@article{m2014sertoli,
  title = {Sertoli Cell Tumor of the Testis in Association with Peutz-Jeghers Syndrome Sometimes Requires a High Index of Suspicion},
  author = {García González M. and Moreno Álvarez A. and Dargallo Carbonell T. and Solar Boga A. and Suarez Dono I. and Mosquera Reboredo J. and Vela Nieto D.},
  year = 2014,
  url = {https://ibimapublishing.com/articles/PRIJ/2014/704812/},
  journal = {Pediatrics Research International Journal},
  volume = 2014 (2014),
  pages = 6,
  doi = 10.5171/2014.704812,
  abstract = {Peutz Jeghers Syndrome (PJS) is an autosomal dominant disorder characterized by mucocutaneous pigmentation and hamartomatous polyps throughout the gastrointestinal tract. Pigmented macules appear especially on oral mucosa, lips and fingers. Hamartomatous polyps are found predominantly at the small intestine and colon lesser extent1 and can cause bleeding and abdominal pain secondary to intussusception, intestinal obstruction and infarction. Approximately 80% of patients with PJS have mutations in threonine kinase 11 (STK11) located in 19p13.3 chromosome1,2. This acts as a tumor suppressor gen, leading its mutation to increased risk of cancer at an early age3. Most commonly reported cancers are luminal gastrointestinal and breast. Testicular tumors are less known, but may be present at early age2 and course with estrogenic manifestations in most of cases. We report a case of PJS with intratubular large cell hyalinizing Sertoli Cell (LCHSC) tumor of the testis diagnosed during the follow-up of the patient.},
  keywords = {Peutz-Jeghers syndrome, testicular neoplasm, Sertoli cell tumor, gynecomastia.},
  note = Article ID: 704812
}