Adrenocortical Carcinoma Signs & Symptoms
Adrenocortical carcinoma (ACC) is a rare and aggressive cancer originating in the adrenal glands, which are small endocrine glands located on top of each kidney. Recognizing the diverse and often subtle adrenocortical carcinoma symptoms is crucial for early detection and improved outcomes.

Key Takeaways
- ACC symptoms are often varied, stemming from either excessive hormone production or the physical presence of a growing tumor.
- Common non-specific symptoms include persistent fatigue, weakness, and unexplained weight changes.
- Hormone-related manifestations, such as Cushing’s syndrome (excess cortisol) or androgen excess (virilization), are significant signs of adrenal gland cancer.
- Physical symptoms like abdominal pain, fullness, or flank discomfort can arise as the tumor grows and presses on surrounding structures.
- Due to their gradual onset and non-specific nature, early signs of adrenocortical carcinoma can be challenging to identify, emphasizing the importance of medical evaluation for persistent or worsening symptoms.
Common Adrenocortical Carcinoma Symptoms
Many of the initial adrenocortical carcinoma symptoms are non-specific, making them easy to overlook or attribute to other less serious conditions. However, their persistence and progressive nature warrant medical attention, especially when multiple symptoms appear concurrently. These general indicators often reflect the body’s systemic response to the disease or early metabolic disturbances.
Fatigue and Weakness
Persistent and profound fatigue is a common complaint among individuals with ACC. This isn’t merely tiredness from a busy day but an overwhelming lack of energy that doesn’t improve with rest. The underlying causes can be multifaceted, including the metabolic demands of a growing tumor, hormonal imbalances (such as altered cortisol levels), and the body’s inflammatory response to cancer. This chronic fatigue often significantly impacts daily activities and quality of life, serving as an important, albeit non-specific, indicator of potential underlying health issues.
Unexplained Weight Changes
Significant and unintentional weight changes can be a red flag for various cancers, including ACC. Some individuals may experience unexplained weight loss, often due to the tumor consuming energy and altering metabolism, leading to a state of cachexia. Conversely, others might exhibit weight gain, particularly if the tumor is producing excessive cortisol, leading to manifestations similar to Cushing’s syndrome. This weight gain typically involves central obesity, with increased fat around the abdomen and face, rather than a generalized increase. The key is that these changes occur without intentional dietary or lifestyle modifications.
Hormone-Related Signs of Adrenal Gland Cancer
The adrenal glands are vital endocrine organs responsible for producing various hormones, including cortisol, aldosterone, and androgens. A significant proportion of ACCs (approximately 60-80%, according to medical literature) are “functional,” meaning they produce an excess of one or more of these hormones, leading to distinct signs of adrenal gland cancer. These hormonal imbalances often provide the most specific clues for diagnosis.
Cushing’s Syndrome Manifestations
When an ACC produces excessive cortisol, it leads to Cushing’s syndrome. This condition presents with a characteristic set of symptoms that can be quite striking. Common manifestations include a rounded, “moon face,” a fat pad between the shoulders known as a “buffalo hump,” and central obesity with thin arms and legs. Other signs include fragile skin that bruises easily, purple stretch marks (striae) on the abdomen, high blood pressure, elevated blood sugar levels (diabetes), muscle weakness, and mood changes. Recognizing these specific features is crucial for identifying potential symptoms of ACC in adults, as Cushing’s syndrome is a prominent presentation in many functional ACC cases.
Androgen Excess (Virilization)
Some ACCs produce an excess of androgens (male hormones), leading to virilization, particularly noticeable in females and pre-pubertal males. In adult females, symptoms can include hirsutism (excessive growth of coarse body hair in a male pattern), deepening of the voice, male-pattern baldness, acne, and menstrual irregularities or amenorrhea (absence of menstruation). In young boys, androgen excess can cause precocious puberty, characterized by early development of pubic hair, increased muscle mass, and rapid growth. While less obvious in adult males due to naturally high androgen levels, these changes are significant adrenocortical carcinoma diagnosis symptoms in other populations and warrant immediate investigation.
Physical Symptoms of Tumor Growth
Beyond hormonal effects, the physical presence and growth of an adrenocortical carcinoma can directly cause symptoms as the tumor expands within the abdominal cavity. These mechanical symptoms are often important adrenocortical carcinoma diagnosis symptoms, especially for non-functional tumors that do not produce excess hormones. As the tumor increases in size, it can exert pressure on nearby organs and structures, leading to localized discomfort and other noticeable changes.
