Brain MRIs may be of low value in most children diagnosed with isolated growth hormone deficiency

2021 ◽  
Vol 34 (3) ◽  
pp. 333-340
Author(s):  
Jessica Schmitt ◽  
Paul Thornton ◽  
Avni N. Shah ◽  
A. K. M. Falzur Rahman ◽  
Elizabeth Kubota ◽  
...  

Abstract Objectives Brain MRIs are considered essential in the evaluation of children diagnosed with growth hormone deficiency (GHD), but there is uncertainty about the appropriate cut-off for diagnosis of GHD and little data about the yield of significant abnormal findings in patients with peak growth hormone (GH) of 7–10 ng/mL. We aimed to assess the frequency of pathogenic MRIs and associated risk factors in relation to peak GH concentrations. Methods In this retrospective multicenter study, charts of patients diagnosed with GHD who subsequently had a brain MRI were reviewed. MRIs findings were categorized as normal, incidental, of uncertain significance, or pathogenic (pituitary hypoplasia, small stalk and/or ectopic posterior pituitary and tumors). Charges for brain MRIs and sedation were collected. Results In 499 patients, 68.1% had normal MRIs, 18.2% had incidental findings, 6.6% had uncertain findings, and 7.0% had pathogenic MRIs. Those with peak GH<3 ng/mL had the highest frequency of pathogenic MRIs (23%). Only three of 194 patients (1.5%) with peak GH 7–10 ng/mL had pathogenic MRIs, none of which altered management. Two patients (0.4%) with central hypothyroidism and peak GH<4 ng/mL had craniopharyngioma. Conclusions Pathogenic MRIs were uncommon in patients diagnosed with GHD except in the group with peak GH<3 ng/mL. There was a high frequency of incidental findings which often resulted in referrals to neurosurgery and repeat MRIs. Given the high cost of brain MRIs, their routine use in patients diagnosed with isolated GHD, especially patients with peak GH of 7–10 ng/mL, should be reconsidered.

Author(s):  
Gary Butler ◽  
Jeremy Kirk

Embryology 72Anatomy 73Physiology 74Growth hormone deficiency (GHD) 76Diagnosis of GHD 78Treatment of GHD 81Adult GHD 82ACTH deficiency 84CHARGE syndrome 86Gonadotropin deficiency 86Thyroid-stimulating hormone deficiency (central hypothyroidism) 90Prolactin deficiency 92Posterior pituitary 94Further reading ...


2020 ◽  
Vol 4 (Supplement_1) ◽  
Author(s):  
Hsin-Yuan Chang ◽  
Fu-Sung Lo

Abstract Background:Intracranial germ cell tumors are rare extragonadal neoplasms. These patients may present with headache, visual impairment and endocrine disorder, depending on the size and location of the tumor. The aim of this study is to assess the clinical features of patients with germinomas in our hospital. Methods:We performed a retrospective chart review of 58 children diagnosed with intracranial germ cell tumors from January, 1990 to December, 2018. The initial clinical presentation, tumor markers (beta-hCG and alpha-fetoprotein, etc.), pituitary function, and brain images were reviewed and further analyzed. Results:Total 58 patients (45 boys and 13 girls) were included in the study. The mean age at diagnosis was 13.44 ± 2.64 years, ranging from 6.51 to 17.92 years. The initial complaints were weakness (n= 30, 51.7%), eye manifestation (n=27, 46.6%), polyuria (n=27, 46.6%), headache (n= 22, 27.9%), nausea or vomiting (n=16, 27.6%), dizziness or vertigo (n=16, 27.6%), and short stature (n= 8, 15.7%), respectively. Laboratory data showed central hypothyroidism (n = 14, 42.4%), central diabetes insipidus (n=14, 66.7%), hypogonadotropic hypogonadism (n= 4, 40%), and growth hormone deficiency (n=14, 73.7%). Conclusions:Germinomas may present with neurologic signs such as weakness, visual impairment, headache, nausea or vomiting. Some patiens presented short stature or polyuria due to central hypothyroidism, diabetes insipidus and growth hormone deficiency. Some atypical manifestations were also noted, such as psychological presentations and incontinence.


