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neuroendocrine tumor

ICD-10 Codes

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Description

What are Neuroendocrine Tumors?

Neuroendocrine tumors (NETs) are a group of uncommon tumors that start in neuroendocrine cells1. These cells have traits similar to both nerve and endocrine cells, allowing them to receive and send messages through hormones to help the body function4.

Types of Neuroendocrine Tumors

Neuroendocrine tumors can occur in various parts of the body, including:

  • The gastrointestinal tract (48%)2
  • Lungs (25%)2
  • Pancreas
  • Other organs

These tumors can grow slowly (indolent) or quickly (aggressive), and may progress to neuroendocrine cancer5.

Characteristics of Neuroendocrine Tumors

Neuroendocrine tumors are rare, slow-growing cancers that often occur without symptoms6. However, some hormonal neuroendocrine symptoms include severe diarrhea, severe gastric ulcers, or uncontrolled blood sugar that responds poorly to treatment3.

Key Points

  • Neuroendocrine tumors start in cells of the neuroendocrine system
  • Can grow slowly (indolent) or quickly (aggressive)
  • May progress to neuroendocrine cancer
  • Often occur without symptoms
  • Hormonal neuroendocrine symptoms include severe diarrhea, gastric ulcers, and uncontrolled blood sugar

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Additional Characteristics

  • Neuroendocrine tumors (NETs) are a group of uncommon tumors that start in neuroendocrine cells.
  • These cells have traits similar to both nerve and endocrine cells, allowing them to receive and send messages through hormones to help the body function.
  • Neuroendocrine tumors can occur in various parts of the body, including: The gastrointestinal tract (48%), Lungs (25%), Pancreas, Other organs.
  • These tumors can grow slowly (indolent) or quickly (aggressive), and may progress to neuroendocrine cancer.
  • Neuroendocrine tumors are rare, slow-growing cancers that often occur without symptoms.
  • Some hormonal neuroendocrine symptoms include severe diarrhea, severe gastric ulcers, or uncontrolled blood sugar that responds poorly to treatment.
  • Neuroendocrine tumors start in cells of the neuroendocrine system.
  • Can grow slowly (indolent) or quickly (aggressive).
  • May progress to neuroendocrine cancer.
  • Often occur without symptoms.
  • Hormonal neuroendocrine symptoms include severe diarrhea, gastric ulcers, and uncontrolled blood sugar.

Signs and Symptoms

Common Signs and Symptoms of Neuroendocrine Tumors

Neuroendocrine tumors (NETs) can exhibit a wide range of symptoms, which vary depending on the location and severity of the tumor. Here are some common signs and symptoms associated with NETs:

  • General symptoms: Extreme fatigue [7], weakness, and weight loss [3, 4]
  • Gastrointestinal symptoms: Diarrhea or constipation, abdominal swelling, nausea, and vomiting [4, 6]
  • Cardiovascular symptoms: Fast or irregular heartbeat, dizziness, and shaking [5, 8]
  • Neurological symptoms: Headache, blurred vision, confusion, anxiety, and tremors [5, 6]
  • Skin symptoms: Flushing of the skin, especially on the face and neck [8]

Specific Symptoms Based on Tumor Location

The symptoms of NETs can also vary depending on their location in the body. For example:

  • Insulinomas: Headaches, dizziness, sweating, confusion, anxiety, trembling, palpitations, eyesight changes, feeling hungry or weak, and fits [6]
  • Carcinoid syndrome: Flushing of the skin, diarrhea, wheezing, abdominal pain, fast or irregular heartbeat, fatigue, low blood pressure, and heart valve problems [2]

When to Seek Medical Attention

If you are experiencing any of these symptoms, it is essential to seek medical attention promptly. Early diagnosis and treatment can significantly improve outcomes for NET patients.

