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16 Cards in this Set
- Front
- Back
How is it diagnosed?
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At appendectomy
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How common?
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2 to 5/1000 operations
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Of all intestinal malignancies it is the _____ most common?
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Second
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Secrete what?
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Serotonin, chromogranin A, other vasoactive substances
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Most common age?
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40s
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Carcinoid syndrome
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Episodic flushing, wheezing, diarrhea, right-sided heart disease
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Location of most appendiceal carcinoids
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Distal one-third
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Staging includes
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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.
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Which serum/urine marker is most sensitive?
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Chromogranin A
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Outcome data
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<2 cm - no recurrences noted with 26 years of follow up, 2-3 cm - 3 of 14, and 4 of 9 >3cm.
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Survival
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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%
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Risk of lymph node involvement
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<1.0 cm - 0%, 1-2 cm - 7.5%, >2 cm - 33%
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Another paper on risk of LN involvement (from MGH)
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<1 cm - 15%, 1-2 cm - 47%, >2 cm - 86%.
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Survival in second paper Mullen MGH
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100% - <1 cm, 92% 1-2 cm, 91% >2 cm @ 10 years, despite the fact that 86% had LN mets
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Indications for right colectomy
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>2 cm, 1-2 cm with mesoappendiceal invasion, positive or unclear margins, higher proliferative rate, angioinvasion, and mixed histology (goblet cell, adenocarcinoid).
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Pediatric literature
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Longitudinal follow up for children with tumors less than 2 cm indicates that appendectomy is curative.
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