Tumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler
Tumour-induced hypoglycaemia is a rare complication/condition mainly seen in adults. It is caused due to increased production of insulin or insulin-like growth factor (IGF) 2 tumour cells. We present a 3-year-old paediatric patient with non-islet cell tumour induced hypoglycaemia (NICTH) secondary t...
Guardado en:
Autores principales: | , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Karger Publishers
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/955aebcb69334412ac8c14df6bfa46f4 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:955aebcb69334412ac8c14df6bfa46f4 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:955aebcb69334412ac8c14df6bfa46f42021-12-02T12:40:24ZTumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler2673-17972673-173810.1159/000520177https://doaj.org/article/955aebcb69334412ac8c14df6bfa46f42021-12-01T00:00:00Zhttps://www.karger.com/Article/FullText/520177https://doaj.org/toc/2673-1797https://doaj.org/toc/2673-1738Tumour-induced hypoglycaemia is a rare complication/condition mainly seen in adults. It is caused due to increased production of insulin or insulin-like growth factor (IGF) 2 tumour cells. We present a 3-year-old paediatric patient with non-islet cell tumour induced hypoglycaemia (NICTH) secondary to rhabdomyosarcoma. She presented with abdominal mass and refractory hypoglycaemia, requiring high glucose infusion and steroids. Critical sample analysis during hypoglycaemia showed suppression of insulin, IGF-1, C-peptide, growth hormone, and ketones, with a high cortisol level. CT scan of abdomen and pelvis showed a huge retroperitoneal mass, later diagnosed as rhabdomyosarcoma. In a resource-limited setting, where IGF-2 is not possible, low serum insulin and IGF-1 levels during hypoglycaemia aids in diagnosis of NICTH. This is one of the first few reported paediatric cases with NICTH from India, and we believe that reporting this case would add more information to the existing literature. Thus, NICTH should be suspected in all malignancies presenting with intractable hypoglycaemia irrespective of their age.Jayati JoshipuraVani H.N.Nabanita KoraKarger Publishersarticlehypoglycaemiasarcomapediatric endocrinologyDiseases of the endocrine glands. Clinical endocrinologyRC648-665ENDubai Diabetes and Endocrinology Journal, Pp 1-3 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
hypoglycaemia sarcoma pediatric endocrinology Diseases of the endocrine glands. Clinical endocrinology RC648-665 |
spellingShingle |
hypoglycaemia sarcoma pediatric endocrinology Diseases of the endocrine glands. Clinical endocrinology RC648-665 Jayati Joshipura Vani H.N. Nabanita Kora Tumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler |
description |
Tumour-induced hypoglycaemia is a rare complication/condition mainly seen in adults. It is caused due to increased production of insulin or insulin-like growth factor (IGF) 2 tumour cells. We present a 3-year-old paediatric patient with non-islet cell tumour induced hypoglycaemia (NICTH) secondary to rhabdomyosarcoma. She presented with abdominal mass and refractory hypoglycaemia, requiring high glucose infusion and steroids. Critical sample analysis during hypoglycaemia showed suppression of insulin, IGF-1, C-peptide, growth hormone, and ketones, with a high cortisol level. CT scan of abdomen and pelvis showed a huge retroperitoneal mass, later diagnosed as rhabdomyosarcoma. In a resource-limited setting, where IGF-2 is not possible, low serum insulin and IGF-1 levels during hypoglycaemia aids in diagnosis of NICTH. This is one of the first few reported paediatric cases with NICTH from India, and we believe that reporting this case would add more information to the existing literature. Thus, NICTH should be suspected in all malignancies presenting with intractable hypoglycaemia irrespective of their age. |
format |
article |
author |
Jayati Joshipura Vani H.N. Nabanita Kora |
author_facet |
Jayati Joshipura Vani H.N. Nabanita Kora |
author_sort |
Jayati Joshipura |
title |
Tumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler |
title_short |
Tumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler |
title_full |
Tumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler |
title_fullStr |
Tumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler |
title_full_unstemmed |
Tumour-Not So Sweet, Tumour-Induced Hypoglycemia: A Rare Case of Refractory Hypoglycemia in a Toddler |
title_sort |
tumour-not so sweet, tumour-induced hypoglycemia: a rare case of refractory hypoglycemia in a toddler |
publisher |
Karger Publishers |
publishDate |
2021 |
url |
https://doaj.org/article/955aebcb69334412ac8c14df6bfa46f4 |
work_keys_str_mv |
AT jayatijoshipura tumournotsosweettumourinducedhypoglycemiaararecaseofrefractoryhypoglycemiainatoddler AT vanihn tumournotsosweettumourinducedhypoglycemiaararecaseofrefractoryhypoglycemiainatoddler AT nabanitakora tumournotsosweettumourinducedhypoglycemiaararecaseofrefractoryhypoglycemiainatoddler |
_version_ |
1718393753326059520 |