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A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration

Local lipohypertrophy due to recombinant human growth hormone (rhGH) administration is a rare phenomenon. Here, we report a case of an 11-year-old girl who presented with a paraumbilical swelling, approximately one year after the start of rhGH treatment for short stature due to the presumed diagnosi...

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Autores principales: Koppen, Ilan J. N., Bakx, Roel, de Kruiff, Chris C., van Trotsenburg, A. S. Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075607/
https://www.ncbi.nlm.nih.gov/pubmed/27803832
http://dx.doi.org/10.1155/2016/9648043
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author Koppen, Ilan J. N.
Bakx, Roel
de Kruiff, Chris C.
van Trotsenburg, A. S. Paul
author_facet Koppen, Ilan J. N.
Bakx, Roel
de Kruiff, Chris C.
van Trotsenburg, A. S. Paul
author_sort Koppen, Ilan J. N.
collection PubMed
description Local lipohypertrophy due to recombinant human growth hormone (rhGH) administration is a rare phenomenon. Here, we report a case of an 11-year-old girl who presented with a paraumbilical swelling, approximately one year after the start of rhGH treatment for short stature due to the presumed diagnosis of partial growth hormone insensitivity. Ultrasound imaging revealed an asymmetric distribution of subcutaneous fat tissue at the rhGH administration site, indicating local lipohypertrophy. After sparing her routine injection site and alternating other sites, the swelling disappeared within 6 months. Although the precise cause of local lipohypertrophy resulting from rhGH administration is still unclear, it might be related to the presumed diagnosis of partial growth hormone insensitivity.
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spelling pubmed-50756072016-11-01 A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration Koppen, Ilan J. N. Bakx, Roel de Kruiff, Chris C. van Trotsenburg, A. S. Paul Case Rep Pediatr Case Report Local lipohypertrophy due to recombinant human growth hormone (rhGH) administration is a rare phenomenon. Here, we report a case of an 11-year-old girl who presented with a paraumbilical swelling, approximately one year after the start of rhGH treatment for short stature due to the presumed diagnosis of partial growth hormone insensitivity. Ultrasound imaging revealed an asymmetric distribution of subcutaneous fat tissue at the rhGH administration site, indicating local lipohypertrophy. After sparing her routine injection site and alternating other sites, the swelling disappeared within 6 months. Although the precise cause of local lipohypertrophy resulting from rhGH administration is still unclear, it might be related to the presumed diagnosis of partial growth hormone insensitivity. Hindawi Publishing Corporation 2016 2016-10-10 /pmc/articles/PMC5075607/ /pubmed/27803832 http://dx.doi.org/10.1155/2016/9648043 Text en Copyright © 2016 Ilan J. N. Koppen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Koppen, Ilan J. N.
Bakx, Roel
de Kruiff, Chris C.
van Trotsenburg, A. S. Paul
A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration
title A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration
title_full A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration
title_fullStr A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration
title_full_unstemmed A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration
title_short A Child with Local Lipohypertrophy following Recombinant Human Growth Hormone Administration
title_sort child with local lipohypertrophy following recombinant human growth hormone administration
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075607/
https://www.ncbi.nlm.nih.gov/pubmed/27803832
http://dx.doi.org/10.1155/2016/9648043
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