Zobrazeno 1 - 10
of 192
pro vyhledávání: '"gastrointestinal amyloidosis"'
Autor:
Giuseppe Davide Albano, Stefania Zerbo, Simone Di Franco, Elisabetta Orlando, Eleonora Formisano, Antonina Argo, Beatrice Belmonte
Publikováno v:
Forensic Sciences, Vol 4, Iss 3, Pp 453-462 (2024)
Amyloidosis is defined as a rare group of 30 protein-folding diseases characterized by the extracellular deposition of a specific soluble precursor protein that aggregates in the form of insoluble fibrils. The gastrointestinal tract (GI) is a common
Externí odkaz:
https://doaj.org/article/bc9caa25efe642b28d0657676bc98bb1
Autor:
Sandica Bucurica, Andreea-Simona Nancoff, Miruna Valeria Moraru, Ana Bucurica, Calin Socol, Daniel-Vasile Balaban, Mihaela Raluca Mititelu, Ionela Maniu, Florentina Ionita-Radu, Mariana Jinga
Publikováno v:
Biomedicines, Vol 12, Iss 11, p 2630 (2024)
Amyloidosis is a group of diseases characterized by the extracellular deposition of abnormally folded, insoluble proteins that lead to organ dysfunction. While it commonly affects the cardiovascular system, gastrointestinal (GI) tract involvement is
Externí odkaz:
https://doaj.org/article/35cbfcfbec9e45dba869694109b192cf
Autor:
Sameer Abdul Rauf, Hussain Haider Shah, Rahul Khatri, Mansoor Ul Haq, Tirth Dave, Javaria Parwez Ali, Syed Khizar Ali
Publikováno v:
Clinical Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Key Clinical Message This case highlights the importance of considering tuberculosis as an underlying cause of gastrointestinal amyloidosis, even in patients previously treated for the infection. Clinicians should maintain a high index of suspicion f
Externí odkaz:
https://doaj.org/article/d879160feaf24fcb8ede1c95c421e2e1
Akademický článek
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Publikováno v:
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Gastrointestinal (GI) amyloidosis is a rare complication of multiple myeloma (MM). Due to its nonspecific clinical presentation and endoscopic appearance, an early and accurate diagnosis of GI amyloidosis is difficult. Here, we re
Externí odkaz:
https://doaj.org/article/881ecb23b2b442af916295b8fc8e51d4
Publikováno v:
Case Reports in Gastroenterology, Vol 13, Iss 3, Pp 462-467 (2019)
Amyloidosis of the gastrointestinal tract is an uncommon disorder characterized by the extracellular deposition of an abnormal fibrillar protein. It is rarely proven by biopsy. Amyloid deposition interferes with organ structure and its function. We r
Externí odkaz:
https://doaj.org/article/60c9b96b3f38400fa74b063496a727f1
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Satoshi Fukai, Suguru Hayase, Atsushi Ozeki, Yuya Maruyama, Hisahito Endo, Taisuke Ito, Yoshimasa Ishii, Koji Kono
Publikováno v:
福島医学雑誌. 73(1):7-11
本邦では消化管アミロイドーシスと非閉塞性腸管虚血(non-occlusive mesenteric ischemia ;以下,NOMI と略記)の併発例が数例報告されており,消化管へのアミロイド沈着がNOMIの危険因子となる
Autor:
Toshiro Fukui, Yuji Tanimura, Yasushi Matsumoto, Shunsuke Horitani, Takashi Tomiyama, Kazuichi Okazaki
Publikováno v:
Case Reports in Gastroenterology, Vol 12, Iss 3, Pp 737-746 (2018)
Amyloid light-chain (AL) amyloidosis is associated with plasma cell disorder and monoclonal light chains. This type of amyloidosis is the prominent type involving the gastrointestinal tract. Monoclonal gammopathy of undetermined significance (MGUS) i
Externí odkaz:
https://doaj.org/article/7eaa79c502d446deb5cdc73699f721f3
Publikováno v:
Case Reports in Gastroenterology, Vol 12, Iss 2, Pp 317-321 (2018)
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition of nonbranching fibrils in various tissues, ultimately leading to a variety of clinical presentations including isolated or multiorgan dysfunction. Amy
Externí odkaz:
https://doaj.org/article/bf13f61c41444b99b0b641d017c3186e