Introduction
Short stature is a common health problem encountered by pediatrician, its causes range from genetic or constitutional short stature to pathological
causes like gastrointestinal diseases.
Short stature is defined as a standing height that is more than two standard deviations below the mean for age and sex in a genetically relevant
population.(1) It is a pathological and psychological issue that leads family to seek medical help. It is documented that around 20-
30% of patients with celiac disease could present with short stature only.(1,2)
Celiac is an autoimmune disorder of the small intestine that occurs in genetically predisposed people of all ages from middle
infancy onward. It is caused by intolerance to gluten and dietary proteins present in wheat, rye and barley.(3,4)
Performing endoscopy to rule out celiac disease in patients with short stature is important. In our study, though we focus on this issue, we emphasize
other endoscopic findings in short stature that might or might not affect growth and stature.
Methods
A retrospective review of 32 records of children referred to the pediatric gastrointestinal clinic in Prince Ali Hospital in Al-Karak with short
stature was done. It was conducted over a six months period between August 2011 and February 2012. All patients were subjected to full history and
physical examination.
The following investigations were done to all patients to exclude organic causes: complete blood count, kidney function test, liver function test,
thyroid function test, tissue transglutaminase antibodies and abdominal ultrasound.
Upper gastrointestinal endoscopy was done to all patients whom we were not able to reach for a diagnosis, mainly to rule out celiac disease, and before
being labeled to have genetic or constitutional short stature.
Results
There were 32 children included in this study, (14 females and 18 males) with a mean age of 7.75 years, ranges from 2.5-13 years.
Normal gross endoscopy was noticed in the majority of patients (25 patients, 78%), most of them had normal histopathological reports (19 patiens, 79%).
Nevertheless, four patients out of 25 (16%) were diagnosed to have celiac disease by histopathology report. One of those 25 patients
was diagnosed to have giardiasis (4%) and another with H. pylori gastritis (4%) while the rest were normal (19 patients, 79%).
Abnormal endoscopy was noticed in six patients only out of 32 patients, showing D2 effacement and scalloped folds. Two of them were diagnosed to have
celiac disease in histopathological reports (33%), one was diagnosed to have H. pylori gastritis and another with lymphonodular hyperplasia, and the
other two were normal (Table I). One patient showed antral nodularity and was diagnosed to have H. pylori gastritis (3%).
Table I:
Number of celiac disease patients in regard to endoscopic findings.
Endoscopic finding
|
No. of patients
|
Celiac
|
Scalloping of folds
|
6
|
2 (33%)
|
Normal
|
25
|
4 (16%)
|
Antral nodularity
|
1
|
0
|
Other relevant associated symptoms, that are related to celiac were followed in this study like diarrhea which was noticed in three of the patients, in
addition to their short stature, but it was not the chief complaint to parents; one of them only showed to be celiac (9%).
Tissue transglutaminase antibodies are important serological diagnostic tool for celiac which were followed as well. Five of the patients were having
positive tissue transglutaminase antibodies (15%), two of them were proved to be celiac by histopathology report (40%).
Total number of patients with celiac disease in this study were six (18.75%), regardless their gross endoscopic appearance (Table II).
Table II:
Histopathological findings in patients with short stature
Histopathology
|
Normal gross endoscopy (25 patients)
|
Abnormal gross endoscopy (7)
|
Normal
|
19
|
2
|
Celiac
|
4
|
2
|
H. pylori
|
1
|
2
|
Lymphonodular hyperplasia
|
0
|
1
|
Giardiasis
|
1
|
0
|
None of the mentioned causes except for celiac explained short stature so were considered as coincidetal findings.
Discussion
Celiac disease is a chronic gastrointestinal disorder in which ingestion of gluten leads to damage of the small intestinal mucosa by an autoimmune
mechanism in genetically susceptible individuals.(3,4) Its prevalence has been ranged from 1-130 to 1-681 in general population
according to the population being studied.(3,5,6,7) It is believed to be the most common chronic intestinal inflammatory
disease, being more prevalent among Western Europeans and least among people of purely African-Caribbean, Chinese or Japanese background. (5,7)
Celiac has wide spectrum of gastrointestinal and extraintestinal manifestation including: chronic diarrhea, impaired growth, recurrent abdominal pain,
anemia, low bone density and psychiatric and behavioral disturbances.(5,7,8)
Most of the published studies were focusing on the prevalence of Celiac disease among children with short stature. Our study, though acting the same,
it emphasizes other endoscopic findings in short stature as well, regardless weather they would or would not affect their growth.
As expected, the most common finding in our study was normal gross endoscopy. Not surprisingly, 16% showed Celiac disease in histopathology reports, as
its well established that normal endoscopy does not rule out Celiac and biopsies should be obtained.(3) Here, the incidence of Celiac
disease was matching others around the world.(1,2,9,10,11,12) Noticeably, all had the same ethnic background and come
from developing areas. Other reports that showed higher incidence(13) or lower incidence(5) were from different
backgrounds confirming the diversity of Celiac disease.
