Adrenal gland cancers are rare but complex tumors that require highly specialized evaluation and treatment. Because the adrenal glands regulate essential hormones that control blood pressure, metabolism, stress response, and electrolyte balance, tumors in these glands can affect multiple organs and body systems. Early diagnosis, proper hormonal assessment, and precise surgical intervention are crucial for achieving the best possible outcomes.
Dr. Lovedeep Singh Chauhan , Consultant Surgical Oncologist in punjab at Max Super Speciality Hospital, Mohali, offers comprehensive evaluation and advanced surgical management for adrenal gland cancers. With expertise in minimally invasive and robotic cancer surgery, he provides evidence-based treatment tailored to each patient’s condition, tumor type, and overall health status.
The adrenal glands are small, triangular-shaped endocrine glands located above each kidney. Despite their small size, they perform vital hormonal functions that influence almost every organ system.
The outer layer produces steroid hormones, including:
The inner part produces catecholamines such as:
These hormones regulate heart rate, blood pressure, and the body’s fight-or-flight response.
Adrenal gland cancer refers to malignant tumors that originate within the adrenal gland. The most common primary adrenal cancer is adrenocortical carcinoma (ACC), though other tumors such as malignant pheochromocytoma may arise from the adrenal medulla. In some cases, cancers from other organs such as the lung, kidney, or melanoma may spread (metastasize) to the adrenal glands.
Because adrenal cancer is rare, it requires management by a surgical oncologist experienced in endocrine malignancies and complex abdominal surgeries.
Adrenal tumors may be benign (non-cancerous) or malignant (cancerous). A detailed evaluation helps distinguish between them.
ACC is a rare but aggressive cancer arising from the adrenal cortex. It may produce excess cortisol or other hormones, or it may be non-functioning. Early-stage ACC can be curable with complete surgical removal.
Pheochromocytomas arise from the adrenal medulla and often produce excessive catecholamines. While most are benign, a small percentage are malignant. These tumors can cause severe fluctuations in blood pressure and require careful preoperative preparation.
With increasing use of CT and MRI scans, many adrenal tumors are detected incidentally during imaging for unrelated conditions. Most are benign, but tumors larger than 4–6 cm or hormonally active lesions require surgical consideration.
The adrenal glands are a common site for metastasis from cancers such as lung carcinoma, renal cell carcinoma, and melanoma. Surgical removal may be considered in selected patients when disease is limited.
The presentation of adrenal cancer varies depending on whether the tumor produces hormones.
Patients may experience:
These symptoms often result from excess cortisol (Cushing’s syndrome) or catecholamines.
Some tumors do not produce hormones and may present with:
Because symptoms may be subtle, early imaging and endocrine evaluation play a critical role in diagnosis.
A comprehensive diagnostic workup is essential before initiating treatment.
Contrast-enhanced CT scan of the abdomen is the primary imaging modality for evaluating adrenal masses. It helps determine tumor size, characteristics, and invasion into nearby structures. MRI may provide further characterization, especially in hormonally active tumors. PET-CT scans are used in selected cases to assess metastasis or recurrence.
Because adrenal tumors may produce excess hormones, laboratory tests include:
Proper hormonal assessment is critical, especially before surgery, to prevent life-threatening complications.
Adrenal biopsy is rarely required and is usually reserved for suspected metastatic disease where imaging is inconclusive.
Surgery remains the cornerstone of treatment for most adrenal cancers.
Adrenalectomy involves removal of the affected adrenal gland. The approach depends on tumor size, location, and suspicion of invasion.
Laparoscopic and robotic adrenalectomy are preferred for appropriately selected tumors. Benefits include:
For large tumors or those invading surrounding organs, an open surgical approach may be required to achieve complete tumor clearance.
Dr. Lovedeep Singh Chauhan specializes in advanced minimally invasive cancer surgery, ensuring oncological safety while promoting quicker recovery.
Adrenal cancer management often requires coordination between:
At Max Super Speciality Hospital, Mohali, patients benefit from a multidisciplinary tumor board approach where individualized treatment plans are formulated.
Recovery varies depending on the surgical approach and tumor type. Most patients undergoing minimally invasive adrenalectomy are discharged within 2–4 days. Light activities can usually be resumed within two weeks.
Patients with hormonally active tumors may require temporary steroid supplementation after surgery. Regular follow-up is essential to monitor hormone levels and detect recurrence early.
The prognosis of adrenal gland cancer depends on several key factors:
Adrenal gland cancers require not only surgical skill but also deep understanding of endocrine physiology and oncological principles. Dr. Lovedeep Singh Chauhan brings extensive experience in managing complex abdominal and endocrine malignancies.
Trained in Surgical Oncology from premier institutions, he performs both laparoscopic and robotic cancer surgeries with precision and adherence to oncological safety standards.
Every treatment decision is based on established guidelines and individualized assessment. Patients receive clear explanations regarding risks, benefits, and expected outcomes.
From diagnosis to postoperative recovery and long-term surveillance, patients receive coordinated care under one roof at Max Super Speciality Hospital, Mohali.