Interruption Syndrome Pituitary Stalk: About 8O Cases
Soumeya Nora Fedala1
Ali El Mahdi Haddam2
1. Department of endocrinology bab el oued hospital, Algeria
2. Department of endocrinology bologhine hospital, Algeria
International Journal of Clinical Case Reports, 2015, Vol. 5, No. 28 doi: 10.5376/ijccr.2015.05.0028
Received: 04 Apr., 2015 Accepted: 13 Jun., 2015 Published: 03 Jul., 2015
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Preferred citation for this article:
Soumeya Nora Fedala, Farida Chentli, Djamila Meskine and Ali El Mahdi Haddam, 2015, Interruption Syndrome Pituitary Stalk: About 8O Cases, International Journal of Clinical Case Reports, 5(28) 1-8 (doi: 10.5376/ijccr.2015.05.0028)
Summary We report the study of 80 patients (65 M, 15 F) with Interruption Syndrome Pituitary Stalk. They had consulted for delay stature n: 65 and polyuropolydipsic syndrome n: 2. The mean age at diagnosis was 7±2.8 years. Delivery dystocia was noted in 18.7%. Neonatal hypoxia has been reported in 5%. The average size of patients was -.3±DS/M (Sempe). Micropenis ± cryptorchidism was present in 50%. Pituitary hypoplasia represents 91.2% of abnormality. The post pituitary gland is ectopic in 37.5%: infundibular place (90%) Tubercinerum (10%). In 3.7%, it is not found. The number of ectopic and unseen post pituitary gland is significantly higher (p<10-6) when the stalk is discontinued (n: 28). Than when pituitary gland is normally (n=3).
When the post pituitary gland is ectopic or unseen (n: 37), malformations of HH are associated generally (81, 08%).
Pituitary is more severely reduced when the post pituitary gland is ectopic or invisible and that the stalk is interrupted than when it is normal: 1.5mm±0.6 vs. 1.8±3 mm (p: 0.01).
Hormonal assessment revealed IGH in 100%. It was associated with others pituitary deficiencies in 68.7%. Diabetes insipidus was found in 05 cases.
Multiple pituitary deficiencies are more common when there are at least two malformations anomalies. Reassessment revealed other hormonal deficiencies in 22, 5% of patients with a mean of 05 years.
The genetic study performed showed no molecular defect (PROP 1 PIT1, LHX3, LHX4, HESX1).
SITP MRI; GH deficiency; Multiple hormone deficiencies; Malformatives abnormalities; Monitoring