Spontaneous adrenal hemorrhage after rupture of adenoma: case report and review of 78 cases

Introduction: Spontaneous adrenal hemorrhage (SAH) in the absence of trauma or anticoagulant therapy is rare. This entity presents an insidious clinical picture, making diagnosis difficult and treatment challenging. We present a case of SAH and a review of 78 related cases. Case presentation: A 32-year-old previously healthy woman presented with sudden, severe lower back pain and nonspecific symptoms resembling a urinary tract infection. After imaging studies, an SAH was detected. Due to persistent hemorrhage and abdominal tenderness, she underwent emergency surgical treatment, which showed a ruptured adrenal capsule caused by an adrenal tumor. Malignancy was ruled out, and an adrenal adenoma was identified as the cause. Our review of 78 cases of SAH found a predominance in men ( n = 33, 53%) with unilateral hemorrhage ( n = 57, 86%). The leading etiology was primary adrenal tumors ( n = 26, 40%), and most cases were treated with adrenalectomy. The overall mortality rate was 8%. Clinical discussion: This case highlights the importance of recognizing SAH as a differential diagnosis in patients with atypical clinical presentations. Furthermore, it highlights the importance of early detection, the necessity of timely surgical intervention, and the need for close follow-up to assess adrenal function and monitor clinical progress. Conclusions: SAH is a rare and potentially life-threatening condition. It can present as a surgical emergency and may be caused by an adrenal adenoma. Early identification is crucial to prevent complications.

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Publication Details

Journal
International Journal of Surgery Case Reports
Published
2026-03-03
DOI
https://doi.org/10.1097/rc9.0000000000000186
Primary Topic
Adrenal and Paraganglionic Tumors
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article
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article

Spontaneous adrenal hemorrhage after rupture of adenoma: case report and review of 78 cases

Jair Diaz-Martinez, Mario Alberto Reza-Salgado, Samantha Avonce-Soriano, Juan Arturo Hernández-Gámez et al.
International Journal of Surgery Case Reports
Adrenal and Paraganglionic Tumors
article

Spontaneous adrenal hemorrhage after rupture of adenoma: case report and review of 78 cases

Jair Diaz-Martinez, Mario Alberto Reza-Salgado, Samantha Avonce-Soriano, Juan Arturo Hernández-Gámez, Aldo Cárdenas-Ziga
article en

Abstract

Introduction: Spontaneous adrenal hemorrhage (SAH) in the absence of trauma or anticoagulant therapy is rare. This entity presents an insidious clinical picture, making diagnosis difficult and treatment challenging. We present a case of SAH and a review of 78 related cases. Case presentation: A 32-year-old previously healthy woman presented with sudden, severe lower back pain and nonspecific symptoms resembling a urinary tract infection. After imaging studies, an SAH was detected. Due to persistent hemorrhage and abdominal tenderness, she underwent emergency surgical treatment, which showed a ruptured adrenal capsule caused by an adrenal tumor. Malignancy was ruled out, and an adrenal adenoma was identified as the cause. Our review of 78 cases of SAH found a predominance in men ( n = 33, 53%) with unilateral hemorrhage ( n = 57, 86%). The leading etiology was primary adrenal tumors ( n = 26, 40%), and most cases were treated with adrenalectomy. The overall mortality rate was 8%. Clinical discussion: This case highlights the importance of recognizing SAH as a differential diagnosis in patients with atypical clinical presentations. Furthermore, it highlights the importance of early detection, the necessity of timely surgical intervention, and the need for close follow-up to assess adrenal function and monitor clinical progress. Conclusions: SAH is a rare and potentially life-threatening condition. It can present as a surgical emergency and may be caused by an adrenal adenoma. Early identification is crucial to prevent complications.

International Journal of Surgery Case Reports
Hospital Regional de Alta Especialidad del Bajío (MX)
Good health and well-being
Openalex Percentile: Top 35%
Adrenal and Paraganglionic Tumors
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