Skok P, Knehtl M, Ceranić D, Glumbić I
Department of Gastroenterology and Endoscopy, Maribor University Hospital, Maribor, Slovenia.
Z Gastroenterol. 2009 Mar;47(3):292-5. doi: 10.1055/s-2008-1027628. Epub 2009 Mar 11.
Splenic rupture and hemorrhage into the abdominal cavity is an extremely unusual and rare complication of internal disease. Hemopathies, inflammatory or infiltrative diseases affecting the spleen are possible causes for such a complication. Splenomegaly is a factor, which may significantly increase the risk of rupture.
The authors present the case of a 52-year-old patient with established systemic amyloidosis. In the past he had received treatment for undefined hepatic disease and anemia, which was established during the treatment of pathological vertebral fractures. Unfortunately, during the initial treatment he did not consent to a liver biopsy, which would have determined the etiology of the disease. Systemic infiltrative disease, affecting the spleen and other organs, was confirmed posthumously. Described are those forms of amyloidosis which usually represent an unfavorable course of the disease.
Presented is a patient with a rare form of primary amyloidosis and fatal complication, spleenic rupture.
脾破裂并腹腔内出血是一种极为罕见的内科疾病并发症。血液系统疾病、影响脾脏的炎症或浸润性疾病可能是导致这种并发症的原因。脾肿大是一个因素,它可能会显著增加破裂风险。
作者介绍了一名52岁患有系统性淀粉样变性病的患者。过去,他曾接受过针对不明肝病和贫血的治疗,贫血是在病理性椎体骨折治疗期间确诊的。遗憾的是,在初始治疗期间,他不同意进行肝活检,而肝活检本可确定疾病的病因。死后证实存在影响脾脏和其他器官的系统性浸润性疾病。文中描述了那些通常代表疾病不良病程的淀粉样变性形式。
本文介绍了一名患有罕见原发性淀粉样变性形式及致命并发症——脾破裂的患者。