2012 ◽  
Vol 32 (1) ◽  
pp. 81-84
Author(s):  
SK Kota ◽  
S Jammula ◽  
PR Tripathy ◽  
Siva Krishna Kota ◽  
LK Meher ◽  
...  

Langerhans cell histiocytosis is a multi system disorder with a certain predilection for involving hypothalamic pituitary axis. We hereby report a 7 year old girl presenting with polyuria, polydipsia and growth retardation. The girl had a past history of pain in right hip joint and nodular region over chest. Water deprivation test confirmed the diagnosis of central diabetes inspidus. Other investigations revealed Growth hormone deficiency and central hypothyroidism. X-ray and MRI hip revealed absent right inferior pubic ramus with bone marrow biopsy confirming the diagnosis of histiocytosis. Patient was treated with nasal Arginine Vasopressin spray, subcutaneous growth hormone and oral thyroxine. Key words: Histiocytosis; Diabetes inspidus; Growth hormone deficiency; Central hypothyroidism DOI: http://dx.doi.org/10.3126/jnps.v32i1.5343 J. Nepal Paediatr. Soc. Vol.32(1) 2012 81-84


Author(s):  
Fariba Naderi ◽  
Samira Rajabi Eslami ◽  
Sohrab Afshari Mirak ◽  
Mohammad Khak ◽  
Jalaladin Amiri ◽  
...  

AbstractGrowth hormone deficiency (GHD) is a major problem among children with short stature. In this study, the role of brain magnetic resonance imaging (MRI) in defining the underlying defects among short children with GHD is evaluated.In a cross-sectional study, data of 158 children were evaluated. Growth hormone (GH) levels were measured using stimulating tests and brain MRI with gadolinium contrast was applied, as well.Some 25.3% of patients had GHD with a mean age of 8.01±3.40 years. MRI results showed 35 as normal, four with pituitary hypoplasia, and one with microadenoma. The MRI results were significantly associated with GH levels and presence of other endocrine disorders. There was a significant association between prenatal disorders and patients’ bone age delay.In patients with severe GHD and patients with multiple pituitary hormone deficiencies, MRI is more likely to be abnormal, and bone age is much delayed in patients with history of prenatal disorders.


Author(s):  
Himanshu Sharma ◽  
Naincy Purwar ◽  
Anshul Kumar ◽  
Rahul Sahlot ◽  
Umesh Garg ◽  
...  

Abstract Objectives Congenital idiopathic growth hormone deficiency (GHD) is associated with various MRI abnormalities, including sellar and extrasellar abnormalities. However, it remains contentious whether MRI brain findings could provide an additional avenue for precisely predicting the differentiation of GHD based on severity and type {isolated GHD or multiple pituitary hormone deficiencies (MPHD)}. This study aimed to ascertain the abnormality that is the best predictor of severity and type of GHD amongst the different MRI findings. Methods We conducted an analytical cross-sectional study, including 100 subjects diagnosed with idiopathic GHD. Patients were grouped into severe GHD, partial GHD, and MPHD and into groups based on the presence of pituitary hypoplasia, extrasellar brain abnormalities (EBA), and presence of ectopic posterior pituitary or pituitary stalk abnormalities (EPP/PSA) or both. Results Sixty six percentage of subjects had isolated GHD, 34% had MPHD, 71% had severe GHD, and 29% had partial GHD. Pituitary hypoplasia was the most common finding, observed in 53% of patients, while 23% had EBA, and 25% had EPP/PSA. Pituitary hypoplasia was observed to be the best predictor of severity of GHD with an odds ratio (OR) of 10.8, followed by EPP/PSA (OR=2.8), and EBA was the weakest predictor (OR=1.8). Pituitary hypoplasia was the only finding to predict MPHD (OR=9.2) significantly. On ROC analysis, a Pituitary height SDS of −2.03 had the best detection threshold for both severe GHD and MPHD. Conclusions We observed Pituitary hypoplasia to be not only the most frequent MRI abnormality but also the best predictor of severe GHD and MPHD amongst various sellar and extrasellar abnormalities.


2008 ◽  
Vol 146A (3) ◽  
pp. 384-388 ◽  
Author(s):  
Anwar Baban ◽  
Luca Moresco ◽  
Maria Teresa Divizia ◽  
Andrea Rossi ◽  
Roberto Ravazzolo ◽  
...  

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