A Rare Case of Haemoperitoneum Secondary to Spontaneous Splenic Rupture in a Patient with AL Amyloidosis

Jayalakshmi Manjunath, Pooja Chandrakant Patil, P. Venkategowda, Rakshith Katikere Sudarshan
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引用次数: 0

Abstract

Haemoperitoneum due to spontaneous splenic rupture is a rare condition. We present a case of AL-type amyloidosis and chronic kidney disease (CKD) who is presented with diffuse abdominal pain. A contrast-enhanced CT scan of the abdomen revealed moderate to large amounts of free fluid in the peritoneum, indicating splenic rupture causing haemoperitoneum. The patient underwent emergency exploratory laparotomy and splenectomy. After the operation, the patient was closely monitored in the ICU and was transferred to the ward on postoperative day 3. He was discharged home on day 6. This case report highlights a rare occurrence of haemoperitoneum secondary to spontaneous splenic rupture in a patient with AL amyloidosis.
AL 淀粉样变性患者自发性脾破裂继发腹腔积血的罕见病例
自发性脾破裂引起的腹腔积血是一种罕见病。我们报告了一例因弥漫性腹痛而就诊的 AL 型淀粉样变性和慢性肾脏病(CKD)患者。腹部对比增强 CT 扫描显示腹腔内有中量至大量游离液体,表明脾破裂导致腹腔积血。患者接受了急诊剖腹探查术和脾脏切除术。术后,患者在重症监护室接受了严密监护,并于术后第 3 天转入病房。术后第 6 天,患者出院回家。本病例报告重点介绍了一名 AL 淀粉样变性患者因自发性脾破裂导致腹腔积血的罕见病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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