Tumors of the pancreas

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  • benign tumors occur very rarely
    • lipoma, cystadenomas, dermoid cysts, teratomas , apudomas
    • cystadenomas tend to malignate, they are removed
  • malignant tumors – we distinguish ampular tumors and then pancreatic cancer

Regional pancreatic lymph nodes[edit | edit source]

  • upper group - overhead and body
  • lower group - under the head and body
  • anterior group - pancreatoduodenal, pyloric and proximal mesenteric nodes
  • posterior group - posterior pancreatoduodenal, pericholedochal, mesenteric
  • lienal group - nodules in the hilus of the spleen

Ampullar (periampullar) tumors[edit | edit source]

  • most often it is a well-differentiated adenocarcinoma with papillary exophytic manifestations
  • used to be a rare rarity, today it is the fifth most common cause of cancer death
  • affects people over 50 years of age
  • prognostically favorable is that it soon manifests as obstructive jaundice - therefore it is indicated up to 4 times more *often for resection than pancreatic head cancer
  • metastases occur later

Carcinoma[edit | edit source]

Searchtool right.svg For more information see Pancreatic carcinoma.
Pancreatic head carcinoma after contrast application of CT
  • according to the location we recognize - carcinoma of the head, body and cauda pancreas
  • occurrence
    • is increasingly common (currently about 2 times more than in the interwar period)
    • make up over 10% of GIT malignancies, over 3% of all malignancies
  • causes - a number of predisposing factors are known - obesity , alcohol, smoking , DM , biliopancreatic reflux, chronic pancreatitis
  • localization - 65-70% is in the head, 15% in the body, 5% in the cauda area
  • histology - 90% are adenocarcinomas of the ductal epithelium, acinar cell carcinoma has a very poor prognosis

stages of the tumor process[edit | edit source]

  • stage I - T1 or 2, N0, M0
  • stage II - T3 (infiltration into the stomach, blood vessels), N0, M0
  • stage III - any T, N1, M0
  • stage IV - any T, N, but M1

Clinical picture[edit | edit source]

  • initially presents as:
    • "discomfort" syndrome - anorexia, fullness, weight loss and indigestion
    • these symptoms should lead to the suspicion of pancreatic malignancy
  • pain - in the abdomen and banded in the back
  • in head tumor - obstructive jaundice - typical painless onset

Diagnosis[edit | edit source]

Imaging methods are crucial in diagnosis:

  • contrast X-ray - typical enlargement of the duodenal window "C"
  • USG - identifies the tumor mass, enables FNAB
  • ERCP - imaging functions and pancreatic juice collection for cytology
  • CT
  • arteriography - important for determining tumor operability (infiltration of ports or mesenterics - almost this precludes radical performance)
  • oncomarkers - CEA, CA 19-9, CA 50
  • differential diagnosis(dif.dg) - benign tumors, pancreatic pseudocysts, chronic pancreatitis

Therapy[edit | edit source]

Therapy is optimally surgical:

  • Whipple surgery - in case of head injury - cephalic partial duodenopancreatectomy
  • cauda involvement - left resection of the pancreas
  • total duodenopancreatectomy, tube connection gastrojejunoanastomosis
  • palliative:
    • in bile duct oppression - biliary anastomoses (see above)
    • at imminent duodenal oppression - gastrojejunoanastomosis
  • postoperative measures - glycemic control , or iatrogenic DM therapy - this diabetes is very difficult to control due to the absence of glucagon! - great tendency to hypoglycemia !!!
  • pancreatic enzyme substitution
  • adjuvant - percutaneous conventional RT, it is not very sensitive to CHT, it is used only palliatively

Prognosis[edit | edit source]

  • very unfavorable, operational lethality is 5-15%
  • in early diagnosable cancer, 5-year survival is still only 3%



Links[edit | edit source]

Source[edit | edit source]