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Background <p>Adrenal haemangiomas are exceptionally rare benign vascular tumours, usually discovered incidentally and measuring only a few centimetres. But in rare cases, lesions exceeding 20&#xa0;kg are distinctly uncommon and pose major diagnostic and operative challenges.</p> Case presentation <p>A 67-year-old woman presented with six months of progressive abdominal distension, early satiety, and exertional dyspnea on a four years background of intermittent left loin pain. Her medical history includes HTN, T2DM, AF and heart failure. No surgical history was reported. Imaging revealed a giant left retroperitoneal mass displacing adjacent viscera. Hormonal evaluation showed hypothyroidism, consistent with a non-functional adrenal lesion. Tumour markers were negative. After multidisciplinary discussion, open trans-abdominal excision was performed. Operative time was 4&#xa0;h 45&#xa0;min with an estimated blood loss of 500 mL. Two units of packed red blood cells and two units of plasma were transfused pre-operatively and the same post-operatively. She underwent midline laparotomy. The tumour, densely adherent to aorta, inferior vena cava and ureter, was removed en‑bloc using meticulous dissection and a radiofrequency scissor. Concomitant umbilical hernia was repaired with a 30 × 30&#xa0;cm pre‑peritoneal polypropylene underlay mesh (5&#xa0;cm overlap). The excised specimen weighed 20.1&#xa0;kg, verified intra-operatively. Histopathology confirmed a cavernous haemangioma without atypia or malignancy. Post-operative recovery was uneventful. Follow-up at two months with ultrasound showed no recurrence.</p> Conclusions <p>Although giant adrenal cavernous haemangioma is benign, it can mimic other retroperitoneal tumours and demands meticulous pre-operative optimisation and multidisciplinary planning. Surgical excision remains the treatment of choice, and structured long-term surveillance is advised.</p>

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A 20.1 kg adrenal cavernous haemangioma presenting as a giant retroperitoneal mass: diagnostic difficulties and operative strategy - a case report

  • 期刊论文

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  • 发表日期：

    2026年2月2日

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  • Ali Taghi,
  • Fares Issa,
  • Ahmad Alhamid,
  • Aya Alayyoubi,
  • Mohammad Atia,
  • Areen Glore,
  • Baraa Basbous

摘要

Background

Adrenal haemangiomas are exceptionally rare benign vascular tumours, usually discovered incidentally and measuring only a few centimetres. But in rare cases, lesions exceeding 20 kg are distinctly uncommon and pose major diagnostic and operative challenges.

Case presentation

A 67-year-old woman presented with six months of progressive abdominal distension, early satiety, and exertional dyspnea on a four years background of intermittent left loin pain. Her medical history includes HTN, T2DM, AF and heart failure. No surgical history was reported. Imaging revealed a giant left retroperitoneal mass displacing adjacent viscera. Hormonal evaluation showed hypothyroidism, consistent with a non-functional adrenal lesion. Tumour markers were negative. After multidisciplinary discussion, open trans-abdominal excision was performed. Operative time was 4 h 45 min with an estimated blood loss of 500 mL. Two units of packed red blood cells and two units of plasma were transfused pre-operatively and the same post-operatively. She underwent midline laparotomy. The tumour, densely adherent to aorta, inferior vena cava and ureter, was removed en‑bloc using meticulous dissection and a radiofrequency scissor. Concomitant umbilical hernia was repaired with a 30 × 30 cm pre‑peritoneal polypropylene underlay mesh (5 cm overlap). The excised specimen weighed 20.1 kg, verified intra-operatively. Histopathology confirmed a cavernous haemangioma without atypia or malignancy. Post-operative recovery was uneventful. Follow-up at two months with ultrasound showed no recurrence.

Conclusions

Although giant adrenal cavernous haemangioma is benign, it can mimic other retroperitoneal tumours and demands meticulous pre-operative optimisation and multidisciplinary planning. Surgical excision remains the treatment of choice, and structured long-term surveillance is advised.