Abdominal Pain and Fullness
As an ACC grows, it can become large enough to cause noticeable abdominal symptoms. Patients may experience persistent or intermittent abdominal pain, which can range from a dull ache to more severe discomfort. This pain often results from the tumor pressing on adjacent organs, nerves, or the capsule of the adrenal gland itself. A feeling of abdominal fullness, bloating, or a palpable mass in the abdomen can also occur. In some cases, the tumor may be felt during a physical examination, particularly if it has reached a substantial size. These physical indicators are critical for identifying potential signs of adrenal gland cancer.
Flank or Back Discomfort
Given the location of the adrenal glands high in the abdomen, near the kidneys and spine, a growing ACC can cause discomfort or pain in the flank or back region. This pain may be localized to one side, corresponding to the affected adrenal gland, and can sometimes radiate. The discomfort can arise from the tumor directly invading surrounding tissues, stretching the adrenal capsule, or pressing on nearby nerves. This symptom, while not exclusive to ACC, becomes particularly concerning when it is persistent, unexplained, and accompanied by other general or hormone-related symptoms, prompting further investigation into what are ACC symptoms in a broader context.
Recognizing Early Adrenocortical Carcinoma Symptoms
Identifying early signs of adrenocortical carcinoma is often challenging because the initial symptoms are frequently subtle, non-specific, and can mimic those of many other common conditions. The rarity of ACC also means it’s not typically the first diagnosis considered. However, understanding the insidious nature of its onset is key to improving diagnostic timeliness. Paying close attention to persistent or gradually worsening changes in one’s body can be crucial for early intervention.
Subtle Changes in Appearance
Many of the hormonal manifestations of ACC, particularly those related to Cushing’s syndrome or androgen excess, often begin with very subtle changes in appearance that may go unnoticed or be dismissed initially. For instance, a slight rounding of the face, mild weight gain around the abdomen, or a barely perceptible increase in body hair might be the first indicators. These changes are often so gradual that individuals or their close contacts may not recognize them as significant until they become more pronounced. Learning how to recognize ACC symptoms often involves being attuned to these minor, yet persistent, shifts in one’s physical presentation over time.
Gradual Onset of Symptoms
The symptoms of ACC in adults typically develop slowly over several months, rather than appearing suddenly. This gradual onset contributes significantly to diagnostic delays, as individuals may adapt to the changes or attribute them to aging, stress, or other minor ailments. For example, fatigue might progressively worsen, or abdominal discomfort might slowly become more frequent. It is the persistence and progressive nature of these symptoms, rather than their initial severity, that should raise suspicion. Any unexplained symptom that persists for several weeks or months, especially when combined with other subtle changes, warrants a thorough medical evaluation to rule out serious conditions like adrenocortical carcinoma.
Frequently Asked Questions
What is adrenocortical carcinoma?
Adrenocortical carcinoma (ACC) is a rare and aggressive cancer that originates in the outer layer (cortex) of the adrenal glands. These small glands, located above the kidneys, produce vital hormones. ACC can either produce excessive hormones (functional tumors) or grow without significant hormonal activity (non-functional tumors). Its rarity, with an incidence of about 0.7 to 2 cases per million people per year, often contributes to diagnostic challenges, making awareness of its varied symptoms particularly important for early detection and treatment.
Why are ACC symptoms so varied?
The wide range of ACC symptoms stems from two primary factors: the adrenal gland’s role in hormone production and the physical growth of the tumor. Many ACCs are functional, meaning they overproduce hormones like cortisol or androgens, leading to distinct syndromes such as Cushing’s or virilization. Additionally, as the tumor grows, it can physically press on surrounding organs, causing symptoms like abdominal pain or a palpable mass. The specific hormones produced and the tumor’s size and location determine the unique combination of adrenocortical carcinoma symptoms an individual experiences.
When should I see a doctor for potential ACC symptoms?
You should consult a doctor if you experience any persistent, unexplained symptoms, especially if they are progressive or if you notice a combination of several symptoms mentioned in this article. This includes chronic fatigue, unexplained weight changes, new onset of high blood pressure or diabetes, changes in body hair or voice, or persistent abdominal/flank pain. Given the rarity and aggressive nature of ACC, prompt medical evaluation for concerning symptoms is crucial for early diagnosis and improving treatment outcomes. Do not self-diagnose; seek professional medical advice.







