Back to Search Start Over

High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.

Authors :
Noriega-Iriondo, Maria Fernanda
Colon-Otero, Gerardo
Kipp, Benjamin R.
Copland, John A.
Ferber, Matthew J.
Marlow, Laura A.
Roberts, Maegan E.
Robertson, Matthew W.
Dinh, Tri A.
Attia, Steven
Geiger, Xochiquetzal J.
Riegert-Johnson, Douglas L.
Source :
Hereditary Cancer in Clinical Practice; 2015, Vol. 13 Issue 1, p76-87, 12p
Publication Year :
2015

Abstract

A 46-year-old female presents with a pelvic mass and is diagnosed as having a high-grade endometrial stromal sarcoma. During surgery, she is noted to have areas of intussusception of the small bowel secondary to large hamartomatous polyps. The patient had a previous history of small bowel obstruction secondary to what had been thought to be hyperplastic polyps but represented hamartomatous polyps on further review. Additional examination revealed the presence of subtle hyperpigmented macules on the fingers leading to a diagnosis of Peutz-Jeghers Syndrome (PJS). The diagnosis was confirmed by the presence of a germ-line STK11 mutation. Immunohistochemistry analysis of the tumor showed decreased expression of STK-11 as compared to one of the patient's hamartomatous polyps. Next generation sequencing of the tumor specimen failed to demonstrate a "second hit" somatic mutation in STK-11. This case represents the first case of endometrial stromal sarcoma associated with PJS and illustrates the importance of increased awareness of this condition among oncologists. PJS is associated with dysregulation of the mTOR pathway; treatment with an mTOR inhibitor was not effective in this case. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17312302
Volume :
13
Issue :
1
Database :
Complementary Index
Journal :
Hereditary Cancer in Clinical Practice
Publication Type :
Academic Journal
Accession number :
101039358
Full Text :
https://doi.org/10.1186/s13053-015-0027-0