A 57-year-old man presented with chronic fatigue, weakness, irritability, and lack
of concentration. Physical examination revealed pale skin with grooved and brittle
nails. In addition, hyperpigmented mucocutaneous lesions were noted in the mouth.
Laboratory investigation was remarkable for iron deficiency anemia. Esophagogastroduodenoscopy
(EGD) disclosed a large polypoid mass in the gastric cardia ([Fig. 1 a]). Chromoendoscopy with methylene blue (1 % dilution) revealed a Kudo pit pattern
3 L (large roundish and tubular pits; [Fig. 1 b]) which was confirmed by narrow-band imaging (Olympus, Tokyo, Japan; [Fig. 1 c]). Confocal laser endomicroscopy (EC-3870 CIFK, Pentax, Tokyo, Japan) showed disorganization
of glands with suspicion of different cell types but there was a lack of atypia ([Fig. 1 d]). Endocytoscopy (XEC-120-U, Olympus, Tokyo, Japan) of the polyp revealed normal
cells without nuclear or cytoplasmic changes ([Fig. 1 e]), and endoscopic ultrasound showed enlargement of the mucosa but no muscularis infiltration
([Fig. 1 f]). Subsequently, an oral double-balloon endoscopy (Fujinon, Omiya, Japan) disclosed
multiple polyps in the jejunum, most of them smaller than 10 mm in diameter ([Fig. 1 g]). Endoscopic examination was completed with ileocolonoscopy, which revealed multiple
polyps ranging in size from 2 mm to 25 mm ([Fig. 1 h]). Following genetic analysis, which disclosed mutation of the serine threonine kinase
11 (STK11)/LKB1 gene, a diagnosis of Peutz–Jeghers syndrome was made.
Fig. 1 (a) Large polypoid mass in the gastric cardia visualized on esophagogastroduodenoscopy.
(b) Large, round, tubular pits demonstrating a Kudo pit pattern 3L on chromoendoscopy
(1 % methylene blue). (c) The pit pattern was confirmed on narrow-band imaging. (d) Disorganized glandular pattern with possibility of different cell types but no cellular
atypia seen on confocal laser endomicroscopy. (e) No signs of atypia on endocytoscopy. (f) Enlarged mucosa seen on endoscopic ultrasound. (g) Multiple small polyps visualized in the jejunum on oral double-balloon endoscopy.
(h) Ileocolonoscopy showing multiple polyps (2 – 25 mm in size).
Peutz–Jeghers syndrome, an autosomal dominant condition, is characterized by hamartomatous
polyps in the gastrointestinal tract and mucocutaneous melanin pigmentation, and is
caused by a germline mutation of the STK11 gene. Patients are at an increased risk of developing different types of gastrointestinal
and nongastrointestinal tumors. Most authorities recommend polypectomy for gastric/colonic
polyps larger than 10 mm, and surgery is recommended for symptomatic or rapidly growing
small intestinal polyps and asymptomatic polyps greater than 10 – 15 mm in diameter
[1].
In our patient, all the polyps greater than 5 mm in diameter were removed in multiple
sessions from the stomach, jejunum (using double-balloon endoscopy), and colon. Histopathological
analysis revealed hamartomatous polyps. Follow-up EGD and colonoscopy were performed
after 6 months. In keeping with international guidelines, surveillance endoscopy of
the stomach, small bowel, and colon will now be performed every 2 years.
Competing interests: None
Endoscopy_UCTN_Code_CCL_1AB_2AD_3AB
