
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Peutz-Jeghers syndrome history and symptoms
Introduction
Overview
Overview
The hallmark of Peutz-Jeghers syndrome is hamatomatous polyps. A positive history of mucucutaneous hyperpigmentation and rectal bleeding is suggestive of Peutz-Jeghers syndrome. The most common symptoms of Peutz-Jeghers syndrome include abdominal pain, fatigue, and weight loss.
History and Symptoms
History and Symptoms
Individuals with Peutz-Jeghers syndrome may have positive history of:[1]
- Peutz-Jeghers syndrome in family
- Mucucutaneous hyperpigmentation of the oral mucosa
- Rectal bleeds
- Abdominal pain
- Fatigue
Symptoms of Peutz-Jeghers syndrome include the following:[1][2]_Genetic_and_Rare_Diseases_Information_Center_(GARD)_–_an_NCATS_Program-3|[3]
- Mucocutaneous hyperpigmentation (mouth, hands, and feet)
- Rectal bleeding
- Melena
- Rectal prolapse
- Abdominal pain
- Weight loss
- Gynecomastia in males
- Menstrual irregularities in females
- Hematemesis
- Fatigue
| Percentage of symptom occurrence in Peutz-Jeghers syndrome | |
|---|---|
| Symptoms | Percentage (%) |
| Abnormal Pigmentation | 80 to 90 |
| GI Bleeding | 30 to 79 |
| Abdominal Pain | 5 to 29 |
References
References
- ↑ 1.0 1.1 Kopacova, Marcela; Tacheci, Ilja; Rejchrt, Stanislav; Bures, Jan (2009). “Peutz-Jeghers syndrome: Diagnostic and therapeuticapproach”. World Journal of Gastroenterology. 15 (43): 5397. doi:10.3748/wjg.15.5397. ISSN 1007-9327.
- ↑ Giardiello, F; Trimbath, J (2006). “Peutz-Jeghers Syndrome and Management Recommendations”. Clinical Gastroenterology and Hepatology. 4 (4): 408–415. doi:10.1016/j.cgh.2005.11.005. ISSN 1542-3565.
- _Genetic_and_Rare_Diseases_Information_Center_(GARD)_–_an_NCATS_Program_3-0|↑ “Peutz-Jeghers syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program”.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]
