Gastrointestinal amyloidosis occurring in three different patterns: Case serie
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Dosyalar
Tarih
2019
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
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Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Systemic amyloidosis is a rare disease characterized by extracellular accumulation of amyloid protein in one or more organs. In
patients with systemic amyloidosis, the most frequently affected organs are kidney and heart, followed by the nervous system,
soft tissues, and lungs. Small bowel and liver involvement are also frequent in systemic amyloidosis. Gastrointestinal (GI) findings
are common, and the degree of organ involvement determines the symptoms. Patients usually have nonspecific findings such
as abdominal pain, nausea, diarrhea, and dysphagia, which may delay the appropriate diagnosis. Liver involvement occurs in the
majority of patients, but the symptoms typically do not happen unless a marked hepatic amyloid deposition occurs. Diagnosis is by
tissue biopsy. Treatment and prognosis depend on the underlying disease. GI system involvement is a sign of poor prognosis. In this
case series, five patients who were diagnosed with gastrointestinal system amyloidosis in our clinic are presented.
Açıklama
Anahtar Kelimeler
Kaynak
Annals of Medical Research
WoS Q DeÄŸeri
Scopus Q DeÄŸeri
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Künye
Riza Caliskan, A., Furkan Cagin, Y., Bilgic, Y., Yildirim, O., Ali Erdogan, M., Seckin, Y., Alan, S., & Karadag Soylu, N. (2021). Gastrointestinal amyloidosis occurring in three different patterns: Case serie . Annals of Medical Research
