J.C is an 82-year-old white man who was evaluated by GI specialist due to abdominal discomfort, loss of appetite, weight lost, weakness and occasional nausea.
Past Medical History (PMH):
Patient is Diabetic, controlled with Metformin 500 mg by mouth twice a day, Lantus 15 units SC bedtime. Hypertensive, controlled with Olmesartan 20 mg by mouth once a day. Atrial Fibrillation, controlled with Rivaroxaban 15 mg by mouth once a day and bisoprolol 10 mg by mouth once a day.
Labs:
Hb 12.7 g/dl; Hct 38.8% WBC 8.2; Glycemia 74mg/dl; Creatinine 0.8 mg/dl; BUN 9.8 mg/dl; AST 21 U/L ALT 17 U/L; Bil T 1.90 mg/dl; Ind 0.69 mg/dl; Dir 1.21 mg/dl.
Diagnostic test:
Endoscopic Ultrasound of the Pancreas. Solid mass in the head of pancreas 4 cms, infiltrating Wirsung duct. The solid mass impress to infiltrate the superior mesenteric vein. Perilesional node is detected, 1.5 cms, metastatic aspect. Fine needle aspiration (FNA) biopsy: Ductal adenocarcinoma.
Case study questions:
- Please name the potential most common sites for metastasis on J.C and why?
- What are tumor cell markers and why tumor cell markers are ordered for a patient with pancreatic cancer?
- Based on the case study described, proceed to classify the tumor based on the TNM Stage classification. Why this classification important?
- Discussed characteristic of malignant tumors regarding it cells, growth and ability to spread.
- Describe the carcinogenesis phase when a tumor metastasizes.
- Choose the tissue level that is affected on the patient discussed above: Epithelial, Connective, Muscle or Neural. Support your answer.
Submission Instructions:
- Your initial post should be at least 500 words, formatted and cited in current APA style with support from at least 2 academic sources.
Metastasis Sites in Pancreatic Cancer:
- Liver: Liver metastases are common in pancreatic cancer due to the close anatomical proximity of the liver to the pancreas and the rich blood supply the liver receives from the portal vein, facilitating dissemination of cancer cells.
- Lymph Nodes: Lymphatic spread is common in pancreatic cancer, with lymph nodes in the peripancreatic, celiac, and superior mesenteric regions being commonly involved. The peripancreatic lymph nodes are typically the first sites of metastasis.
- Lungs: Hematogenous spread can lead to metastasis in the lungs. The lungs are a frequent site of metastasis for many cancers due to their extensive vascular supply and large surface area for potential colonization by circulating tumor cells.
- Peritoneum: Direct extension or seeding of tumor cells into the peritoneal cavity can lead to peritoneal metastasis. This often results in the development of carcinomatosis, characterized by widespread dissemination of tumor nodules throughout the peritoneal cavity.
- Bone: Although less common than liver or lymph node metastases, pancreatic cancer can spread to bones, particularly the vertebrae, pelvis, and long bones, through hematogenous dissemination. Bone metastases can cause pain, pathological fractures, and other skeletal-related complications.
Tumor Cell Markers:
Tumor cell markers are substances produced by cancer cells or by the body in response to cancer. In pancreatic cancer, commonly measured tumor markers include:
- CA 19-9: This is the most widely used tumor marker for pancreatic cancer. Elevated levels are associated with advanced disease and can be used for prognosis, monitoring response to treatment, and detecting recurrence.
- CEA (carcinoembryonic antigen): While not specific to pancreatic cancer, elevated CEA levels may be seen in pancreatic cancer and can also be used for monitoring treatment response and detecting recurrence.
- CA 125: Elevated CA 125 levels may be seen in pancreatic cancer, particularly in cases with peritoneal metastasis.
Tumor markers are ordered for patients with pancreatic cancer to aid in diagnosis, assess disease extent and stage, monitor treatment response, detect recurrence, and guide clinical management decisions.
TNM Stage Classification:
Based on the TNM stage classification:
- T: T4 (Tumor extends beyond the pancreas)
- N: N1 (Regional lymph node metastasis)
- M: M1 (Distant metastasis)
This classification is important because it helps determine the prognosis, guide treatment decisions, and standardize communication among healthcare providers regarding the extent of the disease.
Characteristics of Malignant Tumors:
Malignant tumors exhibit several characteristic features:
- Abnormal Cell Growth: Malignant cells proliferate uncontrollably, leading to the formation of a mass or tumor.
- Invasion: Malignant cells have the ability to invade nearby tissues and structures, disrupting normal organ function.
- Metastasis: Malignant tumors can spread to distant sites in the body via lymphatic or hematogenous routes, forming secondary tumors at these sites.
- Angiogenesis: Malignant tumors induce the formation of new blood vessels (angiogenesis) to supply nutrients and oxygen, facilitating tumor growth and metastasis.
Carcinogenesis Phase of Metastasis:
The process of metastasis involves several steps:
- Local Invasion: Cancer cells acquire the ability to invade neighboring tissues and structures by breaking down the extracellular matrix and basement membranes through the secretion of proteolytic enzymes.
- Intravasation: Some cancer cells enter blood vessels or lymphatic vessels, allowing them to travel to distant sites in the body.
- Survival in Circulation: Cancer cells must survive in the circulation, which can be hostile due to shear forces, immune surveillance, and lack of attachment to extracellular matrix components.
- Extravasation: Cancer cells exit the circulation and invade the surrounding tissues at distant sites, often guided by chemotactic signals from the microenvironment.
- Colonization: Once at a distant site, cancer cells establish secondary tumors through proliferation and interaction with the local microenvironment.
Affected Tissue Level:
In the case described, the tissue level affected is Epithelial. Pancreatic cancer arises from the epithelial cells lining the ducts of the pancreas, leading to the development of ductal adenocarcinoma, which is the most common type of pancreatic cancer.