Relevant bibliographies by topics / Primary intracranial fibrous histiocytomas

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Academic literature on the topic 'Primary intracranial fibrous histiocytomas'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Primary intracranial fibrous histiocytomas"

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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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Koşucu, Polat, Ali Aydın Yavuz, Melek Nur Yavuz, Abdülkadir Reis, and Ali Ahmetoğlu. "Primary intracranial malignant fibrous histiocytoma." European Journal of Radiology Extra 47, no. 2 (2003): 78–81. http://dx.doi.org/10.1016/s1571-4675(03)00091-9.

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Ochalski, Pawel G., James T. Edinger, Michael B. Horowitz, et al. "Intracranial angiomatoid fibrous histiocytoma presenting as recurrent multifocal intraparenchymal hemorrhage." Journal of Neurosurgery 112, no. 5 (2010): 978–82. http://dx.doi.org/10.3171/2009.8.jns081518.

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Angiomatoid fibrous histiocytoma (AFH) is a rare soft-tissue neoplasm that most commonly appears in the limbs, typically affecting children and young adults. The tumor has a propensity for local recurrence and recurrent hemorrhage but rarely for remote metastasis. To date, only 2 reports have documented an intracranial occurrence of the tumor (1 of which was believed to be metastatic disease). This is the second report of primary intracranial AFH. Additionally, hemorrhage from an intracranial AFH lesion has yet to be reported, and little is known about the radiographic characteristics and biol
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Deb, Prabal, Vikram Singh, Vibha Dutta, HS Bhatoe, and VijaiMohan Chandran. "Primary intracranial benign fibrous histiocytoma: Report of an unusual case." Journal of Cancer Research and Therapeutics 10, no. 1 (2014): 200. http://dx.doi.org/10.4103/0973-1482.131417.

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Ideguchi, Makoto, Koji Kajiwara, Koichi Yoshikawa, et al. "Benign fibrous histiocytoma of the skull with increased intracranial pressure caused by cerebral venous sinus occlusion." Journal of Neurosurgery 111, no. 3 (2009): 504–8. http://dx.doi.org/10.3171/2008.11.jns081206.

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The authors present a very rare case of benign fibrous histiocytoma of the skull with increased intracranial pressure caused by sinus occlusion. A 33-year-old woman was referred for investigation of a right occipital protrusion with tenderness and double vision. She had only mild divergence insufficiency and bilateral papilledema neurologically. Imaging findings showed that the skull tumor was located at the right occipital bone with bone disruption and a compressed right sigmoid sinus. When planning the resection, caution was required to spare the collateral flow so as to manage the intracran
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Bin Abdulqader, Sarah, Khalid Altuhaini, Raghad Tallab, et al. "Primary Intracranial Angiomatoid Fibrous Histiocytoma: Two Case Reports and Literature Review." World Neurosurgery 143 (November 2020): 398–404. http://dx.doi.org/10.1016/j.wneu.2020.07.225.

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Mazur-Hart, David J., Brannan E. O'Neill, Brandi W. Pang, et al. "Operative Technique: Angiomatoid Fibrous Histiocytoma—Unique Case and Management." Journal of Neurological Surgery Reports 83, no. 03 (2022): e110-e118. http://dx.doi.org/10.1055/s-0042-1754320.

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Abstract Objective We describe the first jugular foramen angiomatoid fibrous histiocytoma (AFH) case and the first treatment with preoperative endovascular embolization. AFH is a rare intracranial neoplasm, primarily found in pediatric patient extremities. With an increase in AFH awareness and a well-described genetic profile, intracranial prevalence has also subsequently increased. Study Design We compare this case to previously reported cases using PubMed/Medline literature search, which was performed using the algorithm [“intracranial” AND “angiomatoid fibrous histiocytoma”] through Decembe
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Berry, Allen D., Stephen L. Reintjes, and John J. Kepes. "Intracranial malignant fibrous histiocytoma with abscess-like tumor necrosis." Journal of Neurosurgery 69, no. 5 (1988): 780–84. http://dx.doi.org/10.3171/jns.1988.69.5.0780.

