Spontaneous Splenic Artery Rupture as the First Symptom of Systemic Amyloidosis
Author(s) -
Øyvind Bruserud,
Tor Henrik Anderson Tvedt,
Aymen Ahmed,
Olav Karsten Vintermyr,
Tor Hervig,
Anne Berit Guttormsen,
Håkon Reikvam
Publication year - 2021
Publication title -
case reports in critical care
Language(s) - English
Resource type - Journals
eISSN - 2090-6439
pISSN - 2090-6420
DOI - 10.1155/2021/6676407
Subject(s) - medicine , amyloidosis , dyscrasia , shock (circulatory) , spleen , splenic artery , laparotomy , coagulopathy , surgery , pathology , plasma cell , bone marrow
Spontaneous splenic rupture is a life-threatening condition leading to a rapidly progressing hypovolemic shock due to intra-abdominal blood loss, with a mortality rate of about 10%. Spontaneous splenic rupture can be caused by widely different disorders including acute and chronic infections, neoplastic disorders, and inflammatory noninfectious disorders. In this case report, we present a 67-year-old male patient with hemorrhagic shock caused by an acute bleeding from the splenic artery. The patient was massively transfused with blood products and fluids and underwent laparotomy for hemostatic control and clinical stabilization. Multiorgan involvement by amyloid light-chain amyloidosis (AL-amyloidosis) caused by plasma cell dyscrasia, specifically with infiltration of the spleen artery, was found to be the underlying cause of his life-threatening bleeding. Based on this case, we discuss the features of serious spleen bleeding, massive transfusion therapy in the intensive care setting, and AL-amyloidosis pathophysiology and treatment.
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