ArticleCureus2025
Bilateral Spontaneous Renal Hematoma or Wünderlich Syndrome: A Rare and Life-Threatening Clinical Entity.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Wünderlich syndrome (WS) is an unusual clinical condition defined by spontaneous perirenal space hemorrhage or subcapsular renal hemorrhage without antecedent of traumatic history, often triggered by various factors. It manifests mainly as abdominal pain and fever. As the signs and symptoms are nonspecific, imaging studies are essential for diagnosing and ruling out differential diagnoses. We present a case of a 42-year-old female with no previous pathological or traumatic history, who was admitted with abdominal pain and episodes of fever, attributed to bilateral spontaneous renal hematomas. We conducted a comprehensive clinical history to rule out metabolic, autoimmune, infectious, traumatic, or congenital factors. Laboratory tests for autoimmune, infectious, coagulation, and metabolic causes were all negative. An abdominal contrast-enhanced computed tomography revealed a bilateral renal hemorrhage, ruling out other abdominal causes of pain and confirming a bilateral WS. The patient underwent fluoroscopy-guided drainage and biopsy because we did not have an accurate diagnosis based on the imaging reports, which indicated either pure hematomas or renal abscesses. We ruled out any tumoral or infectious process with the drainage samples. After a thorough consideration and elimination of all possible causes, we arrived at the diagnosis of an idiopathic bilateral WS, an infrequent medical occurrence.
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