References:

[1] - Not provided in the context [2] - Carcinoid syndrome may include flushing of the skin... [3] - New, growing lump or mass [4] - Other symptoms of a neuroendocrine tumor [5] - Symptoms of functional neuroendocrine tumors [6] - Insulinomas [7] - Symptoms of neuroendocrine tumors (NETs) can vary depending on their location and severity. [8] - flushing of the skin, especially the face and neck

Additional Symptoms

Diagnostic Tests

Diagnostic Tests for Neuroendocrine Tumors

Diagnosing neuroendocrine tumors (NETs) can be a complex process, involving various tests and procedures to determine the location, size, and type of tumor. Here are some of the diagnostic tests used to diagnose NETs:

  • Blood tests: Blood tests can help diagnose some types of NETs by checking for specific biomarkers in the blood. For example, Chromogranin A (CgA) is a blood test used to diagnose NETs [5]. However, it's essential to note that certain medications can interfere with test results [5].
  • Imaging tests: Imaging tests such as ultrasound, computed tomography (CT), and magnetic resonance imaging (MRI) are used to take pictures of the body's anatomy and locate the tumor. For example, endoscopic ultrasonography may be used to diagnose a NET in the pancreas [6].
  • Biopsy: A biopsy involves taking a sample of fluid or tissue from the tumor for examination under a microscope.
  • Laboratory tests: Laboratory tests examine blood, urine, or tumor tissue to determine the type and severity of the tumor.
  • Endoscopic ultrasonography: This test uses an endoscope with a built-in ultrasound probe to visualize the tumor in the pancreas or other organs.

Diagnostic Testing for Neuroendocrine Tumors

Laboratory tests, imaging tests, and biopsies are used to diagnose NETs. These tests can help determine the location, size, and type of tumor [8].

  • Pathology: Pathological examination of tissue samples is essential in diagnosing NETs.
  • Syndrome-specific biochemical testing: This test is used to diagnose specific syndromes associated with NETs.
  • Nonsyndrome-specific biochemical testing: This test is used to diagnose NETs without a specific syndrome.

References

[1] Blood tests can help to diagnose some types of neuroendocrine tumours. You might also have one to check your general health [7]. [2] The tests and procedures you might undergo to diagnose a neuroendocrine tumor will depend on where your tumor is located in your body [3]. [3] For example, they might use endoscopic ultrasonography to diagnose a neuroendocrine tumor in your pancreas. Biopsy: Providers do biopsies to obtain fluid or tissue from the tumor [6]. [4] Diagnostic Testing for Neuroendocrine Tumors · Laboratory tests examine blood, urine, or tumor tissue. · Imaging tests and take pictures of your body's anatomy ( ... ) [8] [5] Chromogranin A (CgA) is a blood test used in the diagnosis of neuroendocrine tumors. Learn which common medications interfere with tests results [5]. [6] For example, they might use endoscopic ultrasonography to diagnose a neuroendocrine tumor in your pancreas. Biopsy: Providers do biopsies to obtain fluid or tissue from the tumor [6] [7] Blood tests can help to diagnose some types of neuroendocrine tumours. You might also have one to check your general health [7]. [8] Diagnostic Testing for Neuroendocrine Tumors · Laboratory tests examine blood, urine, or tumor tissue. · Imaging tests and take pictures of your body's anatomy ( ... ) [8] [9] by MJ Raphael · 2017 · Cited by 134 — How are neuroendocrine tumours diagnosed? · Pathology · Syndrome-specific biochemical testing · Nonsyndrome-specific biochemical testing · Diagnostic imaging [9]

Additional Diagnostic Tests

  • Blood tests
  • Biopsy
  • Laboratory tests
  • Imaging tests
  • Pathology
  • Endoscopic ultrasonography
  • Syndrome-specific biochemical testing
  • Nonsyndrome-specific biochemical testing

Treatment

Treatment Options for Neuroendocrine Tumors

Neuroendocrine tumors (NETs) can be treated with various drug therapies, depending on the type and stage of the cancer. Here are some of the most common treatment options:

  • Somatostatin analogs: These drugs mimic the action of somatostatin, a hormone that helps regulate cell growth. Octreotide is a commonly used somatostatin analog that can help slow down tumor growth and reduce hormone production [3][4].
  • Chemotherapy: Chemotherapy uses strong drugs to kill cancer cells. It can be given through a vein in the arm or taken as a pill, and is often used for fast-growing or advanced NETs [2][4].
  • Targeted therapy: Targeted therapies work by blocking specific molecules that help cancer cells grow. For example, cabozantinib has been shown to improve outcomes in patients with previously treated extra-pancreatic and pancreatic NETs [8].
  • mTOR inhibitors: Everolimus is an mTOR inhibitor that can help slow down tumor growth by blocking a protein called mTOR, which helps regulate cell growth [9].

