Bibliografías temáticas / Cystic angiomatosis radiology

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Literatura académica sobre el tema "Cystic angiomatosis radiology"

Autor: Grafiati
Publicado: 7 de junio de 2025
Última modificación: 2 de agosto de 2025

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Artículos de revistas sobre el tema "Cystic angiomatosis radiology"

1

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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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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4

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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5

Cohen, M. D., B. Rougraff, and P. Faught. "Cystic angiomatosis of bone: MR findings." Pediatric Radiology 24, no. 4 (1994): 256–57. http://dx.doi.org/10.1007/bf02015448.

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6

Vanhoenacker, F. M., A. M. De Schepper, H. De Raeve, and Z. Berneman. "Cystic angiomatosis with splenic involvement: unusual MRI findings." European Radiology 13, S6 (2003): L35—L39. http://dx.doi.org/10.1007/s00330-002-1805-4.

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7

Levey, David S., L. M. MacCormack, David J. Sartoris, Parviz Haghighi, Donald Resnick, and Roger Thorne. "Cystic angiomatosis: case report and review of the literature." Skeletal Radiology 25, no. 3 (1996): 287–93. http://dx.doi.org/10.1007/s002560050082.

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8

Ishida, Tsuyoshi, Howard D. Dorfman, German C. Steiner, and Alex Norman. "Cystic angiomatosis of bone with sclerotic changes mimicking osteoblastic metastases." Skeletal Radiology 23, no. 4 (1994): 247–52. http://dx.doi.org/10.1007/bf02412356.

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9

Joshi, Anagha R., Kiran Kulkarni, and Ankita U. Shah. "Labrune Syndrome: A Very Rare Association of Leukoencephalopathy, Cerebral Calcifications, and Cysts." Indian Journal of Radiology and Imaging 31, no. 03 (2021): 772–75. http://dx.doi.org/10.1055/s-0041-1736398.

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AbstractLeukoencephalopathy, cerebral calcifications, and cysts (LCC) form a very rare association which is named as “Labrune syndrome” after Labrune who reported the first case in 1996. To the best of our knowledge only eight to 10 cases have been reported in literature to date. We report a case of a 26-year-old male with onset of neurological symptoms in late adolescence (at 19 years of age) and presented with complains of continued seizures for 7 years, giddiness with imbalance, and slowly progressive motor symptoms. MRI brain revealed multiple calcifications in bilateral basal ganglia, cer
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10

Janevska, Vesna, Vlado Janevski, Oliver Stankov, Liljana Spasevska, Slavica Kostadinova-Kunovska, and Julija Zhivadinovik. "Non-Tumor Cystic Lesions of the Adrenal Gland." PRILOZI 36, no. 3 (2015): 51–59. http://dx.doi.org/10.1515/prilozi-2015-0078.

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Abstract Adrenal cystic lesions are uncommon but due to the improved radiologic imaging techniques their appearance seems to increase. Material and Methods: We analyzed the clinical and radiological findings of 10 patients with adrenal cysts and the pathological features of the operative material. Standard dissection procedure and paraffin embedded tissue sections were made, stained by HE and immunohistochemically with CD34, CD 31, Factor 8, Podoplanin, CKWS and AE1/AE3 Results: The mean age of the patients was 40.6 years; female to male ratio was 2.3:1. All the cysts were diagnosed as cystic
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