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Case Reports
. 2015 May;44(4):676-8.
doi: 10.1097/MPA.0000000000000311.

HNPCC-associated pheochromocytoma: expanding the tumor spectrum

Affiliations
Case Reports

HNPCC-associated pheochromocytoma: expanding the tumor spectrum

Brian P Riff et al. Pancreas. 2015 May.
No abstract available

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Conflict of interest statement

The Authors Declare No Conflict of Interest

Figures

Figure 1
Figure 1
1A: Hematoxylin and eosin stained section of pheochromocytoma with marked cytologic atypia 1B: Tumor shows diffuse cytoplasmic staining for synaptophysin 1C: Tumor demonstrates presence of mismatch repair proteins MLH-1 1D: Tumor demonstrates presence of PMS-2 1E: Tumor shows loss of mismatch repair proteins MSH-2 (1E) 1F: Tumor shows loss of mismatch repair proteins MSH-6 (1F). * All photos at 400X.

References

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    1. Ligtenberg Marjolijn JL, et al. Heritable somatic methylation and inactivation of MSH2 in families with HNPCC due to deletion of the 3′ exons of TACSTD1. Nature genetics. 2008;41(1):112–117. - PubMed
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    1. Arnason Thomas, et al. Loss of expression of DNA mismatch repair proteins is rare in pancreatic and small intestinal neuroendocrine tumors. Archives of Pathology & Laboratory Medicine. 2011;135(12):1539–1544. - PubMed
    1. Kidd Mark, et al. Microsatellite instability and gene mutations in transforming growth factor-beta type II receptor are absent in small bowel carcinoid tumors. Cancer. 2005;103(2):229–236. - PubMed

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