therapy has been executed.

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Berres-Wehrle, Frauke, Khaled Mukkadam, Daniel Baumhoer, and Michael M. Bornstein. "Peripheres odontogenes Fibrom im Oberkiefer bei einem 26-jährigen Patienten." SWISS DENTAL JOURNAL SSO – Science and Clinical Topics 131, no. 11 (2021): 924–25. http://dx.doi.org/10.61872/sdj-2021-11-04.

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Peripheral odontogenic fibroma (POF) is a rare and benign neoplasm consisting of a mature fibroblastic spindle cell proliferation and variable inclusions of odontogenic epithelium. It can occur in both the maxilla and mandible.

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Mohamedali, Rasheeda, Nilay Nishith, Rahul Raj, et al. "Unveiling Rare Breast Neoplasms: Diagnostic Challenges and Insights." Discoveries 12, no. 4 (2024): e200. https://doi.org/10.15190/d.2024.19.

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Breast neoplasm encompasses a diversified range of different diseases characterized by unique biological and pathological features, clinical presentation, response to treatments, clinical behavior, and outcome. The histological variability has profound prognostic implications, thus playing a pivotal role in diagnosing breast neoplasm. Special histologies can occur rarely, and most information on outcomes and treatments is mainly derived from small series and case reports. Thus, reporting such unusual occurrences is of utmost importance. This is a retrospective study of four years in which 11 c

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Hallin, Magnus, Yurina Miki, Andrew J. Hayes, Robin L. Jones, Cyril Fisher, and Khin Thway. "Acral myxoinflammatory fibroblastic sarcoma with hybrid features of hemosiderotic fibrolipomatous tumor occurring 10 years after renal transplantation." Rare Tumors 10 (January 1, 2018): 203636131878262. http://dx.doi.org/10.1177/2036361318782626.

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Myxoinflammatory fibroblastic sarcoma is a rare malignant soft tissue neoplasm that typically arises on the distal extremities of adults. It usually behaves in a low-grade manner and its characteristic histology is of a lobulated proliferation of moderately atypical spindled to epithelioid cells, vacuolated cells, and enlarged or bizarre cells with prominent nucleoli, dispersed within myxoid stroma containing a mixed inflammatory cell infiltrate. The etiology of myxoinflammatory fibroblastic sarcoma remains unknown with no definite causal factors identified. We describe a case of myxoinflammat

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Jain, Ekta, Lata Kini, Rita Alaggio, and Sarangarajan Ranganathan. "Myxoinflammatory Fibroblastic Sarcoma of Eyeball in an Infant: A Rare Presentation." International Journal of Surgical Pathology 28, no. 3 (2019): 306–9. http://dx.doi.org/10.1177/1066896919879497.

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Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare soft tissue neoplasm most commonly occurring in the distal extremities of adult patients. It is a low-grade neoplasm with high rate of local recurrence but low rate of metastasis. We describe a case of MIFS of eyeball in an infant. An enucleation surgery was performed, and on the basis of histopathological and immunohistochemical evaluation, a diagnosis of MIFS was rendered. Till date more than 400 cases of MIFS have been reported with only a single case report of MIFS in an adult in iris. To the best of our knowledge, ours is the first ca

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Ieremia, Eleni, and Khin Thway. "Myxoinflammatory Fibroblastic Sarcoma: Morphologic and Genetic Updates." Archives of Pathology & Laboratory Medicine 138, no. 10 (2014): 1406–11. http://dx.doi.org/10.5858/arpa.2013-0549-rs.

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Myxoinflammatory fibroblastic sarcoma (MIFS) is a malignant mesenchymal neoplasm most frequently arising in the distal extremities of adults, which usually behaves in a low-grade manner but is capable of metastasizing to local and distant sites, rarely leading to death. It is a rare tumor whose unusual morphology can lead to erroneous histologic diagnosis, either as a nonneoplastic (infectious or inflammatory) process or as a variety of neoplastic diseases. While its exact origin is uncertain, ultrastructural studies have shown at least some of the constituent cells to be modified fibroblasts.

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Shetty, Rohan, Shubha Bhat, Rajesh Ballal, Pramod Makannavar, and Anil Kumar K. N. "AGGRESSIVE MESENTRIC FIBROMATOSIS: A RARE CASE REPORT AND REVIEW OF LITERATURE." Journal of Health and Allied Sciences NU 03, no. 01 (2013): 79–82. http://dx.doi.org/10.1055/s-0040-1703641.

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AbstractMesentric fibromatosis is a proliferative fibroblastic neoplasm of the small intestinal mesentery with varied clinical presentation. Giant mesentric fibromatosis is uncommon and its rarity poses a diagnostic and therapeutic challenge. This paper presents a recurrent aggressive fibromatosis in a 38 year old male patient, who had initially undergone a laparotomy outside for mass abdomen but only pus was evacuated and definitive diagnosis was not made.

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Kamble, Pradnya, Jayashree Chaudhari, and Manisha Khare. "Superficial CD34 Positive Fibroblastic Tumor: A rare mesenchymal tumor of borderline malignant potential." Journal of Pathology of Nepal 14, no. 2 (2024): 2232–35. https://doi.org/10.3126/jpn.v14i2.64485.

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Superficial CD34 positive fibroblastic tumor is a rare soft tissue tumor first brought to light by Jodi M Carter in 2014. Several cases have been reported since, and they have been newly included in the recent WHO classification under the fibroblastic and myofibroblastic tumors category. It is a mesenchymal neoplasm of borderline malignant potential predominantly found in middle-aged adults with a median age of 37 years and most commonly located in the lower extremities. It is a spindle cell tumor with pleomorphic epithelioid cells, low mitotic activity, and strong diffuse positivity for CD34

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Części książek na temat "Rare fibroblastic neoplasm"

Baki, Ahmet. "Soft-Tissue Tumors of the Head and Neck Region." In Advances in Soft Tissue Tumors [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.102026.

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Fibroblastic and myofibroblastic neoplasms in the head and neck region are a rare group of tumors ranging from benign lesions to malignant lesions. Due to the difficult anatomy of the head and neck region, even neoplasms without metastatic potential can pose significant therapeutic challenges in this region. In this section, the most common soft-tissue neoplasms in the head and neck region will be discussed.

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