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Gotowe bibliografie tematyczne / Cystic angiomatosis

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Gotowa bibliografia na temat „Cystic angiomatosis”

Autor: Grafiati

Data publikacji: 7 czerwca 2025

Data aktualizacji: 2 sierpnia 2025

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Artykuły w czasopismach na temat "Cystic angiomatosis"

1

Clayer, Mark. "Skeletal Angiomatosis in Association with Gastro-Intestinal Angiodysplasia and Paraproteinemia: A Case Report." Journal of Orthopaedic Surgery 10, no. 1 (2002): 85–88. http://dx.doi.org/10.1177/230949900201000115.

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Skeletal-extraskeletal angiomatosis is defined as a benign vascular proliferation involving the medullary cavity of bone and at least one other type of tissue. It has also been known as cystic angiomatosis in which multiple cystic lesions are scattered diffusely throughout the skeleton often with similar angiomatous changes in other tissues, usually the spleen. A case of skeletal angiomatosis in association with gastro-intestinal angiodysplasia and paraproteinemia is reported.

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Lateur, L., C. J. Simoens, S. Gryspeerdt, I. Samson, V. Mertens, and B. Van Damme. "Skeletal cystic angiomatosis." Skeletal Radiology 25, no. 1 (1996): 92–95. http://dx.doi.org/10.1007/s002560050042.

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Fleckenstein, J., John T. Milliken, J. S. Lee, and S. J. Ballentine. "Cystic angiomatosis of the bone, liver, and spleen." American Journal of Clinical Pathology 156, Supplement_1 (2021): S125—S126. http://dx.doi.org/10.1093/ajcp/aqab191.268.

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Abstract Introduction/Objective Cystic angiomatosis is a very rare entity characterized by multifocal cystic angiomatous lesions of the skeletal system, occasionally involving visceral organ systems. Clinical presentation and progression are extremely variable. Cases with liver involvement are even rarer, and have been described as invariably fatal. The pathogenesis of this disorder is poorly understood, and no treatments are currently available. Methods/Case Report A 24 year old man with history of polysubstance abuse and untreated hepatitis C presented with acute abdominal pain. Imaging reve

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Mohan, Sandeep, Rahul Krishnan, Sernam Kuttiyil, S. Archa, Hamdi Nizar Ahamed, and Rashik Ismail. "A Rare Case of Systemic Cystic Angiomatosis in an Elderly Female Initially Misdiagnosed as Vascular Neoplasm: A Case Report and Literature Review." Journal of Orthopaedic Case Reports 15, no. 1 (2025): 8–12. https://doi.org/10.13107/jocr.2025.v15.i01.5104.

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Introduction: Systemic cystic angiomatosis is an exceedingly rare condition characterized by widespread cystic vascular lesions involving multiple organs. Its clinical presentation can be non-specific, often leading to diagnostic challenges. This report discusses the case of a 72-year-old female with a long-standing history of diabetes mellitus who presented with non-specific symptoms, ultimately diagnosed with systemic cystic angiomatosis after an initial misdiagnosis of vascular neoplasia. The role of advanced imaging techniques and a multidisciplinary, individualized management approach is

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Goutoudi, P. C., N. K. Sferopoulos, V. Papavasiliou, and A. Konstantinidis. "Cystic angiomatosis of bone." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 81, no. 1 (1996): 89–92. http://dx.doi.org/10.1016/s1079-2104(96)80155-7.

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Boyse, Tedric D., and Jon A. Jacobson. "Case 45: Cystic Angiomatosis." Radiology 223, no. 1 (2002): 164–67. http://dx.doi.org/10.1148/radiol.2231001598.

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International, Journal of Medical Science and Innovative Research (IJMSIR). "Cystic Angiomatosis: A Radiological Dilemma." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 2 (2024): 61–67. https://doi.org/10.5281/zenodo.15378249.

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<strong>Abstract</strong> Cystic angiomatosis is a rare benign disorder with multifocal hemangiomatous or lymphangiomatous lesions of the axial or appendicular skeleton, spleen, liver, and lungs. Patients usually are asymptomatic and are incidentally detected on radiographs. The spectrum clinical presentation may include splenomegaly, hepatomegaly, cystic hygromas or effusions, and pathological fracture depending on the affected area, they may also have neurological symptoms with vertebral localization and skull lesions. This case report illustrates the prompt and accurate diagnosis of cystic

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Najm, Aurélie, Elise Soltner-Neel, Benoît Le Goff, Pascale Guillot, Yves Maugars, and Jean-Marie Berthelot. "Cystic angiomatosis, a heterogeneous condition." Medicine 95, no. 43 (2016): e5213. http://dx.doi.org/10.1097/md.0000000000005213.

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Shivaram, Giridhar M., Reetesh K. Pai, Kevin B. Ireland, and Kathryn J. Stevens. "Temporal progression of skeletal cystic angiomatosis." Skeletal Radiology 36, no. 12 (2007): 1199–204. http://dx.doi.org/10.1007/s00256-007-0378-3.

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REID, A. B., I. L. REID, G. JOHNSON, M. HAMONIC, and P. MAJOR. "Familial Diffuse Cystic Angiomatosis of Bone." Clinical Orthopaedics and Related Research 238 (January 1989): 211–18. http://dx.doi.org/10.1097/00003086-198901000-00031.

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Części książek na temat "Cystic angiomatosis"

1

Campanacci, Mario. "Lymphangioma, Cystic Angiomatosis." In Bone and Soft Tissue Tumors. Springer Vienna, 1999. http://dx.doi.org/10.1007/978-3-7091-3846-5_37.

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Kumar, Vivek, Trishala Meghal, Yanyu Helen Sun, and Yiwu Huang. "Systemic Cystic Angiomatosis Mimicking Metastatic Cancer: A Case Report and Review of Literature." In Top 25 Clinical Case Reports. Avid Science, 2019. http://dx.doi.org/10.29290/tccr.2.4.2019.2-17.

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Neumann, Hartmut P. H., Jijrg Laubenberger, Ulrich Wetterauer,, and Berton Zbar. "von Hippel-Lindau syndrome." In Inherited Disorders of the Kidney. Oxford University PressNew York, NY, 1998. http://dx.doi.org/10.1093/oso/9780192624734.003.0026.

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Abstract von Rippel-Lindau syndrome (VHL) is a cancer-prone inherited disorder of adulthood involv ing many organs and organ systems (Figs 26.1 and 26.2, Table 26.1). The reported prevalence in different populations was 1: 38000-1: 53000 (Maher et al. 1991; Neumann and Wiestler 1991). The disease predominantly affects the eyes (retinal angiomatosis), central nervous system (hae mangioblastoma of the cerebellum, brainstem, and spinal cord), adrenal glands and paraganglia (phaeochromocytoma), kidneys (renal cysts, renal cell carcinoma), and pancreas (pancreatic cysts). Rare manifestations involv

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