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✓ A case of a malignant fibrous histiocytoma (MFH) in the right temporal lobe of a 75-year-old man is reported. The tumor involved the brain and the overlying dura as one continuous mass and had undergone extensive liquefaction necrosis of its center that had a gross appearance similar to that of an abscess. The preoperative computerized tomography scan with injection of contrast material showed the lesion to have central and peripheral enhancement suggestive of metastatic tumor, glioblastoma multiforme, or abscess. Microscopically, the tumor showed the typical features of a MFH with marked ac
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Hansen, Jakob Møller, Vibeke Andrée Larsen, David Scheie, Arie Perry, and Jane Skjøth-Rasmussen. "Primary intracranial angiomatoid fibrous histiocytoma presenting with anaemia and migraine-like headaches and aura as early clinical features." Cephalalgia 35, no. 14 (2015): 1334–36. http://dx.doi.org/10.1177/0333102415583988.

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A 17-year-old female with migraine with aura complained of fatigue and was diagnosed with anemia. Three years later, changes in her headache pattern prompted hospital referral. Brain MRI showed a bi-lobed extra-axial intracerebral tumor encroaching both parieto-occipital regions. The resection specimen yielded a rare diagnosis of primary intracranial angiomatoid fibrous histiocytoma (AFH). Tumor removal resulted in cessation of her migraine and anemia. AFH may cause systemic symptoms – in this case fatigue and anemia – long before focal neurological symptoms are present. This is the first repo
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Maruno, Motohiko, A. K. M. Ghulam Muhammad, Junji Taguchi, et al. "Giant cell type of primary intracranial malignant fibrous histiocytoma: a case report." Brain Tumor Pathology 23, no. 1 (2006): 65–70. http://dx.doi.org/10.1007/s10014-006-0200-2.

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Book chapters on the topic "Primary intracranial fibrous histiocytomas"

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Pehlivanoglu, Suray, and Sebnem Pehlivanoglu. "Craniosynostosis: Clinical Characteristics, Molecular Mechanisms and Treatment." In Molecular Approaches in Medicine. Nobel Tip Kitabevleri, 2024. http://dx.doi.org/10.69860/nobel.9786053359524.6.

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Craniosynostosis is a congenital condition marked by the early fusion of one or more cranial sutures. Cranial sutures are fibrous tissues that connect the skull bones. They play a crucial role in ensuring bone formation at the edges of the calvarial bones, which move apart to facilitate the passage of the head through the birth canal and allow for future brain growth. The premature fusion limits skull growth perpendicular to the affected sutures, potentially resulting in abnormal head shapes, increased intracranial pressure, and developmental delays. The prevalence of craniosynostosis is about
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Harmon, Angus J. Patterson ,David C. "Bone tumours and soft tissue sarcomas." In Oncology. Oxford University PressNew York, NY, 2001. http://dx.doi.org/10.1093/oso/9780192629821.003.0020.

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Abstract The commonest malignant primary bone tumours are the matrix-producing tumours, osteosarcoma and chondrosarcoma. Less frequently seen is the small round cell tumour, Ewing’s sarcoma. Malignant fibrous histiocytomas, primary bone lymphomas, and malignant giant cell tumours are rare but well recognized.
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Sathornsumetee, Sith, Rakesh Jalali, Manfred Westphal, and Christian Mawrin. "Mesenchymal, non-meningothelial tumors involving the central nervous system." In Oxford Textbook of Neuro-Oncology, 2nd ed. Oxford University PressOxford, 2025. https://doi.org/10.1093/med/9780198869702.003.0017.

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Abstract Central nervous system mesenchymal, non-meningothelial tumors are rare soft tissue or chondro-osseous tumors that uniquely or frequently involve the brain and spinal cord. In the 2021 World Health Organization (WHO) classification of tumors involving the central nervous system, these neoplasms have been categorized to align with their counterparts in the WHO classification of bone and soft tissue tumors. The most common type is solitary fibrous tumor. Some entities such as leiomyoma no longer exist in the current classification as their diagnostic criteria are similar to bone and soft
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Journal articles
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