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16 Cards in this Set

  • Front
  • Back
How is it diagnosed?
At appendectomy
How common?
2 to 5/1000 operations
Of all intestinal malignancies it is the _____ most common?
Second
Secrete what?
Serotonin, chromogranin A, other vasoactive substances
Most common age?
40s
Carcinoid syndrome
Episodic flushing, wheezing, diarrhea, right-sided heart disease
Location of most appendiceal carcinoids
Distal one-third
Staging includes
Unnecessary unless there is evidence of intraabdominal spread, tumor >2 cm, incomplete resection, or symptoms. CT or MRI. Octreotide scan is the most sensitive. If suspicion for carcinoid syndrome, then obtain assays for 5-HIAA (urine) and serum chromogranin A.
Which serum/urine marker is most sensitive?
Chromogranin A
Outcome data
<2 cm - no recurrences noted with 26 years of follow up, 2-3 cm - 3 of 14, and 4 of 9 >3cm.
Survival
SEER database - <3 cm without regional nodal or distant metastases - 100%, 2-3 cm with regional node involvement or >3cm no nodes - 78%, Distant disease - 32%
Risk of lymph node involvement
<1.0 cm - 0%, 1-2 cm - 7.5%, >2 cm - 33%
Another paper on risk of LN involvement (from MGH)
<1 cm - 15%, 1-2 cm - 47%, >2 cm - 86%.
Survival in second paper Mullen MGH
100% - <1 cm, 92% 1-2 cm, 91% >2 cm @ 10 years, despite the fact that 86% had LN mets
Indications for right colectomy
>2 cm, 1-2 cm with mesoappendiceal invasion, positive or unclear margins, higher proliferative rate, angioinvasion, and mixed histology (goblet cell, adenocarcinoid).
Pediatric literature
Longitudinal follow up for children with tumors less than 2 cm indicates that appendectomy is curative.