A 14-year-old girl had been enjoying good health until December 2001, when she received
a minor blunt trauma against the left side of the body during gymnastic exercises.
Thereafter, she developed intermittent pain in the epigastrium, as well as fatigue,
dizziness, and paleness. There was no melena or bright red blood per rectum, but the
color of the stool changed to maroon. In June 2002, gastroscopy and colonoscopy revealed
no abnormalities. Because of persistent symptoms and iron-deficiency anemia, upper
endoscopy was repeated in October 2002, again with no obvious source for the bleeding
being found.
After another 2 months, she was admitted to hospital for further evaluation of obscure
gastrointestinal bleeding. On presentation, the patient reported continuing symptoms.
The physical examination did not reveal any abnormalities, apart from pale lips. Laboratory
tests showed reduced values for hemoglobin (8.8 g/dl; normal range 12 - 16 g/dl),
mean corpuscular hemoglobin (21 pg; normal range 27 - 32 pg), mean corpuscular volume
(70 fl; normal range 82 - 92 fl), total protein (5.4 g/dl; normal range 6.0 - 8.0
g/dl), albumin (3.2 g/dl; normal range 3.5 - 5.0 g/dl) and serum ferritin (< 5 ng/ml;
normal range 10 - 120 ng/ml).
A capsule endoscopy (CE) examination was carried out, which identified a large tumor
with an irregular surface 11 min after the pylorus had been passed (Figure [1]). A push enteroscopy examination was performed, which confirmed a neoplasia 50 -
80 cm after the ligament of Treitz (Figure [2]). Biopsies showed that the lesion was an ulcerated mesenchymal neoplasm with leiomyomatous
differentiation.
Figure 1 Capsule-endoscopic image of an irregular tumor of the jejunum with an unclear malignant
status, with a mucin layer.
Figure 2 Confirmation of the tumor on push enteroscopy.
In January 2003, the girl underwent laparoscopic resection of the tumor. Histology
showed a completely resected mesenchymal tumor of the jejunal wall, measuring 4 cm
in diameter, with infiltration of the mucosa and superficial ulceration, but with
no vascular invasion (Figure [3 a]). Immunohistochemistry confirmed leiomyomatous differentiation (Figure [3 b]). The patient was discharged 8 days after surgery in good condition.
Figure 3 a Histology shows a spindle-cell neoplasm immediately under the intestinal epithelium
(hematoxylin-eosin, original magnification × 40). b Immunohistochemistry reveals strong reactivity for desmin, confirming leiomyomatous
differentiation (immunoalkaline phosphatase, original magnification × 200).
Three years after the resection, there have been no signs of recurrence of the tumor
and there have been no further symptoms.
Two studies have been published focusing on CE in children [1,2]. Taking these together,
CE was safely performed in 42 children over the age of 10 and showed a high diagnostic
yield. The main indication for CE in the two trials was a clinical suspicion of Crohn’s
disease. In the small group of children who had obscure gastrointestinal bleeding
(n = 4), CE confirmed a diagnosis of vascular malformations in three cases [1]. In
the present case, CE revealed a tumor of the jejunum with unclear malignant status
1 year after the onset of the initial symptoms. Leiomyomas of the intestine are rarely
found in pediatric patients and usually appear in late adult life. To date, there
have only been a few reports on smooth-muscle tumors of the small bowel in immunocompetent
children [3-6].
Endoscopy_UCTN_Code_CCL_1AB_2AZ_3AB
Endoscopy_UCTN_Code_CCL_1AC_2AC
