Klinik Araştırma

Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience

Cilt: 32 Sayı: 6 31 Aralık 2022
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Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience

Öz

ABSTRACT Intracranial pathologies can affect pituitary hormone levels whether they are primarily related to the pituitary gland or not. In pituitary hormone deficiencies, the size and location of the pituitary gland may be normal, as well as one or more hormone effects may be observed after hypoplasia, partial empty sella, ectopic neurohypophysis, Rathke's cleft cyst, adenomas and other pituitary masses or surgeries. In early puberty, the pituitary dimensions are usually increased, rarely hypoplasia and rathke cleft cyst are seen as MRI findings. Non-pituitary pathologies cause especially early puberty, single or multiple pituitary hormone deficiency. In this study, we aimed to categorize the patients with pituitary/cranial lesions and hormonal pathology and to determine their frequency and distribution in the single pediatric endocrinology clinic for ten years. The data of 485 patients, 186 (38.3%) male, were retrospectively analyzed. Their mean age was 9.3 ± 3.2 years. The incidental pituitary lesion was found in 28 (5.77%) of all cases. There was no hormonal influence in 20 (71.4%) of them. In most of the 454 cases with hormonal disorders, MRI (Magnetic Resonance Imaging) findings were normal in most of the 454 cases with hormonal disorders (71.8%). The most common hormonal pathologies were precocious puberty and isolated Growth Hormone deficiency, 57.9% and 26.4% respectively. Non-pituitary lesions (n=23, 5%) were most frequently accompanied by early puberty (39.1%). The hypothalamus-pituitary axis may be affected by primary lesions in its own region, or it may be seen as a result of other cranial pathologies. Cranial evaluation is also important in addition to pituitary imaging in pituitary hormone disorders.

Anahtar Kelimeler

Pituitary Hormone Disorders, Central Nervous System Lesions, Precocious Puberty, Magnetic Resonance Imaging.

Kaynakça

  1. 1. Sizonenko PC, Clayton PE, Cohen P, Hintz RL, Tanaka T, Laron Z. Diagnosis and management of growth hormone deficiency in childhood and adolescence. Part 1: diagnosis of growth hormone deficiency. Growth Horm IGF Res. 2001;11(3):137-165.
  2. 2. Latronico AC, Brito VN, Carel JC. Causes, diagnosis, and treatment of central precocious puberty. Lancet Diabetes Endocrinol. 2016;4(3):265-274.
  3. 3. Baldeweg SE, Ball S, Brooke A, et al. SOCIETY FOR ENDOCRINOLOGY CLINICAL GUIDANCE: Inpatient management of cranial diabetes insipidus. Endocr Connect. 2018;7(7):G8-G11.
  4. 4. Zhu J, Feldman HA, Eugster EA, et al. PRACTICE VARIATION IN THE MANAGEMENT OF GIRLS AND BOYS WITH DELAYED PUBERTY. Endocr Pract. 2020;26(3):267-284.
  5. 5. Bosch I Ara L, Katugampola H, Dattani MT. Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome. Front Pediatr. 2021;8:600962. Published 2021 Feb 2.
  6. 6. Higham CE, Johannsson G, Shalet SM. Hypopituitarism. Lancet. 2016;388(10058):2403-2415.
  7. 7. Melmed S, Casanueva FF, Hoffman AR, et al. Diagnosis and treatment of hyperprolactinemia: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011;96(2):273-288.
  8. 8. Hage M, Kamenický P, Chanson P. Growth Hormone Response to Oral Glucose Load: From Normal to Pathological Conditions. Neuroendocrinology. 2019;108(3):244-55.
  9. 9. Sari S, Sari E, Akgun V, et al. Measures of pituitary gland and stalk: from neonate to adolescence. J Pediatr Endocrinol Metab. 2014;27(11-12):1071-1076.
  10. 10. Bellotto E, Monasta L, Pellegrin MC, et al. Pattern and Features of Pediatric Endocrinology Referrals: A Retrospective Study in a Single Tertiary Center in Italy. Front Pediatr. 2020;8:580588. Published 2020 Oct 2.

Kaynak Göster

APA
Gül Şiraz, Ü. (2022). Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience. Genel Tıp Dergisi, 32(6), 714-718. https://doi.org/10.54005/geneltip.1200537
AMA
1.Gül Şiraz Ü. Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience. Genel Tıp Derg. 2022;32(6):714-718. doi:10.54005/geneltip.1200537
Chicago
Gül Şiraz, Ülkü. 2022. “Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience”. Genel Tıp Dergisi 32 (6): 714-18. https://doi.org/10.54005/geneltip.1200537.
EndNote
Gül Şiraz Ü (01 Aralık 2022) Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience. Genel Tıp Dergisi 32 6 714–718.
IEEE
[1]Ü. Gül Şiraz, “Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience”, Genel Tıp Derg, c. 32, sy 6, ss. 714–718, Ara. 2022, doi: 10.54005/geneltip.1200537.
ISNAD
Gül Şiraz, Ülkü. “Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience”. Genel Tıp Dergisi 32/6 (01 Aralık 2022): 714-718. https://doi.org/10.54005/geneltip.1200537.
JAMA
1.Gül Şiraz Ü. Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience. Genel Tıp Derg. 2022;32:714–718.
MLA
Gül Şiraz, Ülkü. “Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience”. Genel Tıp Dergisi, c. 32, sy 6, Aralık 2022, ss. 714-8, doi:10.54005/geneltip.1200537.
Vancouver
1.Ülkü Gül Şiraz. Intracranial Pathologies and Endocrine Results: Single Pediatric Endocrinology Center Experience. Genel Tıp Derg. 01 Aralık 2022;32(6):714-8. doi:10.54005/geneltip.1200537