Zobrazeno 1 - 10
of 498
pro vyhledávání: '"gorham-stout disease"'
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5066-5070 (2024)
Gorham-Stout disease is a rare condition characterized by the massive osteolysis replaced with vascular or lymphatic proliferation and fibrous tissue. We report the case of a 13-year-old boy complaining of occasional lower back pain. Spinal X-ray sho
Externí odkaz:
https://doaj.org/article/93081a22c2db47229ef4793f692b1afc
Publikováno v:
Journal of the Korean Society of Radiology, Vol 85, Iss 2, Pp 451-455 (2024)
A 45-year-old male patient with spontaneous chylothorax and osteolysis in the right 1st and 2nd ribs was diagnosed with Gorham–Stout disease based on clinical manifestations and bone biopsy. The chylothorax temporarily decreased after a successfu
Externí odkaz:
https://doaj.org/article/983d3d8a72ef4024a478036cb0488121
Autor:
Michio Ozeki, Saori Endo, Shiho Yasue, Akifumi Nozawa, Ryuta Asada, Akiko M. Saito, Hiroya Hashimoto, Takumi Fujimura, Yohei Yamada, Tatsuo Kuroda, Shigeru Ueno, Shoji Watanabe, Shunsuke Nosaka, Mikiko Miyasaka, Akihiro Umezawa, Kentaro Matsuoka, Takanobu Maekawa, Satoshi Hirakawa, Taizo Furukawa, Shigehisa Fumino, Tatsuro Tajiri, Junkichi Takemoto, Ryota Souzaki, Yoshiaki Kinoshita, Akihiro Fujino
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionIntractable lymphatic anomalies (LAs) include cystic lymphatic malformation (LM; macrocystic, microcystic, or mixed), generalized lymphatic anomaly, and Gorham–Stout disease. LAs can present with severe symptoms and poor prognosis. Thus
Externí odkaz:
https://doaj.org/article/75d954cef4394ed4b3e0cce1df803598
Akademický článek
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Autor:
H. Ikrou, A. Ibenyahia, N. Boutbagha, M. Hachmi, M. Makloul, F. Ammor, I. lefquih, M. Maidi, S. Wakrim, O. Halloumi, S. Abdala, H. Serhane
Publikováno v:
Rare, Vol 2, Iss , Pp 100047- (2024)
Complex lymphatic anomalies (CLA) are an extremely rare group of disorders resulting from embryogenic lymphatic malformations that are characterized by overlapping clinical, anatomic location, imaging features, and complications. Due to their low inc
Externí odkaz:
https://doaj.org/article/d01ca347137740c0abb57153bdc90a87
Autor:
Yuna Lee, Seunghyun Lee, Saebeom Hur, Yun Soo Jeong, Dong In Suh, Jangsup Moon, Man Jin Kim, Young Hun Choi, Jung-Eun Cheon
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background To describe the radiological features of Gorham–Stout disease (GSD) as evaluated using plain radiography and dynamic contrast-enhanced magnetic resonance lymphangiography (DCMRL) imaging techniques. Methods Clinical and conventi
Externí odkaz:
https://doaj.org/article/6fdd1346398f43ed935bc9cc9ebeab24
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background Gorham-Stout disease (GSD) is a very rare disorder characterized by massive osteolysis of poorly understood aetiology. The association between GSD involving the skull base and cerebrospinal fluid (CSF) leakage has been reported in
Externí odkaz:
https://doaj.org/article/172eb448c3034d54b7c7a8c94785021c
Autor:
Lorenzo M. Fernandes, Jeffrey Tresemer, Jing Zhang, Jonathan J. Rios, Joshua P. Scallan, Michael T. Dellinger
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Complex lymphatic anomalies (CLAs) are sporadically occurring diseases caused by the maldevelopment of lymphatic vessels. We and others recently reported that somatic activating mutations in KRAS can cause CLAs. However, the mechanisms by which activ
Externí odkaz:
https://doaj.org/article/ba2b069fed614929b94de62055977d42
Akademický článek
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Akademický článek
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