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Updated: Feb 17, 2026

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
[A Case of Adrenal Leiomyosarcoma]
Ayumu Taniguchi1, Takeshi Ujike1, Kazutoshi Fujita1
1The Department of Urology, Osaka University Graduate School of Medicine.
A rare adrenal leiomyosarcoma, initially suspected as adrenocortical carcinoma, was diagnosed in a 61-year-old man presenting with abdominal pain. Surgical excision confirmed the diagnosis, with no recurrence observed during 16 months of follow-up.
Area of Science:
- Oncology
- Radiology
- Pathology
Background:
- Adrenal masses require accurate diagnosis to differentiate between benign and malignant conditions.
- Imaging modalities like CT and MRI are crucial for characterizing adrenal lesions.
- Positron emission tomography (PET) can aid in assessing metabolic activity of adrenal tumors.
Observation:
- A 61-year-old male presented with abdominal pain and a 7 cm left adrenal mass on enhanced CT and MRI.
- The mass exhibited heterogeneous enhancement and abnormal fluorodeoxyglucose (FDG) uptake on PET scan.
- No endocrinological abnormalities were detected preoperatively.
Findings:
- Preoperative diagnosis suggested left adrenocortical carcinoma (cT2N0M0).
- Pathological examination of the resected specimen revealed leiomyosarcoma of the adrenal gland.
- The patient remained disease-free with no local recurrence or metastasis at 16 months post-surgery.
Implications:
- This case highlights the importance of considering rare adrenal tumors beyond adrenocortical carcinoma.
- Accurate pathological diagnosis is essential for appropriate treatment and patient management.
- Successful surgical management of adrenal leiomyosarcoma can lead to favorable long-term outcomes.
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