Which condition is associated with the presence of Peutz-Jeghers syndrome?

Peutz-Jeghers syndrome is a genetic condition characterized by the presence of hamartomatous polyps, particularly in the gastrointestinal tract, along with mucocutaneous pigmentation. The hallmark feature of this syndrome is the development of GI polyposis, which can lead to complications such as bowel obstruction and an increased risk for certain types of cancer. The polyps often occur in the small intestine but can also be found in the colon and stomach.

While the other options hint at various medical conditions, they do not specifically relate to Peutz-Jeghers syndrome. The inheritance pattern of Peutz-Jeghers syndrome is autosomal dominant, ruling out the relevance of an autosomal recessive inheritance option. Hormonal imbalances and autoimmune disorders do not pertain to this syndrome's defining features or associated conditions. Thus, the correct association with Peutz-Jeghers syndrome is indeed GI polyposis, making it a key aspect of the condition's clinical presentation.