Celiac disease has different serological markers that help in diagnosis. Most importantly is tissue transglutaminase that was documented to be 80-100%
sensitive to detect Celiac disease.(3,14)
This was not the case in our study as only 15% of our patients were having positive tissue transglutaminase which was much less than others, (1,14) with only two of them being diagnosed as Celiac disease. This can be explained by the fact that it was done to
patients with short stature only and not those with suspicion of Celiac regardless the presentation.
The endoscopic findings and their correlation to Celiac disease were the main concern in many studies which includes decrease in duodenal folds
scalloping, mucosal fissure and mosaic appearance.(7) Some emphasizes that they can’t be the only indicator as they are not specific
nor sensitive(7) while others were appreciating these findings as highly sensitive and specific.(3,15,16,17)
Its worth to mention, though not included in our study, that Celiac disease is known to have patchy pattern in small intestine involvement in both
adult and children. All recent data determines the importance of obtaining biopsies not only from the D2 but also from the duodenal bulb to enhance the
yield of the diagnosis.(4)
Lastly, some limitations were encountered in this study like the relatively small size of the sample which might encourage larger prospective studies
in the future.
Conclusion
Short stature is a common health problem and a well-known feature of Celiac disease which should be excluded to prevent serious and long term
complications. Investigations should be performed to rule out organic causes including intestinal biopsy which is the gold standard for diagnosis and
should be performed in every child with no apparent endocrine causes.
References
1. Hashemi J, Hajiani E, Shahbazin H, et al. Prevalence of celiac disease in Iranian children with idiopathic short stature. World J Gastroenterol 2008; 14(48): 7376-7380.
2. Rabia M, Naeemullah S, Baqai M T, Shabbir A. Clinical presentation of celiac disease in children from 2 to 14 years. Journal of Rawalpindi Medical College (JRMC) 2012; 16(2): 112-114.
3. Medhat A, Abd El-Salam Nadia, Hassany S M, Hussein H I, Blum H E. Frequency of celiac disease in Egyptian patients with chronic diarrhea:
Endoscopic, histopathologic and immunologic evaluation. Journal of physiology and pathophysiology 2011; 2(1):1-5.
4. Rashid M, MacDonald A. Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice. BMC Gastroenterology 2009; 9(78).
5. Queiroz MS, Nery M, Cancado EL, et al. Prevalence of celiac disease in Brazilian children of short stature. Brazilian Journal of Medical and Biological Research 2004; 37:55-60.
6. Maki M, Mustalahti K, Kokkonen J, et al.
Prevalence of celiac disease among children in Finland. N Eng J Med 2003; 348(25):2517-24.
7. Green PHR, Murray JA. Routine duodenal biopsies to exclude celiac disease? Gastrointestinal Endoscopy 2003; 58(1): 92-95.
8. Farrell RJ, Kelly CP. Celiac sprue. New England Journal of Medicine 2002; 346: 180-188.
9. Shaltout AA, Khuffash FA, Hilal AA, El Ghanem MM. Pattern of protracted diarrhea among children in Kuwait. Ann Trop Paediatr1989; 9
(1): 30-32.
10. Abdullah AMA, El Mouzan MI, Al Herbish AS, Al Sohaibani MO. P1024 Endoscopic Doudenal Biopsy: Experience in A Developing Country. Journal of Pediatric Gastroenterology and Nutrition 2004; 39: 446-447.
11. Sari S, Dalgic B. Evaluation of patients with short stature consulted for suspicion of celiac disease. Turkiye Klinikleri J Pediatr Sci 2005; 1(10): 41-43.
12. Sabir OME, Gadour MOEH. Upper
gastrointestinal endoscopy in Sudanese infants and children. Sudan JMS 2007; 2 (2):91-95
13. Rosenbach Y, Dinari G, Zahavi I, Nitzan M. Short stature as the major manifestation of celiac disease in older children. Clinical Pediatrics 1986; 25(1): 13-16.
14. Oxentenko AS, Grisolano SW, Murray JA, et al. The insensitivity of endoscopic markers in celiac disease. Am J Gastroenterol
2002; 97(4): 933-8.
15. Corazza GR, Caletti GC, Lazzari R. Scalloped duodenal folds in childhood celiac disease. Gastrointest Endosc 1993; 39(4): 543-5
16. Savas N, Akbulut S, Saritas U, Koseoglu T. Correlation of clinical and histopathological with endoscopic findings of celiac disease in the
Turkish population. Dig Dis Sci 2007; 52(5):1299-303.
17. Brocchi E, Corazza G R, Caletti G, et al. Endoscopic Demonstration of Loss of Duodenal Folds in the Diagnosis of Celiac Disease. N Engl J Med 1988; 319: 741-744.