Timing and Choice of Treatment

The timing and choice of treatment for NETs are critical factors in determining the best course of action. According to experts, effective drug therapy relies on choosing the right treatment at the right time [1]. This may involve using somatostatin analogs as a first-line treatment, followed by chemotherapy or targeted therapy if necessary.

References

[1] Effective drug therapy for neuroendocrine tumors relies on timing and choice. Our experts offer all options, from somatostatin analogs to NET chemotherapy. [2] Chemotherapy uses strong drugs to kill tumor cells. It can be given through a vein in your arm or taken as a pill. Chemotherapy ... [3] Octreotide is a drug that mimics somatostatin and tricks the tumors into halting growth and hormone production. This is the standard initial ... [4] Chemotherapy uses cytotoxic drugs to destroy NET cells. You might have it for a NET that is fast growing or that has spread to other parts of the body. [5] by AD Herrera-Martínez · 2019 · Cited by 84 — Medical treatment options for EAS include: (1) Tumor-directed drugs including somatostatin analogs (octreotide, pasireotide) and dopamine agonists that decrease ... [6] Active surveillance · Surgery · Chemotherapy · Targeted Therapy · Radiation therapy · Peptide radionuclide therapy · Somatostatin analogs · Liver-directed therapies. [7] Aug 22, 2024 — The targeted drugs used to treat pancreatic neuroendocrine tumors (NETs) by blocking angiogenesis (the growth of new blood vessels that nourish ... [8] Oct 22, 2023 — “Cabozantinib significantly improved outcomes in patients with previously treated extra-pancreatic and pancreatic neuroendocrine tumors and may ... [9] Drugs used to treat Neuroendocrine Carcinoma ; Generic name: everolimus systemic; Brand names: Afinitor, Zortress; Drug class: mTOR inhibitors, selective ...

Recommended Medications

💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.

Differential Diagnosis

Understanding Differential Diagnosis in Neuroendocrine Tumors

The differential diagnosis of neuroendocrine tumors (NETs) refers to the process of ruling out other possible conditions that may present with similar symptoms or characteristics. In the context of NETs, differential diagnosis is crucial for accurate diagnosis and treatment.

Key Points:

  • Differential Diagnosis in NETs: The differential diagnosis of NETs involves considering a range of possibilities, including other types of tumors, metastatic disease, and non-neoplastic conditions.
  • Clinical Presentation: The clinical presentation of NETs can vary widely, making differential diagnosis challenging. Symptoms may include abdominal pain, weight loss, diarrhea, or flushing, among others.
  • Imaging Studies: Imaging studies such as CT scans, MRI, or PET scans can help identify the location and extent of the tumor, but may not always distinguish between different types of NETs.
  • Histopathological Examination: Histopathological examination of tissue samples is essential for accurate diagnosis. This involves examining the microscopic appearance of the tumor cells and assessing their differentiation grade.

Differential Diagnosis Considerations:

  • Metastatic Disease: Metastatic disease from other primary tumors, such as breast or lung cancer, can mimic NETs.
  • Other Types of Tumors: Other types of tumors, such as carcinoid tumors or paragangliomas, may present with similar symptoms and imaging characteristics.
  • Non-Neoplastic Conditions: Non-neoplastic conditions, such as inflammatory bowel disease or pancreatitis, can also mimic NETs.

References:

  • [1] The differential diagnosis of neuroendocrine neoplasms of the larynx is broad and includes lesions of epithelial, mesenchymal, and neuroectodermal origin. (Source: 10)
  • [2] Well-differentiated neuroendocrine tumors are typically slow-growing and may be difficult to distinguish from other types of NETs. (Source: 11)
  • [3] Poorly differentiated neuroendocrine tumors are more aggressive and may require different treatment approaches. (Source: 11)

Conclusion

Differential diagnosis in neuroendocrine tumors is a complex process that requires careful consideration of clinical presentation, imaging studies, histopathological examination, and other factors. Accurate differential diagnosis is essential for providing appropriate treatment and improving patient outcomes.

Additional Information

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