Myxedema crisis and ovarian hyperstimulation in a child with Down syndrome

Author:

Abraham Maria Susan1,Sampathkumar Geethalakshmi2,Narayanan Rajeshwari3,Jagannathan Prahada3

Affiliation:

1. Department of Family Medicine , Dr. Kamakshi Memorial Hospital , Chennai , Tamil Nadu , 600100 , India

2. Department of Endocrinology , Dr. Kamakshi Memorial Hospital , Chennai , Tamil Nadu , 600100 , India

3. Department of Paediatrics , Dr. Kamakshi Memorial Hospital , Chennai , Tamil Nadu , 600100 , India

Abstract

Abstract Objectives Myxedema crisis, a fatal complication of severe hypothyroidism, is extremely rare in children and treatment guidelines are lacking. Since availability of intravenous levothyroxine is limited in resource poor settings, myxedema crisis can be treated with oral levothyroxine and/or oral liothyronine (if necessary), in the absence of cardiac risk factors, thus hastening the recovery and significantly decreasing the associated morbidity and mortality. In the background of untreated hypothyroidism, a possible association of ovarian hyperstimulation syndrome (OHSS) and reactive pituitary hyperplasia should be kept in mind, thus preventing unnecessary interventions. Case presentation A 13-year-old girl child with Down syndrome, presented with myxedema crisis, as initial presentation of untreated hypothyroidism. Conclusions Annual screening, timely diagnosis of hypothyroidism, and early initiation of thyroid hormone supplementation will prevent associated physical and neurocognitive morbidity in children, especially those with Down syndrome. Importance of oral liothyronine supplementation in myxedema crisis, has been highlighted in this case report.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Divecha, CA, Tullu, MS, Deshmukh, CT, Karande, S. Myxedema coma in a pediatric patient with Down syndrome. J Pediatr Intensive Care 2020;9:70–3. https://doi.org/10.1055/s-0039-1698812.

2. Mathew, V, Misgar, RA, Ghosh, S, Mukhopadhyay, P, Roychowdhury, P, Pandit, K, et al.. Myxedema coma: a new look into an old crisis. J Thyroid Res 2011;2011:493462. https://doi.org/10.4061/2011/493462.

3. Root, JM, Vargas, M, Garibaldi, LR, Saladino, RA. Pediatric patient with altered mental status and hypoxemia: case report. Pediatr Emerg Care 2017;33:486–8. https://doi.org/10.1097/pec.0000000000000722.

4. Simşek, E, Simşek, T, Savaş-Erdeve, S, Erdoğmuş, B, Döşoğlu, M. Pituitary hyperplasia mimicking pituitary macroadenoma in two adolescent patients with long-standing primary hypothyroidism: case reports and review of literature. Turk J Pediatr 2009;51:624–30.

5. Schutt-Aine, JC. Hypothyroid myxedema and hyponatremia in an eight-year-old child: a case report. J Natl Med Assoc 1980;72:705–8.

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