Literature DB >> 15073433

Neonatal identification of pituitary aplasia: a life-saving diagnosis. Review of five cases.

Salvatore Scommegna1, Daniela Galeazzi, Simonetta Picone, Edoardo Farinelli, Rocco Agostino, Alessandro Bozzao, Brunetto Boscherini, Stefano Cianfarani.   

Abstract

BACKGROUND: Neonatal onset hypopituitarism is a life-threatening, potentially treatable endocrine disease. A possible cause is congenital absence of the anterior pituitary gland, a condition very rarely reported in the literature.
METHODS: A series of 5 cases of children with pituitary aplasia referred to the Centre of Paediatric Endocrinology 'Rina Balducci', Tor Vergata University, Rome, is presented.
RESULTS: Major clinical features in our patients were respiratory distress on the first day of life, in spite of uneventful pregnancy, labour and delivery, metabolic acidosis, non-cholestatic jaundice, hypotonia, severe hypoglycaemia, hypogenitalism, and midline defects. Diagnosis was established by endocrine tests during hypoglycaemia and hypothalamic-pituitary MRI scan. Symptoms disappeared soon after replacement therapy was started.
CONCLUSION: We stress the importance of performing baseline endocrine tests as soon as possible during hypoglycaemia and MRI of the brain aimed at visualizing the hypothalamic-pituitary area in neonates with hypogenitalism and severe unexplained hypoglycaemia, so that the irreversible neurological and developmental consequences of panhypopituitarism can be prevented by adequate replacement therapy. Copyright 2004 S. Karger AG, Basel

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Year:  2004        PMID: 15073433     DOI: 10.1159/000077661

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  7 in total

1.  Prenatal MR imaging of the normal pituitary stalk.

Authors:  A Righini; C Parazzini; C Doneda; F Arrigoni; F Triulzi
Journal:  AJNR Am J Neuroradiol       Date:  2009-02-04       Impact factor: 3.825

2.  Congenital adenohypophysis aplasia: clinical features and analysis of the transcriptional factors for embryonic pituitary development.

Authors:  T Arrigo; M Wasniewska; F De Luca; M Valenzise; F Lombardo; D Vivenza; T Vaccaro; E Coradi; A Biason-Lauber
Journal:  J Endocrinol Invest       Date:  2006-03       Impact factor: 4.256

3.  Focal congenital hyperinsulinism in a patient with septo-optic dysplasia.

Authors:  Raja Padidela; Ritika R Kapoor; Yuva Moyo; Clare Gilbert; Sarah E Flanagan; Sian Ellard; Khalid Hussain
Journal:  Nat Rev Endocrinol       Date:  2010-09-14       Impact factor: 43.330

4.  Diagnostic pitfalls in the assessment of congenital hypopituitarism.

Authors:  Paolo Cavarzere; Paolo Biban; Rossella Gaudino; Silvia Perlini; Lorenzo Sartore; Lorenza Chini; Davide Silvagni; Franco Antoniazzi
Journal:  J Endocrinol Invest       Date:  2014-08-01       Impact factor: 4.256

5.  Three Japanese patients with congenital pituitary hormone deficiency and ophthalmological anomalies.

Authors:  Kuniko Takanashi; Yashuto Suzuki; Ayumu Noro; Minako Sugiyama; Masanori Nakanishi; Tetsuro Nagashima; Akie Nakamura; Ishizu Katsura; Toshihiro Tajima
Journal:  Pediatr Rep       Date:  2011-07-18

6.  Congenital hypopituitarism: how to select the patients for genetic analyses.

Authors:  Giuseppe Crisafulli; Tommaso Aversa; Giuseppina Zirilli; Filippo De Luca; Romina Gallizzi; Malgorzata Wasniewska
Journal:  Ital J Pediatr       Date:  2018-04-06       Impact factor: 2.638

7.  A rare cause of respiratory distress and edema in neonate: Panhypopituitarism.

Authors:  Fatma Dursun; Heves Kirmizibekmez; Fazilet Metin
Journal:  North Clin Istanb       Date:  2017-08-26
  7 in total

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