The first symptom of adrenocortical carcinoma is a deepening of voice. Some women also experience vaginal bleeding, irregular periods, or swelling of the breasts. However, most men do not show any signs of the disease and initially develop the condition incidentally. A doctor will perform imaging tests and blood tests to confirm the diagnosis. If the tumors are located near the adrenal cortex, surgery may be recommended to remove the tumor.
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Although some men have a genetic predisposition to adrenocortical cancer, the vast majority of cases are sporadic. The cancer is typically diagnosed during childhood and peaks in adulthood. It usually begins as a solitary tumor in children and men. While men tend to have a higher percentage of nonfunctioning tumors, women are more likely to have a functioning adrenocortical gland.
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The disease is atypical of the common adrenocortical tumors. A small percentage of patients with adrenocortical cancer develop atypical symptoms, such as hypertension and unintended weight loss. Other than the atypical signs of the cancer, most patients do not have any recognizable symptoms. A biopsy can be done to rule out a primary diagnosis of adrenocortical cancer.
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Symptoms of adrenocortical cancer are similar in men to those of other types. In women, symptoms of the disease include a deepening of the voice, swelling of the sex organs, and vaginal bleeding. There are no specific signs for men, though. Almost all patients have symptoms of the condition, which can range from vaginal bleeding to irregular menstrual cycles.
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If adrenocortical cancer has spread to other organs, the patient may have no symptoms or asymptomatic disease. In some cases, adrenocortical cancers may be benign, but there are instances when they spread to other organs. The patient may feel thirsty and have decreased energy. But they are usually small. The patient's symptoms and prognosis are dependent on the specific cancer.
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Men with adrenocortical cancers are rare and do not cause symptoms. There are no specific signs and symptoms. Most adrenocortical cancer is not a life-threatening condition, but if you have any of the symptoms listed above, you should visit a doctor as soon as possible. While the tumors are benign, the symptoms of adrenocortical carcinomas may not be. Moreover, the cancer is sometimes difficult to detect.
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The disease may also affect the adrenal glands. There are several types of adrenocortical tumors. The most common type is nonfunctioning, but can still be fatal. In addition to the cancer, there are also gastrointestinal disorders and neurological disorders. The tumors may even spread to the bones or other organs. If a cellular cancer in your adrenocortical gland is suspected, a doctor will examine it to determine whether it is a primary or secondary tumor.
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Adenomas are the most common type of adrenocortical tumor. The tumors are less than four centimeters in diameter. Most patients have adenomas that do not affect the adrenal glands. The cancer is inoperable and has no symptoms, but it may affect the adrenals. Various treatments may be necessary. The cancer is asymptomatic.
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The symptoms of adrenocortical cancer vary from person to person. In men, the condition may be accompanied by a deepening of the voice or chest pain. In women, the enlarged breasts and abdominal pain can also be signs of adrenocortical carcinoma. In women, the cancer may result in abnormal menstrual periods and vaginal bleeding. In either case, a doctor will need to determine whether the adenomas are malignant.
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Other symptoms of adrenocortical cancer may include abdominal pain, or a lump in the abdomen. Unlike in men, these symptoms are not indicative of adrenocortical carcinoma, but are indicators of the disease. It can be detected in its early stages with a PET or MIBG scan. If the cancer is nonfunctioning, there are no symptoms.
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Adrenocortical cancer symptoms can occur in both men and women. The symptoms of adrenocortical cancer may include excess facial and body hair growth, weight gain, and fluid retention. The symptoms of adrenocoriasis may be difficult to diagnose in a woman because she is more vulnerable to the disease. The adrenocortical tumor is usually found on an imaging test, but it can also be detected in other ways.
