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Case reports

Mesenteric Arterial Thrombosis Revealing Relapse of Nephrotic Syndrome in Young Women

, ORCID Icon, ORCID Icon, , ORCID Icon, , & show all
Pages 633-639 | Received 25 May 2023, Accepted 19 Aug 2023, Published online: 29 Sep 2023
 

Abstract

Background

Nephrotic syndrome (NS) is associated with a hypercoagulable state and may be complicated by thrombotic events. Venous thrombosis is well-acknowledged, while arterial thrombosis is rather unusual.

Case Presentation

We present the case of a 20-year-old woman with a 12-year history of idiopathic NS revealed by extensive cerebral venous thrombosis with pulmonary embolism treated with anticoagulation therapy and oral corticosteroid therapy followed by mycophenolate mofetil (MMF). The thrombophilia assessment did not show any abnormalities. The evolution was marked by the occurrence of several NS relapses controlled by oral corticosteroid therapy until 2017. Subsequently, the patient had not presented a relapse of her disease. The anticoagulant treatment and the MMF were therefore stopped. One year later, the patient presented with severe diffuse acute abdominal pain associated with postprandial vomiting and bilateral lower limb edema. Laboratory results confirmed a NS relapse. An abdominal CT scan revealed acute thrombosis of the superior mesenteric artery with acute mesenteric ischemia. Intraoperative exploration showed mesenteric ischemia with extensive necrosis of the small intestine making their resections incompatible with life. The patient died after 48 hours.

Conclusion

Mesenteric arterial thrombosis, which is a rare but life-threatening NS complication, should always be considered, especially in the case of acute non-specific digestive symptoms.

Abbreviations

NS, nephrotic syndrome; MMF, mycophenolate mofetil.

Acknowledgment

We express our gratitude to the staff of the department of Pediatrics of Charles Nicolle Hospital who were involved in the patient’s care.

Statement of Ethics: Ethical approval is not required for this study in accordance with local or national Guidelines. Written informed consent for publication of clinical details and accompanying images was obtained from the family of the patient (parents).

Author Contributions

All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis, and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.

Disclosure

The authors have no conflicts of interest to declare for this work.

Additional information

Funding

The authors declared that no funding was involved in supporting this work.