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By Martínez-Muñoz Elsa, Baena-Del Valle Javier, Barrios-Barreto Rina, Herrera-Lomonaco Sandra, Redondo-Bermúdez César and Miranda-Marzola María del Carmen


Introduction: amyloidosis is the extracellular accumulation of amyloid material,\ud which causes damage in the functioning of organs and tissues. It is characterized\ud by the presence of protein folding, which acquire the capacity of self-assembly\ud creating unusual configurations.\ud Case reports: the case reports of two female patients are presented. Both with\ud 47 years of age, who died without clinical diagnosis. Due to not evident cause\ud of the deaths, clinical autopsies were carried out. Massive presence of amyloid\ud in different organs was found, which was confirmed with the Congo red staining\ud method and the assessment in the polarized light microscopy. Multiple organ\ud dysfunction syndromes secondary to the presence of systemic amyloidosis was\ud diagnosed and in both patients was considered as the cause of death.\ud Conclusion: the clinical symptoms of the amyloidosis are variable and nonspecific,\ud depending of the extracellular deposits and its location in the body. It\ud is a challenge to do a diagnosis. It is recommended to consider the diagnostic\ud possibility of the amyloidosis in patients with suggestive symptoms of damage\ud in the function of the organ and it is required the histological confirmation. Rev.\ud cienc.biomed. 2014;5(1):123-129\ud KEYWORDS\ud Amyloid, Amyloid beta-protein precursor, Amyloidosis, Autopsy

Topics: Amyloid, Amyloid beta-protein precursor, Amyloidosis, Autopsy, Medicine (General), R5-920, Medicine, R
Publisher: Universidad de Cartagena
Year: 2014
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